Kolling Institute, University of Sydney, Sydney, NSW, Australia; Royal North Shore Hospital, Sydney, NSW, Australia.
Royal North Shore Hospital, Sydney, NSW, Australia; The George Institute for Global Health, UNSW Sydney, Sydney, NSW, Australia.
Adv Chronic Kidney Dis. 2021 Jul;28(4):298-308. doi: 10.1053/j.ackd.2021.02.006.
Large-scale randomized trials have demonstrated the remarkable capacity of sodium-glucose cotransporter 2 inhibitors to reduce the risk of cardiovascular outcomes and kidney disease progression, irrespective of the presence or absence of type 2 diabetes mellitus. Although the results of these trials have transformed clinical practice guidelines, the mechanisms underpinning the wide-ranging benefits of this class of agents remain incompletely understood and subject to ongoing investigation. Improvements in cardiometabolic risk factors such as glucose, blood pressure, body weight, and albuminuria likely contribute. However, other direct effects on physiological and cellular function, such as restoration of tubuloglomerular feedback, improvements in kidney and cardiac oxygenation and energy efficiency, as well as restoration of normal autophagy are also likely to be important. This review summarizes the rationale and potential mechanisms for cardiorenal protection with sodium-glucose cotransporter 2 inhibitors in people with and without diabetes, their relative importance, and the experimental and clinical lines of evidence supporting these hypotheses.
大规模随机临床试验表明,钠-葡萄糖共转运蛋白 2 抑制剂具有显著降低心血管结局和肾脏疾病进展风险的能力,无论是否存在 2 型糖尿病。尽管这些试验的结果改变了临床实践指南,但该类药物广泛获益的机制仍不完全了解,仍在不断研究中。改善血糖、血压、体重和蛋白尿等心血管代谢危险因素可能有一定作用。然而,其他对生理和细胞功能的直接影响,如肾小管-肾小球反馈的恢复、肾脏和心脏氧合及能量效率的改善,以及正常自噬的恢复,也可能很重要。这篇综述总结了钠-葡萄糖共转运蛋白 2 抑制剂在有或没有糖尿病的患者中具有心脏肾脏保护作用的基本原理和潜在机制、它们的相对重要性,以及支持这些假说的实验和临床证据。