Department of Cardiology and Cardiovascular Research Institute, Renmin Hospital of Wuhan University, 238 Jiefang Road, Wuhan, 430060, Hubei, China.
Hubei Key Laboratory of Cardiology, Wuhan, 430060, Hubei, China.
Cardiovasc Diabetol. 2024 Jul 15;23(1):252. doi: 10.1186/s12933-024-02312-0.
Sodium-glucose cotransporter type 2 inhibitors (SGLT2i) were initially recommended as oral anti-diabetic drugs to treat type 2 diabetes (T2D), by inhibiting SGLT2 in proximal tubule and reduce renal reabsorption of sodium and glucose. While many clinical trials demonstrated the tremendous potential of SGLT2i for cardiovascular diseases. 2022 AHA/ACC/HFSA guideline first emphasized that SGLT2i were the only drug class that can cover the entire management of heart failure (HF) from prevention to treatment. Subsequently, the antiarrhythmic properties of SGLT2i have also attracted attention. Although there are currently no prospective studies specifically on the anti-arrhythmic effects of SGLT2i. We provide clues from clinical and fundamental researches to identify its antiarrhythmic effects, reviewing the evidences and mechanism for the SGLT2i antiarrhythmic effects and establishing a novel paradigm involving intracellular sodium, metabolism and autophagy to investigate the potential mechanisms of SGLT2i in mitigating arrhythmias.
钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)最初被推荐作为口服抗糖尿病药物用于治疗 2 型糖尿病(T2D),通过抑制近曲小管中的 SGLT2 并减少钠和葡萄糖的肾重吸收。虽然许多临床试验表明 SGLT2i 在心血管疾病方面具有巨大的潜力。2022 年 AHA/ACC/HFSA 指南首次强调 SGLT2i 是唯一能够涵盖心力衰竭(HF)从预防到治疗的整个管理的药物类别。随后,SGLT2i 的抗心律失常特性也引起了关注。尽管目前尚无专门针对 SGLT2i 抗心律失常作用的前瞻性研究。我们从临床和基础研究中提供线索,以确定其抗心律失常作用,综述 SGLT2i 抗心律失常作用的证据和机制,并建立一个涉及细胞内钠、代谢和自噬的新范式,以研究 SGLT2i 减轻心律失常的潜在机制。