Department of Endocrinology, Institute of Postgraduate Medical Education and Research, Kolkata, 700020, India.
Department of Endocrinology, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Indian Heart J. 2023 Mar-Apr;75(2):122-127. doi: 10.1016/j.ihj.2023.03.003. Epub 2023 Mar 11.
To provide a pooled effect of sodium-glucose cotransporter-2 inhibitors (SGLT2i) on cardiovascular outcomes in patients with heart failure with preserved ejection fraction (HFpEF: ≥50%) or/and mildly reduced EF (HFmrEF: 41-49%) regardless of baseline diabetes.
We systemically searched PubMed/MEDLINE, Embase, Web of Science databases and clinical trial registries using appropriate keywords till August 28, 2022, to identify randomized controlled trials (RCTs) or post-hoc analysis of RCTs, reporting cardiovascular death (CVD) and/or urgent visits/hospitalization for heart failure(HHF) in patients with HFmrEF/HFpEF receiving SGLTi vs. placebo. Hazard ratios (HR) with 95% confidence intervals (CI) for outcomes were pooled together using generic inverse variance method with fixed-effects model.
We identified six RCTs, pooling data retrieved from 15,769 patients with HFmrEF/HFpEF. Pooled analysis showed that compared to placebo, SGLT2i use was significantly associated with improved CVD/HHF outcomes in HFmrEF/HFpEF (pooled HR 0.80, 95% CI: 0.74, 0.86, p < 0.001, I = 0%). When separately analyzed, benefits of SGLT2i remained significant across HFpEF (N = 8891, HR 0.79, 95% CI: 0.71, 0.87, p < 0.001, I = 0%) and HFmrEF (N = 4555, HR 0.77, 95% CI: 0.67, 0.89, p < 0.001, I = 40%). Consistent benefits were observed also in HFmrEF/HFpEF subgroup without baseline diabetes (N = 6507, HR 0.80, 95% CI: 0.70, 0.91, p < 0.001, I = 0%). Sensitivity analysis including the DELIVER and EMPEROR-Preserved trials found a trend towards significant beneficial effects on CV deaths with no heterogeneity (HR 0.90, 95% CI: 0.79, 1.02, p = 0.08, I = 0%).
This meta-analysis established the place of SGLT2i as a foundational therapy among patients with HF with preserved and mildly reduced EF regardless of diabetes.
无论基线是否患有糖尿病,评估钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)对射血分数保留的心力衰竭(HFpEF:≥50%)或/和轻度射血分数降低的心力衰竭(HFmrEF:41-49%)患者心血管结局的汇总效果。
我们系统性地检索了 PubMed/MEDLINE、Embase、Web of Science 数据库和临床试验注册库,使用了适当的关键词,截至 2022 年 8 月 28 日,以确定接受 SGLTi 与安慰剂治疗的 HFmrEF/HFpEF 患者的心血管死亡(CVD)和/或心力衰竭紧急就诊/住院(HHF)的随机对照试验(RCT)或 RCT 的事后分析。使用固定效应模型的通用逆方差法汇总结局的风险比(HR)及其 95%置信区间(CI)。
我们共纳入了 6 项 RCT,共纳入了 15769 例 HFmrEF/HFpEF 患者的数据。汇总分析显示,与安慰剂相比,SGLT2i 可显著改善 HFmrEF/HFpEF 患者的 CVD/HHF 结局(汇总 HR 0.80,95%CI:0.74,0.86,p<0.001,I=0%)。当单独分析时,SGLT2i 的获益在 HFpEF(N=8891,HR 0.79,95%CI:0.71,0.87,p<0.001,I=0%)和 HFmrEF(N=4555,HR 0.77,95%CI:0.67,0.89,p<0.001,I=40%)患者中仍然显著。在无基线糖尿病的 HFmrEF/HFpEF 亚组(N=6507,HR 0.80,95%CI:0.70,0.91,p<0.001,I=0%)中也观察到了一致的获益。敏感性分析纳入了 DELIVER 和 EMPEROR-Preserved 试验,发现 CV 死亡的获益有显著趋势,但存在异质性(HR 0.90,95%CI:0.79,1.02,p=0.08,I=0%)。
本荟萃分析确定了 SGLT2i 作为射血分数保留和轻度降低的心力衰竭患者的基础治疗药物的地位,无论是否患有糖尿病。