Department of Pharmacy, China Medical University and China Medical University Beigang Hospital, Yunlin County, Taiwan, ROC.
Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan, ROC.
Cardiovasc Diabetol. 2020 Jun 5;19(1):73. doi: 10.1186/s12933-020-01048-x.
Clinical trials have shown the cardiovascular protective effect of sodium-glucose cotransporter-2 (SGLT2) inhibitors and reduced hospitalization for heart failure. However, no study has investigated the association between SGLT2 inhibitors and the risk of arrhythmias. This study aimed to evaluate the risk of new-onset arrhythmias (NOA) and all-cause mortality with the use of SGLT2 inhibitors.
This was a population-based cohort study utilizing Taiwan's National Health Insurance Research Database. Each patient aged 20 years and older who took SGLT2 inhibitors was assigned to the SGLT2 inhibitor group, whereas sex-, age-, diabetes mellitus duration-, drug index date-, and propensity score-matched randomly selected patients without SGLT2 inhibitors were assigned to the non-SGLT2 inhibitor group. The study outcome was all-cause mortality and NOA.
A total of 399,810 patients newly diagnosed with type 2 DM were enrolled. A 1:1 matching propensity method was used to match 79,150 patients to 79,150 controls in the non-SGLT2 inhibitors group for analysis. The SGLT2 inhibitor group was associated with a lower risk of all-cause mortality [adjusted hazard ratio (aHR) 0.547; 95% confidence interval (CI) 0.482-0.621; P = 0.0001] and NOA (aHR 0.830; 95% CI 0.751-0.916; P = 0.0002).
Patients with type 2 DM prescribed with SGLT2 inhibitors were associated with a lower risk of all-cause mortality and NOA compared with those not taking SGLT2 inhibitors in real-world practice.
临床试验已经证实钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂具有心血管保护作用,并降低心力衰竭住院率。然而,目前尚无研究探讨 SGLT2 抑制剂与心律失常风险之间的关系。本研究旨在评估 SGLT2 抑制剂的使用与新发心律失常(NOA)和全因死亡率之间的相关性。
这是一项基于人群的队列研究,利用了台湾全民健康保险研究数据库。将年龄≥20 岁、服用 SGLT2 抑制剂的患者纳入 SGLT2 抑制剂组,将性别、年龄、糖尿病病程、药物起始日期和倾向评分匹配的未服用 SGLT2 抑制剂的随机患者纳入非 SGLT2 抑制剂组。研究结局为全因死亡率和 NOA。
共纳入 399810 例新诊断为 2 型糖尿病的患者。采用 1:1 倾向评分匹配方法,将 79150 例患者匹配至非 SGLT2 抑制剂组中 79150 例对照。SGLT2 抑制剂组的全因死亡率风险降低[校正后的危险比(aHR)0.547;95%置信区间(CI)0.482-0.621;P=0.0001],新发心律失常风险也降低[aHR 0.830;95%CI 0.751-0.916;P=0.0002]。
与未服用 SGLT2 抑制剂的患者相比,在真实世界实践中,服用 SGLT2 抑制剂的 2 型糖尿病患者的全因死亡率和 NOA 风险较低。