Lin Yu-Min, Liao Kuang-Ming, Yu Tsung, Wu Jheng-Yan, Lai Chih-Cheng
Division of Cardiology, Department of Internal Medicine, Chi Mei Medical Centre, Chiali, Tainan, Taiwan.
Department of Internal Medicine, Chi Mei Medical Centre, Chiali, Tainan, Taiwan.
Nat Commun. 2025 May 14;16(1):4471. doi: 10.1038/s41467-025-59616-2.
Tirzepatide, a dual agonist of glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptors, has shown promise in improving metabolic and cardiovascular profiles in patients with obesity. However, its potential benefits in patients with heart failure with preserved ejection fraction (HFpEF) remain unclear. We conducted a real-world, retrospective cohort study using the TriNetX global database. A total of 14,154 patients with HFpEF were included after 1:1 propensity score matching. Tirzepatide use was associated with significantly lower risks of the primary composite outcome of heart failure exacerbation and all-cause mortality (HR 0.52), as well as reductions in major adverse cardiovascular events (HR 0.64) and major adverse kidney events (HR 0.44). Subgroup analyses demonstrated consistent benefits across different strata. Sensitivity analyses using alternative exposure definitions confirmed the robustness of the findings. These results support the potential clinical utility of tirzepatide in HFpEF management and warrant further investigation in randomized controlled trials.
替尔泊肽是一种葡萄糖依赖性促胰岛素多肽(GIP)和胰高血糖素样肽-1(GLP-1)受体的双重激动剂,已显示出改善肥胖患者代谢和心血管状况的前景。然而,其在射血分数保留的心力衰竭(HFpEF)患者中的潜在益处仍不明确。我们使用TriNetX全球数据库进行了一项真实世界的回顾性队列研究。在进行1:1倾向评分匹配后,共纳入了14154例HFpEF患者。使用替尔泊肽与心力衰竭加重和全因死亡率的主要复合结局风险显著降低(风险比0.52)相关,同时主要不良心血管事件(风险比0.64)和主要不良肾脏事件(风险比0.44)也有所减少。亚组分析表明,在不同亚组中均有一致的益处。使用替代暴露定义的敏感性分析证实了研究结果的稳健性。这些结果支持替尔泊肽在HFpEF管理中的潜在临床应用价值,并值得在随机对照试验中进一步研究。