GLP-1 agonists associated with lower all-cause mortality in adults with obesity and elevated CRP (matched cohort study)
This matched cohort study compared 50,009 adults with obesity and C-reactive protein levels of 3-10 mg/L who received GLP-1 receptor agonists to a similar-sized group receiving metformin, orlistat, or phentermine. Over a median follow-up of up to 3,650 days, GLP-1 exposure was associated with a 39% lower hazard of the composite outcome of all-cause mortality, myocardial infarction, and ischemic stroke, with the strongest effect on all-cause mortality (39% lower hazard). Ischemic stroke, arrhythmias, and heart failure with reduced ejection fraction showed modest reductions, while myocardial infarction and heart failure with preserved ejection fraction did not differ significantly.
What this changes
The finding has not established an approved change to our evidence assessment.
Source date: Sep 21, 2026 · Discovered: Sep 22, 2026 · Assessed: — · Research update
What it does not prove
- Limitations have not yet been verified. Read the primary source.
Extracted from supplied source material; model confidence is not a measured probability of correctness.
Study details
- Design
- Cohort
- Sample size
- 100,018
- Duration
- 121 months
- Population
- Adults with body mass index ≥30 kg/m² and C-reactive protein (CRP) levels of 3-10 mg/L
- Primary outcome
- All-cause mortality, acute myocardial infarction, and ischemic stroke (composite outcome)
- Effect size
- Primary composite outcome: HR 0.799 (95% CI 0.772-0.825); All-cause mortality: HR 0.608 (95% CI 0.578-0.640)
- Significance
- Significant
- Journal
- The American journal of cardiology
- Published
- Sep 21, 2026
Sources
Primary source
- The American journal of cardiology ↗Peer reviewed
Assessment history
9/24/2026 · SUPERSEDED: Source updated; assessment withdrawn pending review.
Discussion (0)
One thread per scientific event, no matter how many outlets covered it.
No comments yet
Be the first to weigh in on this evidence.