Pahud de Mortanges Aurélie, Salvador Dante, Laimer Markus, Muka Taulant, Wilhelm Matthias, Bano Arjola
Faculty of Medicine, University of Bern, Bern, Switzerland.
Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.
Front Pharmacol. 2021 Nov 5;12:751214. doi: 10.3389/fphar.2021.751214. eCollection 2021.
Sodium glucose cotransporter 2 inhibitors (SGLT2-is) are antidiabetic drugs that improve glycemic control by limiting urinary glucose reuptake in the proximal tubule. SGLT2-is might suppress atherosclerotic processes and ameliorate the prognosis of patients with diabetes mellitus diagnosed with or at high risk of atherosclerotic cardiovascular disease (ASCVD). In this mini review, we examine the role of SGLT2-is in the development and progression of atherosclerosis throughout its spectrum, from subclinical atherosclerosis to ASCVD. -PubMed and Google Scholar were searched for publications related to SGLT2-is and atherosclerosis. All types of articles were considered, including clinical trials, animal studies, observations, and reviews and meta-analyses. Data were examined according to their impact and clinical relevance. -We first review the underlying mechanisms of SGLT2-is on the development and progression of atherosclerosis, including favorable effects on lipid metabolism, reduction of systemic inflammation, and improvement of endothelial function. We then discuss the putative impact of SGLT2-is on the formation, composition, and stability of atherosclerotic plaque. Furthermore, we evaluate the effects of SGLT2-is in subclinical atherosclerosis assessed by carotid intima media thickness and pulse wave velocity. Subsequently, we summarize the effects of SGLT2-is in ASCVD events, including ischemic stroke, angina pectoris, myocardial infarction, revascularization, and peripheral artery disease, as well as major adverse cardiovascular events, cardiovascular mortality, heart failure, and chronic kidney disease. Moreover, we examine factors that could modify the role of SGLT2-is in atherosclerosis, including sex, age, diabetes, glycemic control, ASCVD, and SGLT2-i compounds. Additionally, we propose future directions that can improve our understanding of SGLT2-is and atherosclerosis.
钠-葡萄糖协同转运蛋白2抑制剂(SGLT2抑制剂)是一类抗糖尿病药物,通过限制近端小管对尿葡萄糖的重吸收来改善血糖控制。SGLT2抑制剂可能会抑制动脉粥样硬化进程,并改善已诊断患有动脉粥样硬化性心血管疾病(ASCVD)或有ASCVD高风险的糖尿病患者的预后。在这篇小型综述中,我们研究了SGLT2抑制剂在动脉粥样硬化从亚临床动脉粥样硬化到ASCVD整个病程的发生和发展中所起的作用。我们检索了PubMed和谷歌学术中与SGLT2抑制剂和动脉粥样硬化相关的出版物。考虑了所有类型的文章,包括临床试验、动物研究、观察性研究以及综述和荟萃分析。根据其影响力和临床相关性对数据进行了审查。我们首先回顾SGLT2抑制剂对动脉粥样硬化发生和发展的潜在机制,包括对脂质代谢的有利影响、全身炎症的减轻以及内皮功能的改善。然后我们讨论SGLT2抑制剂对动脉粥样硬化斑块形成、成分和稳定性的假定影响。此外,我们评估SGLT2抑制剂在通过颈动脉内膜中层厚度和脉搏波速度评估的亚临床动脉粥样硬化中的作用。随后我们总结SGLT2抑制剂在ASCVD事件中的作用,包括缺血性中风、心绞痛、心肌梗死、血运重建和外周动脉疾病,以及主要不良心血管事件、心血管死亡率、心力衰竭和慢性肾脏病。此外,我们研究了可能改变SGLT2抑制剂在动脉粥样硬化中作用的因素,包括性别、年龄、糖尿病、血糖控制、ASCVD和SGLT2抑制剂化合物。此外,我们提出了未来的研究方向,以增进我们对SGLT2抑制剂和动脉粥样硬化的理解。