Mechanisms of SGLT2 Inhibitors in Heart Failure and Their Clinical Value

被引:20
|
作者
Xie, Yafei [1 ,2 ]
Wei, Yujie [1 ,2 ]
Li, Dan [1 ,2 ]
Pu, Jie [1 ,2 ]
Ding, Hong [2 ]
Zhang, Xiaowei [1 ,2 ,3 ]
机构
[1] Lanzhou Univ, Second Coll Clin Med, Lanzhou, Peoples R China
[2] Lanzhou Univ, Hosp 2, Dept Cardiol, Lanzhou, Peoples R China
[3] Lanzhou Univ, Hosp 2, Dept Cardiol, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
SGLT2; inhibitors; heart failure; diabetes; CONSENSUS DECISION PATHWAY; REDUCED EJECTION FRACTION; EMPA-REG; CARDIOVASCULAR OUTCOMES; NA+/H+ EXCHANGER; GLUCOSE TRANSPORTERS; EMPAGLIFLOZIN; DAPAGLIFLOZIN; MORTALITY; CANAGLIFLOZIN;
D O I
10.1097/FJC.0000000000001380
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sodium-glucose cotransporter 2 (SGLT2) inhibitors are widely used to treat diabetes mellitus. Abundant evidence has shown that SGLT2 inhibitors can reduce hospitalization for heart failure (HF) in patients with or without diabetes. An increasing number of studies are being conducted on the mechanisms of action of SGLT2 inhibitors in HF. Our review summarizes a series of clinical trials on the cardioprotective effects of SGLT2 inhibitors in the treatment of HF. We have summarized several classical SGLT2 inhibitors in cardioprotection research, including empagliflozin, dapagliflozin, canagliflozin, ertugliflozin, and sotagliflozin. In addition, we provided a brief overview of the safety and benefits of SGLT2 inhibitors. Finally, we focused on the mechanisms of SGLT2 inhibitors in the treatment of HF, including ion-exchange regulation, volume regulation, ventricular remodeling, and cardiac energy metabolism. Exploring the mechanisms of SGLT2 inhibitors has provided insight into repurposing these diabetic drugs for the treatment of HF.
引用
收藏
页码:4 / 14
页数:11
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