Forschergruppe Diabetes e.V. at Munich Helmholtz Centre, Germany.
Forschergruppe Diabetes e.V. at Munich Helmholtz Centre, Germany.
Diabetes Res Clin Pract. 2020 Mar;161:108054. doi: 10.1016/j.diabres.2020.108054. Epub 2020 Feb 6.
Based on cardiovascular (CV) outcome trials (CVOTs) being available on the brink of the 2020ies, CV safety assessed by major adverse CV event outcomes has been established for the classes of glucagon-like-peptide-1 receptor agonists (GLP1 RAs), sodium-glucose-co-transporter-2 inhibitors (SGLT2-is), and dipeptidyl-peptidase-4 inhibitors (DPP4is) in patients at very high CV risk. This should be relevant to the whole population with diabetes in general as well as the fact that no new serious and unexpected side effects have emerged within these trials. At the same time, treatment paradigm shifting CV benefit has been confirmed for two classes of diabetes medications (SGLT2is & GLP1 RAs), with important additional benefit of SGLT2is reducing heart failure and hard renal endpoints, both in patients with such diseases, but also in patients being in primary prevention. Moreover, the "soft" renal outcome of albuminurea progression seems to be attenuated by all three classes of drugs discussed in this overview. Still ongoing CVOTs are not expected to essentially change the current notions, with the potential of some differentiation regarding subgroups of primary heart failure populations in relation to treatment with SGLT2is.
基于心血管(CV)结局试验(CVOT)在 21 世纪 20 年代即将问世,通过主要不良 CV 事件结局评估的 CV 安全性已在极高 CV 风险患者中确立了胰高血糖素样肽-1 受体激动剂(GLP1 RAs)、钠-葡萄糖共转运蛋白-2 抑制剂(SGLT2-is)和二肽基肽酶-4 抑制剂(DPP4is)的类别。这应该与一般糖尿病的整个人群以及这些试验中没有出现新的严重和意外的副作用这一事实有关。与此同时,两种糖尿病药物类别(SGLT2is 和 GLP1 RAs)的治疗模式转移 CV 获益已得到证实,SGLT2is 还具有重要的额外获益,可降低心力衰竭和肾脏硬终点的发生风险,无论患者是否患有此类疾病,即使是在一级预防中也是如此。此外,所有三种讨论的药物类别似乎都可以减轻白蛋白尿进展的“软性”肾脏结局。仍在进行的 CVOT 预计不会从根本上改变当前的观念,而在与 SGLT2is 治疗相关的原发性心力衰竭人群亚组方面可能存在一些差异。