Do sensor glucose levels accurately predict plasma glucose concentrations during hypoglycemia and hyperinsulinemia?

被引:111
作者
Monsod, TP
Flanagan, DE
Rife, F
Saenz, R
Caprio, S
Sherwin, RS
Tamborlane, WV
机构
[1] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06510 USA
[2] Yale Univ, Pediat Pharmacol Res Unit, Sch Med, New Haven, CT USA
[3] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Gen Clin Res Ctr, New Haven, CT 06510 USA
关键词
D O I
10.2337/diacare.25.5.889
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - The MiniMed Continuous Glucose Monitoring System (CGMS) measures subcutaneous interstitial glucose levels that are calibrated against three or more fingerstick glucose levels daily. The objective of the present Study was to examine whether the relationship between plasma and interstitial fluid glucose is altered by changes in plasma glucose and insulin levels and how such alterations might influence CGMS performance. RESEARCH DESIGN AND METHODS - Arterialized plasma glucose, sensor glucose, and interstitial fluid glucose were measured by microdialysis in 11 healthy subjects during a 1.0 mU (.) k(-1 .) min(-1) Stepped euglycemic-hypoglycemic-hyperglycemic (plasma glucose similar to5, 3.1, and 8.6 mmolA, respectively) insulin clamp that raised plasma insulin to -360-390 pmol/l. RESULTS - When the CGMS was calibrated versus plasma glucose levels before insulin infusion. basal sensor and plasma glucose were similar (5.0 +/- 0.3 vS. 5.2 +/- 0.3 mmol/l, respectively); dialysate alucose was 3.3 +/- 0.9 mmol/l. During the hyperinsulinemic-euglycemia study (plasma glucose 4.9 +/- 0.3 mmol/l), dialysate glucose fell by 30-35%, accompanied by a significant reduction in sensor glucose (to 3.7 +/- 0.6 mmol/l; P < 0.001 vs. plasma). Subsequently, sensor levels remained lower than plasma values during mild hypoglycemia (2.5 +/- 0.6 vs. 3.1 +/- 0.3 mmo/l P < 0.01) and during recovery from hypoglycemia (7.3 +/- 1.2 vs. 8.6 +/- 0.6 P < 0.01)- However, when the CGMS was calibrated against plasma glucose levels before and during each Step of the clamp, sensor glucose levels increased throughout the study and did not differ from plasma glucose values during hypoglycemia. CONCLUSIONS - Although hyperinsulinema may contribute to modest discrepancies between plasma and sensor glucose levels, the CGMS is able to accurately track acute changes in plasma glucose when calibrated across a range of plasma glucose and insulin levels.
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页码:889 / 893
页数:5
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共 13 条
  • [1] Interstitial glucose concentration and glycemia: implications for continuous subcutaneous glucose monitoring
    Aussedat, B
    Dupire-Angel, M
    Gifford, R
    Klein, JC
    Wilson, GS
    Reach, G
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 278 (04): : E716 - E728
  • [2] Continuous glucose monitoring used to adjust diabetes therapy improves glycosylated hemoglobin: a pilot study
    Bode, BW
    Gross, TM
    Thornton, KR
    Mastrototaro, JJ
    [J]. DIABETES RESEARCH AND CLINICAL PRACTICE, 1999, 46 (03) : 183 - 190
  • [3] Boland EA, 2001, DIABETES, V50, pA377
  • [4] MICRODIALYSIS MEASUREMENT OF THE ABSOLUTE GLUCOSE-CONCENTRATION IN SUBCUTANEOUS ADIPOSE-TISSUE ALLOWING GLUCOSE MONITORING IN DIABETIC-PATIENTS
    BOLINDER, J
    UNGERSTEDT, U
    ARNER, P
    [J]. DIABETOLOGIA, 1992, 35 (12) : 1177 - 1180
  • [5] CAPLIN NJ, 2000, J PEDIAT ENDOCRIN S4, V13, P31
  • [6] Continuous subcutaneous glucose monitoring in children with type 1 diabetes
    Chase, HP
    Kim, LM
    Owen, SL
    MacKenzie, TA
    Klingensmith, GJ
    Murtfeldt, R
    Garg, SK
    [J]. PEDIATRICS, 2001, 107 (02) : 222 - 226
  • [7] COUNTERREGULATION OF HYPOGLYCEMIA - SKELETAL-MUSCLE GLYCOGEN-METABOLISM DURING 3 HOURS OF PHYSIOLOGICAL HYPERINSULINEMIA IN HUMANS
    COHEN, N
    ROSSETTI, L
    SHLIMOVICH, P
    HALBERSTAM, M
    HU, MZ
    SHAMOON, H
    [J]. DIABETES, 1995, 44 (04) : 423 - 430
  • [8] EFFECTS OF PHYSIOLOGICAL HYPERINSULINEMIA ON COUNTERREGULATORY RESPONSE TO PROLONGED HYPOGLYCEMIA IN NORMAL HUMANS
    DAVIS, SN
    SHAVERS, C
    COLLINS, L
    CHERRINGTON, AD
    PRICE, L
    HEDSTROM, C
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (03): : E402 - E410
  • [9] Kaufman F R, 2000, Diabetes Technol Ther, V2 Suppl 1, pS49
  • [10] KERR D, 2000, DIABETOLOGIA S1, V44, P917