Glucagon Response to Oral Glucose Challenge in Type 1 Diabetes: Lack of Impact of Euglycemia

被引:28
作者
Kramer, Caroline K. [1 ,2 ]
Borgono, Carla A. [3 ]
Van Nostrand, Paula [1 ]
Retnakaran, Ravi [1 ,2 ,4 ]
Zinman, Bernard [1 ,2 ,4 ]
机构
[1] Mt Sinai Hosp, Leadership Sinai Ctr Diabet, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Div Endocrinol, Toronto, ON, Canada
[3] Univ Toronto, Div Gen Internal Med, Toronto, ON, Canada
[4] Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada
关键词
BETA-CELL FUNCTION; GLYCEMIC CONTROL; POSTPRANDIAL HYPERGLYCEMIA; INSULIN; SECRETION; SUPPRESSION; COUNTERREGULATION; MELLITUS; CHILDREN;
D O I
10.2337/dc13-2339
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Previous studies have demonstrated aberrant glucagon physiology in the setting of type 1 diabetes (T1D) but have not addressed the potential impact of ambient glycemia on this glucagon response. Thus, our objective was to evaluate the impact of euglycemia versus hyperglycemia on the glucagon response to an oral glucose challenge in T1D. RESEARCH DESIGN AND METHODS Ten adults with T1D (mean age 56.6 +/- 9.0 years, duration of diabetes 26.4 +/- 7.5 years, HbA(1c) 7.5% +/- 0.77, and BMI 24.1 kg/m(2) [22.6-25.4]) underwent 3-h 50-g oral glucose tolerance tests (OGTTs) on two separate days at least 24 h apart in random order under conditions of pretest euglycemia (plasma glucose [PG] between 4 and 6 mmol/L) and hyperglycemia (PG between 9 and 11 mmol/L), respectively. RESULTS Glycemic excursion on the OGTT was similar between the euglycemic and hyperglycemic tests (P = 0.72 for interaction between time postchallenge and glycemic setting). Interestingly, glucagon levels increased in response to the OGTT under both glycemic conditions (P < 0.001) and there were no differences in glucagon response between the euglycemic and hyperglycemic days (P = 0.40 for interaction between time postchallenge and glycemic setting). In addition, the incretin responses to the OGTT (glucose-dependent insulinotropic polypeptide, glucagon-like peptide-1, glucagon-like peptide-2) were also not different between the euglycemic and hyperglycemic settings. CONCLUSIONS In patients with T1D, there is a paradoxical increase in glucagon in response to oral glucose that is not reversed when euglycemia is achieved prior to the test. This abnormal glucagon response likely contributes to the postprandial hyperglycemia in T1D irrespective of ambient glycemia.
引用
收藏
页码:1076 / 1082
页数:7
相关论文
共 20 条
[1]   Impaired glucose tolerance (IGT) is associated with reduced insulin-induced suppression of glucagon concentrations [J].
Ahrén, B ;
Larsson, H .
DIABETOLOGIA, 2001, 44 (11) :1998-2003
[2]   Editorial: The role of glucagon in postprandial hyperglycemia - The jury's still out [J].
Bollyky, Jennifer ;
Greenbaum, Carla J. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (08) :2879-2881
[3]   Too much glucagon, too little insulin - Time course of pancreatic islet dysfunction in new-onset type 1 diabetes [J].
Brown, Rebecca J. ;
Sinah, Ninet ;
Rother, Kristina I. .
DIABETES CARE, 2008, 31 (07) :1403-1404
[4]  
DINNEEN S, 1995, DIABETOLOGIA, V38, P337, DOI 10.1007/BF00400639
[5]   Vildagliptin Reduces Glucagon during Hyperglycemia and Sustains Glucagon Counterregulation during Hypoglycemia in Type 1 Diabetes [J].
Farngren, Johan ;
Persson, Margaretha ;
Schweizer, Anja ;
Foley, James E. ;
Ahren, Bo .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2012, 97 (10) :3799-3806
[6]   Impaired β-cell function, incretin effect, and glucagon suppression in patients with type 1 diabetes who have normal fasting glucose [J].
Greenbaum, CJ ;
Prigeon, RL ;
D'Alessio, DA .
DIABETES, 2002, 51 (04) :951-957
[7]   Inappropriate glucagon response after oral compared with isoglycemic intravenous glucose administration in patients with type 1 diabetes [J].
Hare, Kristine J. ;
Vilsboll, Tina ;
Holst, Jens J. ;
Knop, Filip K. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2010, 298 (04) :E832-E837
[8]   Regulation of α-cell function by the β-cell in isolated human and rat islets deprived of glucose:: the "switch-off" hypothesis [J].
Hope, KM ;
Tran, POT ;
Zhou, HR ;
Oseid, E ;
Leroy, E ;
Robertson, RP .
DIABETES, 2004, 53 (06) :1488-1495
[9]   Four Weeks of Treatment With Liraglutide Reduces Insulin Dose Without Loss of Glycemic Control in Type 1 Diabetic Patients With and Without Residual β-Cell Function [J].
Kielgast, Urd ;
Krarup, Thure ;
Holst, Jens Juul ;
Madsbad, Sten .
DIABETES CARE, 2011, 34 (07) :1463-1468
[10]   The separate and combined impact of the intestinal hormones, GIP, GLP-1, and GLP-2, on glucagon secretion in type 2 diabetes [J].
Lund, Asger ;
Vilsboll, Tina ;
Bagger, Jonatan I. ;
Holst, Jens J. ;
Knop, Filip K. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2011, 300 (06) :E1038-E1046