心血管疾病的SGLT2抑制剂预防房颤:一项随机对照试验的荟萃分析

IF 6.1 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Damiano Fedele, Marcello Casuso Alvarez, Angelo Maida, Nicolò Vasumini, Sara Amicone, Lisa Canton, Michele Di Leo, Marco Basile, Tommaso Manaresi, Francesco Angeli, Matteo Armillotta, Luca Bergamaschi, Carmine Pizzi
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引用次数: 0

摘要

目的:钠-葡萄糖共转运蛋白-2 (SGLT2)抑制剂预防心房颤动(AF)的能力已经在各种研究中进行了评估,结果相互矛盾。本研究旨在确定SGLT2抑制剂是否对房颤具有保护作用,这取决于进行随机对照试验(RCT)的基线临床状况。方法和结果:进行了一项试验水平的荟萃分析,包括52项随机对照试验(112031例患者),比较SGLT2抑制剂和安慰剂,并报告每组中发生房颤的患者数量。采用随机效应模型对房颤发生的95%置信区间(95% ci)的风险比(RR)进行汇总。根据每个试验的纳入标准(糖尿病、慢性肾病、心力衰竭伴射血分数降低(HFrEF)、轻度降低的射血分数(HFmrEF)和保存的射血分数(HFpEF))对rct进行分类,进行亚组分析。总体而言,SGLT2抑制剂可预防AF (RR=0.86, 95%CI 0.77-0.96)。在亚组分析中,SGLT2抑制剂的af预防能力受到HF的影响,在招募9141名HFrEF患者的rct中得以保留,而在招募12877名HFmrEF/HFpEF患者的rct中则没有影响(组间p值差异=0.01)。荟萃回归显示,当更多的高血压或高EF患者入组时,SGLT2抑制剂预防房颤的效果降低(p值结论:SGLT2抑制剂预防房颤。其保护作用在HFrEF亚组中得到证实,但在招募HFmrEF/HFpEF患者的随机对照试验中未得到证实,可能表明在这些情况下导致房颤的病理生理不同。然而,考虑到试验水平分析的局限性,这些发现是探索性的,有待于患者水平数据的证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevention of atrial fibrillation with SGLT2 inhibitors across the spectrum of cardiovascular disorders: a meta-analysis of randomized controlled trials.

Aims: The ability of sodium-glucose co-transporter 2 (SGLT2) inhibitors to prevent atrial fibrillation (AF) has been evaluated in various studies with conflicting results. This study aimed to determine whether SGLT2 inhibitors have a protective effect against AF depending on the baseline clinical condition in which the randomized controlled trials (RCTs) were conducted.

Methods and results: A trial-level meta-analysis was performed including 52 RCTs (112 031 patients) comparing SGLT2 inhibitors with placebo and reporting the number of patients who developed AF in each arm. Risk ratios (RRs) for AF development with 95% confidence intervals (95% CIs) were pooled using a random-effects model. Subgroup analyses were performed by classifying RCTs according to the inclusion criteria of each trial [diabetes, chronic kidney disease, heart failure with reduced ejection fraction (HFrEF), mildly reduced EF (HFmrEF), and preserved EF (HFpEF)]. Overall, SGLT2 inhibitors prevented AF (RR = 0.86, 95% CI 0.77-0.96). In the subgroup analysis, the AF-preventive ability of SGLT2 inhibitors was influenced by HF, being preserved in RCTs recruiting 9141 patients with HFrEF, but not in those recruiting 12 877 subjects with HFmrEF/HFpEF (P-value for group difference = 0.01). Meta-regression showed a reduced efficacy of SGLT2 inhibitors in preventing AF when more patients with hypertension or higher EF were enrolled (P < 0.01 for both).

Conclusion: Sodium-glucose co-transporter 2 inhibitors prevent AF. Their protective effect was confirmed in the HFrEF subgroup, but not in RCTs recruiting patients with HFmrEF/HFpEF, possibly indicating a different pathophysiology leading to AF among these conditions. However, given the limitations of a trial-level analysis, these findings are exploratory, pending confirmation from patient-level data.

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来源期刊
European Heart Journal - Cardiovascular Pharmacotherapy
European Heart Journal - Cardiovascular Pharmacotherapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
10.10
自引率
14.10%
发文量
65
期刊介绍: The European Heart Journal - Cardiovascular Pharmacotherapy (EHJ-CVP) is an international, peer-reviewed journal published in English, specifically dedicated to clinical cardiovascular pharmacology. EHJ-CVP publishes original articles focusing on clinical research involving both new and established drugs and methods, along with meta-analyses and topical reviews. The journal's primary aim is to enhance the pharmacological treatment of patients with cardiovascular disease by interpreting and integrating new scientific developments in this field. While the emphasis is on clinical topics, EHJ-CVP also considers basic research articles from fields such as physiology and molecular biology that contribute to the understanding of cardiovascular drug therapy. These may include articles related to new drug development and evaluation, the physiological and pharmacological basis of drug action, metabolism, drug interactions, and side effects.
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