Effect of GLP-1 receptor agonists on weight and cardiovascular outcomes: A review.
Medicine (Baltimore) · 2024
Last updated 2026-05-28GLP-1 receptor agonists (GLP-1 RAs) are medications originally developed for type 2 diabetes that have been approved for weight loss due to their ability to help people lose significant and sustained weight. Two examples, semaglutide and liraglutide, have shown promise not only in weight loss but also in improving cardiovascular risk factors and outcomes in obese patients. These drugs work by mimicking a natural hormone that helps regulate appetite and blood sugar.
AI summary of the abstract below.
| Journal | Medicine (Baltimore), 2024 |
|---|---|
| Citations | 10 |
| Relative citation ratio | 2.40 |
| NIH percentile | 79 |
| Molecules | — |
| Conditions studied | Obesity, Cardiovascular Risk Reduction |
Abstract
Diet and lifestyle modifications remain the foundation of obesity treatment, but they have historically proven insufficient for significant, long-term weight loss. As a result, there is a high demand for new pharmacologic treatments to promote weight loss and prevent life-threatening diseases associated with obesity. Researchers are particularly interested in 1 type of drug, glucagon-like peptide 1 receptor agonists (GLP-1 RAs), because of its promising potential in addressing the limitations of non-pharmacologic treatments. In addition to their role in weight loss, these drugs have shown promising early evidence of cardiovascular benefits in obese patients, further enhancing their clinical relevance. Semaglutide and liraglutide, which were initially approved for the treatment of type 2 diabetes, have since been approved by the Food and Drug Administration as weight loss medications due to their effectiveness in promoting significant and sustained weight loss. In this narrative review, we will explore the mechanism of GLP-1 RAs, their effects on weight loss, cardiovascular risk factors and outcomes, common adverse effects, and strategies for managing these effects.
Verbatim abstract via PubMed 39496023 ↗