Obesity

Cardiovascular Outcomes With Tirzepatide Versus GLP ‐1 Receptor Agonists in Overweight or Obesity: A Systematic Review and Meta‐Analysis

Diabetes Obes MetabPublished Systematic review and meta-analysis of randomised and observational studies

Pooled result · MACEResult — go to the resultHazard ratio 0.85 95% CI 0.70–1.04

Authors' conclusion

Tirzepatide was not associated with a statistically significant reduction in MACEs.

Study context

Population
Adults with overweight or obesity; studies searched through 30 March 20268 studies (1 RCT, 7 observational)
Participants
323,439 adults
Comparison
Tirzepatide vs GLP-1 RAs
Outcome
MACE
Methodological detailsadjusted hazard ratios when available, risk of bias assessed with RoB 2 and ROBINS-I
  • Adjusted hazard ratios when available
  • Risk of bias assessed with RoB 2 and ROBINS-I

Pooled result

As reported in the abstract

Hazard ratio

0.85

95% CI 0.70–1.04

Tirzepatidevs GLP-1 RAs
HR 0.85 (95% CI 0.70–1.04)

Further pooled results

All-cause mortality

HR, tirzepatide vs GLP-1 RAs; directionally consistent with major adverse cardiovascular events (MACE)
HR 0.90, 95% CI 0.79-1.02

CV mortality

HR, tirzepatide vs GLP-1 RAs; directionally consistent with MACE
HR 0.88, 95% CI 0.76-1.00

All-cause mortality, T2D subgroup

Lower estimated risk in patients with T2D
HR 0.85, 95% CI 0.76-0.94
  • Exploratory subgroup analysis

HF, T2D subgroup

Lower estimated risk in patients with T2D
HR 0.75, 95% CI 0.58-0.97
  • Exploratory subgroup analysis

Original publication

Cardiovascular Outcomes With Tirzepatide Versus GLP ‐1 Receptor Agonists in Overweight or Obesity: A Systematic Review and Meta‐Analysis. Diabetes Obes Metab. Published 6 July 2026. doi:10.1111/dom.71051

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

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