Heart failure & cardiomyopathies

Semaglutide and cardiovascular outcomes in patients with obesity and prevalent heart failure: a prespecified analysis of the SELECT trial

LancetPublished Secondary analysis of the SELECT randomised trial

Authors' conclusion

In patients with atherosclerotic cardiovascular diease and overweight or obesity, treatment with semaglutide 2.4 mg reduced MACE and composite heart failure endpoints compared with placebo in those with and without clinical heart failure, regardless of heart failure subtype.

Study context

Population
Adults ≥45 years, BMI ≥27 kg/m², established CVD, with and without HF history (HFpEF, HFrEF, unclassified)4,286 (24.3%) with HF history
Participants
17,604 adults
Comparison
Semaglutide 2.4 mg once weekly vs placebo, by HF history and subtype
  • Semaglutiden = 8,803
  • Placebon = 8,801reference
Methodological detailsprespecified analysis, double-blind, placebo-controlled, multicentre, event-driven, phase 3, 41 countries
  • Prespecified analysis
  • Double-blind
  • Placebo-controlled
  • Multicentre
  • Event-driven
  • Phase 3
  • 41 countries

Primary result

As reported in the abstract

Semaglutide vs placebo in patients with HF at random assignment
Semaglutide vs PlaceboHazard ratio (95% CI)
MACE, HF
0.72(0.60–0.87)
HF composite endpoint, HF
0.79(0.64–0.98)
CV death, HF
0.76(0.59–0.97)
All-cause death, HF
0.81(0.66–1.00)
MACE, HFrEF
0.65(0.49–0.87)
Composite HF endpoint, HFrEF
0.79(0.58–1.08)
MACE, HFpEF
0.69(0.51–0.91)
Composite HF endpoint, HFpEF
0.75(0.52–1.07)

Further findings

Major adverse cardiovascular events (MACE) and HF composite, by baseline age, sex, BMI, NYHA status, diuretic use (subgroups)

No significant differences in benefits across subgroups

Safety

Serious adverse events

Less frequent with semaglutide vs placebo, regardless of HF subtype

Original publication

Semaglutide and cardiovascular outcomes in patients with obesity and prevalent heart failure: a prespecified analysis of the SELECT trial. Lancet. Published 24 August 2024. doi:10.1016/s0140-6736(24)01498-3

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