Hu Ying
Department of Endocrinology, Lankenau Hospital, Main Line Health System, Wynnewood, PA 19096, USA.
Chronic Dis Transl Med. 2019 Mar 15;5(1):25-36. doi: 10.1016/j.cdtm.2019.01.001. eCollection 2019 Mar.
Treatment intended to lower cardiovascular (CV) risk in patients with diabetes has always been a primary goal of diabetes treatment. Due to the subdued effects of reducing hemoglobin A1c (HbA1c) on macrovascular complications, controlling other CV risk factors such as hypertension and hyperlipidemia instead of hyperglycemia has been the mainstay treatment to improve CV outcome in patients with type 2 diabetes mellitus (T2DM) until recent years. This review is intended to summarize and compare the results from the available cardiovascular outcome trials (CVOTs) for the two classes of glucose lowering drug: sodium-glucose co-transporter 2 inhibitor (SGLT2i) and glucagon-like peptide-1 receptor agonist (GLP-1 RA). The results including the EMPA-REG, CANVAS program and DECLARE-TIMI 58 trials for SGLT2i, and the ELIXA, LEADER, SUSTAIN-6, EXSCEL and HARMONY trials for GLP-1 RA were summarized. The potential mechanisms of these CV beneficial effects and the optimal CV risk reduction treatment in patients with T2DM based on patient risk stratification and evidence from these CVOTs in real-world setting were discussed.
旨在降低糖尿病患者心血管(CV)风险的治疗一直是糖尿病治疗的主要目标。由于降低糖化血红蛋白(HbA1c)对大血管并发症的作用有限,直到近年来,控制高血压和高脂血症等其他CV风险因素而非高血糖一直是改善2型糖尿病(T2DM)患者CV结局的主要治疗方法。本综述旨在总结和比较两类降糖药物:钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)和胰高血糖素样肽-1受体激动剂(GLP-1 RA)的现有心血管结局试验(CVOT)结果。总结了SGLT2i的EMPA-REG、CANVAS项目和DECLARE-TIMI 58试验以及GLP-1 RA的ELIXA、LEADER、SUSTAIN-6、EXSCEL和HARMONY试验的结果。讨论了这些CV有益作用的潜在机制以及基于患者风险分层和这些现实世界CVOT证据的T2DM患者最佳CV风险降低治疗方法。