Vildagliptin Reduces Glucagon during Hyperglycemia and Sustains Glucagon Counterregulation during Hypoglycemia in Type 1 Diabetes

被引:89
作者
Farngren, Johan [1 ]
Persson, Margaretha [2 ]
Schweizer, Anja [3 ]
Foley, James E. [4 ]
Ahren, Bo [1 ]
机构
[1] Lund Univ, Dept Clin Sci, SE-22184 Lund, Sweden
[2] Lund Univ, Dept Clin Sci, SE-20041 Malmo, Sweden
[3] Novartis Pharma AG, CH-4002 Basel, Switzerland
[4] Novartis Pharmaceut, E Hanover, NJ 07936 USA
基金
瑞典研究理事会;
关键词
IMPROVES GLYCEMIC CONTROL; DRUG-NAIVE PATIENTS; GLUCOSE COUNTERREGULATION; CELL-FUNCTION; SECRETION; INSULIN; METFORMIN; EFFICACY; COMBINATION; MONOTHERAPY;
D O I
10.1210/jc.2012-2332
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Context: The dipeptidyl peptidase-4 inhibitor, vildagliptin, inhibits glucagon secretion at hyperglycemia but appears to enhance glucagon counterregulation during hypoglycemia in type 2 diabetes. Objective: The objective of the investigation was to study whether vildagliptin also improves alpha-cell function in type 1 diabetes (T1D). Patients and Methods: The study was a single-center, double-blind, randomized, placebo-controlled crossover study involving 28 patients with C-peptide negative and antibody positive T1D [ 21 males, seven females, glycosylated hemoglobin 57.9 mmol/mol (7.5%)]. Patients received vildagliptin (50 mg twice a day) or placebo as an add-on to their insulin therapy for 4 wk each. On d 28 of the respective treatment period, patients were served a standard meal (500 kcal) to raise the circulating incretin hormone levels followed by a hyperinsulinemic hypoglycemic clamp at 2.5 mmol/liter. Main Outcome Measure: The increase in plasma glucagon levels during the 30-min hypoglycemic clamp (min 165-195 of the test) was measured. Results: During the meal, glucagon levels were lower with vildagliptin than with placebo (120 min area under the curve(glucagon) 2.4 +/- 0.2 vs. 2.6 +/- 0.2 nmol/liter x minutes, P = 0.022 for between group difference). In contrast, during hypoglycemia, the glucagon counterregulation was not reduced by vildagliptin (increase in glucagon 1.5 +/- 1.0 pmol/liter with vildagliptin vs. 1.7 +/- 0.8 pmol/liter with placebo, P = NS). In addition, the counterregulatory responses in epinephrine, norepinephrine, cortisol, and pancreatic polypeptide were not different between the treatments. During the 4-wk treatment period, vildagliptin reduced the mean glycosylated hemoglobin, whereas there was no change with placebo [ between group difference was -3.4 +/- 1.0 mmol/mol (-0.32 +/- 0.09%; P = 0.002)] from baseline of 57.9 mmol/mol (7.5%). Conclusions: Vildagliptin, although inhibiting glucagon secretion during hyperglycemia, does not compromise the glucagon counterregulatory response during hypoglycemia in T1D. (J Clin Endocrinol Metab 97: 3799-3806, 2012)
引用
收藏
页码:3799 / 3806
页数:8
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