
Glucagon-like peptide-1 receptor agonists, such as semaglutide, are currently recommended for cardiovascular (CV) prevention only in patients with diabetes and high CV risk.1 They have also shown a >15% mean weight reduction benefit in patients without diabetes; however, it was previously unknown if they reduce CV risks in this population.2
The Semaglutide Effects on Cardiovascular Outcomes in People with Overweight or Obesity trial (SELECT) is a multicenter, double-blind, randomized, placebo-controlled trial that was presented at the American Heart Association’s Scientific Sessions on October 11, 2023, by Michael Lincoff, MD.3 SELECT enrolled 17,604 nondiabetic patients with a body mass index ≥27 and established CV disease (previous myocardial infarction, stroke, or symptomatic peripheral arterial disease). The primary CV end point (death from CV causes, nonfatal myocardial infarction, or nonfatal stroke) occurred in 569 of the 8803 patients (6.5%) in the once-weekly semaglutide 2.4-mg group and in 701 of the 8801 patients (8.0%) in the placebo group (hazard ratio, 0.80; 95% CI, 0.72-0.90; P<.001), a 20% relative risk reduction.
The incidence of serious adverse events (AEs) was higher in the placebo group (33.4% vs 36.4%; P<.001). However, AEs leading to discontinuation of semaglutide or placebo (mainly gastrointestinal symptoms) were more common in the semaglutide group (16.6% vs 8.2%; P<.001).