Exenatide treatment for 6 months improves insulin sensitivity in adults with type 1 diabetes

Diabetes Care. 2014;37(3):666-70. doi: 10.2337/dc13-1473. Epub 2013 Nov 5.

Abstract

Objective: Exenatide treatment improves glycemia in adults with type 2 diabetes and has been shown to reduce postprandial hyperglycemia in adolescents with type 1 diabetes. We studied the effects of exenatide on glucose homeostasis in adults with long-standing type 1 diabetes.

Research design and methods: Fourteen patients with type 1 diabetes participated in a crossover study of 6 months' duration on exenatide (10 μg four times a day) and 6 months off exenatide. We assessed changes in fasting and postprandial blood glucose and changes in insulin sensitivity before and after each study period.

Results: High-dose exenatide therapy reduced postprandial blood glucose but was associated with higher fasting glucose concentrations without net changes in hemoglobin A1c. Exenatide increased insulin sensitivity beyond the effects expected as a result of weight reduction.

Conclusions: Exenatide is a promising adjunctive agent to insulin therapy because of its beneficial effects on postprandial blood glucose and insulin sensitivity in patients with type 1 diabetes.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Intramural

MeSH terms

  • Adult
  • Blood Glucose / drug effects
  • Body Weight / drug effects
  • Cross-Over Studies
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 1 / drug therapy*
  • Drug Administration Schedule
  • Exenatide
  • Fasting / blood
  • Female
  • Glycated Hemoglobin / metabolism
  • Humans
  • Hyperglycemia / drug therapy
  • Hypoglycemic Agents / administration & dosage*
  • Insulin Resistance / physiology
  • Male
  • Middle Aged
  • Peptides / administration & dosage*
  • Postprandial Period / drug effects
  • Venoms / administration & dosage*

Substances

  • Blood Glucose
  • Glycated Hemoglobin A
  • Hypoglycemic Agents
  • Peptides
  • Venoms
  • Exenatide