Exenatide treatment for 6 months improves insulin sensitivity in adults with type 1 diabetes.
Diabetes Care · 2014
Last updated 2026-05-28In a 6-month study of 14 adults with type 1 diabetes, taking exenatide (10 μg four times a day) reduced blood sugar spikes after meals but increased fasting blood sugar levels. While overall blood sugar control (measured by hemoglobin A1c) did not change, the drug improved insulin sensitivity beyond what would be expected from weight loss alone.
AI summary of the abstract below.
| Journal | Diabetes Care, 2014 |
|---|---|
| Citations | 62 |
| Relative citation ratio | 2.03 |
| NIH percentile | 74 |
| Molecules | exenatide |
| Conditions studied | Type 2 Diabetes |
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.
Verbatim abstract via PubMed 24194508 ↗
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