Ojeda-Fernández Luisa, Torrigiani Ginevra, Molteni Mauro, Fortino Ida, Cimminiello Claudio, Baviera Marta
Laboratory of Cardiovascular Prevention, Department of Health Policy, Istituto Di Ricerche Farmacologiche Mario Negri IRCCS, Via Mario Negri 2, 20156, Milan, Italy.
Department of Statistics and Quantitative Methods, Università Degli Studi Di Milano-Bicocca, Milan, Italy.
Clin Res Cardiol. 2025 May 13. doi: 10.1007/s00392-025-02674-9.
Evidence on the impact of GLP-1 RAs on HF hospitalization (HHF) and mortality has been inconsistent across clinical trials in patients with diabetes. We investigated the association between GLP-1 RAs and these outcomes in a real-world setting.
We selected individuals aged 45 years and older already treated with metformin living in Lombardy, Italy, and then split them into two groups if they initiated GLP-1 RAs or other antidiabetic drugs, between 2019 and 2021. A multivariable Cox proportional hazard regression model was performed to assess the association of GLP-1 RAs on HHF and all-cause death as hazard ratios (HRs) with 95% CI compared to the Other ADs group, stratifying by history of HF. The role of GLP-1 RAs was also investigated using the Inverse Probability Treatment Weighting (IPTW) and in the subgroup analyses.
In total, 9795 patients in the GLP-1 RAs group (302 with HF; 9493 without) and 6018 in the Other ADs group (405 with HF; 5613 without) were included in the analysis. GLP-1 RAs use was significantly associated with a lower risk of HHF in patients with a history of HF (HR 0.65; CI 95% 0.426-0.987) and in those without (HR 0.52; CI 95% 0.371-0.733). A lower risk for all-cause death was also observed in GLP-1 RAs users (with HF: HR 0.45; CI 95% 0.320-0.638; without HF: HR 0.44; CI 95% 0.383-0.514). The results of the IPTW and subgroup analyses confirmed those of the main analysis.
Our findings showed a benefit of GLP-1 RAs on HHF and all-cause death in patients with diabetes regardless of HF history. Although, our study presents several limitations, if confirmed through dedicated randomized trial, this could further expand the role of GLP-1RAs in cardiovascular prevention".
在糖尿病患者的临床试验中,关于胰高血糖素样肽-1受体激动剂(GLP-1 RAs)对心力衰竭住院(HHF)和死亡率影响的证据并不一致。我们在真实世界环境中研究了GLP-1 RAs与这些结局之间的关联。
我们选择了居住在意大利伦巴第地区、年龄在45岁及以上且已接受二甲双胍治疗的个体,然后在2019年至2021年期间,如果他们开始使用GLP-1 RAs或其他抗糖尿病药物,将他们分为两组。采用多变量Cox比例风险回归模型,以评估与其他抗糖尿病药物组相比,GLP-1 RAs对HHF和全因死亡的关联,以风险比(HRs)及95%置信区间表示,并按心力衰竭病史进行分层。还使用逆概率治疗加权法(IPTW)及在亚组分析中研究了GLP-1 RAs的作用。
分析共纳入了GLP-1 RAs组的9795例患者(302例有心力衰竭;9493例无心力衰竭)和其他抗糖尿病药物组的6018例患者(405例有心力衰竭;5613例无心力衰竭)。在有心力衰竭病史的患者中,使用GLP-1 RAs与较低的HHF风险显著相关(HR 0.65;95%置信区间0.426 - 0.987),在无心力衰竭病史的患者中也是如此(HR 0.52;95%置信区间0.371 - 0.733)。在使用GLP-1 RAs的患者中也观察到较低的全因死亡风险(有心力衰竭:HR 0.45;95%置信区间0.320 - 0.638;无心力衰竭:HR 0.44;95%置信区间0.383 - 0.514)。IPTW和亚组分析的结果证实了主要分析的结果。
我们的研究结果表明,无论有无心力衰竭病史,GLP-1 RAs对糖尿病患者的HHF和全因死亡均有益处。尽管我们的研究存在一些局限性,但如果通过专门的随机试验得到证实,这可能会进一步扩大GLP-1 RAs在心血管预防中的作用。