Xu Dan, Chandler Owain, Wee Cleo, Ho Chau, Affandi Jacquita S, Yang Daya, Liao Xinxue, Chen Wei, Li Yanbing, Reid Christopher, Xiao Haipeng
Faculty of Health Sciences, CCRE, Curtin School of Population Health, Curtin University, Perth, WA, Australia.
Faculty of Health Sciences, Curtin Medical School, Curtin University, Perth, WA, Australia.
Front Med (Lausanne). 2021 Aug 23;8:712671. doi: 10.3389/fmed.2021.712671. eCollection 2021.
Sodium-glucose cotransporter-2 inhibitors (SGLT2i) are a relatively novel class of drug for treating type 2 diabetes mellitus (T2DM) that inhibits glucose reabsorption in the renal proximal tubule to promote glycosuria and reduce blood glucose levels. SGLT2i has been clinically indicated for treating T2DM, with numerous recent publications focussing on both primary and secondary prevention of cardiovascular and renal events in Type 2 diabetic patients. The most recent clinical trials showed that SGLT2i have moderately significant beneficial effects on atherosclerotic major adverse cardiovascular events (MACE) in patients with histories of atherosclerotic cardiovascular disease. In this review and analysis, SGLT2i have however demonstrated clinically significant benefits in reducing hospitalisation for heart failure and worsening of chronic kidney disease (CKD) irrespective of pre-existing atherosclerotic cardiovascular disease or previous heart failure history. A meta-analysis suggests that all SGLT2 inhibitors demonstrated the therapeutic benefit on all-cause and cardiovascular mortality, as shown in EMPAREG OUTCOME study with a significant decrease in myocardial infarction, without increased stroke risk. All the above clinical trial recruited type 2 diabetic patients. This article aims to postulate and review the possible primary prevention role of SGLT2i in healthy individuals by reviewing the current literature and provide a prospective overview. The emphasis will include primary prevention of Type 2 Diabetes, Heart Failure, CKD, Hypertension, Obesity and Dyslipidaemia in healthy individuals, whom are defined as healthy, low or intermediate risks patients.
钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)是一类相对新型的用于治疗2型糖尿病(T2DM)的药物,它通过抑制肾近端小管中的葡萄糖重吸收来促进糖尿并降低血糖水平。SGLT2i已被临床用于治疗T2DM,近期有大量出版物聚焦于2型糖尿病患者心血管和肾脏事件的一级和二级预防。最新的临床试验表明,SGLT2i对有动脉粥样硬化性心血管疾病病史的患者的动脉粥样硬化主要不良心血管事件(MACE)具有中度显著的有益作用。然而,在本次综述和分析中,无论患者先前是否存在动脉粥样硬化性心血管疾病或心力衰竭病史,SGLT2i在降低心力衰竭住院率和慢性肾脏病(CKD)恶化方面均显示出具有临床意义的益处。一项荟萃分析表明,所有SGLT2抑制剂均对全因死亡率和心血管死亡率显示出治疗益处,如在EMPAREG OUTCOME研究中所示,心肌梗死显著减少,且中风风险未增加。上述所有临床试验均招募2型糖尿病患者。本文旨在通过回顾当前文献,推测和综述SGLT2i在健康个体中可能的一级预防作用,并提供前瞻性概述。重点将包括对健康个体(定义为健康、低风险或中度风险患者)的2型糖尿病、心力衰竭、CKD、高血压、肥胖和血脂异常的一级预防。