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替尔泊肽与严重肢体不良事件:来自PAD和糖尿病患者多中心真实世界分析的见解

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

作者信息

Wu Jheng-Yan, Tu Wan-Ling, Yu Tsung, Liao Kuang-Ming, Lin Yu-Min

机构信息

Department of Nutrition, Chi Mei Medical Centre, Tainan, Taiwan; Department of Public Health, College of Medicine, National Cheng Kung University, Tainan, Taiwan.

Department of Nutrition Therapy, E-Da Hospital, Kaohsiung, Taiwan.

出版信息

Diabetes Res Clin Pract. 2025 Apr;222:112083. doi: 10.1016/j.diabres.2025.112083. Epub 2025 Mar 4.

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.

摘要

目的

外周动脉疾病(PAD)是一种主要的糖尿病并发症,也是截肢的主要原因。虽然胰高血糖素样肽-1受体激动剂(GLP-1 RAs)可提供心血管和肢体保护,但双重GLP-1/葡萄糖依赖性促胰岛素多肽(GIP)受体激动剂替尔泊肽对主要肢体不良事件(MALEs)的影响仍不明确。本研究使用真实世界数据评估替尔泊肽与PAD合并糖尿病患者发生MALE风险的相关性。

方法

这项回顾性队列研究分析了TriNetX数据库中8046例倾向评分匹配的PAD合并糖尿病患者(4023例使用替尔泊肽,4023例为对照)。主要结局为MALEs,次要结局包括全因死亡率、急性卒中、急性心肌梗死(AMI)和主要不良心血管事件(MACEs)。采用Cox模型和Kaplan-Meier曲线进行分析。

结果

替尔泊肽显著降低了MALE风险(风险比:0.44,95%置信区间:0.33-0.59,p<0.001),并与较低的死亡率、卒中和MACEs相关。两组间AMI风险相似(风险比:0.85,p=0.29)。亚组分析证实了一致的结果,但既往有卒中史的患者除外。

结论

替尔泊肽显著降低了PAD合并糖尿病患者的MALE风险,提示其具有潜在的治疗作用。需要进一步的前瞻性研究来验证这些发现。

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