钠-葡萄糖共转运体-2 抑制剂与 2 型糖尿病患者心房颤动的风险:一项基于人群的队列研究。

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Talip E Eroglu, Ruben Coronel, Patrick C Souverein
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引用次数: 0

摘要

目的:钠-葡萄糖共转运体-2 抑制剂(SGLT-2is)具有直接的心脏效应,这种效应可能与其降糖的肾脏效应无关。先前的研究表明,SGLT2-is 可减轻心力衰竭并防止心律失常性心源性死亡。我们的目标是确定与其他二线至三线抗糖尿病药物相比,SGLT2-is 是否能减少 2 型糖尿病患者的心房颤动:我们利用英国临床实践研究数据链(UK Clinical Practice Research Datalink)中的数据开展了一项基于人群的新用户主动比较队列研究。我们确定了一组在 2013 年 1 月至 2020 年 9 月期间开始使用新型抗糖尿病药物的患者。该队列包括首次使用非胰岛素类抗糖尿病药物的患者,以及改用或加用治疗史上未曾使用过的抗糖尿病药物的患者。不包括在进入组群前任何时候诊断为房颤或心房扑动的患者。使用时间依赖性协变量的 Cox 回归分析来估算 SGLT-2-is 与其他二线至三线抗糖尿病药物的房颤危险比 (HR) 和 95% 置信区间 (95%-CIs)。根据性别、糖尿病病程进行了分层分析(结论:SGLT-2-is 与心房颤动的相关性较低:与其他二线至三线抗糖尿病药物相比,SGLT-2 类药物可降低 2 型糖尿病患者发生房颤的风险。这种风险的降低在男女患者中均有发生,但在女性患者中更为明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sodium-glucose cotransporter-2 inhibitors and the risk of atrial fibrillation in patients with type 2 diabetes: a population-based cohort study.

Aims: Sodium-glucose cotransporter-2 inhibitors (SGLT-2is) have a direct cardiac effect that is likely to be independent of its glucose lowering renal effect. Previous research has shown that SGLT2-is mitigate heart failure and prevent arrhythmic cardiac death. Our objective is to determine whether SGLT-2is reduce atrial fibrillation (AF) in comparison to other second-to third-line antidiabetic drugs in type 2 diabetes.

Methods and results: We conducted a population-based, new-user active comparator cohort study using data from the UK Clinical Practice Research Datalink. We identified a cohort of patients initiating a new antidiabetic drug class between January 2013 and September 2020. This cohort included patients initiating their first ever non-insulin antidiabetic drug, as well as those who switched to or added-on an antidiabetic drug class not previously used in their treatment history. Individuals with a diagnosis of AF or atrial flutter at any time before cohort entry were excluded. Cox regression analysis with time-dependent covariates was used to estimate hazard ratios (HRs) and 95% confidence intervals (95% CIs) of AF comparing SGLT-2-is with other second-line to third-line antidiabetic drugs. Stratified analyses were performed according to sex, diabetes duration (<5 or ≥ 5 years), body mass index (BMI), HbA1c, and presence of heart failure.The cohort comprised 142 447 patients. SGLT-2is were associated with a statistically significant reduced hazard of AF compared to other second-line to third-line antidiabetic drugs (adjusted HR: 0.77 [95% CI: 0.68-0.88]). This reduced risk was present in both sexes but was more prominently among women (adjusted HRwomen: 0.60 [95% CI: 0.45-0.79]; HRmen: 0.85 [95% CI: 0.73-0.98]; P-value interaction: 0.012). There was no evidence for effect modification when stratifying on duration of diabetes, BMI, HbA1c, or presence of heart failure.

Conclusion: SGLT-2is were associated with a reduced risk of AF in patients with type 2 diabetes compared to other second-line to third-line antidiabetic drugs. This reduced risk occurs in both sexes but more prominently among women.

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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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