Treatment with exenatide once weekly or twice daily for 30 weeks is associated with changes in several cardiovascular risk markers.
Vasc Health Risk Manag · 2012
Last updated 2026-05-28In a 30-week study of 211 people with type 2 diabetes, those taking exenatide once weekly saw reductions in harmful blood fats like apolipoprotein B and triglycerides, as well as lower levels of a marker for inflammation called high sensitivity C-reactive protein. The once-weekly dose also increased protective HDL-2 cholesterol and shifted harmful small, dense LDL cholesterol to a less risky form, with these benefits occurring even when accounting for changes in blood sugar control and weight.
AI summary of the abstract below.
| Journal | Vasc Health Risk Manag, 2012 |
|---|---|
| Citations | 43 |
| Relative citation ratio | 1.34 |
| NIH percentile | 61 |
| Molecules | exenatide |
| Conditions studied | Cardiovascular Risk Reduction |
Abstract
BACKGROUND: Cyslipidemia and type 2 diabetes are two of the most significant risk factors for the development of cardiovascular disease. Measurement of lipoprotein subclasses provides important information about derangements in lipid metabolism and helps refine cardiovascular risk assessment. Exenatide, a glucagon-like peptide 1 receptor agonist, improved glycemic control, obesity, hypertension, and dyslipidemia in patients with type 2 diabetes in clinical trials.
METHODS: In the DURATION-1 trial, patients with type 2 diabetes were treated with exenatide once weekly or twice daily for 30 weeks. This post hoc analysis evaluated the impact of exenatide on lipoprotein subclasses in 211 DURATION-1 patients using vertical auto profile methodology and the Statistical Package for the Social Sciences general linear model adjusted for glycosylated hemoglobin (HbA(1c)) and weight.
RESULTS: Baseline lipids and high sensitivity C-reactive protein were normal overall based on the standard lipid panel. Once-weekly exenatide reduced apolipoprotein B and the apolipoprotein B to apolipoprotein A1 ratio (P < 0.05), independent of glycemic improvement and weight loss. A significant shift in lipoprotein pattern away from small, dense low-density lipoprotein-4 cholesterol was also observed (P < 0.05). Exenatide once weekly increased high-density lipoprotein-2 cholesterol, even after adjustment for changes in HbA(1c) and weight (P < 0.05). Triglycerides, very low-density lipoprotein cholesterol, and high sensitivity C-reactive protein were reduced with both the once-weekly and twice-daily exenatide regimens (P < 0.05).
CONCLUSION: In this post hoc analysis, exenatide significantly improved a number of cardiovascular risk markers. Continuous exenatide exposure with exenatide once weekly elicited a greater response than did immediate-release exenatide twice daily, generally independent of glycemic improvement and weight loss. Thus, in addition to improving glycemic control, exenatide induced favorable changes in lipid and lipoprotein metabolism and decreased systemic inflammation.
Verbatim abstract via PubMed 23166441 ↗
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