Department of Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic, 9500 Euclid Ave, Desk JB1 Cleveland, OH, USA.
Beth Israel Deaconess Medical Center, 330 Brookline Ave Boston, MA, USA.
Eur Heart J. 2018 Jul 1;39(25):2368-2375. doi: 10.1093/eurheartj/ehx668.
Despite extensive clinical efforts to achieve stricter glycaemic control over the past few decades, cardiovascular (CV) disease remains the leading cause of death among diabetic patients. Recently, sodium-glucose cotransporter-2 (SGLT-2) inhibitors and glucagon-like peptide-1 receptor (GLP-1-R) agonists have gained attention due to their apparent effects in reducing CV mortality. Four CV randomized controlled trials: EMPA-REG, CANVAS, LEADER, and SUSTAIN-6, found a decrease in CV events among patients with type 2 diabetes on empagliflozin, canagliflozin, liraglutide, and semaglutide, respectively. In light of this data, the US Food and Drug Administration has recently approved empagliflozin for CV mortality reduction in type 2 diabetic patients, making it the first diabetes medication approved for such an indication. The purpose of this review is to summarize the results of novel anti-hyperglycaemic medication trials, and shed light on their mode of action and cardioprotective pathways.
尽管在过去几十年中,人们进行了广泛的临床努力以实现更严格的血糖控制,但心血管(CV)疾病仍然是糖尿病患者死亡的主要原因。最近,钠-葡萄糖共转运蛋白 2(SGLT-2)抑制剂和胰高血糖素样肽-1 受体(GLP-1-R)激动剂因其在降低 CV 死亡率方面的明显效果而受到关注。四项 CV 随机对照试验:EMPA-REG、CANVAS、LEADER 和 SUSTAIN-6 分别发现,在接受恩格列净、卡格列净、利拉鲁肽和司美格鲁肽治疗的 2 型糖尿病患者中,CV 事件减少。有鉴于此,美国食品和药物管理局最近批准恩格列净可降低 2 型糖尿病患者的 CV 死亡率,使其成为第一种为此类适应症获批的糖尿病药物。本文旨在总结新型降糖药物试验的结果,并阐明其作用机制和心脏保护途径。