Division of Endocrinology and Metabolic Diseases, Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
Diabetes Unit, Department of Advanced Medical and Surgical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
Diabetes Obes Metab. 2019 Nov;21(11):2576-2580. doi: 10.1111/dom.13847. Epub 2019 Aug 28.
A meta-analysis of cardiovascular outcome trials (CVOTs) comparing glucagon-like peptide-1 receptor agonists (GLP-1RAs) and placebo concerning cardiorenal outcomes in patients with type 2 diabetes (T2D) is presented. An electronic search without language restrictions up to June 15, 2019 was conducted to determine eligible trials. A meta-analysis of available trial data was undertaken, using a random-effects model to calculate overall hazard ratios (HRs) and 95% confidence intervals (CIs). Data from seven CVOTs, comprising 56 004 patients (68.9% with established cardiovascular disease) were included. GLP-1RA reduced major cardiovascular events (MACE) by 13% (HR, 0.87; 95% CI, 0.80-0.96; P = 0.011) with a non-significant heterogeneity between subgroups of patients with and without cardiovascular disease (CVD) (P = 0.220). GLP-1RA also reduced the risk of cardiovascular death by 12%, of non-fatal stroke by 16%, of hospitalization for heart failure by 9%, of all-cause mortality by 11%, and the broad composite kidney outcome by 17%; the latter appeared to be driven only by a reduction in macroalbuminuria (HR, 0.76 [0.68-0.86]; P = 0.003). GLP-1RAs have moderate benefits concerning MACE, and also reduce hospitalization for heart failure and all-cause mortality; they also robustly reduce the incidence of macroalbuminuria, without affecting the progression of diabetic renal disease.
本文呈现了一项荟萃分析,比较了 2 型糖尿病(T2D)患者中胰高血糖素样肽-1 受体激动剂(GLP-1RAs)与安慰剂在心血管结局试验(CVOTs)中的心肾结局。我们进行了一项无语言限制的电子检索,检索时间截至 2019 年 6 月 15 日,以确定合格的试验。使用随机效应模型计算总体风险比(HR)和 95%置信区间(CI),对可用试验数据进行了荟萃分析。纳入了来自 7 项 CVOTs 的数据,包括 56004 名患者(68.9%有明确的心血管疾病)。GLP-1RA 降低了 13%的主要心血管事件(MACE)(HR,0.87;95%CI,0.80-0.96;P=0.011),而有或无心血管疾病(CVD)的患者亚组之间无显著异质性(P=0.220)。GLP-1RA 还降低了 12%的心血管死亡风险,16%的非致死性卒中风险,9%的心衰住院风险,11%的全因死亡率风险,以及 17%的广泛复合肾脏结局风险;后者似乎仅归因于白蛋白尿的减少(HR,0.76 [0.68-0.86];P=0.003)。GLP-1RA 在心肾结局方面有适度获益,还降低了心衰住院和全因死亡率,并且还能稳健地降低白蛋白尿的发生率,而不会影响糖尿病肾病的进展。