Glucagon-like Peptide-1 Receptor Agonists and Cardiovascular Events: Class Effects versus Individual Patterns.
Trends Endocrinol Metab · 2018
Last updated 2026-05-28Some GLP-1 drugs, like liraglutide and semaglutide, reduced major heart-related events and death in people with Type 2 diabetes, while others, such as lixisenatide and extended-release exenatide, did not show these benefits. The review compares these drugs to help doctors choose the most effective options for improving heart health in their patients.
AI summary of the abstract below.
| Journal | Trends Endocrinol Metab, 2018 |
|---|---|
| Citations | 51 |
| Relative citation ratio | 1.85 |
| NIH percentile | 71 |
| Molecules | — |
| Conditions studied | Cardiovascular Risk Reduction |
Abstract
Several new glucose-lowering medications have been approved, such as dipeptidyl peptidase-4 inhibitors, glucagon-like peptide-1 receptor agonists (GLP-1RAs), and sodium glucose cotransporter-2 inhibitors. Among GLP-1RAs, lixisenatide, a short-acting drug, did not show cardiovascular (CV) benefits in patients with Type 2 diabetes mellitus (T2D) and acute coronary syndrome. Extended-release exenatide was also not significantly better for CV outcomes. By contrast, once daily liraglutide and once weekly semaglutide, both long-acting GLP-1RAs, decreased the incidence of major adverse CV events and mortality. This Review attempts to explain favorable CV results with some, but not all, GLP-1RAs, to aid in their differential prescription with the aim of further reducing the adverse CV burden of T2D.
Verbatim abstract via PubMed 29463450 ↗