Type 2 & other diabetes

Comparative effectiveness of GLP-1 receptor agonists on cardiovascular outcomes among adults with type 2 diabetes and moderate cardiovascular risk: emulation of a target trial

Diabetes Res Clin PractPublished Target trial emulation

Authors' conclusion

Among GLP-1RAs, semaglutide and liraglutide were associated with the greatest cardiovascular risk reduction in patients with T2D at moderate cardiovascular risk.

Study context

Population
Adults with T2D at moderate cardiovascular risk initiating a GLP-1 RA, 01/01/2014–12/31/2021, claims dataafter inverse probability of treatment weighted (IPTW)
Participants
35,572 / 4,376 / 8,843 / 33,063
Exposure
Dulaglutide vs exenatide vs liraglutide vs semaglutide
  • Dulaglutiden = 35,572reference
  • Exenatiden = 4,376
  • Liraglutiden = 8,843
  • Semaglutiden = 33,063
Outcome
Time to MACE (MACE):
  • MI
  • Stroke
  • All-cause mortality
Methodological detailsretrospective cohort study using claims data, propensity scores, inverse probability of treatment weighted (IPTW) Cox models
  • Retrospective cohort study using claims data
  • Propensity scores
  • Inverse probability of treatment weighted (IPTW) Cox models

Main finding

As reported in the abstract

MACE
Each group vs dulaglutideHazard ratio (95% CI)
Semaglutide
0.85(0.78–0.93)
Liraglutide
0.84(0.72–0.97)

Observational data: associations, not effects.

Further findings

OutcomeHR (95% CI)
Expanded MACE (MACE, hospitalization for HF, revascularization)Semaglutidevs Dulaglutide0.92 (0.87–0.96)
All-cause mortalitySemaglutidevs Dulaglutide0.81 (0.71–0.92)
All-cause mortalityLiraglutidevs Dulaglutide0.79 (0.64–0.99)
StrokeSemaglutidevs Dulaglutide0.82 (0.70–0.97)
RevascularizationSemaglutidevs Dulaglutide0.93 (0.88–0.99)

Original publication

Comparative effectiveness of GLP-1 receptor agonists on cardiovascular outcomes among adults with type 2 diabetes and moderate cardiovascular risk: emulation of a target trial. Diabetes Res Clin Pract. Published 20 September 2025. doi:10.1016/j.diabres.2025.112910

Composed by AI from the published abstract and checked against it. How Briefs are made →

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