Pradhan Akshyaya, Vohra Shweta, Vishwakarma Pravesh, Sethi Rishi
Department of Cardiology, King George's Medical University, Lucknow, Uttar Pradesh, India.
J Family Med Prim Care. 2019 Jun;8(6):1855-1862. doi: 10.4103/jfmpc.jfmpc_232_19.
SGLT-2 inhibitors are a novel class of anti-diabetic agents which act by inhibiting glucose reabsorption in proximal convoluted tubules of kidney. Apart from maintaining glucose homeostasis they exert a number of positive effects on the cardiovascular system like weight loss, decreasing blood pressure, preserving renal function, reducing triglycerides, natriuresis and improving endothelial dysfunction. In large clinical trials, all the three prototype agents - Empaglifozin, Canaglifozin and dapaglifozin have shown reductions in major adverse cardiovascular events including cardiovascular deaths, non fatal MI, stroke and heart failure (HF) hospitalizations. The reduction in heart failure hospitalization is a surprising finding and trials of these drug are now underway for HF also. More surprising is the fact that the benefits are comparable or even better that achieved by recently approved novel drugs for HF. In this review, we briefly discuss the pathophysiology of HF in diabetes, describe the prototype SGLT-2 molecules available, their data from large cardiovascular outcome trials till date and their role in current practice of diabetes management.
钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂是一类新型抗糖尿病药物,其作用机制是抑制肾脏近端曲小管中的葡萄糖重吸收。除了维持血糖稳态外,它们还对心血管系统产生许多积极影响,如减轻体重、降低血压、保护肾功能、降低甘油三酯、促进尿钠排泄以及改善内皮功能障碍。在大型临床试验中,三种原型药物——恩格列净、卡格列净和达格列净均显示出主要不良心血管事件减少,包括心血管死亡、非致死性心肌梗死、中风和心力衰竭(HF)住院治疗。心力衰竭住院率的降低是一个令人惊讶的发现,目前这些药物针对心力衰竭的试验也正在进行。更令人惊讶的是,这些益处与最近批准的用于治疗心力衰竭的新型药物相当,甚至更好。在这篇综述中,我们简要讨论糖尿病中心力衰竭的病理生理学,描述现有的SGLT-2原型分子、它们截至目前来自大型心血管结局试验的数据以及它们在当前糖尿病管理实践中的作用。