The George Institute for Global Health, University of New South Wales, Sydney, NSW 2042, Australia.
Department of Cardiology, Royal Prince Alfred Hospital, Sydney, NSW 2050, Australia.
Cells. 2021 Oct 9;10(10):2699. doi: 10.3390/cells10102699.
Sodium glucose cotransporter 2 (SGLT2) inhibitors are a class of medication with broad cardiovascular benefits in those with type 2 diabetes, chronic kidney disease, and heart failure. These include reductions in major adverse cardiac events and cardiovascular death. The mechanisms that underlie their benefits in atherosclerotic cardiovascular disease (ASCVD) are not well understood, but they extend beyond glucose lowering. This narrative review summarises the ASCVD benefits of SGLT2 inhibitors seen in large human outcome trials, as well as the mechanisms of action explored in rodent and small human studies. Potential pathways include favourable alterations in lipid metabolism, inflammation, and endothelial function. These all require further investigation in large human clinical trials with mechanistic endpoints, to further elucidate the disease modifying benefits of this drug class and those who will benefit most from it.
钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂是一类具有广泛心血管益处的药物,适用于 2 型糖尿病、慢性肾脏病和心力衰竭患者。这些益处包括降低主要不良心脏事件和心血管死亡的风险。其在动脉粥样硬化性心血管疾病(ASCVD)中的获益机制尚不完全清楚,但不仅仅局限于降低血糖。本文综述了大型人类结局试验中观察到的 SGLT2 抑制剂在 ASCVD 方面的获益,以及在啮齿动物和小样本人类研究中探索的作用机制。潜在的途径包括脂质代谢、炎症和内皮功能的有利改变。这些都需要在具有机制终点的大型人类临床试验中进一步研究,以进一步阐明这类药物的疾病改善益处以及哪些患者将从中获益最大。