Peng Xiaodong, Li Linling, Zhang Mengxia, Zhao Qianqian, Wu Kui, Bai Rong, Ruan Yanfei, Liu Nian
Department of Cardiology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Front Physiol. 2020 Aug 4;11:912. doi: 10.3389/fphys.2020.00912. eCollection 2020.
Sodium-glucose cotransporter 2 inhibitors (SGLT2i) are a novel class of glucose-lowering agents that significantly improve the prognosis of patients with type 2 diabetes (T2D) and heart failure. SGLT2i has recently been implicated in the treatment of atrial fibrillation (AF) with clinical data demonstrating that these agents decrease the incidence of AF events in patients with T2D. Fundamental findings have suggested that SGLT2i may alleviate atrial electrical and structural remodeling. The underlying mechanisms of SGLT2i are likely associated with balancing the sodium and calcium handling disorders and mitigating the mitochondrial dysfunction in atrial myocytes. This review illustrates the advances in understanding the underlying mechanisms of SGLT2i as an evolving treatment modality for AF.
钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)是一类新型降糖药物,可显著改善2型糖尿病(T2D)和心力衰竭患者的预后。最近有临床数据表明SGLT2i可降低T2D患者房颤(AF)事件的发生率,提示其可用于AF的治疗。基础研究结果表明,SGLT2i可能减轻心房电重构和结构重构。SGLT2i的潜在机制可能与平衡钠和钙处理紊乱以及减轻心房肌细胞的线粒体功能障碍有关。本文综述了对SGLT2i作为AF一种不断发展的治疗方式的潜在机制的认识进展。