WO2025064603A1 - Procédés, dispositifs, et systèmes d'ajustement de valeurs de hba1c vérifiées en laboratoire - Google Patents

Procédés, dispositifs, et systèmes d'ajustement de valeurs de hba1c vérifiées en laboratoire Download PDF

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WO2025064603A1
WO2025064603A1 PCT/US2024/047375 US2024047375W WO2025064603A1 WO 2025064603 A1 WO2025064603 A1 WO 2025064603A1 US 2024047375 W US2024047375 W US 2024047375W WO 2025064603 A1 WO2025064603 A1 WO 2025064603A1
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level
hbalc
time period
glucose
glycated hemoglobin
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Yongjin Xu
Timothy C. Dunn
Shridhara Alva Karinka
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Abbott Diabetes Care Inc
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Abbott Diabetes Care Inc
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A61B5/14532—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue for measuring glucose, e.g. by tissue impedance measurement
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A61B5/14546—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue for measuring analytes not otherwise provided for, e.g. ions, cytochromes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/74—Details of notification to user or communication with user or patient; User input means
    • A61B5/746—Alarms related to a physiological condition, e.g. details of setting alarm thresholds or avoiding false alarms
    • G—PHYSICS
    • G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
    • G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
    • G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
    • G16H10/40—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for data related to laboratory analysis, e.g. patient specimen analysis

Definitions

  • glycosylated hemoglobin also referred to as glycated hemoglobin
  • HbAl Most of hemoglobin is a type called HbA.
  • HbAl glycosylated HbA is formed, which is referred to as HbAl.
  • HbAl has three components: HbAl a, HbAlb, and HbAlc. Because a glucose binds more strongly and to a higher degree to HbAlc than HbAl a and HbAlb, a measure of HbAlc in blood (HbAlc test) is often used as an indication of a subject’s average blood glucose level over a 120 day period (the average lifespan of a red blood cell).
  • the HbAlc test is performed by drawing a blood sample from a subject at a medical professional’s office, which is then analyzed in a laboratory.
  • the HbAlc test may be used as a screening and diagnostic test for pre-diabetes and diabetes.
  • a subject’s glucose exposure as determined by HbAlc levels is one of the primary factors used in making diagnosis and/or therapy decisions. That is, a normal or healthy glucose exposure is correlated to an HbAlc level or range assuming a 120 day red blood cell lifespan.
  • a subject’s laboratory HbAlc level (also referred to in the art as a measured HbAlc) is compared to this normal or health range when diagnosing and/or treating the subject.
  • the red blood cell lifespan does not vary within a subject to a great degree (except for some subjects with specific diseases), the red blood cell lifespan for individual subjects can be between about 50 days to about 170 days. Therefore, a laboratory HbAlc level for a subject with a longer red blood cell lifespan overestimates glucose exposure and for a subject with a shorter red blood cell lifespan underestimates glucose exposure. Therefore, the diagnoses and treatments (and even if treatment should occur) are based an incorrect glucose exposure.
  • FIG. 1 illustrates that individual RBC lifespan can affect HbAlc and diabetes treatment.
  • 31% of laboratory HbAlc can be misleading and resulting in undertreatment or overtreatment.
  • FIG. 2 illustrates an example time line illustrating collection of at least one HbAlc value and a plurality of glucose levels for a time period.
  • FIG. 3 illustrates an example of a physiological parameter analysis system for providing physiological parameter analysis in accordance with some of the embodiments of the present disclosure.
  • FIG. 4 illustrates an example of a physiological parameter analysis system for providing physiological parameter analysis in accordance with some of the embodiments of the present disclosure.
  • FIG. 5 illustrates an example of a cHbAlc report that may be generated as an output by a physiological parameter analysis system in accordance with some of the embodiments of the present disclosure.
  • FIG. 6A illustrates an example of a method of determining a personalized-target glucose range in accordance with some of the embodiments of the present disclosure.
  • FIG. 6B illustrates an example of a personalized-target glucose range report that may be generated as an output by a physiological parameter analysis system in accordance with some of the embodiments of the present disclosure.
  • FIG. 7 illustrates an example of a personalized-target average glucose report that may be generated as an output by a physiological parameter analysis system in accordance with some of the embodiments of the present disclosure.
  • FIG. 8 illustrates an example of a glucose pattern insight report that may be generated as an output by a physiological parameter analysis system in accordance with some of the embodiments of the present disclosure.
  • FIG. 9 illustrates an example of an in vivo analyte monitoring system in accordance with some of the embodiments of the present disclosure.
  • FIG. 10 is a plot of the glucose monitoring data (right y-axis) for 200 days, the three HbAlc values (left y-axis), and the estimated HbAlc values (left y-axis) based on the 14- day eHbAlc model.
  • FIG. 11 is the plot of FIG. 10 with a cHbAlc (left y-axis) for the first 100 days determined using k giy and k age per the methods described herein.
  • FIG. 12 is the plot of FIG. 11 with the cHbAlc (extension from day 100 to day 200, left y-axis) for the following 100 days using the k giy and k age determined relative to FIG. 10 per the methods described herein.
  • FIG. 14 is a plot of laboratory HbAlc compared to aHbAlC (“aAlC”) by RBC lifespan.
  • FIG. 16A is a cross-plot and correlation of the mean 14-day intracellular glucose (I)G values with the aHbAlc was prepared
  • FIG. 16B is a cross-plot of the originally- collected data of 14-day mean plasma glucose (PG) and laboratory HbAlc.
  • FIGS. 17A and 17B are examples of a glucose pattern insight report for the same subject using the measured PG and the PG e ff, respectively.
  • FIG. 18 shows summary performance characteristics of an exemplary glucose monitoring system.
  • the disclosed subject matter is directed to a method for determining a recommended time for obtaining laboratory glycated hemoglobin measurements can include receiving at least one glucose level for a subject during at least one time period; receiving a first measured glycated hemoglobin (HbAlc) level for the subject corresponding to a beginning of a first time period of the at least one time period; determining a first calculated glycated hemoglobin (HbAlc) level corresponding to the first time period; determining for the first time period a second calculated glycated hemoglobin (HbAlc) level using a first offset value; determining for the first time period a third calculated glycated hemoglobin (HbAlc) level using a second offset value; calculating a first difference between the first calculated glycated hemoglobin (HbAlc) level and the second calculated glycated hemoglobin
  • the first calculated HbAlc level, second calculated HbAlc level, and third calculated HbAlc level is determined using Equation A: Equation A where k age is a red blood cell elimination constant, where k giy is a red blood cell glycation rate constant, where KM is a constant value, where [G z ] is an average glucose level over a corresponding time period z, where [G] is an average glucose level over a corresponding time period i, where [Gj] is an average glucose level over a corresponding time period j, where ti is a length of time interval of a corresponding time period i, where tj is a length of time interval of a corresponding time period j, where t z is a length of time interval of a corresponding time period z; wherein the first offset value is a first predetermined offset of k age ; wherein the second offset value level is a second predetermined offset of k giy
  • the method can further include generating a second alert notification in response to a determination that the first difference and the second different are equal to or below the first predetermined threshold value.
  • the first alert notification can include generating a prompt.
  • the first difference or the second difference can be above the first predetermined threshold value for the first time period, and the method can further comprise receiving a second measured glycated hemoglobin (HbAlc) level corresponding to the first time period.
  • HbAlc glycated hemoglobin
  • the method can further include treating the subject based on the second measured glycated hemoglobin (HbAlc) level, wherein treating the subject comprises administering and/or adjusting a pharmaceutical compound, an insulin dosage, a glycation-medication dosage, an exercise regime, a meal intake, or a combination thereof.
  • HbAlc glycated hemoglobin
  • the method can further include adjusting a therapeutic profile or treatment regimen based on the second glycated hemoglobin (HbAlc) level, outputting a first a therapeutic profile or treatment regimen based on the second glycated hemoglobin (HbAlc) level, and/or administering a pharmaceutical compound to the subject based on the second measured glycated hemoglobin (HbAlc) level.
  • a duration of the first time period can be about one day in length, and wherein tj is 1, ti is 1 and tz is 1.
  • a duration of the first time period can be about 1 hour to about 24 hours
  • the least one glucose level can be at least two glucose levels
  • ti can be the of number of hours between received glucose levels divided by the number of hours in time period i.
  • the duration of the first time period can be greater than around 1 hour and/or less than around 24 hours.
  • a duration between glucose measurements can be about 4 hours.
  • the first predetermined threshold is approximately 0.2% (NGSP).
  • the received glucose level can be received from a continuous glucose monitoring system and can include receiving a mean absolute relative difference for the first time period from the continuous glucose monitoring system.
  • the glucose measurements can be received when the mean absolute relative difference from the continuous glucose monitoring system is less than 8%.
  • the first predetermined threshold can be at least 0.15% (NGSP) in response to a determination that the received mean absolute relative difference is less than a second predetermined threshold.
  • NGSP 0.15%
  • the first predetermined threshold can be at least 0.25% (NGSP) in response to a determination that the received mean absolute relative difference is more than a third predetermined threshold.
  • NGSP 0.25%
  • the Km can be 460-480 mg/dL.
  • Km is the Michaelis constant that relates to the affinity of an enzyme for a substrate.
  • the Km can be at least around 100 mg/dL, at least around 200 mg/dL, or at least around 460 mg/dL.
  • the Km can be no greater than around 700 mg/dL, no greater than around 600 mg/dL, or no greater than around 480 mg/dL.
  • the first estimated initial value can be at least around 0.0052 day' 1 and/or to no greater than around 0.05 day' 1 , optionally around 1/105 day -1 .
  • the first estimated initial value may be an initial estimated value of k age .
  • the second estimated initial value can be at least around 3.6xl0' 6 dL/mg/day and/or no greater than around 9.9xl0' 6 dL/mg/day, optionally around 6.2x10-6 dL * mg * day -1 .
  • the second estimated initial value may be an initial estimated value of k giy .
  • the steps for determining if a time period is a recommended time period can be repeated to determine a recommended time period from a plurality of time periods.
  • the method can further include determining a fourth calculated glycated hemoglobin (HbAlc) level corresponding to a second time period; determining for the second time period a fifth calculated glycated hemoglobin (HbAlc) level using a third offset value; determining for the second time period a sixth calculated glycated hemoglobin (HbAlc) level using a fourth offset value; calculating a third difference between the fourth calculated glycated hemoglobin (HbAlc) level and the fifth calculated glycated hemoglobin (HbAlc) level; calculating a fourth difference between the fourth calculated glycated hemoglobin (HbAlc) level and the sixth calculated glycated hemoglobin (HbAlc) level; and wherein the generating a fourth calculated glycated hemoglobin
  • the disclosed subject matter is directed to a system for determining a time for obtaining laboratory glycated hemoglobin measurements can include an analyte monitoring device configured to measure a glucose level; one or more processors; and a memory operatively coupled to the one or more processors and having instructions stored thereon which, when executed by the one or more processors, causes the one or more processors to: receive at least one glucose level for a subject during at least one time period; receive a first measured glycated hemoglobin (HbAlc) level for the subject corresponding to a beginning of a first time period of the at least one time period; determining a first calculated glycated hemoglobin (HbAlc) level corresponding to the first time period; determine for the first time period a second calculated glycated hemoglobin (HbAlc) level using a first offset value; determine for the first time period a third
  • the first calculated HbAlc level, second calculated HbAlc level, and third calculated HbAlc level is determined using
  • Equation A where k age is a red blood cell elimination constant, where k giy is a red blood cell glycation rate constant, where KM is a constant value, where [G z ] is an average glucose level over a corresponding time period z, where [G] is an average glucose level over a corresponding time period i, where [Gj] is an average glucose level over a corresponding time period j, where ti is a length of time interval of a corresponding time period i, where tj is a length of time interval of a corresponding time period j, where t z is a length of time interval of a corresponding time period z; wherein the first offset value is a first predetermined offset of k age ; wherein the second offset value level is a second predetermined offset of k giy .
  • the system can further include instructions which causes the one or more processors to generate a second alert notification in response to a determination that the first difference and the second different are equal to or below the first predetermined threshold value.
  • the first alert notification can include generating a prompt.
  • the first difference or the second difference can be above the first predetermined threshold value for the first time period, and the method can further comprise receiving a second measured glycated hemoglobin (HbAlc) level corresponding to the first time period.
  • HbAlc glycated hemoglobin
  • the system can further include instructions which causes the one or more processors to treat the subject based on the second measured glycated hemoglobin (HbAlc) level, wherein treating the subject comprises administering and/or adjusting a pharmaceutical compound, an insulin dosage, a glycationmedication dosage, an exercise regime, a meal intake, or a combination thereof.
  • HbAlc glycated hemoglobin
  • the system can further include instructions which causes the one or more processors to adjust a therapeutic profile or treatment regimen based on the second glycated hemoglobin (HbAlc) level, output a first a therapeutic profile or treatment regimen based on the second glycated hemoglobin (HbAlc) level, and/or administer a pharmaceutical compound to the subject based on the second measured glycated hemoglobin (HbAlc) level.
  • a duration of the first time period can be about one day in length, and wherein tj is 1, ti is 1 and tz is 1.
  • a duration of the first time period can be about 1 hour to about 24 hours
  • the least one glucose level can be at least two glucose levels
  • ti can be the of number of hours between received glucose levels divided by the number of hours in time period i.
  • the duration of the first time period can be greater than around 1 hour and/or less than around 24 hours.
  • a duration between glucose measurements can be about 4 hours.
  • the first predetermined threshold is approximately 0.2% (NGSP).
  • the received glucose level can be received from a continuous glucose monitoring system and can include receiving a mean absolute relative difference for the first time period from the continuous glucose monitoring system.
  • the glucose measurements can be received when the mean absolute relative difference from the continuous glucose monitoring system is less than 8%.
  • the first predetermined threshold can be at least 0.15% (NGSP) in response to a determination that the received mean absolute relative difference is less than a second predetermined threshold.
  • NGSP 0.15%
  • the first predetermined threshold can be at least 0.25% (NGSP) in response to a determination that the received mean absolute relative difference is more than a third predetermined threshold.
  • NGSP 0.25%
  • the Km can be 460-480 mg/dL.
  • Km is the Michaelis constant that relates to the affinity of an enzyme for a substrate.
  • the Km can be at least around 100 mg/dL, at least around 200 mg/dL, or at least around 460 mg/dL.
  • the Km can be no greater than around 700 mg/dL, no greater than around 600 mg/dL, or no greater than around 480 mg/dL.
  • the first estimated initial value can be at least around 0.0052 day' 1 and/or no greater than around 0.05 day' 1 , optionally around 1/105 day -1 .
  • the first estimated initial value may be an initial estimated value of k age .
  • the second estimated initial value can be at least around 3.6xl0' 6 dL/mg/day and/or no greater than around 9.9xl0' 6 dL/mg/day, optionally around 6.2x10-6 dL * mg * day -1 .
  • the second estimated initial value may be an initial estimated value of k giy .
  • the system can include further instructions which causes the one or more processors to: determine a fourth calculated glycated hemoglobin (HbAlc) level corresponding to a second time period; determine for the second time period a fifth calculated glycated hemoglobin (HbAlc) level using a third offset value; determine for the second time period a sixth calculated glycated hemoglobin (HbAlc) level using a fourth offset value; calculate a third difference between the fourth calculated glycated hemoglobin (HbAlc) level and the fifth calculated glycated hemoglobin (HbAlc) level; calculate a fourth difference between the fourth calculated glycated hemoglobin (HbAlc) level and the sixth calculated glycated hemoglobin (HbAlc) level; and wherein the first alert notification to obtain the second measured glycated hemoglobin (HbAlc) level for the subject is in response to a determination that at least one of the
  • the present disclosure generally describes methods, devices, and systems for determining physiological parameters related to the kinetics of red blood cell glycation, elimination, and generation within the body of a subject.
  • Such physiological parameters can be used, for example, to calculate a more reliable calculated HbAlc (cHbAlc), adjusted HbAlc (aHbAlc), and/or a personalized target glucose range, among other things, for subject-personalized diagnoses, treatments, and/or monitoring protocols.
  • HbAlc level HbAlc value
  • aHbAlc value and “aHbAlc”
  • cHbAlc level cHbAlc value
  • cHbAlc are used interchangeably.
  • High glucose exposure in specific organs is a critical factor for the development of diabetes complications.
  • a laboratory HbAlc (also referred to in the art as a measured HbAlc) is routinely used to assess glycemic control, but studies report a disconnect between this glycemic marker and diabetes complications in some individuals.
  • the exact mechanisms for the failure of laboratory HbAlc to predict diabetes complications are not often clear but likely in some cases to be related to inaccurate estimation of intracellular glucose exposure in the affected organs.
  • Formula 1 illustrates the kinetics of red blood cell hemoglobin glycation (or referred to herein simply as red blood cell glycation), red blood cell elimination, and red blood cell generation, where “G” is free glucose, “R” is a non-glycated red blood cell, and “GR” is s glycated red blood cell hemoglobin.
  • the rate at which glycated red blood cell hemoglobin (GR) are formed is referred to herein as a red blood cell hemoglobin glycation rate constant k g iy typically having units of dL*mg' 1 *day' 1 ).
  • Formula 2 illustrates the mechanism in more detail where glucose transporter 1 (GLUT1) facilitates glucose (G) transport into the red blood cell. Then, the intracellular glucose (GI) interacts with the hemoglobin (Hb) to produce glycated hemoglobin (HbG) where the hemoglobin glycation reaction rate constant is represented by kg (typically having units of dL*nng'l*day' 1 ). A typical experiment measured k g value is 1.2xl0' 3 dL/mg/day. Hemoglobin glycation reaction is a multi-step non-enzymatic chemical reaction, therefore k g should be a universal constant.
  • the rate constant for the glucose to be transported into the red blood cell and glycated the Hb into HbG is k giy .
  • k age describes red blood cell elimination (along with hemoglobin), also described herein as the red blood cell turnover rate.
  • HbAlc mirrors intracellular glucose exposure in organs affected by diabetes complications.
  • laboratory HbAlc may not always reflect intracellular glucose exposure. While variation in RBC cross-membrane glucose uptake is likely to be relevant to the risk of estimating diabetes complications in susceptible organs, red blood cell lifespan is unique to RBCs and therefore irrelevant to the complication risk in other tissues.
  • HbAlc a measure of personalized HbAlc has been developed, which takes into account individual variations in both RBC turnover and cellular glucose uptake.
  • the current work aims to extend this model by adjusting for a standard RBC lifespan of 100 days (equivalent to RBC turnover rate of 1% per day, or mean RBC age of 50 days) to establish a new clinical marker, which we term adjusted HbAlc (aHbAlc).
  • aHbAlc is the most relevant glycemic marker for estimating organ exposure to hyperglycemia and risk of future diabetes-related complications.
  • HbAlc is a commonly used analyte indicative of the fraction of the glycated hemoglobin found in red blood cells. Therefore, a kinetic model can be used, for example, to derive a calculated HbAlc based on at least the glucose levels measured for a subject. However, the kinetic model can also be applied to HbAl.
  • HbAlc is uniformly used herein, but HbAl could be substituted except in instances where specific HbAlc values are used. In such instances, specific HbAl values could be used to derive similar equations.
  • the glycation process has first order dependencies on concentrations of both hemoglobin in red blood cells and intracellular glucose, an assumption that is widely adopted.
  • Newly-generated red blood cells have a negligible amount of glycated hemoglobin.
  • the maximum rate Vmax should be proportional to the GLUT1 level on the membrane. Both k c and Vmax can vary individually. Under equilibrium, Equation 3 is derived.
  • Equation 4 is derived.
  • Equation 6 (C — [Hb])/C, Equation 6 is derived.
  • Equation 1 can be transformed to Equation 7.
  • Equation 8 Solving this differential equation and integrating from time 0 to t, Equation 8 is derived, for the HbAlc value HbAlco at the end of an interval t, given a starting HbAlc (HbAlco) and assuming a constant glucose level during the time interval.
  • HbAlc t EA + (HbAlco - EA) ⁇ e’ ⁇ e) 1
  • HbAlc value HbAlc z (at the end of time interval t2) can be expressed by Equation 9 for numerical calculations.
  • HbAlc The value HbAlc, is equivalent to calculated HbAlc
  • cHbAlc at the end of time interval t z .
  • cHbAlc is the preferred term introduced by our work. Note that EA, and D, are both affected by k giy , k age and the glucose level. In addition, Di depends on the length of the time interval t ( -.
  • Embodiments of the present disclosure provide kinetic modeling of red blood cell glycation, elimination, and generation within the body of a subject.
  • the physiological parameters k giy , k age , and/or K can be derived from the equations described herein given at least one laboratory HbAlc value (also referred to as HbAlc level measurement) and a plurality of glucose levels (also referred to as glucose level measurements) over a time period immediately before the HbAlc measurement.
  • HbAlc level measurement also referred to as HbAlc level measurement
  • glucose level measurements also referred to as glucose level measurements
  • the number of laboratory HbAlc values 202a, 202b, 202c needed to calculate k giy , k age , and/or K depends on the frequency and duration of the plurality of glucose levels, and the dynamics over time of the HbAlc values and glucose levels.
  • one laboratory Hb Al c 202b can be used along with a plurality of glucose measurements over time period 206 to calculate k giy , k age , and/or K.
  • Such embodiments are applicable to subjects with steady daily glucose measurements for a long time period 206.
  • Embodiments where one laboratory HbAlc value 202b can be used include a time period 206 about 100 days to about 300 days (or longer) with glucose levels being measured at least about 72 times (e.g., about every 20 minutes) to about 96 times per day (e.g., about every 15 minutes) or more often. Further, in such embodiments, the time between glucose level measurements may be somewhat consistent where an interval between two glucose level measurements should not be more than about an hour. Some missing data glucose measurements are tolerable when using only one laboratory HbAlc value. Increases in missing data may lead to more error.
  • the time period 206 may be shortened if a subject has an existing glucose level monitoring history with stable, consistent glucose profile. For example, for a subject who has been testing for a prolonged time (e.g., 6 months or longer) but, perhaps, at less frequent or regimented times, the existing glucose level measurements can be used to determine and analyze a glucose profile.
  • the three in combination may be used to calculate one or more physiological parameters (k giy , k age , and/or K) at time t ( -.
  • two laboratory HbAlc values may be used with a first laboratory HbAlc value 202a at the beginning of a time period 206, a second laboratory HbAlc value 202b at the end of the time period 206, and a plurality of glucose levels 204a measured during the time period 206.
  • Equation 9 may be used to calculate one or more physiological parameters (k giy , k age , and/or K) at time tl .
  • Glucose levels may be measured over a time period of about a few days to about 300 days or more (e.g., about one week or more, about 10 days or more, about 14 days or more, about 30 days or more, about 60 days or more, about 90 days or more, about 120 days or more, and so on).
  • the frequency of such glucose levels may be, on average, about 14,400 times daily (e.g., about every 10 seconds) (or more often) to about 3 times daily (e.g., about every 8 hours) (e.g., 1,440 times daily (e.g., about every minute), about 288 times daily (e.g., about every 5 minutes), about 144 times daily (e.g., about every 10 minutes), about 96 times daily (e.g., about every 15 minutes), about 72 times daily (e.g., about every 20 minutes), about 48 times daily (e.g., about every 30 minutes), about 24 times daily (e.g., about every 1 hour), about 12 times daily (e.g., about every 2 hours), about 8 times daily (e.g., about every 3 hours), about 6 times daily (e.g., about every 4 hours), about 4 times daily (e.g., about every 6 hours), and so on). In some instances, less frequent monitoring (like once or twice daily) may be used where the glucose measurements occur at about the same time (
  • one or more of the foregoing actions may be taken when the error (e.g., error from the HbAlc assay) associated with k giy , k age . and/or K is at or greater than about 15%, preferably at or greater than about 10%, preferably at or greater than about 7%, and preferably at or greater than about 5%.
  • the error e.g., error from the HbAlc assay
  • K is at or greater than about 15%, preferably at or greater than about 10%, preferably at or greater than about 7%, and preferably at or greater than about 5%.
  • a lower error may be preferred to have more stringent monitoring and less error in the analyses described herein.
  • one or more physiological parameters (k giy , k age , and/or K) at time t t may be used to determine one or more parameters or characteristics for a subject’s personalized diabetes management (e.g., a cHbAlc at the end of time period 208, a personalized-target glucose range, and/or a treatment or change in treatment for the subject in the near future), each described in more detail further herein.
  • a HbAlc value may be measured at time t 2 and the one or more physiological parameters recalculated and applied to a future time period (not illustrated).
  • the one or more physiological parameter and/or the one or more parameters or characteristics for a subject’s personalized diabetes management can be measured and/or calculated for two or more times (e.g., and t 2 ) and compared. For example, k giy at and t 2 may be compared. In another example, cHbAlc at t2 and at a future time may be compared. Some embodiments, described further herein, may use such comparisons to (1) monitor progress and/or effectiveness of a subject’s personalized diabetes management and, optionally, alter the subject’s personalized diabetes management, (2) identify an abnormal or diseased physiological condition, and/or (3) identify subjects taking supplements and/or medicines that effect red blood cell production and/or effect metabolism.
  • the generally accepted average RBC lifespan may change. While the reference RBC lifespan may be outside these ranges, the k re f age preferably reflects a reference average RBC lifespan of 85 days to 135 days, or 85 days to 110 days, or 90 days to 110 days, or 95 days to 125 days, or 110 days to 135 days. Most preferably, the k re age reflects a reference RBC lifespan of 85 days to 110 days, or 90 days to 110 days, or 100 days. Herein, k re f age equals 0.01 day' 1 for all examples. However, embodiments of the present disclosure are not limited to this specific k re age .
  • the aHbAlc for a subject can be calculated via Equation 10 using the HbAlc level for said subject, the k age for said subject, and the k re f age .
  • HbAlc may be cHbAlc described herein or a laboratory HbAlc.
  • HbAlc may be cHbAlc described herein or a laboratory HbAlc.
  • the aHbAlc for a subject can then be used for diagnoses, treatments, and/or monitoring protocols of said subject.
  • the subject may be diagnosed with diabetes, pre-diabetes, or another abnormal or diseased physiological condition based, at least in part, on the aHbAlc described herein.
  • the subject may be monitored and/or treated with insulin self-monitoring and/or injections, continuous insulin monitoring and/or injections, and the like based, at least in part, on the aHbAlc described herein.
  • the aHbAlc described herein may be used for determining and/or administering a personalized treatment for subject triage, determining and/or administering a personalized treatment for titration of diabetes medication, determining and/or administering a personalized closed-loop or hybrid-closed loop control system, determining and/or administering a personalized treatment using glycation medications, determining of physiological age, identifying if and/or what supplements and/or medicines are present during testing, and the like, and any combination thereof.
  • aHbAlc is a better individual biomarker than HbAlc for the risk of complications in people with diabetes.
  • the aHbAlc can be higher and lower than laboratory HbAlc and which will make significant differences in diabetes diagnosis and management.
  • HbAlc is artificially low and give people illusion of good glycemic control.
  • slower than normal RBC turnover will lead to artificially high HbAlc and lead to over-zealous treatment and may cause dangerous hypoglycemia.
  • a k age of 0.0125 day"’ or RBC lifespan of 80 days
  • laboratory HbAlc 7% would lead to aHbAlc of 8.6%.
  • a laboratory HbAlc of 7% without adjustment for RBC turnover rate indicates good glycemic control.
  • said HbAlc value is an underestimate, where the more accurate value adjusted for RBC turnover rate (aHbAlc) of 8.6%, which indicates a higher complication risk for said subject.
  • a k age of 0.0077 day' 1 (or RBC lifespan of 130 days) and a seemingly high laboratory HbAlc 9% would lead to aHbAlc of 7.1%.
  • the seemingly high laboratory HbAlc of 9% would indicate a poor glycemic control and significant complication risk.
  • the person has low complication risk by aHbAlc of 7.1%.
  • Working from the laboratory HbAlc value of 9%, said subject would likely receive treatment that could the subject at risk for hypoglycemia because the aHbAlc is 7.1%.
  • aHbAlc can be estimated with Equation 11. For example, when the laboratory HbAlc is 8% and a high K value of 6xl0' 4 day' 1 is determined, an aHbAlc estimation of 7%. This adjustment is usually conservative and, therefore, safe to use when k age is not yet available. In this example, unnecessary, and potentially harmful, treatment may be given based on the laboratory HbAlc value when no treatment should be given based on the aHbAlc value.
  • the estimated aHbAlc is 8.9%.
  • treatment may not be given when relying solely on the laboratory HbAlc value but should be given because of the high aHbAlc.
  • the k re f age herein is a predetermined value used as a reference average RBC turnover rate that describes the RBC lifespan.
  • k ref age is calculated the same way using the desired reference average RBC lifespan.
  • the k age of a subject can be determined by a variety of methods including, but not limited to, methods described in herein; in US Pat. App. Pub. No. 2018/0235524; in US Prov. Pat. App. No. 62/750,957; and in US Prov. Pat. App. No. 62/939,956; each of which is incorporated herein by reference in their entirety for all purposes.
  • the HbAlc may be measured in a laboratory and/or calculated (e.g., as described herein as cHbAlc) based, at least in part, on glucose monitoring data.
  • said glucose monitoring data is continuous with little to no missed readings to provide higher accuracy in the calculated HbAlc level.
  • the HbAlc level may be referred to in the art as calculated or estimated.
  • eAG/AlC Conversion Calculator provided by the American Diabetes Association
  • GMI glucose management indicator
  • Glucose management indicator e.g., methods described in Glucose management indicator (GMI): A new term for estimating A1C from continuous glucose monitoring Diabetes 41(11): 2275-2280 Nov 2018
  • methods described in Mechanistic modeling of hemoglobin glycation and red blood cell kinetics enables personalized diabetes monitoring Sci. Transl. Med. 8, 359ral30 Oct 2016; US Pat. App. Pub. No.
  • Methods of the present disclosure include determining (e.g., measuring and/or calculating based on glucose monitoring) a HbAlc level for a subject; determining a RBC elimination rate constant (also referred to as RBC turnover rate and k age , typically having units of day"’) for the subject; and calculating an adjusted HbAlc value (aHbAlc) for the subject based on the HbAlc level, the k age , and a defined reference ka9e (krefd9e) Then, the subject may be diagnosed, treated, and/or monitored based on the aHbAlc.
  • a nonlimiting example method of the present disclosure may comprise: providing (or taking) a plurality of blood glucose measurements for the subject; calculating a HbAlc for the subject based, at least in part, on the plurality of blood glucose measurements; providing (or determining) a k age for a subject; and calculating an aHbAlc for the subject based on the HbAlc level, the k age , and a k re f age . Then, the subject may be diagnosed, treated, and/or monitored based on the aHbAlc.
  • Another nonlimiting example method of the present disclosure may comprise: providing (or measuring) a HbAlc for a subject based; providing (or determining) a k age for a subject; and calculating an aHbAlc for the subject based on the HbAlc level, the k age , and a k re f age . Then, the subject may be diagnosed, treated, and/or monitored based on the aHbAlc.
  • one or more other subject-specific parameters may be used in addition to the one or more physiological parameters.
  • subject-specific parameters may include, but are not limited to, an existing medical condition (e.g., cardiovascular disease, heart valve replacement, cancer, and systemic disorder such as autoimmune disease, hormone disorders, and blood cell disorders), a family history of a medical condition, a current treatment, an age, a race, a gender, a geographic location (e.g., where a subject grew up or where a subject currently lives), a diabetes type, a duration of diabetes diagnosis, and the like, and any combination thereof.
  • an existing medical condition e.g., cardiovascular disease, heart valve replacement, cancer, and systemic disorder such as autoimmune disease, hormone disorders, and blood cell disorders
  • a family history of a medical condition e.g., a current treatment, an age, a race, a gender, a geographic location (e.g., where a subject grew up or where a subject currently lives), a diabetes type, a duration of diabetes diagnosis, and
  • determining the one or more physiological parameters (k giy , k age , and/or K) for a subject may be performed using a physiological parameter analysis system.
  • FIG. 3 illustrates an example of a physiological parameter analysis system 310 for providing physiological parameter analysis in accordance with some of the embodiments of the present disclosure.
  • the physiological parameter analysis system 310 includes one or more processors 312 and one or more machine-readable storage media 314.
  • the one or more machine-readable storage media 314 contains a set of instructions for performing a physiological parameter analysis routine, which are executed by the one or more processors 312.
  • the instructions include receiving inputs 316 (e.g., one or more glucose levels, one or more HbAlc levels, one or more physiological parameters (k giy , k age , and/or K) previously determined, or more other subject-specific parameters, and/or one or more times associated with any of the foregoing), determining outputs 318 (e.g., one or more physiological parameters (k giy , k age , and/or K), an error associated with the one or more physiological parameters, one or more parameters or characteristics for a subject’s personalized diabetes management (e.g., cHbAlc, aHbAlc, a personalized-target glucose range, an average-target glucose level, a supplement or medication dosage, among other parameters or characteristics), and the like), and communicating the outputs 318.
  • inputs 316 e.g., one or more glucose levels, one or more HbAlc levels, one or more physiological parameters (k giy , k age , and/or K)
  • communication of the inputs 316 may be via a user-interface (which may be part of a display), a data network, a server/cloud, another device, a computer, or any combination thereof, for example.
  • communication of the outputs 318 may be to a display (which may be part of a user-interface), a data network, a server/cloud, another device, a computer, or any combination thereof, for example.
  • a “machine-readable medium”, as the term is used herein, includes any mechanism that can store information in a form accessible by a machine (a machine may be, for example, a computer, network device, cellular phone, personal digital assistant (PDA), manufacturing tool, any device with one or more processors, and the like).
  • a machine-accessible medium includes recordable/non-recordable media (e.g., read-only memory (ROM), random access memory (RAM), magnetic disk storage media, optical storage media, flash memory devices, and the like).
  • the one or more processors312 and the one or more machine- readable storage media 314 may be in a single device (e.g., a computer, network device, cellular phone, PDA, an analyte monitor, and the like).
  • a physiological parameter analysis system may include other components.
  • FIG. 4 illustrates another example of a physiological parameter analysis system 410 for providing physiological parameter analysis in accordance with some of the embodiments of the present disclosure.
  • the physiological parameter analysis system 410 includes health monitoring device 420 with subject interface 420A and analysis module 420B, the health monitoring device 420 is, or may be, operatively coupled to data network 422. Also provided in physiological parameter analysis system 410 is a glucose monitor 424 (e.g., in vivo and/or in vitro (ex vivo) devices or system) and a data processing terminal/personal computer (PC) 426, each operatively coupled to health monitoring device 420 and/or data network 422. Further shown in FIG. 4 is server/cloud 428 operatively coupled to data network 422 for bidirectional data communication with one or more of health monitoring device 420, data processing terminal/PC 426 and glucose monitor 424. Physiological parameter analysis system 410 within the scope of the present disclosure can exclude one or more of server/cloud 428, data processing terminal/PC 426 and/or data network 422.
  • analysis module 420B is programmed or configured to perform physiological parameter analysis and, optionally, other analyses (e.g., cHbAlc, aHbAlc, personalized target glucose range, and others described herein). As illustrated, analysis module 420B is a portion of the health monitoring device 420 (e.g., executed by a processor therein). However, the analysis module 420B may alternatively be associated with one or more of server/cloud 428, glucose monitor 424, and/or data processing terminal/PC 426.
  • analyses e.g., cHbAlc, aHbAlc, personalized target glucose range, and others described herein.
  • analysis module 420B is a portion of the health monitoring device 420 (e.g., executed by a processor therein). However, the analysis module 420B may alternatively be associated with one or more of server/cloud 428, glucose monitor 424, and/or data processing terminal/PC 426.
  • server/cloud 428, glucose monitor 424, and/or data processing terminal/PC 426 may comprise machine-readable storage medium(media) with a set of instructions that cause one or more processors to execute the set of instructions corresponding to the analysis module 420B.
  • the health monitoring device 420, the data processing terminal/PC 426, and the glucose monitor 424 are illustrated as each operatively coupled to the data network 422 for communication to/from the server/cloud 428, one or more of the health monitoring device 420, the data processing terminal/PC 426, and the glucose monitor 424 can be programmed or configured to directly communicate with the server/cloud 428, bypassing the data network 422.
  • the physiological parameter analysis can be performed by one or more of the health monitoring device 420, data processing terminal/PC 426, glucose monitor 424, and server/cloud 428, with the resulting analysis output shared in the physiological parameter analysis system 410.
  • Measuring Glucose and HbAlc Levels The measurement of the plurality of glucose levels through the various time periods described herein may be done with in vivo and/or in vitro (ex vivo) methods, devices, or systems for measuring at least one analyte, such as glucose, in a bodily fluid such as in blood, interstitial fluid (ISF), subcutaneous fluid, dermal fluid, sweat, tears, saliva, or other biological fluid.
  • ISF interstitial fluid
  • subcutaneous fluid such as glucose
  • dermal fluid such as in blood, interstitial fluid (ISF)
  • sweat interstitial fluid
  • tears saliva
  • in vivo and in vitro methods, devices, or systems may be used in combination.
  • Examples of in vivo methods, devices, or systems measure glucose levels and optionally other analytes in blood or ISF where at least a portion of a sensor and/or sensor control device is, or can be, positioned in a subject’s body (e.g., below a skin surface of a subject).
  • Examples of devices include, but are not limited to, continuous analyte monitoring devices and flash analyte monitoring devices. Specific devices or systems are described further herein and can be found in US Patent No. 6,175,752 and US Patent Application Publication No. 2011/0213225, the entire disclosures of each of which are incorporated herein by reference for all purposes
  • In vitro methods, devices, or systems include sensors that contact the bodily fluid outside the body for measuring glucose levels.
  • an in vitro system may use a meter device that has a port for receiving an analyte test strip carrying bodily fluid of the subject, which can be analyzed to determine the subject’s glucose level in the bodily fluid. Additional devices and systems are described further below.
  • the frequency and duration of measuring the glucose levels may vary from, on average, about 3 times daily (e.g., about every 8 hours) to about 14,400 times daily (e.g., about every 10 seconds) (or more often) and from about a few days to over about 300 days, respectively.
  • the glucose levels may be used to determine the one or more physiological parameters (k giy , k age , and/or K) and, optionally, other analyses (e.g., cHbAlc, aHbAlc, personalized target glucose range, and others described herein). In some instance, such analyses may be performed with a physiological parameter analysis system.
  • the glucose monitor 424 may comprise a glucose sensor coupled to electronics for (1) processing signals from the glucose sensor and (2) communicating the processed glucose signals to one or more of health monitoring device 420, server/cloud 428, and data processing terminal/PC 426.
  • HbAlc levels are measured in a laboratory using a blood sample from a subject.
  • laboratory tests include, but are not limited to, a chromatography-based assay, an antibody-based immunoassay, and an enzyme-based immunoassay.
  • HbAlc levels may also be measured using electrochemical biosensors.
  • the frequency of HbAlc level measurements may vary from, on average, monthly to annually (or less often if the average glucose level of the subject is stable).
  • HbAlc levels may be measured with a laboratory test where the results are input to the server/cloud 428, the subject interface 420 A, and/or a display from the testing entity, a medical professional, the subject, or other user. Then, the HbAlc levels may be received by the one or more of health monitoring device 420, server/cloud 428, and data processing terminal/PC 426 for analysis by one or more methods described herein. Calculated HbAlc (cHbAlc)
  • a plurality of glucose measurements may be taken for a following time period and used for calculating HbAlc during and/or at the end of the following time period.
  • one or more physiological parameters k gty , k age , and/or K) may be calculated at time G based on measurements of the plurality of glucose levels 204a over time period 206, a laboratory HbAlc level 202b at the end of time period 206, and optionally a laboratory HbAlc level 202a at the beginning of time period 206.
  • Equation 9 can be used to determine a cHbAlc value (HbAlc, of Equation 9) where HbAlco is the laboratory HbAlc level 202b at the end of time period 206 (which is the beginning of time period 208), [G,] are the glucose levels or averaged glucose levels at times t, measured over time period 208 (or the portion of time period 208 where cHbAlc is determined during the time period 208), and the provided one or more physiological parameters (k giy , k age , and/or K) corresponding to time G are used.
  • HbAlco is the laboratory HbAlc level 202b at the end of time period 206 (which is the beginning of time period 208)
  • [G,] are the glucose levels or averaged glucose levels at times t, measured over time period 208 (or the portion of time period 208 where cHbAlc is determined during the time period 208)
  • the provided one or more physiological parameters k g
  • a subject’s cHbAlc may be determined for several successive time periods based on the one or more physiological parameters (k giy , k age , and/or K) determined with the most recent laboratory HbAlc level and the intervening measurements of glucose levels.
  • the HbAlc may be measured periodically (e.g., every 6 months to a year) to recalculate the one or more physiological parameters.
  • the time between evaluating a laboratory HbAlc may depend on (1) the consistency of the measurements of glucose levels, (2) the frequency of the measurements of glucose levels, (3) a subject’s and corresponding family’s diabetic history, (4) the length of time the subject has been diagnosed with diabetes, (5) changes to a subject’s personalized diabetes management (e.g., changes in medications/dosages, changes in diet, changes in exercise, and the like), and combinations thereof.
  • a subject with consistent measurements of glucose levels e.g., a [G] with less than 5% variation
  • frequent measurements of glucose levels e.g., continuous glucose monitoring
  • HbAlc levels less frequently e.g., a subject who recently (e.g., within the last 6 months) changed the dosage of a glycation medication even with consistent and frequent measurements of glucose levels.
  • FIG. 5, with reference to FIG. 3, illustrates an example of a cHbAlc report that may be generated as an output 318 by a physiological parameter analysis system 310 of the present disclosure.
  • the illustrated example report includes a plot of average glucose level over time. Also included on the report is the most recently laboratory HbAlc level (open circle) and cHbAlc levels (asterisks) calculated by the physiological parameter analysis system 310. Two cHbAlc levels are illustrated, but one or more cHbAlc levels may be displayed on the report, including a line that continuously tracks cHbAlc.
  • the output 318 of the physiological parameter analysis system 310 may include a single number for a current or most recently calculated cHbAlc, aHbAlc, a table corresponding to the data of FIG. 5, or any other report that provides a subject, healthcare provider, or the like with at least one cHbAlc level.
  • the cHbAlc may be compared to a previous cHbAlc and/or a previous laboratory HbAlc level to monitor the efficacy of a subject’s personalized diabetes management. For example, if a diet and/or exercise plan is being implemented as part of a subject’s personalized diabetes management, with all other factors (e.g., medication and other diseases) equal, then changes in the cHbAlc compared to the previous cHbAlc and/or the previous laboratory HbAlc level may indicate if the diet and/or exercise plan is effective, ineffective, or a gradation therebetween.
  • the cHbAlc may be compared to a previous cHbAlc and/or a previous laboratory HbAlc level to determine if another HbAlc measurement should be taken. For example, in absence of significant glucose profile change, if the cHbAlc changes by 0.5 percentage units or more (e.g., changes from 7.0% to 6.5% or from 7.5% to 6.8%) as compared to the previous cHbAlc and/or the previous laboratory HbAlc level, another laboratory HbAlc level may be tested.
  • a comparison of the cHbAlc to a previous cHbAlc and/or a previous laboratory HbAlc level may indicate if an abnormal or diseased physiological condition is present. For example, if a subject has maintained a cHbAlc and/or laboratory HbAlc level for an extended period of time, then if a change in cHbAlc is identified with no other obvious causes, the subject may have a new abnormal or diseased physiological condition. Indications of what that new abnormal or diseased physiological condition may be gleaned from the one or more physiological parameters (k giy , k age , and/or K). Details of abnormal or diseased physiological conditions relative to the one or more physiological parameters are discussed further herein.
  • the glucose levels in subjects with diabetes is preferably maintained between 70 mg/dL and 180 mg/dL.
  • the kinetic model described herein illustrates that the intracellular glucose levels are dependent on physiological parameters like k giy .
  • the intracellular glucose level is associated with hypoglycemia and hyperglycemia damage to organs, tissues, and cells. Therefore, a measured glucose level may not actually correspond to the actual physiological conditions that relevant to diabetes management in a subject. For example, a subject with a higher than normal k giy uptakes glucose more readily into cells. Therefore, a 180 mg/dL measured glucose level may be too high for the subject and, in the long run, further continue the subject’s diabetes.
  • a subject with a lower than normal k gty uptakes glucose to a lesser degree into cells. Accordingly, at a 70 mg/dL glucose level, the subject’s intracellular glucose level may be much lower making the subject feel weak and, in the long term, lead to the subject being hypoglycemic.
  • a subject s specific k gLy with respect to a glucose reading and/or a corresponding personalized glucose range: (a) adjusting the accepted normal glucose upper and lower limits to arrive at a personalized- target glucose range that is based on k giy , (b) adjusting a subject’s measured glucose level to an effective plasma glucose level that correlates to the accepted normal glucose upper and lower limits, and (c) adjusting a subject’s measured glucose level to an intracellular glucose level that correlates to an accepted normal lower intracellular glucose limit (LIGL) and the an normal upper intracellular glucose limit (UIGL).
  • LIGL normal lower intracellular glucose limit
  • UIGL normal upper intracellular glucose limit
  • Equations 12 and 13 are Equations 12 and 14 rewritten for when both a laboratory HbAlc and an aHbAlc are available.
  • Equation 12 Equation 12 where k ⁇ y is the k giy for a normal person and k g y is the subject’s k gty
  • Equations 12 and 14 are based on k gly because the higher and lower limits of a glucose range are based on an equivalent intracellular glucose level.
  • personalized-target glucose range may alternatively include only the personalized glucose lower limit or the personalized glucose upper limit and use the currently practiced glucose lower or upper limit as the other value in the personalized-target glucose range.
  • the PG e ff level may be used in combination with the accepted normal lower glucose limit and/or the accepted normal glucose upper limit for diagnosing, monitoring, and/or treating a subject. That is, the PG e ff level is interpreted relative to the accepted glucose limits, which herein are considered between 70 mg/dL and 180 mg/dL but may change based on new clinical and/or scientific data and health officials’ recommendations.
  • a subject in a third method for taking into account a subject’s specific k giy with respect to a glucose reading and/or a corresponding personalized glucose range, a subject’s plasma glucose level (e.g., as measured with an analyte sensor configured to measure a glucose level in a bodily fluid where said sensor may be a part of a larger system) is personalized to an intracellular glucose (IG) level using k giy per Equation 17.
  • IG intracellular glucose
  • Equation 17 The subject’s IG level may then be compared to an accepted normal lower intracellular glucose limit (LIGL) and an accepted normal upper intracellular glucose limit (UIGL).
  • LIGL normal lower intracellular glucose limit
  • UIGL accepted normal upper intracellular glucose limit
  • the currently accepted values for LIGL and UIGL are 0.29 mg/dL and 0.59 mg/dL, respectively.
  • the personalized-target glucose range and/or personalized glucose level may be determined and/or implemented in a physiological parameter analysis system.
  • a set of instructions or program associated with a glucose monitor and/or health monitoring device that determines a therapy may use a personalized-target glucose range and/or personalized glucose level in such analysis.
  • a display or subject interface with display may display the personalized-target glucose range and/or personalized glucose level.
  • the personalized-target glucose range and/or personalized glucose level may be updated over time as one or more physiological parameters are recalculated.
  • Equation 18 can be used to calculate a personalized-target average glucose level (GT) from a reference glucose target (RG).
  • the reference target glucose can take any value that physician determines suitable, for example 120 mg/dL.
  • Equation 18 Alternatively or in combination with Equation 18, Equation 19 can be used to calculate a GT based on a laboratory HbAlc and a calculated aHbAlc. Equation 19 Alternatively or in combination with Equations 18 and/or 19, Equation 20 can be used to calculate a GT when the target HbAlc value (AT) is known.
  • AT target HbAlc value
  • a physiological parameter analysis system may determine an average glucose level for the subject during time period 208 and, optionally, display the average glucose level and/or the target average glucose level.
  • the subject may use the current average glucose level and the target average glucose level to self-monitor their progress over time period 208.
  • the current average glucose level may be transmitted (periodically or regularly) to a health care provider using a physiological parameter analysis system for monitoring and/or analysis.
  • the personalized-target average glucose level may be updated over time as updated relevant physiological parameters, calculated values, and/or measured values for one or more of Equations 18-20 are obtained.
  • Insulin pumps along with continuous glucose monitoring may be used for subjects that need tight control of their glucose levels.
  • the target glucose range is individualized and based on k giy . Therefore, in some instances, subjects with a narrower personalize-target glucose range may be stronger candidates for insulin pumps with continuous monitoring. Triage of subjects to be stronger candidates for insulin pumps along with continuous glucose monitoring may be based on a spread of the personalized-target glucose range, and k giy
  • the spread between currently practiced glucose lower or upper limit is about 110 mg/dL. However, as illustrated above, depending on k gty could narrow to about 60 mg/dL or less. Some embodiments may involve triaging a subject to an insulin pump with continuous glucose monitoring when the personalized-target glucose range span is below a threshold that is less than 110 mg/dL.
  • Some embodiments may involve triaging a subject to an insulin pump with continuous glucose monitoring when k giy exceed a threshold greater than 6.2*1 O' 6 dL*mg' 1 *day' 1 .
  • Some embodiments may involve placing a subject to intense hypoglycemia prevention program when k giy is lower than a threshold, e.g. 6.2* 10' 6 dL*mg' 1 *day' 1 .
  • a threshold e.g. 6.2* 10' 6 dL*mg' 1 *day' 1 .
  • triaging a subject to an insulin pump with continuous glucose monitoring may be a stepped triage where first a subject’s glucose levels are monitored continuously for a reasonable time period (e.g., about 5 days, about 10 days, about 15 days, about 30 days, or more). This continuous monitoring time period can be used to assess if the subject is capable of managing glucose levels effectively or if an insulin pump is better, or required.
  • a reasonable time period e.g., about 5 days, about 10 days, about 15 days, about 30 days, or more.
  • Whether the triaging is straight to an insulin pump with continuous glucose monitoring or a stepped triage with monitoring before treatment with the insulin pump may be determined by the level of the indicators (i.e., the personalized-target glucose range span, kgiy, or any combination thereof). For example, if k giy is about 6.4* 10' 6 dL*mg' 1 *day' 1 and the personalized-target glucose range span is about 103 mg/dL, the subject may be more suited for a stepped triage as compared to another subject where the corresponding indicators suggest an insulin pump should be used.
  • triage may be based on a lookup table (e.g., stored in a physiological parameter analysis system of the present disclosure).
  • the lookup table may, for example, correlate multiple values to each other including, but not limited to, one or more physiological parameters (k giy , k age , and/or K), a personalized-target glucose range span, and/or other factors described herein like an existing medical condition, a family history of a medical condition, a current treatment, an age, a race, a gender, a geographic location, a diabetes type, a duration of diabetes diagnosis, and the like, and any combination thereof.
  • physiological parameters k giy , k age , and/or K
  • K personalized-target glucose range span
  • Columns in the lookup table may, for example, define ranges or limits for the foregoing parameters, and the rows may indicate a suggested course of action, which may be an output 318 of a physiological parameter analysis system 310 of FIG. 3.
  • a suggested course of action which may be an output 318 of a physiological parameter analysis system 310 of FIG. 3.
  • two columns may define an upper and lower bound of k giy , where each row corresponds to a suggested course of action, such as “candidate for insulin pump,” “candidate for closed- loop control system,” “candidate for basal/bolus insulin therapy,” “candidate for basal only insulin therapy,” or any such treatment used to control diabetes or effect the subject’s glycation.
  • a subject triage report may simply display the suggested course(s) of action.
  • the subject triage report may, for example, show a map of zones corresponding to the course(s) of action on a plot defined by one or more of the parameters described above relative to the lookup table.
  • Such zones may, in some instances, be defined by the lookup table, labeling each zone representing a recommendation and indicated the glycemic parameter point on the map to show the relevant zone for that subject.
  • the two foregoing subject triage reports are examples based on lookup tables, alternatively, the two foregoing subject triage reports could be based on other correlations between (1) one or more physiological parameters (k giy , k age , and/or K), a personalized- target glucose range span, and/or other factors described herein and (2) a course(s) of action (e.g., a mathematical algorithm or matrix analysis).
  • a subject’s glycation parameters may help healthcare providers and payors to better determine what therapy tools are most appropriate for which subjects. For instance, closed-loop insulin pump systems are expensive to employ and maintain, but subjects who have a high glycation rate may have a very narrow personalized-target glucose range where the safest treatment is keeping their glucose levels within such ranges using a closed-loop insulin pump system.
  • the insulin pumps along with continuous glucose monitoring may be closed-loop systems. In some embodiments, the insulin pumps along with continuous glucose monitoring may be hybrid-loop systems.
  • a physiological parameter analysis system may further include one of the foregoing insulin pumps communicable with one or more of the components in the physiological parameter analysis system 410, for example, the glucose monitor 424 (e.g., a continuous glucose monitoring system) and health monitoring device 420.
  • one or more physiological parameters may be used in titrating dosages of diabetes medication (e.g., insulin) to a subject.
  • a physiological parameter analysis system 310 of the present disclosure may determine or have input (1) one or more physiological parameters, (2) a personalized-target glucose range, (3) a personalized glucose level (e.g., an effective plasma glucose level or an intracellular glucose level), and/or (4) a personalized-target average glucose. Then, when a subsequent glucose level is measured the physiological parameter analysis system 310 may output a recommended diabetes medication dosage.
  • An alternative or complimentary output 318 may be a glucose pattern insight report.
  • glucose pattern insight reports can be found in US Patent Application Publication Nos. 2014/0188400 and 2014/0350369, each incorporated herein by reference.
  • the disclosed analyses and reports in the forgoing applications may be modified based on the one or more physiological parameters k giy , k age , and K) of the present disclosure.
  • FIG. 8 illustrates an example of a glucose pattern insight report that may be an output 318 of a physiological parameter analysis system 310 (e.g., an insulin titration system).
  • the illustrated glucose pattern insights report incorporates an AGP along with a table of glycemic control measures (or “traffic lights”).
  • the report includes an AGP plot over an analysis time period (e.g., about one to about four months) that illustrates the personalized-target average glucose at 120 mg/dL, the average glucose levels for the subject over the analysis time period, the 25th to 75th percentile of glucose levels for the subject over the analysis time period, and the 10th to 90th percentile of glucose levels for the subject over the analysis time period.
  • the glucose pattern insight report may further or alternatively display the personalized-target glucose range and/or personalized glucose level (e.g., an effective plasma glucose level or an intracellular glucose level) relative to the currently accepted glucose range.
  • the glucose pattern insight report may optionally further include one or more of: a laboratory HbAlc level, a cHbAlc level, an adjusted HbAlc level based on either laboratory HbAlc or glucose data, the date range over which the average glucose and related percentiles were determine, and the like.
  • a laboratory HbAlc level e.g., a cHbAlc level
  • an adjusted HbAlc level based on either laboratory HbAlc or glucose data
  • the correlation displays, in this example, as traffic lights (e.g., green (good), yellow (moderate), or high (red)) that correspond to the risk of a condition based on the glycemic control measures.
  • glycemic control measures include, but are not limited to, likelihood of low glucose, likelihood of high glucose, the proximity of the average glucose to the personalized-target average glucose, the adherence of the glucose levels to the personalized- target glucose range and/or the personalized glucose level relative to the currently accepted glucose range, the degree of variability of the average glucose below (or above) to the personalized-target average glucose, the degree of variability of the glucose levels outside (below and/or above) the personalized-target glucose range and/or the personalized glucose level relative to the currently accepted glucose range, and the like.
  • the glucose pattern insights report may be used as part of a diabetes medication titration system, where the traffic lights (or values associated therewith) can drive logic to provide treatment modifications such as changing basal dosages of the diabetes medication or bolus amounts of the diabetes medication associated with meals.
  • the logic driving these traffics lights may provide recommendations to subjects on dosage adjustments.
  • the glucose pattern insights report and related analyses that incorporate the use of the kinetic model described herein may provide better treatment to subjects with diabetes.
  • a subject with a k giy of 5.1*10' 6 dL*mg' 1 *day' 1 may have a personalized-target glucose range of about 90 ⁇ 8 mg/dL to about 250 ⁇ 32 mg/dL. This subject is more sensitive to lower glucose levels and may feel weak, hungry, dizzy, etc. more often if the currently practiced glucose range (70 mg/dL and 180 mg/dL) were used.
  • the analytical logic used for the glucose pattern insights report described herein that uses one or more physiological parameters k giy , k age , and K) may include settings that define the risk of hypoglycemia as traffic lights for “likelihood of low glucose.” For example, if the likelihood of low glucose indicates low risk (e.g., a green traffic light), then it is considered safe to increase insulin. If the likelihood of low glucose indicates moderate risk (e.g., yellow traffic light), then it is considered that the current risk is acceptable but no further increase of insulin should be made. Finally, if the likelihood of low glucose indicates high risk, then it is recommended that insulin should be reduced to get the glucose back to tolerable levels. For a subject with high risk of hypoglycemia because of an increase lower glucose level threshold, the amount of risk associated with moderate and high risk (e.g., how far below the lower glucose level threshold) may be less than a subject with a normal lower glucose level threshold.
  • the output 318 may be values of dosage recommendations.
  • the one or more physiological parameters k giy , k age , and K) and related analyses may be updated periodically (e.g., about every 3 months to annually).
  • the frequency of updates may depend on, among other things, the subject’s glucose level and diabetes history (e.g., how well the subject stays within the prescribed thresholds), other medical conditions, and the like.
  • An insulin titration system may optionally also utilize error associated with the one or more physiological parameters k giy , k age , and K). Error values can be determine using standard statistically techniques by those skilled in the art and may be used as another set of parameters for configuring the titration system. For example, the titration system may use the reduced amount of risk for hypoglycemia (i.e., a smaller tolerance to be below the lower glucose level threshold for indicating moderate and high risk) may be implemented when the lower glucose level of the personalized-target glucose range of about 75 mg/dL with an error of about 7% or less.
  • the reduced amount of risk for hypoglycemia i.e., a smaller tolerance to be below the lower glucose level threshold for indicating moderate and high risk
  • the dosage of diabetes mediation (e.g., via titration) may be updated over time as one or more physiological parameters are recalculated.
  • Closed-loop systems and hybrid closed-loop systems that recommend or administer insulin dosages to a subject have been developed for insulin delivery based on near realtime glucose readings. These systems are often based on models describing the subject’s physiology, glucose sensor dynamics, and glucose sensor error characteristics.
  • the one or more physiological parameters k giy , k age , and K
  • related analyses e.g., personalized-target glucose range, personalized glucose level, personalized- target average glucose, cHbAlc, aHbAlc, and the like
  • Closed-loop systems often are configured to “drive” the subject’s glucose levels inside a target range and/or toward a single glucose target, which may be the personalized- target glucose range, the personalized glucose level relative to the accepted target glucose range, and/or the personalized-target average glucose described herein.
  • a target range which may be the personalized- target glucose range, the personalized glucose level relative to the accepted target glucose range, and/or the personalized-target average glucose described herein.
  • the controller may drive their glucose levels in a way to stay above the lower glucose limit based on k giy , which avoids lower glucose levels that adversely affect them more than subjects with a normal glucose range.
  • subjects with reduced upper glucose limits for their personalized-target glucose range may have the controller of a closed-loop insulin delivery system and hybrid closed-loop insulin delivery system drive glucose to stay below the personalized-upper glucose limit to mitigate hyperglycemic effects.
  • the metrics by which a closed-loop insulin delivery system and hybrid closed-loop insulin delivery system determine a dosage of insulin may be updated over time as one or more physiological parameters are recalculated.
  • the personalized-target glucose range, personalized glucose level, and/or personalized-target average glucose may be updated when one or more physiological parameters are recalculated.
  • Diabetes is a disease caused by a subject’s pancreas being unable to produce sufficient (or any) insulin.
  • a subject’s glycation process may be the source of the body not properly controlling intracellular glucose.
  • Such subjects may be more responsive to treatments that use glycation medications (e.g., azathioprine, meloxicam, nimesulide, piroxicam, mefenamic acid, oxaprozin, D-penicillamine, penicillin G, trimethylphloroglucinol, ranitidine, phloroglucinol dihydrate, epinephrine bitartrate, pyridoxine HCI, toiramate, escitalopram, hydroquinone, tretinoin, colchicine, rutin, and the like) rather than traditional diabetes treatments.
  • glycation medications e.g., azathioprine, meloxicam, nimesulide, piroxicam, mefen
  • Some embodiments may involve monitoring k giy and/or K for a subject on glycation medication and, optionally, changing a glycation medication dosage based on changes to k g iy and/or K. For example, referring to FIG. 2, some embodiments may involve determining k giyl and/or K at a time and a corresponding k giy2 and/or K 2 at a time t 2 (as described above) and treating a subject with glycation medication over time period 208.
  • a dosage and/or type of glycation medication may be altered for a subsequent time period.
  • a corresponding k giy3 and/or /f 3 may be determined at the end of the subsequent time period for comparison to one or more of the previously determined physiological parameters.
  • the time between and t 2 and between t 2 and t 3 should be at least the expected time for the glycation medication to make a measurable change in the parameter being monitored, which may depend on the medication and the dosage.
  • an outputs 18 of the physiological parameter analysis system 310 of FIG. 3 may be a glycation medication report that includes glycation medication and/or dosage recommendations based on k giy and/or K calculated by the physiological parameter analysis system 310. This output 318 may be displayed for a subject, healthcare provider, and/or the like to review and adjust the glycation medication and/or dosage.
  • the dosage recommendations provide a subject and/or automated medication delivery system with the next dosage to be administered.
  • the system guides titration of the medication, where the subject may start with the lowest dosage or a recommended initial dosage.
  • the initial dosage may be defined by the current condition of the subject, the subject’s k giyl and/or and other factors described herein. After an appropriate amount of time has passed for the effects of the current medication dosage to be adequately determined, k giy2 and/or K 2 can be determined based on a new laboratory HbAlc level and the glucose levels measured during the medication dosage.
  • the metrics by which a dosage of glycation medication is determined may be updated over time as one or more physiological parameters are recalculated.
  • a comparison of k giy , k age , and/or K at two or more different time periods provides physiological condition information of the subject. For example, when a clinically significant change to k giy , k age , and/or K is observed over time an abnormal or diseased physiological condition may, and likely, exists.
  • such clinically significant variation can indicate that the glucose transporter level or cell membrane has changed.
  • Such biological changes may indicate a potential metabolic change in the subject’s body resulting from the subject’s physiology under-going a disease state.
  • k age and/or k gen varies significantly over time such that the variation is clinically significant
  • such clinically significant variation can indicate changes to the subject’s immune system because the immune system is designed to recognize cells that need to be removed.
  • a clinically significant variation in k age and/or k gen may also or alternatively be associated with the oxygen sensing mechanism in the body.
  • An increasing k age and/or k gen over time may indicate that the subject’s body needs the red blood cells to carry more oxygen or the oxygen sensing mechanism is not functioning correctly, either reason indicating a physiological state change such as for example, blood loss or a disease condition.
  • clinically significant variation in k age and/or k gen may be associated with bone marrow changes. For example, if the bone marrow suddenly produces a lot more oxygen carrying red blood cells, the subject’s body will respond by killing off or eliminating more red blood cells. That is, a clinically significant increase in k age and/or k gen may be associated with bone marrow abnormality.
  • a hormone disorder can cause a clinically significant variation in kage-. kgen, and K.
  • Hormones can affect heart rate, contraction strength, blood volume, blood pressure, and red blood cell production. Stress hormones such as catecholamines and cortisol stimulate the release of reticulocytes from the bone marrow and possibly also enhance erythropoiesis. Therefore, large fluctuation on hormone level can change k age and/or k gen , and consequently K.
  • deviations from normal of the k giy , k age , and/or K may be an indicator of diabetes or pre-diabetes.
  • k giy , k age , and/or K to measure diabetes or pre-diabetes may be more effective than standard fasting glucose tests and laboratory HbAlc.
  • a subject with a laboratory HbAlc value in the normal range and normal fasting glucose may have low k giy , associated with high glucose values at times in the day other than fasting. Therefore, the subject may be a candidate for earlier diabetes intervention that otherwise may have gone unnoticed based on standard diabetes diagnoses methods.
  • the standard diabetes treatments may be employed to lower their HbAlc.
  • determining that kgiy, is abnormal may be an indication that the problem with their glycation physiology rather than their pancreas, suggesting other more targeted forms of treatment.
  • Embodiments of the present disclosure include displaying the determined k giy , k age , and/or K, the changes in k giy , k age , and/or K over time, and/or possible abnormal or diseased physiological conditions.
  • the physiological parameter analysis provides an indication of a subject’s abnormal or disease condition, as well as an analysis and/or monitoring tool for one or more parameters or characteristics for a subject’s personalized diabetes management.
  • a person’s glycated hemoglobin level can vary over time based upon a variety of internal (e.g., physiological) and external (e.g., environmental) factors. Given these variations, glycated hemoglobin levels measured using a blood sample at a laboratory can be more therapeutically meaningful when taken during certain time periods, and less meaningful when taken in other time periods. According to the embodiments disclosed herein, a relationship between the glucose level and a preferrable time period to obtain a laboratory measured glycated hemoglobin level is described. Benefits of determining recommended times for taking laboratory measured HbAlc levels include reducing the need for extraneous laboratory measurements of glycated hemoglobin, improved or more accurate physiological parameter measurements, and improved treatment options, as disclosed herein.
  • a method for determining a time for obtaining laboratory glycated hemoglobin can include determining a first calculated glycated hemoglobin (HbAlc) level corresponding to the first time period; determining for the first time period a second calculated glycated hemoglobin (HbAlc) level using a first offset value; and determining for the first time period a third calculated glycated hemoglobin (HbAlc) level using a second offset value.
  • equations 5, 6, and 9 can be used to calculate the first and second difference values using an initial laboratory measured HbAlc (i.e., HbAlco) corresponding to a beginning of a time period and received glucose level information corresponding to the time period.
  • Equation A represents a consolidated version of Equations 6, 8, and 8a:
  • a plurality of time periods is represented by the set of numbers 1 to z.
  • the various terms include sub i, j, or z. These sub terms all correspond to time periods in the plurality of time periods 1 to z.
  • [G2] is the average glucose value for the second time period.
  • t? is the time length interval for the third time period.
  • AlcO can be an initial laboratory measured glycated hemoglobin level taken to establish a baseline.
  • AlcO can be the calculated HbAlc value at time tO.
  • the value HbAlcz is equivalent to calculated HbAlc (cHbAlc) at the end of time interval tz.
  • a recommended time period for laboratory measured HbAlc can be determined by calculating three or more glycated hemoglobin levels for each time period in the plurality of time periods. For calculation of each of the three glycated hemoglobin levels, an initial laboratory measured HbAlc (i.e., HbAlco) corresponding to a beginning of a time period and received glucose level information corresponding to the time period can be used. Further, the first calculation can be based upon initial estimation values for ka ge a red blood cell elimination constant, k giy a red blood cell glycation rate constant, and KM a constant value. For example, constant value KM can range from 200-600 mg/dL.
  • the initial estimation for k giy can range from 3.6xl0‘ 6 to 9.9xl0‘ 6 dL/mg/day.
  • the initial estimation for k age can range from 0.0052 to 0.05 day' 1 .
  • a second and third calculation are similarly performed using one offset value for initially estimated values.
  • k giy is set to an initial k giy offset and k age remains the same.
  • the initial k giy offset can range from 3xl0' 7 to IxlO' 6 .
  • the initial k giy offset can be 110% of the initial estimation for k giy .
  • the initial k age offset can range from 0.0005 to 0.005.
  • the initial k age offset can be 110% of the initial estimation for k age .
  • the initial k giy offset can be the same as the initial ka ge offset.
  • the initial k giy offset and the initial k age offset can be 110% of the initial estimations.
  • the initial k giy offset can be different than the initial k age offset.
  • the initial k giy offset can be 110% of the initial estimation and the initial k age offset can be 120% of the initial estimations.
  • the second calculated value for each time period is then compared to the first calculated value for the corresponding time period to determine a first difference value.
  • the third calculated value for each time period is also compared to the first calculated value for the corresponding time period to determine a second difference value.
  • the first and second difference values for each corresponding time period are then compared to a predetermined threshold value. If either the first difference value or the second difference value is equal to or exceeds a predetermined threshold value, the corresponding time is determined to be the recommended time period for obtaining laboratory measured glycated hemoglobin levels.
  • each of those time period where the difference value is equal to or exceeds the predetermined value is a recommended time period for laboratory measured HbAlc. According to embodiments herein, more than one time period can be identified as a recommended time period.
  • First, second, and third are used as terms of convenience and should not be relied upon as a limiting to any particular order. The calculations can be made in any order after glucose levels are received for a particular time period. The calculations can be made all at once or as the glucose levels are received.
  • NGSP National Glycohemoglobin Standardization Program
  • PRLs Primary Reference Laboratories
  • SRLs Secondary Reference Laboratories
  • the SRLs work directly with manufacturers to standardize their methods and provide comparison data for method certification, in order to achieve the desired end result of comparability of fresh sample results with the DCCT Reference.
  • Proficiency testing (PT) data is used to assess the effectiveness of method standardization.
  • two difference values can be calculated for each time period. These calculated difference values can be compared to the predetermined threshold to determine if the corresponding time period is a recommended time period.
  • Both difference values can equal or exceed a predetermined threshold, however only one of the first or second difference value must equal or exceed the predetermined threshold in order for the corresponding time period to be considered a recommended time period.
  • the first difference value is 0.14% NGSP and the second difference value is 0.22% NGSP
  • both the first and second difference values can be compared to a predetermined threshold value or only the larger of the first and second difference values can be compared to a predetermined threshold value.
  • a subject can wear or use an analyte monitoring device.
  • Any reference to analyte monitoring device includes the option of more than one analyte monitoring device at the same time or successively unless context requires one device.
  • the analyte monitoring device can collect from a subject one or more glucose levels (e.g., glucose level information).
  • the analyte monitoring device can transmit the glucose levels, perform the calculations disclosed herein, or a combination thereof.
  • any calculations can be made by one or more processors included on or with an analyte monitoring device, on a separate device (for example, not limitation, a reader device as described herein) with one or more processors and memory, a remote device (for example, not limitation, an electronic medical records database), a remote server (for example, a cloud-based database), or by a combination thereof.
  • the analyte monitoring device can be connected to one or more devices to receive and/or transmit information, as disclosed herein.
  • the analyte monitoring device is a continuous glucose monitoring device.
  • the analyte monitoring device is a lab based device.
  • a time period can include weeks, days, or hours, and is the time period over which average glucose measurements are being received, recorded, or calculated (e.g., based on the analyte level information from the analyte monitoring device).
  • a time period can include 1-2 days, 2-3 days, 24 hours, 1 hour, or any period of time therebetween.
  • a time period can include a minimum of one hour and a maximum of 24 hours. This can be beneficial as HbAlc is slow to change and therefore cannot exhibit a change in value within an hour, and therefore, in determination of Equation A.
  • the time length interval (t z ) for a given time period is set to the approximate number of hours in each time period divided by the total number of hours in a day. For example, for a time period of length of 1 day, the time length interval is 1. Similarly, for a time period of 1 hour, the time length is 1/24. According to the preferred embodiment, the time period can include 1/24, 3, or any fraction between 3 and 1/24, including, without limitation, 1/12, 1/8, 1/6, 1/4, 1/3, 1/2, 1, 1.5, 2, 2.25, 2.5, or 3.
  • a time period can be preset or change after the start of the time period.
  • a time period can be preset at 2 hours before the start of the time period.
  • a time period can start and the duration of the time period is set after the start of the time period at 2 hours.
  • a time period can be static or dynamic.
  • a dynamic time period can be preset at 3 hours and then at the second hour the duration is changed by reducing the time period to 2 hours or by extending the time period to 4 hours.
  • the duration of time periods within the plurality of time periods can vary.
  • an embodiment can comprise a plurality of time periods having a first time period and a second time period, where the first time period has a duration of 24 hours and the second time period has a duration of 12 hours.
  • first time period and second time period can be adjacent or sequential.
  • first time period and second time period can be non-adjacent or nonsequential.
  • a first time period can be from 8:00 am to 8:00 pm day 1 and a second time period can be from 8:00 am to 8:00 pm day 2.
  • a recommended time period for laboratory measured HbAlc can be determined, as described above.
  • the recommended time period for laboratory measured HbAlc can include the 2-3 day time period.
  • the recommended time period for laboratory measured HbAlc can include the 12-hour time period.
  • the predetermined threshold can be the same or different for each time period.
  • a non-limiting example of calculating the calculated glycated hemoglobin levels is provided.
  • the difference between the first calculation and second calculation is compared to the predetermined threshold.
  • the difference between the first calculation and third calculation is compared to the predetermined threshold. If either difference value is equal to or exceeds a predetermined threshold value (e.g., 0.2% NGSP) then the example time period is a recommended time period. If, however, both difference values are below the predetermined threshold value, then the example time period is not a recommended time period. In that instance, three or more glycated hemoglobin levels are calculated for a subsequent time period in the plurality of time periods to determine a recommended time period for laboratory measured HbAlc.
  • a predetermined threshold value e.g. 0.2% NGSP
  • multiple time periods can be employed to monitor a subject.
  • a group of time periods constitutes an observational window.
  • the time periods can be consecutive, there can be gaps between time periods, and combinations thereof.
  • an initial lab measured glycated hemoglobin (HbAlc) level is commonly, but not exclusively, used as an initial value (i.e., AlcO in Equation A above) for using measured glucose values to determine a calculated glycated hemoglobin (cHbAlc) level for each time period.
  • a calculated glycated hemoglobin (cHbAlc) level can alternatively be used as an initial value for determining a subsequent calculated glycated hemoglobin (cHbAlc) level.
  • cHbAlc calculated glycated hemoglobin
  • a subject can obtain a lab measured glycated hemoglobin (HbAlc) level at time tO, which would serve as the initial value AlcO for the first time period, tO.
  • the calculated glycated hemoglobin (cHbAlc) level from the first time period can be used as an initial value (i.e., Alcl) for the second time period, tl.
  • the calculated glycated hemoglobin (cHbAlc) level for the second time period can be used as an initial value (i.e., Alc2) for the third time period, t2.
  • a calculated or lab measured glycated hemoglobin (HbAlc) level can be used as an initial value for any time period, including a first time period or any subsequent time period.
  • the use of a calculated and lab measured glycated hemoglobin (HbAlc) level can alternate over multiple time periods.
  • using a lab-based glycated hemoglobin level measured during the recommended time can provide a more accurate representation of the subject’s HbAlc.
  • a more accurate HbAlc can be beneficial for use in the kinetic models and for providing a superior level of care to a subject, as disclosed herein.
  • Any glycated hemoglobin level measured during a recommended time period is a preferred measured glycated hemoglobin level.
  • Options for care can include treating a person based on the preferred measured glycated hemoglobin level; administering and/or adjusting an insulin dosage, a glycation-medication dosage, an exercise regime, a meal intake, or a combination thereof; and adjusting a therapeutic profile or treatment regimen, outputting a first a therapeutic profile or treatment regimen, or administering a pharmaceutical compound to the subject.
  • one or more output alarms or alert notifications can be generated and/or displayed.
  • output alarms or alert notifications can indicate whether a time period is a recommended time period or whether a time period is not a recommended time period.
  • a message that can be included as part of an output alarm or alert notification can be “Obtain an HbAlc lab test in the next 36 hours” or “Obtain an HbAlc between DATE X and DATE Y ”
  • an output alarm or alert notification does not have to include words and can be a symbol associated with testing.
  • An output alarm or alert notification can prompt a subject to take further action including obtaining a measured glycated hemoglobin level.
  • the output alarm or alert notification can be visual, tactile, verbal, auditory, vibration-based, or a combination thereof.
  • the output alarm or alert notification can be delivered to the subject, the subject’s healthcare provider, a third-party, or a combination thereof. Additional glycated hemoglobin levels can be received from the subject in response to the output alarms or alert notifications.
  • the output alarms or alert notifications and obtained information from the analyte measuring device e.g., glucose levels, calculated hemoglobin levels, date/time information
  • predetermined threshold value can include a range of 0.3% to 0.1%.
  • the predetermined threshold value can be NGSP.
  • a nonlimiting preferred predetermined threshold value can include a range of 0.2% to 0.16%.
  • the predetermined threshold can be selected in part based on the accuracy of the lab measured HbAlc. For example, a typical lab measured HbAlc has a coefficient of variation of approximately 2%, which corresponds to a predetermined threshold value of 0.16% NGSP.
  • the predetermined threshold can be increased or decreased to account for the variation in the measurement.
  • the plurality for time periods can each include a plurality of corresponding predetermined threshold values.
  • the plurality of corresponding predetermined threshold values can each have a unique threshold value. The unique threshold values of one or more threshold values can be a different threshold value.
  • a non-limiting exemplary correlation for the data in FIG. 18 is provided.
  • the highest MARD corresponds to the “Early Middle (Days 7-8)” and is 9.1 and the lowest corresponds to the “Late Middle (Days 9-12)” and is 6.6.
  • MARD of 9.1 can correspond to 0.2% NGSP and MARD of 6.6 can correspond to 0.15% NGSP.
  • the corresponds predetermined threshold is 0.19% NGSP. According to embodiments disclosed herein, this extrapolated value can be used to determine if a time period is recommended.
  • more than one time period can be predicted as likely to be a recommended time period for lab measured HbAlc.
  • the method or system disclosed herein can generate and deliver an output alarm or alert notification any time after making the prediction and before the end of at least one of the time periods predicted to be a recommended time period.
  • a second time period and a third time period can be predicted as a recommended time period.
  • the system or method can generate and deliver an output alarm or alert notification when the prediction is created, during the second time period, during the third time period, or any intermediate point.
  • a prediction is beneficial for giving subjects notice to obtain a lab measured HbAlc value.
  • a subject in a 10-day long observational window can have an increasing first and/or second difference value for the first four days of the study.
  • the method or system disclosed herein can collect data from at least two time periods and determine a trend (e.g., linear extrapolation).
  • the method or system can include a step of, or instructions for, determining a trend or similar information from the collected data.
  • the trend can indicate that, for example, not limitation, at least one of the first and second difference values is likely to be equal to or exceed the predetermined threshold value in the sixth time period.
  • An output alarm or alert notification can then be generated on day five.
  • the output alarm or alert notification can indicate the subject should schedule a laboratory appointment during a determined recommended time period.
  • a confidence rating can be assigned to the predicted recommended time period based on preset amounts, individual historical subject data, or a combination thereof.
  • Preset amounts can be set by a particular subject, a particular subject’s healthcare provider, or by an analyte monitoring device. Preset amounts can be set based on an analyte monitoring device model, averaged data of subjects with similar physiological parameters, or statistics techniques.
  • Individual historical subject data can include the accuracy of prior predictions for an individual subject and/or the degree an individual subject’s glucose or HbAlc levels vary compared to a normal subject.
  • a future time period can be predicted as likely to be a recommended time period.
  • the analyte monitoring device a subject is using can be known to have a 5% error rate for predictions.
  • the output alarm or alert notification can include a moderate confidence rating.
  • the subject can have physiological parameters similar to other subjects who generally have highly accurate predictions.
  • the method or system can upgrade the confidence rating in a output alarm or alert notification to high.
  • a high confidence rating can be assigned where the time periods used in an extrapolation are five or more and a low confidence rating where only two time periods are used in an extrapolation. For the prior examples low, moderate, and high are used as example confidence ratings, these are only for convivence, and embodiments herein are not limited to these three levels.
  • Calculated glycated hemoglobin levels are then determined by relying on estimated constants, average glucose level for each time period, and difference value between the calculated glycated hemoglobin levels.
  • the process of obtaining a baseline measurement, receiving subject glucose measurements, calculating glycated hemoglobin levels, calculating glycated hemoglobin levels with offset values, and comparing the differences of the calculated values is repeated for each 3-day segment. Any time period that satisfies a predetermined threshold value is a recommended time period.
  • the predetermined threshold value is set based on a MARD value for one or more continuous glucose monitor’s monitoring the subject. Each time period can have a different MARD value and thus a different threshold for determining if the time period is a recommended time period. Identifying Supplements and/or Medicines
  • k age and, consequently, K change due to aging. Therefore, kage and/or K (provided a stable or known change in k gty ) may be used as biological markers to calculate a standardized metabolic age. Generally, over time, k age decreases and K increases. Using a correlation between k age and/or K and age in healthy subjects, a new subject’s metabolic age may be calculated. This metabolic age may then be used as an indicator of the new subject’s risk for age-related degenerative conditions like heart disease, Alzheimer’s, or osteoperosis. The risk for age-related degenerative conditions may be used in conjunction with family history of age-related degenerative conditions for proactive screening and/or preventive treatment.
  • a 54-year old subject with a metabolic age of 65 with a family history of cardiovascular disease developing later in life may be tested more often for signs and/or progression of cardiovascular disease than a 54-year old subject with a metabolic age of 50 and a similar family history.
  • embodiments of the present disclosure are used with or as systems, devices, and methods for measuring glucose and, optionally, at least one other analyte in a bodily fluid.
  • the embodiments described herein can be used to monitor and/or process information regarding glucose and, optionally, at least one other analyte.
  • analytes that may be monitored include, but are not limited to, glucose derivatives, HbAlc, reticulocyte count, RBC GLUT1 level, acetyl choline, amylase, bilirubin, cholesterol, chorionic gonadotropin, creatine kinase (e.g., CK-MB), creatine, creatinine, DNA, fructosamine, glutamine, growth hormones, hormones, ketones, ketone bodies, lactate, peroxide, prostate-specific antigen, prothrombin, RNA, thyroid stimulating hormone, and troponin.
  • glucose derivatives HbAlc
  • reticulocyte count reticulocyte count
  • RBC GLUT1 level acetyl choline
  • amylase bilirubin
  • cholesterol chorionic gonadotropin
  • creatine kinase e.g., CK-MB
  • creatine creatinine
  • DNA fructosamine
  • glutamine growth hormones
  • hormones
  • the concentration of drugs may also be monitored.
  • antibiotics e.g., gentamicin, vancomycin, and the like
  • digitoxin digoxin
  • digoxin drugs of abuse
  • theophylline drugs of abuse
  • warfarin drugs of abuse
  • the analyte monitors and/or analyte monitoring systems used with or as systems, devices, and methods for measuring glucose and, optionally, one or more analytes in a bodily fluid may be in vivo analyte monitoring systems or in vitro analyte monitoring systems.
  • systems, devices, and methods of the present disclosure may use both in vivo analyte monitoring systems and in vitro analyte monitoring systems.
  • In vivo analyte monitoring systems include analyte monitoring systems where at least a portion of an analyte sensor is, or can be, positioned in the body of a subject to obtain information about at least one analyte of the body.
  • In vivo analyte monitoring systems can operate without the need for a factory calibration. Examples of in vivo analyte monitoring systems include, but are not limited to, continuous analyte monitoring systems and flash analyte monitoring systems.
  • Continuous analyte monitoring systems are in vivo systems that can transmit data from a sensor control device to a reader device repeatedly or continuously without prompting (e.g., automatically according to a schedule).
  • Flash analyte monitoring systems are in vivo systems that can transfer data from a sensor control device in response to a scan or request for data by a reader device, such as with a near field communication (NFC) or radio frequency identification (RFID) protocol.
  • NFC near field communication
  • RFID radio frequency identification
  • In vivo analyte monitoring systems can include a sensor that, while positioned in vivo, makes contact with the bodily fluid of the subject and senses one or more analyte levels contained therein.
  • the sensor can be part of a sensor control device that resides on the body of the subject and contains the electronics and power supply that enable and control the analyte sensing.
  • the sensor control device and variations thereof, can also be referred to as a “sensor control unit,” an “on-body electronics” device or unit, an “on-body” device or unit, or a “sensor data communication” device or unit, to name a few.
  • analyte monitoring systems can also include one or more reader devices that receive sensed analyte data from the sensor control device. These reader devices can process and/or display the sensed analyte data, in any number of forms, to the subject.
  • Handheld reader devices can be referred to as “handheld reader devices,” “reader devices” (or simply, “readers”), “handheld electronics” (or handhelds), “portable data processing” devices or units, “data receivers,” “receiver” devices or units (or simply receivers), “relay” devices or units, or “remote” devices or units, to name a few.
  • Other devices such as personal computers have also been utilized with or incorporated into in vivo and in vitro monitoring systems.
  • a sensor or portion thereof of an in vivo analyte monitoring system may be the glucose monitor 424, and the reader device may be the health monitoring device 420.
  • the in vivo analyte monitoring system may be, in whole, the glucose monitor 424 that transmits data to a health monitoring device 420, data network 422, data processing terminal/PC 426, and/or server/cloud 428.
  • the determination of one or more physiological parameters may be performed within the in vivo analyte monitoring system, in some instances. Only the physiological parameters may, for example, be determined within the in vivo analyte monitoring system and transmitted to a suitable other component of a physiological parameter analysis system, which may perform other analyses described herein. In some embodiments, the in vivo analyte monitoring system may only produce output signals that correspond to glucose levels that are received by another component of a physiological parameter analysis system.
  • one or more of the other component(s) of the physiological parameter analysis system may determine one or more physiological parameters (e.g., k giy , k age , (or, k gen ), and/or K) and, optionally, perform one or more of the other analyses described herein.
  • physiological parameters e.g., k giy , k age , (or, k gen ), and/or K
  • FIG. 9 illustrates an example of an in vivo analyte monitoring system 960.
  • this example in vivo analyte monitoring system 960 monitors glucose and, optionally, one or more other analytes.
  • the in vivo analyte monitoring system 960 comprises a sensor control device 962 (which may be at least a portion of the glucose monitor 424 of FIG. 4) and a reader device 964 (which may be at least a portion of the health monitoring device 420 of FIG. 4) that communicate with each other over a local communication path (or link) 966, which can be wired or wireless, and unidirectional or bi-directional.
  • path 966 is wireless
  • a near field communication (NFC) protocol, RFID protocol, BLUETOOTH® or BLUETOOTH® Low Energy protocol, WiFi protocol, proprietary protocol, or the like can be used, including those communication protocols in existence as of the date of this filing or their later developed variants.
  • Reader device 964 (e.g., a dedicated reader, a cellular phone or PDA running an app, a smartwatch, or the like) is also capable of wired, wireless, or combined communication with a computer system 968 (which may be at least a portion of the data processing terminal/PC 426 of FIG. 4) over communication path (or link) 970 and with a network 972 (which may be at least a portion of the data network 422 and/or the server/cloud 428 of FIG. 4), such as the internet or the cloud, over communication path (or link) 974.
  • Communication with network 972 can involve communication with trusted computer system 976 within network 972, or though network 972 to computer system 968 via communication link (or path) 978.
  • Communication paths 970, 974, and 978 can be wireless, wired, or both, can be uni-directional or bi-directional, and can be part of a telecommunications network, such as a Wi-Fi network, a local area network (LAN), a wide area network (WAN), the internet, or other data network.
  • communication paths 970 and 974 can be the same path. All communications over paths 966, 970, and 974 can be encrypted and sensor control device 962, reader device 964, computer system 968, and trusted computer system 976 can each be configured to encrypt and decrypt those communications sent and received.
  • Sensor control device 962 can include a housing 980 containing in vivo analyte monitoring circuitry and a power source.
  • the in vivo analyte monitoring circuitry is electrically coupled with an analyte sensor 982 that extends through an adhesive patch 984 and projects away from housing 980.
  • Adhesive patch 984 contains an adhesive layer (not shown) for attachment to a skin surface of the body of the subject. Other forms of body attachment to the body may be used, in addition to or instead of adhesive.
  • Sensor 982 is adapted to be at least partially inserted into the body of the subject, where it can make fluid contact with that subject’s bodily fluid (e.g., subcutaneous (subdermal) fluid, dermal fluid, or blood) and be used, along with the in vivo analyte monitoring circuitry, to measure analyte-related data of the subject.
  • Sensor 982 and any accompanying sensor control electronics can be applied to the body in any desired manner.
  • an insertion device (not shown) can be used to position all or a portion of analyte sensor 982 through an external surface of the subject’s skin and into contact with the subject’s bodily fluid. In doing so, the insertion device can also position sensor control device 962 with adhesive patch 984 onto the skin.
  • insertion device can position sensor 982 first, and then accompanying sensor control electronics can be coupled with sensor 982 afterwards, either manually or with the aid of a mechanical device.
  • Examples of insertion devices are described in US Patent Application Publication Nos. 2008/0009692, 2011/0319729, 2015/0018639, 2015/0025345, and 2015/0173661, all which are incorporated by reference herein in their entireties and for all purposes.
  • sensor control device 962 can apply analog signal conditioning to the data and convert the data into a digital form of the conditioned raw data.
  • this conditioned raw digital data can be encoded for transmission to another device (e.g., reader device 964), which then algorithmically processes that digital raw data into a final form representative of the subject’s measured biometric (e.g., a form readily made suitable for display to the subject or readily used in the analysis module 420B of FIG. 4).
  • This algorithmically processed data can then be formatted or graphically processed for digital display to the subject.
  • sensor control device 962 can algorithmically process the digital raw data into the final form that is representative of the subject’s measured biometric (e.g., analyte level) and then encode and wirelessly communicate that data to reader device 964, which in turn can format or graphically process the received data for digital display to the subject.
  • sensor control device 962 can graphically process the final form of the data such that it is ready for display, and display that data on a display of sensor control device 962 or transmit the data to reader device 964.
  • the final form of the biometric data (prior to graphic processing) is used by the system (e.g., incorporated into a diabetes monitoring regime) without processing for display to the subject.
  • sensor control device 962 and reader device 864 transmit the digital raw data to another computer system for algorithmic processing and display.
  • Reader device 964 can include a display 986 to output information to the subject (e.g., one or more physiological parameter or an output derived therefrom like cHbAlc) and/or to accept an input from the subject, and an optional input component 988 (or more), such as a button, actuator, touch sensitive switch, capacitive switch, pressure sensitive switch, jog wheel or the like, to input data, commands, or otherwise control the operation of reader device 964.
  • display 986 and input component 988 may be integrated into a single component, for example, where the display can measure the presence and location of a physical contact touch upon the display, such as a touch screen subject interface (which may be at least a portion of the subject interface 420A of FIG. 4).
  • input component 988 of reader device 964 may include a microphone and reader device 964 may include software configured to analyze audio input received from the microphone, such that functions and operation of the reader device 964 may be controlled by voice commands.
  • an output component of reader device 964 includes a speaker (not shown) for outputting information as audible signals. Similar voice responsive components such as a speaker, microphone and software routines to generate, process, and store voice driven signals may be included in sensor control device 962.
  • Reader device 964 can also include one or more data communication ports 990 for wired data communication with external devices such as computer system 968.
  • Example data communication ports 990 include, but are not limited to, USB ports, mini USB ports, USB Type-C ports, USB micro-A and/or micro-B ports, RS-232 ports, Ethernet ports, Firewire ports, or other similar data communication ports configured to connect to the compatible data cables.
  • Reader device 964 may also include an integrated or attachable in vitro glucose meter, including an in vitro test strip port (not shown) to receive an in vitro glucose test strip for performing in vitro blood glucose measurements.
  • Reader device 964 can display the measured biometric data wirelessly received from sensor control device 962 and can also be configured to output alarms (e.g., a visual alarm on a display, an auditory alarm, or a combination thereof), alert notifications, glucose levels, etc., which may be visual, audible, tactile, or any combination thereof. Further details and other display embodiments can be found in US Patent Application Publication No. 2011/0193704, for example, which is incorporated herein by reference in its entirety for all purposes.
  • alarms e.g., a visual alarm on a display, an auditory alarm, or a combination thereof
  • alert notifications e.g., glucose levels, etc.
  • Reader device 964 can function as a data conduit to transfer the measured data from sensor control device 962 to computer system 968 or trusted computer system 976.
  • the data received from sensor control device 962 may be stored (permanently or temporarily) in one or more memories of reader device 964 prior to uploading to computer system 968, trusted computer system 976, or network 972.
  • Computer system 968 may be a personal computer, a server terminal, a laptop computer, a tablet, or other suitable data processing device.
  • Computer system 968 can be (or include) software for data management and analysis and communication with the components in analyte monitoring system 960.
  • Computer system 968 can be used by the subject, a medical professional, or other user to display and/or analyze the biometric data measured by sensor control device 962.
  • sensor control device 962 can communicate the biometric data directly to computer system 968 without an intermediary such as reader device 964, or indirectly using an internet connection (also optionally without first sending to reader device 964). Operation and use of computer system 976 is further described in the ‘225 Publication incorporated herein.
  • Analyte monitoring system 960 can also be configured to operate with a data processing module (not shown), also as described in the incorporated ‘225 Publication.
  • Trusted computer system 976 can be within the possession of the manufacturer or distributor of sensor control device 962, either physically or virtually through a secured connection, and can be used to perform authentication of sensor control device 962, for secure storage of the subject’s biometric data, and/or as a server that serves a data analytics program (e.g., accessible via a web browser) for performing analysis on the subject’s measured data.
  • a data analytics program e.g., accessible via a web browser
  • an integrated diabetes management system may include an in vivo analyte monitoring system and a supplement/medication delivery system, and more specifically, an in vivo glucose monitoring system and an insulin delivery system (e.g., an insulin pump).
  • Integrated diabetes management systems may be closed-loop, open-loop, or a hybrid thereof. Closed- loop systems are in full control of analyte measurement times and supplement/medication dosages and times. Open-loop systems allow a subject to be in full control of analyte measurement times and supplement/medication dosages and times. Hybrid systems can rely primarily on a closed-loop system methodology but allows a subject to intervene.
  • in vitro analyte monitoring systems contact a bodily fluid outside of the body.
  • in vitro analyte monitoring systems include a meter device that has a port for receiving the bodily fluid of the subject (e.g., on an analyte test strip/swab or via collection of the bodily fluid), which can be analyzed to determine the subject’s analyte level.
  • a first nonlimiting example embodiment of the present disclosure is a method comprising: determining at least one physiological parameter for a subject selected from the group consisting of: a red blood cell glycation rate constant (k g iy), a red blood cell generation rate constant (k gen ), a red blood cell elimination constant (k a ge), an d an apparent glycation constant (K), based on (1) a plurality of first glucose levels and (2) a laboratory HbAlc level (e.g., one or more laboratory HbAlc levels) using a model that considers cross- membrane glucose transport and glycation; receiving (and/or measuring) a plurality of second glucose levels for the subject over a time period; and deriving a calculated HbAlc (cHbAlc) level (e.g., using Equation 9) for the subject based on the at least one physiological parameter and the plurality of second glucose levels.
  • a red blood cell glycation rate constant k g iy
  • the first nonlimiting example embodiment may further include one or more of: Element 1 : the method further comprising: diagnosing, treating, and/or monitoring the subject based on the cHbAlc level; Element 2: Element 1 and wherein treating the subject occurs and comprises administering and/or adjusting: an insulin dosage, a glycation medication dosage, an exercise regime, a meal intake, or a combination thereof; Element 3 : the method further comprising: displaying the cHbAlc level (e.g., on a system 310, a system 410, a glucose measurement device and/or closed-loop insulin pump system from which the plurality of first and/or second glucose levels were measured, or the like); Element 4: the method further comprising: calculating an adjusted HbAlc (aHbAlc) level for the subject based on the cHbAlc level, the k age , and a defined reference k age (k ref a ge) (e.g., using Equation 10);
  • a second nonlimiting example embodiment of the present disclosure is a method comprising: receiving (and/or measuring) a plurality of first glucose levels for a subject over a first time period; receiving (and/or measuring) a first glycated hemoglobin (HbAlc) level for the subject corresponding to an end of the first time period; determining at least one physiological parameter for the subject selected from the group consisting of a red blood cell glycation rate constant (k g iy), a red blood cell generation rate constant (k gen ), a red blood cell elimination constant (k a ge), an d an apparent glycation constant (K), based on (1) the plurality of first glucose levels and (2) the first HbAlc level using a model that considers cross-membrane glucose transport and glycation; receiving (and/or measuring) a plurality of second glucose levels for the subject over a second time period; and deriving a calculated HbAlc (cHbAlc) level (e.g
  • a third nonlimiting example embodiment of the present disclosure is an analyte sensor configured to measure a glucose level in a bodily fluid; and a monitoring device comprising: one or more processors; and a memory operatively coupled to the one or more processors storing instructions which, when executed by the one or more processors, causes the one or more processors to perform the method of first or second nonlimiting example embodiment optionally including one or more of Elements 1-29.
  • a fourth nonlimiting example embodiment of the present disclosure is closed-loop insulin pump systems comprising: an analyte sensor configured to measure a glucose level in a bodily fluid; an insulin pump; and a monitoring device comprising: one or more processors; and a memory operatively coupled to the one or more processors storing instructions which, when executed by the one or more processors, causes the one or more processors to perform the method of first or second nonlimiting example embodiment (optionally including one or more of Elements 1-29), where, when treatment is administered, said treatment includes administering via the closed-loop insulin pump systems an insulin dosage.
  • a fifth nonlimiting example embodiment is a method comprising: receiving (and/or measuring) a laboratory HbAlc level (e.g., one or more laboratory HbAlc levels) for a subject; determining a red blood cell turnover rate (kage) for the subject (e.g., using a model that considers cross-membrane glucose transport and glycation); and calculating an adjusted HbAlc (aHbAlc) level for the subject based on the HbAlc level, the k age , and a defined reference k age (k re f age ) (e.g., using Equation 10).
  • a laboratory HbAlc level e.g., one or more laboratory HbAlc levels
  • kage red blood cell turnover rate
  • aHbAlc adjusted HbAlc
  • Element 30 the method further comprising: diagnosing, treating, and/or monitoring the subject based on the aHbAlc level
  • Element 31 Element 30 and wherein treating the subject occurs and comprises administering and/or adjusting: an insulin dosage, a glycation medication dosage, an exercise regime, a meal intake, or a combination thereof
  • Element 32 the method further comprising: displaying the aHbAlc level (e.g., on a system 310, a system 410, a glucose measurement device and/or closed-loop insulin pump system from which the plurality of first and/or second glucose levels were measured, or the like)
  • Element 33 the method further comprising: deriving a personalized-target glucose range (e.g., using Equations 13 and 15), a personalized glucose upper limit (e.g., using Equation 15), and/or a personalized glucose lower limit (e.g., using Equation 13), based on the aHbAlc
  • a sixth nonlimiting example embodiment is a method comprising: receiving (and/or measuring) a laboratory HbAlc level (e.g., one or more laboratory HbAlc levels) for a subject; determining an apparent glycation constant (K) for the subject (e.g., using a model that considers cross-membrane glucose transport and glycation); and calculating an adjusted HbAlc (aHbAlc) level for the subject based on the HbAlc level, the K, and a defined reference K (K re f) (e.g., using Equation 11).
  • the sixth nonlimiting example embodiment may further include one or more of Elements 30-47.
  • a seventh nonlimiting example embodiment is a method comprising: receiving (and/or measuring) a plurality of first glucose levels for a subject over a first time period; receiving (and/or measuring) a first glycated hemoglobin (HbAlc) level for the subject corresponding to an end of the first time period; determining at least one physiological parameter for the subject selected from the group consisting of: a red blood cell glycation rate constant k giy ), a red blood cell generation rate constant (k gen ), a red blood cell elimination constant (k a ge), an d an apparent glycation constant (K), based on (1) the plurality of first glucose levels and (2) the first HbAlc level using a model that considers cross-membrane glucose transport and glycation; and calculating an adjusted HbAlc (aHbAlc) level for the subject based on the HbAlc level, the k age , and a defined reference k age (k ref age) (
  • a eighth nonlimiting example embodiment is a method comprising: receiving (and/or measuring) a plurality of first glucose levels for a subject over a first time period; receiving (and/or measuring) a first glycated hemoglobin (HbAlc) level for the subject corresponding to an end of the first time period; determining at least one physiological parameter for the subject selected from the group consisting of: a red blood cell glycation rate constant (k giy ), a red blood cell generation rate constant (k gen ), a red blood cell elimination constant (k a ge , and an apparent glycation constant (K), based on (1) the plurality of first glucose levels and (2) the first HbAlc level using a model that considers cross-membrane glucose transport and glycation; and calculating an adjusted HbAlc (aHbAlc) level for the subject based on the HbAlc level, the K, and a defined reference K K re f ) (e.g.
  • Measuring glucose levels may involve sampling a bodily fluid from the subject using an analyte sensor; and measuring the plurality of first glucose levels with the analyte sensor.
  • the second nonlimiting example embodiment may further include one or more of Elements 30-47.
  • a ninth nonlimiting example embodiment of the present disclosure is an analyte sensor configured to measure a glucose level in a bodily fluid; and a monitoring device comprising: one or more processors; and a memory operatively coupled to the one or more processors storing instructions which, when executed by the one or more processors, causes the one or more processors to perform the method of the fifth or sixth or seventh or eighth nonlimiting example embodiment (optionally including include one or more of Elements 30-47).
  • a tenth nonlimiting example embodiment of the present disclosure is a closed-loop insulin pump systems comprising: an analyte sensor configured to measure a glucose level in a bodily fluid; an insulin pump; and a monitoring device comprising: one or more processors; and a memory operatively coupled to the one or more processors storing instructions which, when executed by the one or more processors, causes the one or more processors to perform the method of the fifth or sixth or seventh or eighth nonlimiting example embodiment (optionally including include one or more of Elements 30-47), where, when treatment is administered, said treatment includes administering via the closed-loop insulin pump systems an insulin dosage.
  • An eleventh nonlimiting example embodiment of the present disclosure is a method comprising: determining at least one physiological parameter for a subject selected from the group consisting of: a red blood cell glycation rate constant (k giy ), a red blood cell generation rate constant (kgen), a red blood cell elimination constant (k age ), and an apparent glycation constant (K), based on (1) a plurality of first glucose levels and (2) a laboratory HbAlc level (e.g., one or more laboratory HbAlc levels) using a model that considers crossmembrane glucose transport and glycation; receiving (and/or measuring) a plurality of second glucose levels for the subject over a time period; and deriving a personalized glucose level (e.g., using Equation 16 or Equation 17) based on the k giy , a defined reference k giy (k re f gi y ), and a measured glucose level.
  • a personalized glucose level e.
  • the eleventh nonlimiting example embodiment may further include one or more of: Element 50: and the method further comprising: diagnosing, treating, and/or monitoring the subject based on the personalized glucose level (e.g., the personalized glucose level relative to a currently accepted glucose range or an intracellular glucose level relative to a currently accepted intracellular glucose level range (i.e., LIGL-UIGL)); Element 51 : Element 50 and wherein treating the subject occurs and comprises administering and/or adjusting: an insulin dosage, a glycation medication dosage, an exercise regime, a meal intake, or a combination thereof; Element 52: the method further comprising: displaying the personalized glucose level (e.g., on a system 310, a system 410, a glucose measurement device and/or closed-loop insulin pump system from which the plurality of first and/or second glucose levels were measured, or the like); and Element 53: the method further comprising: displaying (visually, audibly, and/or haptically (relating to touch)) an alarm when the
  • a twelfth nonlimiting example embodiment of the present disclosure is a method comprising: receiving (and/or measuring) a plurality of first glucose levels for a subject over a first time period; receiving (and/or measuring) a first glycated hemoglobin (Elb Ale) level for the subject corresponding to an end of the first time period; determining at least one physiological parameter for the subject selected from the group consisting of: a red blood cell glycation rate constant (k giy ), a red blood cell generation rate constant (k gen ), a red blood cell elimination constant (k a ge), an d an apparent glycation constant (K), based on (1) the plurality of first glucose levels and (2) the first Elb Ale level using a model that considers cross-membrane glucose transport and glycation; receiving (and/or measuring) a measured glucose level; and deriving a personalized glucose level (e.g., using Equation 16 or Equation 17) based on the k giy ,
  • a thirteenth nonlimiting example embodiment of the present disclosure is an analyte sensor configured to measure a glucose level in a bodily fluid; and a monitoring device comprising: one or more processors; and a memory operatively coupled to the one or more processors storing instructions which, when executed by the one or more processors, causes the one or more processors to perform the method of eleventh or twelfth nonlimiting example embodiment optionally including one or more of Elements 50-53.
  • a fourteenth nonlimiting example embodiment of the present disclosure is closed- loop insulin pump systems comprising: an analyte sensor configured to measure a glucose level in a bodily fluid; an insulin pump; and a monitoring device comprising: one or more processors; and a memory operatively coupled to the one or more processors storing instructions which, when executed by the one or more processors, causes the one or more processors to perform the method of eleventh or twelfth nonlimiting example embodiment (optionally including one or more of Elements 50-53), where, when treatment is administered, said treatment includes administering via the closed-loop insulin pump systems an insulin dosage.
  • the phrase “at least one of’ preceding a series of items, with the terms “and” or “or” to separate any of the items, modifies the list as a whole, rather than each member of the list (i.e., each item).
  • the phrase “at least one of’ allows a meaning that includes at least one of any one of the items, and/or at least one of any combination of the items, and/or at least one of each of the items.
  • the phrases “at least one of A, B, and C” or “at least one of A, B, or C” each refer to only A, only B, or only C; any combination of A, B, and C; and/or at least one of each of A, B, and C.
  • Example 1 The glucose monitoring data for 200 days and three HbAlc values for a single patient was used to verify the model described herein.
  • FIG. 10 is a plot of the glucose monitoring data (right y-axis) for 200 days, the three HbAlc values (left y-axis), and the estimated HbAlc values (left y-axis) based on the 14-day eHbAlc model. As illustrated, the estimated HbAlc derived from the 14-day HbAlc model has very dramatic changes over time. However, it is unlikely that HbAlc can change this fast.
  • FIG. 11 is the plot of FIG. 10 with a cHbAlc (left y-axis) for the first 100 days determined using k giy and k age per the methods described herein.
  • FIG. 12 is the plot of FIG. 11 with the cHbAlc (extension from day 100 to day 200, left y-axis) for the following 100 days using the k giy and k age determined relative to FIG. 11 per the methods described herein.
  • the third HbAlc value was not considered in this method, but the model described herein, predicted the measured value of the third HbAlc value, which illustrates that the model described herein is in close agreement with reality.
  • FIG. 13A is the cross-plot comparison of the estimated HbAlc level (per the 14-day glucose model) compared to laboratory HbAlc level
  • FIG. 13B is the cross-plot comparison of the cHbAlc level (per the methods described herein) compared to laboratory HbAlc level.
  • the 14-day glucose model has an R 2 value of 0.63, while the methods described herein yield a R 2 of 0.88, which illustrates about a 50% reduction in variation.
  • CGM Continuous glucose monitoring
  • laboratory Hb Al c data from 139 type 1 and 148 type 2 diabetes patients, enrolled onto two previous European clinical studies, were used to calculate Elb Al C as detailed below. Both studies were conducted after appropriate ethical approval and participants gave written informed consent.
  • a total of 6 months CGM data were collected using the sensor-based flash glucose monitoring system (FREESTYLE LIBRETM; Abbott Diabetes Care, Witney, UK), while HbAlC was measured by a central laboratory (ICON Laboratories, Dublin, Ireland) at 0, 3, and 6 months of the study. Analysis was conducted with a minimum of 80% CGM coverage and no gaps in glucose data greater than 12 hrs.
  • RBC removal by senescence and eryptosis are complex processes and known to vary both within and across individuals.
  • Previous work attempted to account for average RBC age variation to accurately reflect HbAlC.
  • this work made no adjustment for potential differences in RBC cross-membrane glucose uptake.
  • a kinetic model for glucose levels and hemoglobin A1C provides a novel tool for individualized diabetes management. J Diab Sci Tech. 2020. DOI: 10.1177/1932296819897613; herein “Xu Y et al. 2020”).
  • FIG. 14 is a plot of laboratory HbAlc compared to aHbAlC (“aAlC”) by RBC lifespan.
  • the open squares represent similar lab Ale but different aAlc (solid squares) secondary to variable RBC lifespan.
  • the open stars show different laboratory HbAlc but similar aHbAlc (solid stars).
  • CGM Continuous glucose monitoring
  • laboratory Hb Al c data from 139 type 1 and 148 type 2 diabetes patients, enrolled onto two previous European clinical studies [10, 11], were evaluated to calculate aHbAlc as detailed below. Both studies were conducted after appropriate ethical approval and participants gave written informed consent. A total of 6 months CGM data were collected using the sensor-based flash glucose monitoring system (FreeStyle LibreTM; Abbott Diabetes Care, Witney, UK), while HbAlc was measured by a central laboratory (ICON Laboratories, Dublin, Ireland) at 0, 3, and 6 months of the study.
  • the mean age was 44 years (range 18-70 years), 17 (33%) of whom were females.
  • T2D the mean age was 59 years (range 33-77 years), 28 (35%) of whom were females.
  • the analysis required a minimum of 70% CGM coverage and no gaps in glucose data greater than 48 hours. Each had at least one data section consisting of two HbAlc measurements connected by CGM data. Further, the parameters were successfully estimated for those individuals with sufficient day-to-day glucose variability, as evidenced by the model fit of RBC life converging between 50 and 180 days.
  • RBC turnover rate (ka9e), RBC lifespan (LRBc) and mean RBC age (MARBc)
  • the adjustment is not symmetric, decreasing RBC lifespan corresponds to more aHbAlc adjustment than a comparable increase in RBC lifespan.
  • FIG. 15 shows the adjustment to the laboratory HbAlc at different RBC lifespans. Near the borders of the interquartile range, two subjects with an identical laboratory HbAlc of 63 mmol/mol (7.9%) but different RBC lifespans of 84 and 101 days, would have RBC-lifespan-adjusted aHbAlc values of 78 mmol/mol (9.3%) and 62 mmol/mol (7.8%), respectively, indicating different future risk of diabetes complications.
  • the RBC lifespan can be measured directly, which requires complicated labeling and tracing of RBCs, a process that is difficult to implement in routine clinical practice (6).
  • Example 4 Continuous glucose monitoring (CGM) and laboratory Hb Al c data from 31 type 1 diabetes patients. These individuals all had type 1 diabetes managed by a sensor- augmented pump system. The data set contained on average about 10 laboratory HbAlc values spaced by approximately 1 month for each individual, with continuous glucose monitoring throughout. A total of 304 laboratory HbAlc values were available with paired 14-day periods of CGM for analysis. The intracellular glucose (IG) was determined throughout using the Equation 17.
  • FIG. 16A is a cross-plot and correlation of the mean 14-day IG values with the aHbAlc was prepared
  • FIG. 16B is a cross-plot of the originally-collected data of 14- day mean plasma glucose (PG) and laboratory HbAlc.
  • the IG method has an R 2 value of 0.93, while the original, unadjusted data yielded a R 2 of 0.75, which illustrates a significant reduction in variation.
  • Example 5 Continuous glucose monitoring (CGM) and laboratory Hb Al c data from 31 type 1 diabetes patients. These individuals all had type 1 diabetes managed by a sensor- augmented pump system. The data set contained on average about 10 laboratory HbAlc values spaced by approximately 1 month for each individual, with continuous glucose monitoring throughout. A total of 304 laboratory HbAlc values were available with paired 14-day periods of CGM for analysis. The effective plasma glucose (PG e ff) was determined throughout using the Equation 16.
  • FIGS. 17A and 17B are examples of a glucose pattern insight report for the same subject (an individual with Stage 2, Mild Kidney loss) using the measured plasma glucose (PG) and the PG e ff, respectively.
  • the PG e ff indicates excess glucose exposure in organs and tissues, and therefore a potential source for the kidney damage.
  • the time above target of 180 mg/dL changes from 6.7% for PG to 37.2% for PG e ff, and the time below target of 70 mg/dL decreases from 3.3% to 0.7%.
  • the disclosure of this application also contains a method for determining a time for obtaining laboratory glycated hemoglobin measurements can include receiving at least one glucose level for a subject during at least one time period, receiving a first measured glycated hemoglobin (HbAlc) level for the subject corresponding to a beginning of a first time period of the at least one time period, determining a first calculated glycated hemoglobin (HbAlc) level corresponding to the first time period, determining for the first time period a second calculated glycated hemoglobin (HbAlc) level using a first offset value, determining for the first time period a third calculated glycated hemoglobin (HbAlc) level using a second offset value, calculating a first difference between the first calculated glycated hemoglobin (HbAlc) level and the second calculated glycated hemoglobin (HbAlc) level, calculating a second difference between the first calculated glycated hemoglob
  • a method for determining a time for obtaining laboratory glycated hemoglobin measurements comprising: receiving at least one glucose level for a subject during at least one time period; receiving a first measured glycated hemoglobin (HbAlc) level for the subject corresponding to a beginning of a first time period of the at least one time period; determining a first calculated glycated hemoglobin (HbAlc) level corresponding to the first time period; determining for the first time period a second calculated glycated hemoglobin (HbAlc) level using a first offset value; determining for the first time period a third calculated glycated hemoglobin (HbAlc) level using a second offset value; calculating a first difference between the first calculated glycated hemoglobin (HbAlc) level and the second calculated glycated hemoglobin (HbAlc) level; calculating a second difference between the first calculated glycated hemoglobin (HbAlc
  • Equation A where k age is a red blood cell elimination constant, where k giy is a red blood cell glycation rate constant, where KM is a constant value, where [G z ] is an average glucose level over a corresponding time period z, where [G] is an average glucose level over a corresponding time period i, where [Gj] is an average glucose level over a corresponding time period j, where ti is a length of time interval of a corresponding time period i, where tj is a length of time interval of a corresponding time period j, where t z is a length of time interval of a corresponding time period z; wherein the first offset value is a first predetermined offset of k age ; and wherein the second offset value level is a second predetermined offset of k giy .
  • Clause 3 The method of clause 1 or 2, further: comprising generating a second alert notification if the first difference and the second difference are equal to or below the first predetermined threshold value.
  • Clause 4 The method of clause 3, further: wherein the first alert notification includes generating a prompt.
  • Clause 5 The method of any preceding clause, further: wherein the first difference or the second difference is above the first predetermined threshold value for the first time period and the method further comprises receiving the second measured glycated hemoglobin (HbAlc) level corresponding to the first time period.
  • HbAlc glycated hemoglobin
  • Clause 6 The method of clause 5, further: treating the subject based on the second measured glycated hemoglobin (HbAlc) level, wherein treating the subject comprises administering and/or adjusting an insulin dosage, a glycation-medication dosage, an exercise regime, a meal intake, or a combination thereof.
  • HbAlc glycated hemoglobin
  • Clause 7 The method of clause 5 or 6, further: adjusting a therapeutic profile or treatment regimen based on the second glycated hemoglobin (HbAlc) level, outputting a first a therapeutic profile or treatment regimen based on the second glycated hemoglobin (HbAlc) level, and/or administering a pharmaceutical compound to the subject based on the second measured glycated hemoglobin (HbAlc) level.
  • Clause 8 The method of any preceding clause, further: wherein a duration of the first time period is about one day in length, and wherein tj is 1, ti is 1 and t z is 1.
  • a duration of the first time period is about 1 hour to about 24 hours, wherein the at least one glucose level is obtained from an analyte monitoring device wherein the at least one glucose level is at least two glucose levels, and/or wherein ti is the of number of hours between received glucose levels divided by the number of hours in time period i.
  • Clause 10 The method of clause 9, further: wherein a duration between glucose measurements is about 4 hours.
  • Clause 12 The method of any preceding clause, wherein the received glucose level is received from a continuous glucose monitoring system and includes receiving a mean absolute relative difference for the first time period from the continuous glucose monitoring system. Clause 13. The method of clause 12, wherein the glucose measurements are received when the mean absolute relative difference from the continuous glucose monitoring system is less than 8%.
  • Clause 14 The method of clause 12 or 13, wherein the first predetermined threshold is at least .15% (NGSP) if the received mean absolute relative difference is less than a second predetermined threshold.
  • NGSP .15%
  • Clause 15 The method of any of clauses 12 to 14, wherein the first predetermined threshold is at least .25% (NGSP) if the received mean absolute relative difference is more than a third predetermined threshold.
  • NGSP .25%
  • Clause 17 The method of any preceding clause, wherein the first estimated initial value is 1/105 day' 1 .
  • Clause 18 The method of any preceding clause, wherein the second estimated initial value is 6.2x10-6 dL * mg * day -1 .
  • Clause 20 The method of any preceding clause, wherein the first alert notification identifies as a recommended time period the time period corresponding to the at least one of the first difference, second difference, third difference, or fourth difference which is equal to or exceeds the first predetermined threshold value.
  • a method for determining a recommended time period for obtaining laboratory glycated hemoglobin measurements comprising: receiving at least one glucose level for a subject over at least one time period; receiving a first measured glycated hemoglobin (HbAlc) level for the subject corresponding to a beginning of a first time period of the at least one time period; determining a first calculated glycated hemoglobin (HbAlc) level corresponding to the first time period using equation A; determining for the first time period a second calculated glycated hemoglobin (HbAlc) level using equation A, wherein k age is set to a first predetermined offset value; determining for the first time period a third calculated glycated hemoglobin (HbAlc) level using equation A, wherein k giy is set to a second predetermined offset value;
  • a system for determining a time for obtaining laboratory glycated hemoglobin measurements comprising: an analyte monitoring device configured to measure a glucose level; one or more processors; and a memory operatively coupled to the one or more processors and having instructions stored thereon which, when executed by the one or more processors, causes the one or more processors to: receive at least one glucose level for a subject during at least one time period; receive a first measured glycated hemoglobin (HbAlc) level for the subject corresponding to a beginning of a first time period of the at least one time period; determine a first calculated glycated hemoglobin (HbAlc) level corresponding to the first time period; determine for the first time period a second calculated glycated hemoglobin (HbAlc) level using a first offset value; determine for the first time period a third calculated glycated hemoglobin (HbAlc) level using a second offset value; calculate a first difference between the
  • Equation A where k age is a red blood cell elimination constant, where k giy is a red blood cell glycation rate constant, where KM is a constant value, where [G z ] is an average glucose level over a corresponding time period z, where [G] is an average glucose level over a corresponding time period i, where [Gj] is an average glucose level over a corresponding time period j, where ti is a length of time interval of a corresponding time period i, where tj is a length of time interval of a corresponding time period j, where t z is a length of time interval of a corresponding time period z; wherein the first offset value is a first predetermined offset of k age ; and wherein the second offset value level is a second predetermined offset of k giy .
  • Clause 24 The system of clause 22 or 23, further comprising instructions which causes the one or more processors to generate a second alert notification if the first difference and the second different are equal to or below the first predetermined threshold value.
  • Clause 25 The system of clause 22, further: wherein the first alert notification includes generate a prompt.
  • Clause 26 The system of any of clauses 22 to 25, further: wherein the first difference or the second difference is above the first predetermined threshold value for the first time period and further comprising instructions which causes the one or more processors to receive the second measured glycated hemoglobin (HbAlc) level corresponding to the first time period.
  • Clause 27 The system of clause 26, further comprising instructions which causes the one or more processors to treat the subject based on the second measured glycated hemoglobin (HbAlc) level, wherein treating the subject comprises administering and/or adjusting an insulin dosage, a glycation-medication dosage, an exercise regime, a meal intake, or a combination thereof.
  • Clause 28 The system of clause 26 or 27, further comprising instructions which causes the one or more processors to adjust a therapeutic profile or treatment regimen based on the second glycated hemoglobin (HbAlc) level, output a first a therapeutic profile or treatment regimen based on the second glycated hemoglobin (HbAlc) level, and/or administer a pharmaceutical compound to the subject based on the second measured glycated hemoglobin (HbAlc) level.
  • Clause 29 The system of any of clauses 22 to 28, further: wherein a duration of the first time period is about one day in length, and wherein tj is 1, ti is 1 and t z is 1.
  • Clause 32 The system of any of clauses 22 to 31, further: wherein the first predetermined threshold is approximately 0.2% (NGSP).
  • a system for determining a recommended time period for obtaining laboratory glycated hemoglobin measurements comprising: an analyte monitoring device configured to measure a glucose level; one or more processors; and a memory operatively coupled to the one or more processors and having instructions stored thereon which, when executed by the one or more processors, causes the one or more processors to: receive at least one glucose level for a subject over at least one time period; receive a first measured glycated hemoglobin (HbAlc) level for the subject corresponding to a beginning of a first time period of the at least one time period; determine a first calculated glycated hemoglobin (HbAlc) level corresponding to the first time period using equation A; determine for the first time period a second calculated glycated hemoglobin (HbAlc) level using equation A, wherein k age is set to a first predetermined offset value; determine for the first time period a third calculated glycated hemoglobin (HbA
  • Clause 46 A computer program, computer program product or computer readable medium comprising software code adapted, when executed by a computer system, to perform a method as set out in any of clauses 1 to 21.

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Abstract

Un procédé de détermination d'un temps d'obtention de mesures d'hémoglobine glyquée de laboratoire peut comprendre la réception d'au moins un niveau de glucose pour un sujet pendant au moins une période de temps, la réception d'un premier niveau d'hémoglobine glyquée mesuré (HbAlc) pour le sujet correspondant à un début d'une première période de temps de la ou des périodes de temps, la détermination d'un premier niveau d'hémoglobine glyquée calculé (HbAlc) correspondant à la première période de temps, la détermination pour la première période de temps d'un second niveau d'hémoglobine glyquée calculé (HbAlc) à l'aide d'une première valeur de décalage, la détermination pour la première période de temps a troisième HbAlc) calculé à l'aide d'une deuxième valeur de décalage, calculer une première différence entre le premier niveau d'hémoglobine glyquée (HbAlc) calculé et le deuxième niveau d'hémoglobine glyquée (HbAlc) calculé, calculer une deuxième différence entre le premier niveau d'hémoglobine glyquée (HbAlc) calculé et le troisième niveau d'hémoglobine glyquée (HbAlc) calculé, et générer une notification d'alerte pour obtenir un deuxième niveau d'hémoglobine glyquée (HbAlc) mesuré pour le sujet en réponse à une détermination que la première différence ou la deuxième différence est supérieure à une première valeur seuil prédéterminée.
PCT/US2024/047375 2023-09-21 2024-09-19 Procédés, dispositifs, et systèmes d'ajustement de valeurs de hba1c vérifiées en laboratoire Pending WO2025064603A1 (fr)

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