Division of Cardiology, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan, ROC.
Institute of Medicine, College of Medicine, Chung Shan Medical University, Taichung, Taiwan, ROC.
Transl Stroke Res. 2024 Dec;15(6):1098-1107. doi: 10.1007/s12975-023-01174-0. Epub 2023 Jul 14.
Clinical studies have investigated the effects of using sodium-glucose co-transporter-2 (SGLT2) inhibitors on the development of new-onset stroke (NOS) in patients with type 2 diabetes (T2D) and chronic kidney disease (CKD), but the findings are inconsistent. This study aimed to examine the association between the use of SGLT2 inhibitors and NOS risk in patients with T2D and CKD. We conducted a nationwide retrospective cohort study using data from the Taiwan Health Insurance Review and Assessment Service database for the years 2004 to 2019. The primary outcome was the risk of incident stroke, which was estimated using hazard ratios (HRs) and 95% confidence intervals (CIs). We used multiple Cox regression modeling to analyze the association between SGLT2 inhibitor use and the risk of stroke in patients with T2D and CKD. In a cohort of 113,710 patients with T2D and CKD who were using SGLT2 inhibitors and 227,420 patients with T2D and CKD who were not using SGLT2 inhibitors, after applying a 1:2 sex- and age-matching strategy, 2,842 and 7,169 NOS events were recorded, respectively. The event rate per 10,000 person-months was 10.60 (95% CI 10.21 to 11.03) for SGLT2 inhibitor users and 13.71 (13.39-14.03) for non-SGLT2 inhibitor users. After adjusting for the index year, sex, age, comorbidities, and concurrent medication, there was a decreased risk of NOS for SGLT2 inhibitor users (adjusted HR 0.80; 95% CI 0.77-0.84) compared with non-SGLT2 inhibitor users. The sensitivity test for the propensity score 1:1-matched analyses showed similar results (adjusted HR 0.80; 95% CI 0.76-0.84). The type of SGLT2 inhibitor subgroup analysis for incident stroke showed consistent results. We concluded that the use of SGLT2 inhibitors in patients with T2D and CKD was associated with significantly low rates of NOS. The significantly low rates of NOS in patients with T2D and CKD were greater among females and less than 50 years patients.
临床研究已经调查了使用钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂对 2 型糖尿病(T2D)和慢性肾脏病(CKD)患者新发脑卒中(NOS)发展的影响,但研究结果并不一致。本研究旨在探讨 SGLT2 抑制剂的使用与 T2D 和 CKD 患者 NOS 风险之间的关系。我们使用 2004 年至 2019 年来自台湾健康保险审查和评估服务数据库的数据进行了一项全国性回顾性队列研究。主要结局是卒中的发病风险,使用风险比(HR)和 95%置信区间(CI)进行估计。我们使用多 Cox 回归模型分析了 SGLT2 抑制剂的使用与 T2D 和 CKD 患者卒中风险之间的关系。在接受 SGLT2 抑制剂治疗的 113710 例 T2D 和 CKD 患者和未接受 SGLT2 抑制剂治疗的 227420 例 T2D 和 CKD 患者中,采用 1:2 性别和年龄匹配策略后,分别记录到 2842 例和 7169 例 NOS 事件。SGLT2 抑制剂使用者每 10000 人-月的事件发生率为 10.60(95%CI 10.21-11.03),而非 SGLT2 抑制剂使用者为 13.71(13.39-14.03)。在调整指数年、性别、年龄、合并症和同时使用的药物后,与非 SGLT2 抑制剂使用者相比,SGLT2 抑制剂使用者的 NOS 风险降低(调整后的 HR 0.80;95%CI 0.77-0.84)。倾向评分 1:1 匹配分析的敏感性检验得出了相似的结果(调整后的 HR 0.80;95%CI 0.76-0.84)。SGLT2 抑制剂亚组分析中,对卒中发病的分析结果一致。我们得出结论,在 T2D 和 CKD 患者中使用 SGLT2 抑制剂与 NOS 发生率显著降低有关。在 T2D 和 CKD 患者中,NOS 发生率显著降低的患者主要为女性和年龄小于 50 岁的患者。