Semaglutide and cardiovascular outcomes by frailty status in SELECT (post hoc analysis)
Reported cardiovascular benefit of semaglutide was consistent across frailty strata, with fewer adverse-event discontinuations in more frail patients and more frailty-index improvement than worsening versus placebo. Hypothesis-generating; does not show preserved physical function in phenotypic frailty. Details taken from JAMA Medical News (30 Oct 2026) coverage; stratum-specific hazard ratios not verified.
Evidence
6/10
Moderate Evidence
Sample
—
subjects
Duration
—
study period
Journal
JAMA Cardiology
Sep 2026
Full Abstract
Secondary analysis of the SELECT phase 3 trial (semaglutide vs placebo, >17,000 adults with overweight/obesity and established cardiovascular disease) stratified by a 31-item Rockwood-style frailty index.
Key Findings
- 01
Lower MACE, all-cause hospitalization and all-cause mortality with semaglutide across frailty strata (as described; HRs not verified)
- 02
Fewer discontinuations for adverse events among more frail participants
- 03
Frailty index more likely to improve and less likely to worsen on semaglutide vs placebo
- 04
About two-thirds of participants were frail by index; ~3/4 male; mean age ~62
Structured Methods
- Study Design
- Post hoc analysis of RCT
- Sample Size
- Not reported
- Study Duration
- Not reported
- Methodology
- Post hoc secondary analysis of SELECT (randomized, double-blind, placebo-controlled); 31-item frailty index strata (not frail / more frail / most frail)
- Limitations
- Post hoc and hypothesis-generating. Mean age ~62 and predominantly male; frailty captured by a deficit-accumulation index rather than physical performance, so strength/sarcopenia outcomes are not established. SELECT excluded type 2 diabetes, class IV heart failure and end-stage kidney disease/dialysis. Publication date approximate (September 2026 per JAMA Medical News). HRs not verified.
Citations & References
Ostrominski JW et al. (2026). Semaglutide and cardiovascular outcomes by frailty status in SELECT (post hoc analysis). JAMA Cardiology. https://doi.org/10.1001/jamacardio.2026.3566
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