Evaluation of exenatide versus insulin glargine for the impact on endothelial functions and cardiovascular risk markers.
Diabetes Res Clin Pract · 2014
Last updated 2026-05-28In a 26-week study of 34 people with type 2 diabetes, those taking exenatide saw decreases in high-sensitivity C-reactive protein (27.5%) and endothelin-1 (18.75%), while those on insulin glargine had increases in fibrinogen (13.4%), monocyte chemoattractant protein-1 (30.2%), leptin (47.5%), and endothelin-1 (80%). Both drugs improved blood vessel function, but only exenatide reduced body weight. Changes in body weight were linked to shifts in several heart-related markers in both groups.
AI summary of the abstract below.
| Journal | Diabetes Res Clin Pract, 2014 |
|---|---|
| Citations | 32 |
| Relative citation ratio | 1.06 |
| NIH percentile | 52 |
| Molecules | exenatide |
| Conditions studied | Cardiovascular Risk Reduction, Type 2 Diabetes |
Abstract
AIMS: To demonstrate the efficacy of exenatide versus insulin glargine on endothelial functions and cardiovascular risk markers.
METHODS: Thirty-four insulin and incretin-naive patients with type 2 diabetes mellitus (body mass index 25-45 kg/m(2)) who received metformin for at least two months were randomized to exenatide or insulin glargine treatment arms and followed-up for 26 weeks. Measurements of endothelial functions were done by ultrasonography, cardiovascular risk markers by serum enzyme-linked immunosorbent assay, and total body fat mass by bioimpedance.
RESULTS: Levels of high sensitivity-C-reactive protein and endothelin-1 decreased (27.5% and 18.75%, respectively) in the exenatide arm. However, in the insulin glargine arm, fibrinogen, monocyte chemoattractant protein-1, leptin and endothelin-1 levels (13.4, 30.2, 47.5, and 80%, respectively) increased. Post-treatment flow mediated dilatation and endothelium independent vascular responses were significantly higher in both arms (p=0.0001, p=0.0001). Positive correlation was observed between the changes in body weight and endothelium-independent vasodilatation, leptin, plasminogen activator inhibitor type 1 and endothelin-1 in both arms (r=0.376, r=0.507, r=0.490, r=0.362, respectively).
CONCLUSIONS: Insulin glargine improved endothelial functions, without leading to positive changes in cardiovascular risk markers. Exenatide treatment of 26 weeks resulted in reduced body weight and improvement in certain cardiovascular risk markers and endothelial functions.
Verbatim abstract via PubMed 25458329 ↗
Related research
- Effects of Once-Weekly Exenatide on Cardiovascular Outcomes in Type 2 Diabetes.
- Exenatide once weekly versus placebo in Parkinson's disease: a randomised, double-blind, placebo-controlled trial.
- Efficacy and safety of exenatide once weekly versus sitagliptin or pioglitazone as an adjunct to metformin for treatment of type 2 diabetes (DURATION-2): a randomised trial.
- Efficacy and Safety of Once-Weekly Semaglutide Versus Exenatide ER in Subjects With Type 2 Diabetes (SUSTAIN 3): A 56-Week, Open-Label, Randomized Clinical Trial.
- Exenatide reduces reperfusion injury in patients with ST-segment elevation myocardial infarction.
- Exenatide and the treatment of patients with Parkinson's disease.
- Use of twice-daily exenatide in Basal insulin-treated patients with type 2 diabetes: a randomized, controlled trial.
- Exenatide once weekly versus liraglutide once daily in patients with type 2 diabetes (DURATION-6): a randomised, open-label study.