Exenatide treatment for 6 months improves insulin sensitivity in adults with type 1 diabetes.
rct · Level II
Where this comes from
- Record sourced from PubMed, PMID 24194508.
- Also identified by DOI 10.2337/dc13-1473 and PMC identifier 3931382.
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Abstract
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. 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. 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. 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.
Medical subject headings
- Diabetes Mellitus, Type 1
- Hypoglycemic Agents
- Peptides
- Venoms