Scheen André J
Service de diabétologie, nutrition et maladies métaboliques, CHU Sart Tilman, 4000 Liège.
Unité de pharmacologie clinique, Centre interdisciplinaire de recherche du médicament (CIRM), Liège Université, 4000 Liège, Belgique.
Rev Med Suisse. 2019 Aug 21;15(659):1436-1441.
Some sodium-glucose cotransporter type 2 inhibitors (SGLT2is) and glucagon-like peptide-1 receptor agonists (GLP-1RAs) have proven their ability to reduce major cardiovascular events in patients with type 2 diabetes at high cardiovascular risk. Furthermore, SGLT2is reduce the risk of hospitalization for heart failure and the progression of renal disease. The 2018 ADA-EASD consensus gave the preference to either SGLT2is or GLP-1 RAs to prevent these complications. Underlying protective mechanisms are complex, differ between the two pharmacological classes and are potentially complementary, thus providing a rationale for a combination in patients at very high risk. Some studies already showed positive complementary effects on glucose control, body weight and arterial blood pressure, but not on cardiovascular and/or renal outcomes yet.
一些钠-葡萄糖协同转运蛋白2抑制剂(SGLT2is)和胰高血糖素样肽-1受体激动剂(GLP-1RAs)已证明,它们能够降低心血管疾病高风险的2型糖尿病患者发生主要心血管事件的风险。此外,SGLT2is还能降低心力衰竭住院风险和肾病进展风险。2018年美国糖尿病协会(ADA)和欧洲糖尿病研究协会(EASD)的共识更倾向于使用SGLT2is或GLP-1RAs来预防这些并发症。潜在的保护机制很复杂,在这两类药物之间存在差异,并且可能具有互补性,因此为极高风险患者联合用药提供了理论依据。一些研究已经显示,联合用药对血糖控制、体重和动脉血压有积极的互补作用,但对心血管和/或肾脏结局尚无此类作用。