Department of Pharmacy, College of Pharmaceutical Sciences, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Institute of Public Health, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Diabetes Obes Metab. 2022 Aug;24(8):1623-1637. doi: 10.1111/dom.14741. Epub 2022 May 25.
To examine the comparative effectiveness of glucagon-like peptide-1 receptor agonists (GLP-1RAs) and sodium-glucose cotransporter-2 (SGLT2) inhibitors for select cardiovascular outcomes and to examine whether the relative risks varied across different patient subgroups in patients with type 2 diabetes.
We conducted a nationwide cohort study of patients with type 2 diabetes who initiated GLP-1RAs or SGLT2 inhibitors between 2012 and 2018 in Taiwan. The study outcomes included myocardial infarction and total stroke, further classified into ischaemic or haemorrhagic stroke. We estimated the hazard ratios (HRs) and 95% confidence intervals (CIs) for each outcome, comparing GLP-1RAs with SGLT2 inhibitors using Cox proportional hazards models after 1:1 propensity-score (PS) matching. We also examined if there was effect modification by age, underlying chronic kidney disease, or coexisting cardiovascular disease in prespecified subgroup analyses.
Among 26 032 PS-matched patients, GLP-1RA initiators and SGLT2 inhibitor initiators showed similar risks of myocardial infarction (HR 0.99, 95% CI 0.65-1.52), total stroke (HR 0.90, 95% CI 0.69-1.17), ischaemic stroke (HR 0.86, 95% CI 0.65-1.14) and haemorrhagic stroke (HR 0.88, 95% CI 0.63-1.25). However, GLP-1RA treatment was associated with an increased risk of total stroke (HR 1.76, 95% CI 1.06-2.94) and ischaemic stroke (HR 1.88, 95% CI 1.09-3.23) among patients with chronic kidney disease, but not among patients without chronic kidney disease. GLP-1RA therapy seemed to have a lower risk of haemorrhagic stroke among patients with cardiovascular disease (HR 0.64, 95% CI 0.43-0.97), but not in patients without cardiovascular disease.
Glucagon-like peptide-1 receptor agonists and SGLT2 inhibitors appeared to have comparable effectiveness with regard to several cardiovascular outcomes overall, but their comparative effectiveness may vary in certain patient subgroups.
研究胰高血糖素样肽-1 受体激动剂(GLP-1RA)和钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂在 2 型糖尿病患者中对特定心血管结局的比较疗效,并研究相对风险是否因不同的患者亚组而异。
我们对 2012 年至 2018 年间在台湾开始使用 GLP-1RA 或 SGLT2 抑制剂的 2 型糖尿病患者进行了一项全国性队列研究。研究结果包括心肌梗死和总卒中,进一步分为缺血性或出血性卒中。我们使用 Cox 比例风险模型估计了每个结局的风险比(HR)和 95%置信区间(CI),在 1:1 倾向评分(PS)匹配后,比较 GLP-1RA 与 SGLT2 抑制剂的结果。我们还在预先指定的亚组分析中检查了年龄、潜在的慢性肾脏病或并存的心血管疾病是否存在效应修饰。
在 26032 名经 PS 匹配的患者中,GLP-1RA 起始治疗和 SGLT2 抑制剂起始治疗的心肌梗死(HR 0.99,95%CI 0.65-1.52)、总卒中(HR 0.90,95%CI 0.69-1.17)、缺血性卒中(HR 0.86,95%CI 0.65-1.14)和出血性卒中(HR 0.88,95%CI 0.63-1.25)的风险相似。然而,在患有慢性肾脏病的患者中,GLP-1RA 治疗与总卒中(HR 1.76,95%CI 1.06-2.94)和缺血性卒中(HR 1.88,95%CI 1.09-3.23)的风险增加相关,但在没有慢性肾脏病的患者中没有这种相关性。GLP-1RA 治疗似乎降低了伴有心血管疾病的患者发生出血性卒中的风险(HR 0.64,95%CI 0.43-0.97),但在没有心血管疾病的患者中没有这种相关性。
GLP-1RA 和 SGLT2 抑制剂在总体上对几种心血管结局的疗效似乎相似,但在某些特定患者亚组中,它们的相对疗效可能有所不同。