Cardiovascular Department, Chang Gung Memorial Hospital, Linkou, Taoyuan 333, Taiwan.
Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, 112, Taiwan.
J Clin Endocrinol Metab. 2022 Aug 18;107(9):2493-2499. doi: 10.1210/clinem/dgac402.
Whether sodium-glucose cotransporter 2 inhibitors (SGLT2is) are associated with lower risk of new-onset atrial fibrillation (AF) compared with glucagon-like peptide-1 receptor agonists (GLP-1RAs) in patients with type 2 diabetes was unknown.
We aimed to determine the comparative risk of new-onset AF with SGLT2is vs GLP-1RAs in Asian patients with type 2 diabetes in a real-world setting.
We used medical data from a multicenter health care provider in Taiwan and enrolled 16 566 and 2746 patients treated with an SGLT2i and a GLP-1RA, respectively, from January 1, 2016, to December 31, 2018. Propensity score weighting was used to balance the baseline covariates. The patients were followed from the drug index date until the occurrence of new-onset AF or the end of the follow-up period.
In this study, 54%, 45%, and 1% of the SGLT2i group patients were treated with empagliflozin, dapagliflozin, and canagliflozin, respectively, and 65% and 35% of the GLP-1RA group patients were treated with liraglutide and dulaglutide, respectively. SGLT2is were associated with lower risk of new-onset AF compared with GLP-1RAs after inverse probability of treatment weighting (subdistribution hazard ratio: 0.72; 95% CI, 0.54-0.97; P = 0.028). Subgroup analysis revealed that this finding was consistent among the following high-risk subgroups: older patients, female patients, and patients with cardiovascular disease or chronic kidney disease.
SGLT2is were associated with lower risk of new-onset AF compared with GLP-1RAs among patients with type 2 diabetes mellitus in a real-world practice.
在 2 型糖尿病患者中,钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)与胰高血糖素样肽-1 受体激动剂(GLP-1RA)相比,是否与新发心房颤动(AF)风险降低相关尚不清楚。
我们旨在确定在真实世界环境中,亚洲 2 型糖尿病患者中 SGLT2i 与 GLP-1RA 相比新发 AF 的相对风险。
我们使用来自台湾一家多中心医疗服务提供者的医疗数据,纳入了分别于 2016 年 1 月 1 日至 2018 年 12 月 31 日接受 SGLT2i 和 GLP-1RA 治疗的 16566 例和 2746 例患者。采用倾向评分加权法平衡基线协变量。患者从药物索引日期开始随访,直到新发 AF 发生或随访期结束。
在这项研究中,SGLT2i 组患者中分别有 54%、45%和 1%接受恩格列净、达格列净和卡格列净治疗,GLP-1RA 组患者中分别有 65%和 35%接受利拉鲁肽和度拉鲁肽治疗。经逆概率治疗加权后(亚分布风险比:0.72;95%CI,0.54-0.97;P=0.028),SGLT2i 与 GLP-1RA 相比,新发 AF 的风险较低。亚组分析显示,在以下高风险亚组中,这一发现是一致的:老年患者、女性患者以及患有心血管疾病或慢性肾脏病的患者。
在真实世界实践中,与 GLP-1RA 相比,SGLT2i 与 2 型糖尿病患者新发 AF 的风险较低。