دورية أكاديمية

Quantification of the Glycemic Response to Microdoses of Subcutaneous Glucagon at Varying Insulin Levels.

التفاصيل البيبلوغرافية
العنوان: Quantification of the Glycemic Response to Microdoses of Subcutaneous Glucagon at Varying Insulin Levels.
المؤلفون: El Youssef, Joseph, Castle, Jessica R., Bakhtiani, Parkash A., Haidar, Ahmad, Branigan, Deborah L., Breen, Matthew, Ward, W. Kenneth
المصدر: Diabetes Care; Nov2014, Vol. 37 Issue 11, p3054-3060, 7p, 2 Charts, 2 Graphs
مصطلحات موضوعية: TYPE 1 diabetes, GLUCAGON, HYPOGLYCEMIA, BLOOD sugar, INSULIN research
مستخلص: OBJECTIVE Glucagon delivery in closed-loop control of type 1 diabetes is effective in minimizing hypoglycemia. However, high insulin concentration lowers the hyperglycemic effect of glucagon, and small doses of glucagon in this setting are ineffective. There are no studies clearly defining the relationship between insulin levels, subcutaneous glucagon, and blood glucose. RESEARCH DESIGN AND METHODS Using a euglycemic clamp technique in 11 subjects with type 1 diabetes, we examined endogenous glucose production (EGP) of glucagon (25, 75, 125, and 175 µg) at three insulin infusion rates (0.016, 0.032, and 0.05 units/kg/h) in a randomized, crossover study. Infused 6,6-dideuterated glucose was measured every 10 min, and EGP was determined using a validated glucoregulatory model. Area under the curve (AUC) for glucose production was the primary outcome, estimated over 60 min. RESULTS At low insulin levels, EGP rose proportionately with glucagon dose, from 5 ± 68 to 112 ± 152 mg/kg (P = 0.038 linear trend), whereas at high levels, there was no increase in glucose output (19 ± 53 to 26 ± 38 mg/kg, P = NS). Peak glucagon serum levels and AUC correlated well with dose (r² = 0.63, P < 0.001), as did insulin levels with insulin infusion rates (r² = 0.59, P < 0.001). CONCLUSIONS EGP increases steeply with glucagon doses between 25 and 175 µg at lower insulin infusion rates. However, high insulin infusion rates prevent these doses of glucagon from significantly increasing glucose output and may reduce glucagon effectiveness in preventing hypoglycemia when used in the artificial pancreas. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:01495992
DOI:10.2337/dc14-0803