Research

Hormonal

Once-weekly subcutaneous semaglutide 2.4 mg reduces the risk of major kidney composite endpoints (including macroalbuminuria and persistent eGFR decline) in patients with overweight/obesity and established cardiovascular disease, regardless of diabetes status.

If you have obesity and heart disease but no diabetes, semaglutide 2.4mg weekly offers significant kidney protection. It reduces the risk of serious kidney events like needing dialysis or developing heavy protein in the urine. While there is a temporary initial dip in kidney filtration numbers, long-term outcomes are better than placebo. This is a standard-of-care option for kidney risk reduction in this specific high-risk group.

StrongSupportsHIGH confidence
The incidence of the pre-specified main composite kidney endpoint... was lower with semaglutide (1.8%) versus placebo (2.2%): hazard ratio (HR) = 0.78; 95% confidence interval (CI) 0.63, 0.96; P = 0.02.
Helen M. Colhoun et al. · Nature Medicine · 2024

Why this rating

Large randomized controlled trial (n=17,604) with long follow-up (median 182 weeks) and pre-specified endpoints.

Source

Long-term kidney outcomes of semaglutide in obesity and cardiovascular disease in the SELECT trial

Helen M. Colhoun et al. · Nature Medicine · 2024

DOI 10.1038/s41591-024-03015-5

rct · n=17604Cited 193×
Read the paper
DOI resolved against Crossref · corpus check 2026-06-10

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