Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes
Cleveland Clinic Lerner College of Medicine · University College London
Abstract
Semaglutide, a glucagon-like peptide-1 receptor agonist, has been shown to reduce the risk of adverse cardiovascular events in patients with diabetes. Whether semaglutide can reduce cardiovascular risk associated with overweight and obesity in the absence of diabetes is unknown.
In a multicenter, double-blind, randomized, placebo-controlled, event-driven superiority trial, we enrolled patients 45 years of age or older who had preexisting cardiovascular disease and a body-mass index (the weight in kilograms divided by the square of the height in meters) of 27 or greater but no history of diabetes. Patients were randomly assigned in a 1:1 ratio to receive once-weekly subcutaneous semaglutide at a dose of 2.4 mg or placebo. The primary cardiovascular end point was a composite of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke in a time-to-first-event analysis. Safety was also assessed.
Citation impact
- FWCI
- 441.71
- Percentile
- 100%
- References
- 42
Authors
16- AMA. Michael LincoffCorresponding
Cleveland Clinic Lerner College of Medicine, University College London
- KBKirstine Brown‐Frandsen
Cleveland Clinic Lerner College of Medicine, University College London
- HMHelen M. Colhoun
Cleveland Clinic Lerner College of Medicine, University College London
- JDJohn Deanfield
Cleveland Clinic Lerner College of Medicine, University College London
- SSScott S. Emerson
Cleveland Clinic Lerner College of Medicine, University College London
Topics & keywords
- Semaglutide
- Medicine
- Placebo
- Hazard ratio
- Internal medicine
- Myocardial infarction
- Dulaglutide
- Diabetes mellitus
- Good health and well-being