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Tirzepatide and major adverse limb events: Insights from a multicenter real-world analysis in PAD and diabetes patients.

Diabetes Res Clin Pract · 2025

Last updated 2026-05-28

A study of 8,046 patients with diabetes and peripheral artery disease found that those taking tirzepatide had a 56% lower risk of major limb problems compared to those not taking the drug. Tirzepatide was also linked to lower risks of death, stroke, and major heart events, though it did not significantly change the risk of heart attacks.

AI summary of the abstract below.

JournalDiabetes Res Clin Pract, 2025
Citations22
Relative citation ratio8.62
Molecules tirzepatide
Conditions studied Type 2 Diabetes, Cardiovascular Risk Reduction

Abstract

AIMS: Peripheral artery disease (PAD) is a major diabetic complication and a leading cause of amputation. While GLP-1 receptor agonists (GLP-1 RAs) provide cardiovascular and limb protection, the impact of tirzepatide, a dual GLP-1/GIP receptor agonist, on major adverse limb events (MALEs) remains unclear. This study assessed tirzepatide's association with MALE risk in patients with PAD and diabetes using real-world data. METHODS: This retrospective cohort study analyzed 8,046 propensity score-matched PAD patients with diabetes (4,023 on tirzepatide, 4,023 controls) from the TriNetX database. The primary outcome was MALEs, with secondary outcomes including all-cause mortality, acute stroke, acute myocardial infarction (AMI), and major adverse cardiovascular events (MACEs). Cox models and Kaplan-Meier curves were used for analysis. RESULTS: Tirzepatide significantly reduced MALE risk (HR: 0.44, 95 % CI: 0.33-0.59, p < 0.001) and was associated with lower mortality, stroke, and MACEs. AMI risk was similar between groups (HR: 0.85, p = 0.29). Subgroup analyses confirmed consistent findings, except in those with prior stroke. CONCLUSIONS: Tirzepatide significantly lowered MALE risk in PAD patients with diabetes, suggesting a potential therapeutic role. Further prospective studies are needed to validate these findings.

Verbatim abstract via PubMed 40049522 ↗

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