Pennington Biomedical Research Centre, Baton Rouge, Louisiana.
Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.
Diabetes Obes Metab. 2020 Jul;22(7):1197-1206. doi: 10.1111/dom.14025. Epub 2020 Mar 31.
To compare the cardiovascular risks between users and non-users of sodium-glucose co-transporter-2 (SGLT2) inhibitors based on electronic medical record data from a large integrated healthcare system in South Louisiana.
Demographic, anthropometric, laboratory and medication prescription information for patients with type 2 diabetes who were new users of SGLT2 inhibitors, either as initial treatments or as add-on treatments, were obtained from electronic health records. Mediation analysis was performed to evaluate the association of use of SGLT2 inhibitors and changes of metabolic risk factors with the risk of incident ischaemic heart disease.
A total of 5338 new users of SGLT2 inhibitors were matched with 13 821 non-users. During a mean follow-up of 3.26 years, 2302 incident cases of ischaemic heart disease were defined. After adjusting for multiple confounding factors, patients using SGLT2 inhibitors had a lower risk of incident ischaemic heart disease compared to patients not using SGLT2 inhibitors (hazard ratio [HR] 0.63, 95% confidence interval [CI] 0.54-0.73). Patients using SGLT2 inhibitors also had a lower risk of incident ischaemic heart disease within 6 months (HR 0.36, 95% CI 0.25-0.44), 12 months (HR 0.40, 95% CI 0.32-0.49), 24 months (HR 0.53, 95% CI 0.43-0.60) and 36 months (HR 0.65, 95% CI 0.54-0.73), respectively. Reductions in systolic blood pressure partly mediated lowering risk of ischaemic heart disease among patients using SGLT2 inhibitors.
The real-world data in the present study show the contribution of SGLT2 inhibitors to reducing risk of ischaemic heart disease, and their benefits beyond glucose-lowering.
基于路易斯安那州南部一家大型综合医疗保健系统的电子病历数据,比较钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂使用者与非使用者的心血管风险。
从电子健康记录中获取新使用 SGLT2 抑制剂(初始治疗或附加治疗)的 2 型糖尿病患者的人口统计学、人体测量学、实验室和药物处方信息。进行中介分析,以评估 SGLT2 抑制剂的使用以及代谢风险因素的变化与缺血性心脏病事件风险之间的关联。
共纳入 5338 名新使用 SGLT2 抑制剂的患者,并与 13821 名非使用者进行匹配。在平均 3.26 年的随访期间,定义了 2302 例缺血性心脏病事件。在调整了多种混杂因素后,与未使用 SGLT2 抑制剂的患者相比,使用 SGLT2 抑制剂的患者发生缺血性心脏病的风险较低(风险比[HR]0.63,95%置信区间[CI]0.54-0.73)。使用 SGLT2 抑制剂的患者在 6 个月(HR 0.36,95%CI 0.25-0.44)、12 个月(HR 0.40,95%CI 0.32-0.49)、24 个月(HR 0.53,95%CI 0.43-0.60)和 36 个月(HR 0.65,95%CI 0.54-0.73)时发生缺血性心脏病的风险也较低。收缩压的降低部分解释了使用 SGLT2 抑制剂的患者降低缺血性心脏病风险的机制。
本研究的真实世界数据表明,SGLT2 抑制剂除了具有降血糖作用外,还能降低缺血性心脏病的风险。