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Major adverse cardiovascular and limb events caused by tirzepatide in patients with type 2 diabetes at high cardiovascular risk: A comparison with sitagliptin.

Diabetes Res Clin Pract · 2026

Last updated 2026-05-28

In a study of 31,751 patients with type 2 diabetes, those taking tirzepatide had a lower risk of major heart and limb events over one year compared to those taking sitagliptin (4.3% vs. 6.1%). Tirzepatide was linked to fewer heart-related events, fewer limb-related events, and fewer amputations than sitagliptin.

AI summary of the abstract below.

JournalDiabetes Res Clin Pract, 2026
Citations0
Molecules tirzepatide
Conditions studied Type 2 Diabetes, Cardiovascular Risk Reduction

Abstract

AIMS: To elucidate the overall protective effects of tirzepatide against atherosclerosis-related events, including cardiovascular and lower-extremity events. METHODS: We conducted a retrospective cohort study using the TriNetX global health research network to identify patients with type 2 diabetes (T2D) who initiated tirzepatide or sitagliptin between January 2022 and December 2023. The primary outcome was major adverse cardiovascular and limb events (MACLE), defined as the composite of major adverse cardiovascular events (MACE: all-cause death, myocardial infarction, and stroke) and major adverse limb events (MALE: all-cause death and major lower extremity amputation). Propensity score matching was applied. RESULTS: After matching, 31,751 patients per group were analyzed. At 1 year, the incidence of MACLE was lower with tirzepatide compared to that with sitagliptin (4.3 % vs. 6.1 %; hazard ratio (HR), 0.70; 95 % confidence interval (CI), 0.66-0.76; p < 0.001). Tirzepatide was also associated with a reduced risk of MACE (HR, 0.71; 95 % CI, 0.66-0.76), MALE (HR, 0.39; 95 % CI, 0.34-0.46), and major lower extremity amputation (HR, 0.61; 95 % CI, 0.44-0.84). Consistent benefits were observed across major subgroups. CONCLUSIONS: Tirzepatide was associated with a significantly lower risk of cardiovascular and limb events compared to sitagliptin in patients with T2D.

Verbatim abstract via PubMed 41448390 ↗

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