Duke Clinical Research Institute, 300 W Morgan Street, Durham, NC 27701, USA.
Division of Cardiology, University of Texas Southwestern Medical Center, Dallas, TX 75235-8830, USA.
Heart Fail Clin. 2022 Oct;18(4):597-607. doi: 10.1016/j.hfc.2022.03.007.
Sodium-glucose cotransporter-2 inhibitors (SGLT-2i) improve the risk for heart and kidney failure. However, their effects on major atherosclerotic cardiovascular events (MACE) are less clear. Although outcomes trials of drugs for diabetes were not powered to prove superiority, the totality of trial data yields an estimate of ∼11% relative reduction for MACE (HR 0.89, 95%CI 0.82-0.96) and neutral on stroke (HR 0.92, 95%CI 0.79-1.08). In animal models, SGLT-2i favorably affects plaque size, composition, and inflammatory pathways; human data in this regard are lacking. Ongoing trials are evaluating SGLT-2i efficacy in heart failure, kidney disease, and postmyocardial infarction populations, independent of diabetes status.
钠-葡萄糖共转运蛋白 2 抑制剂(SGLT-2i)可增加心脏和肾脏衰竭的风险。然而,它们对主要动脉粥样硬化性心血管事件(MACE)的影响尚不清楚。尽管糖尿病药物的结局试验没有证明优越性,但试验数据的总体结果估计 MACE 的相对减少约为 11%(HR 0.89,95%CI 0.82-0.96),对中风无影响(HR 0.92,95%CI 0.79-1.08)。在动物模型中,SGLT-2i 可有利地影响斑块大小、组成和炎症途径;在这方面,人体数据尚缺乏。正在进行的试验正在评估 SGLT-2i 在心力衰竭、肾脏疾病和心肌梗死后人群中的疗效,而不考虑糖尿病状况。