College of Medicine & Dentistry, James Cook University, Townsville, QLD, Australia.
Royal Brisbane and Women's Hospital, Faculty of Medicine, University of Queensland, Herston, QLD, Australia.
ESC Heart Fail. 2021 Oct;8(5):4093-4118. doi: 10.1002/ehf2.13483. Epub 2021 Jul 5.
To systematically review randomized controlled trials assessing effects of sodium-glucose cotransporter 2 inhibitors (SGLT2is) on hospitalization for heart failure (HHF) and cardiac structure/function and explore randomized controlled trial (RCT)-derived evidence for SGLT2i efficacy mechanisms in heart failure (HF).
Systematic searches of Medline and Embase were performed. In seven trials [3730-17 160 patients; low risk of bias (RoB)], SGLT2is significantly reduced the relative risk of HHF by 27-39% vs. placebo, including in two studies in patients with HF with reduced ejection fraction with or without type-2 diabetes mellitus (T2DM). Improvements in conventional cardiovascular risk factors, including glycaemic levels, cannot account for these effects. Five trials (56-105 patients; low RoB) assessed the effects of 6-12 months of SGLT2i treatment on left ventricular structure/function; four reported significant improvements vs. placebo, and one did not. Five trials (low RoB) assessed SGLT2i treatment effects on serum N-terminal pro B-type natriuretic peptide levels; significant reductions vs. placebo were reported after 8-12 months (two studies; 3730-4744 patients) but not ≤12 weeks (three studies; 80-263 patients). Limited available RCT-derived evidence suggests various possible cardioprotective SGLT2i mechanisms, including improved haemodynamics (natriuresis and reduced interstitial fluid without blood volume contraction/neurohormonal activation) and vascular function, enhanced erythropoiesis, reduced tissue sodium and epicardial fat/inflammation, decreased sympathetic tone, and beneficial changes in cellular energetics.
Sodium-glucose cotransporter 2 inhibitors reduce HHF regardless of T2DM status, and reversal of adverse left ventricular remodelling likely contributes to this efficacy. Hypothesis-driven mechanistic trials remain sparse, although numerous trials are planned or ongoing.
系统回顾评估钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)对心力衰竭(HF)住院和心脏结构/功能影响的随机对照试验(RCT),并探讨 HF 中 SGLT2i 疗效机制的 RCT 衍生证据。
对 Medline 和 Embase 进行了系统检索。在 7 项试验[3730-17160 例患者;低偏倚风险(RoB)]中,与安慰剂相比,SGLT2i 显著降低了 HHF 的相对风险 27-39%,包括在伴有或不伴有 2 型糖尿病(T2DM)的射血分数降低的 HF 患者的两项研究中。包括血糖水平在内的常规心血管危险因素的改善不能解释这些作用。5 项试验(56-105 例患者;低 RoB)评估了 SGLT2i 治疗 6-12 个月对左心室结构/功能的影响;四项报告与安慰剂相比有显著改善,一项则没有。5 项试验(低 RoB)评估了 SGLT2i 治疗对血清 N 末端 pro B 型利钠肽水平的影响;与安慰剂相比,8-12 个月后报告了显著降低(两项研究;3730-4744 例患者),但在≤12 周时没有(三项研究;80-263 例患者)。有限的 RCT 衍生证据表明,SGLT2i 具有多种可能的心脏保护机制,包括改善血液动力学(利尿和减少间质液而不引起血容量收缩/神经激素激活)和血管功能、增强红细胞生成、减少组织钠和心外膜脂肪/炎症、降低交感神经张力以及细胞能量代谢的有益变化。
SGLT2i 可降低 HHF,无论 T2DM 状态如何,并且逆转不良的左心室重构可能有助于这种疗效。尽管计划或正在进行许多试验,但基于假说的机制试验仍然很少。