替西帕肽优于西马鲁肽治疗糖尿病CABG患者的脑血管预后:一项倾向匹配患者的全球网络研究。

IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Shriya Chunduri, Ghassan Bidaoui, Mohammad H Hussein, Milee Patel, Ahmed Abdelmaksoud, Mohamed Mohamed, Abdallah Attia, Danielle Tatum, Jamil Borgi, Eman A Toraih
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引用次数: 0

摘要

目的:比较替西帕肽(一种GLP-1/GIP受体双激动剂)与西马鲁肽(一种GLP-1受体激动剂)在改善2型糖尿病(T2DM)行冠状动脉旁路移植术(CABG)患者术后预后的有效性。方法:我们使用TriNetX全球研究网络进行了回顾性分析,确定了2022年至2024年间接受孤立性冠脉搭桥的226,742例T2DM成年人。其中,3,669人接受替西帕肽治疗,19,521人接受西马鲁肽治疗。经过1:1的倾向得分匹配,分析了3667对匹配的结果。主要结局包括脑血管和心血管事件、术后并发症、医疗保健利用和全因死亡率,评估间隔为6个月和3年。使用Benjamini-Hochberg程序调整多重检验的p值。结果:替西帕肽与两个随访点脑血管事件发生风险均显著降低相关,包括脑血管病(11.8% vs. 17.5%, HR = 0.831)、脑梗死(4.6% vs. 7.3%, HR = 0.788)、无梗死脑闭塞(6.8% vs. 10.4%, HR = 0.838)的发生率降低,经多次比较校正后均具有统计学意义(调整后p = 0.0024)。心血管结果也有利于替西肽,显著降低主要不良心血管事件(MACE)(39.7%比49.5%,HR = 0.911)、心肌梗死(7.0%比10.8%,HR = 0.838)和急性冠状动脉疾病(1.1%比2.3%,HR = 0.691);在两个时间点进行校正后,其中一些仍然显著。虽然替西帕肽与较低的手术部位感染、静脉血栓形成和冠脉搭桥特异性并发症发生率相关,但调整后只有静脉血栓形成仍具有统计学意义(校正p = 0.021)。此外,替西肽使用者降低了医疗保健利用率,降低了全因死亡率,3年再入院率(16.4% vs. 23.4%; HR = 0.871)和死亡率(1.9% vs. 4.7%; HR = 0.595)在调整后仍然显著(调整后p = 0.002)。Kaplan-Meier分析证实了持续生存获益。结论:在接受CABG的T2DM患者中,与西马鲁肽相比,替西帕肽可改善脑血管和心血管预后,减少静脉血栓并发症,降低长期死亡率和医疗利用率。这些发现支持双重GLP-1/GIP受体激动作用在高危cabg后人群中的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Superior Cerebrovascular Outcomes with Tirzepatide versus Semaglutide in Diabetic CABG Patients: A Global Network Study of Propensity-Matched Patients.

Purpose: To compare the effectiveness of tirzepatide (a dual GLP-1/GIP receptor agonist) versus semaglutide (a GLP-1 receptor agonist) in improving postoperative outcomes among patients with type 2 diabetes mellitus (T2DM) undergoing coronary artery bypass grafting (CABG).

Methods: We conducted a retrospective analysis using the TriNetX global research network, identifying 226,742 adults with T2DM who underwent isolated CABG between 2022 and 2024. Among these, 3,669 received tirzepatide and 19,521 received semaglutide. After 1:1 propensity score matching, 3,667 matched pairs were analyzed. Primary outcomes included cerebrovascular and cardiovascular events, postoperative complications, healthcare utilization, and all-cause mortality, assessed at 6-month and 3-year intervals. P-values were adjusted for multiple testing using the Benjamini-Hochberg procedure.

Results: Tirzepatide was associated with significantly lower risks of cerebrovascular events at both follow-up points, including reduced incidence of cerebrovascular disease (11.8% vs. 17.5%; HR = 0.831), cerebral infarction (4.6% vs. 7.3%; HR = 0.788), and cerebral occlusion without infarction (6.8% vs. 10.4%; HR = 0.838)-all of which remained statistically significant after multiple comparison correction (adjusted p = 0.0024). Cardiovascular outcomes also favored tirzepatide, with significant reductions in major adverse cardiovascular events (MACE) (39.7% vs. 49.5%; HR = 0.911), myocardial infarction (7.0% vs. 10.8%; HR = 0.838), and acute coronary disease (1.1% vs 2.3%; HR = 0.691); several of these remained significant after correction at both timepoints. While tirzepatide was associated with lower rates of surgical site infection, venous thrombosis, and CABG-specific complications, only venous thrombosis remained statistically significant after adjustment (adjusted p = 0.021). Additionally, tirzepatide users had reduced healthcare utilization and lower all-cause mortality, with 3-year readmission (16.4% vs. 23.4%; HR = 0.871) and mortality (1.9% vs. 4.7%; HR = 0.595) both remaining significant after adjustment (adjusted p = 0.002). Kaplan-Meier analysis confirmed sustained survival benefit.

Conclusion: In patients with T2DM undergoing CABG, tirzepatide was associated with improved cerebrovascular and cardiovascular outcomes, reduced venous thrombotic complications, and lower long-term mortality and healthcare utilization compared to semaglutide. These findings support the therapeutic potential of dual GLP-1/GIP receptor agonism in high-risk post-CABG populations.

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来源期刊
Cardiovascular Drugs and Therapy
Cardiovascular Drugs and Therapy 医学-心血管系统
CiteScore
8.30
自引率
0.00%
发文量
110
审稿时长
4.5 months
期刊介绍: Designed to objectively cover the process of bench to bedside development of cardiovascular drug, device and cell therapy, and to bring you the information you need most in a timely and useful format, Cardiovascular Drugs and Therapy takes a fresh and energetic look at advances in this dynamic field. Homing in on the most exciting work being done on new therapeutic agents, Cardiovascular Drugs and Therapy focusses on developments in atherosclerosis, hyperlipidemia, diabetes, ischemic syndromes and arrhythmias. The Journal is an authoritative source of current and relevant information that is indispensable for basic and clinical investigators aiming for novel, breakthrough research as well as for cardiologists seeking to best serve their patients. Providing you with a single, concise reference tool acknowledged to be among the finest in the world, Cardiovascular Drugs and Therapy is listed in Web of Science and PubMed/Medline among other abstracting and indexing services. The regular articles and frequent special topical issues equip you with an up-to-date source defined by the need for accurate information on an ever-evolving field. Cardiovascular Drugs and Therapy is a careful and accurate guide through the maze of new products and therapies which furnishes you with the details on cardiovascular pharmacology that you will refer to time and time again.
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