Comparative Cardiovascular Outcomes of GLP-1 Receptor Agonists Versus Bariatric Surgery: A Systematic Review and Network Meta-Analysis.

Endocrinol Diabetes MetabSep 1, 2026

Erfan Shirmohammadi, Negar Ghasemloo, Navid Ebrahimi et al.

✦ AI-curated · Sources linked

In 30 seconds

This systematic review and network meta-analysis evaluated cardiovascular outcomes of bariatric surgery (BS) versus glucagon-like peptide-1 receptor agonists (GLP-1RAs) in obese patients. Among 932,380 patients, BS significantly reduced major adverse cardiovascular events (MACE) by 34% (HR 0.66), heart failure by 55% (HR 0.45), and myocardial infarction by 47% (HR 0.53) compared to controls, while GLP-1RAs reduced MACE by 15% (HR 0.85) but had non-significant effects on heart failure and myocardial infarction.

Key findings

  • Bariatric surgery reduced major adverse cardiovascular events (MACE) by 34% (HR 0.66; 95% CI 0.60-0.74) compared to controls.
  • Heart failure was reduced by 55% (HR 0.45; 95% CI 0.38-0.53) with bariatric surgery.
  • Myocardial infarction decreased by 47% (HR 0.53; 95% CI 0.45-0.63) with bariatric surgery.
  • GLP-1RAs reduced MACE by 15% (HR 0.85; 95% CI 0.77-0.94) but had non-significant effects on heart failure and myocardial infarction.

Why it matters

Understanding the comparative effectiveness of bariatric surgery and GLP-1RAs on cardiovascular outcomes is crucial for managing obesity-related cardiovascular risks. This information aids clinicians in making informed treatment decisions for patients at high cardiovascular risk.

What to keep in mind

High heterogeneity (I²: 66%-93%) across studies may affect the reliability of the findings.

Source

Published in Endocrinol Diabetes Metab. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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