Gomez-Peralta Fernando, Abreu Cristina
Endocrinology and Nutrition Unit, Hospital General de Segovia, Segovia, Spain,
Drug Des Devel Ther. 2019 Feb 20;13:731-738. doi: 10.2147/DDDT.S165372. eCollection 2019.
Type 2 diabetes mellitus (T2DM) has become one of the leading causes of morbidity and mortality in developed countries. Low efficacy, weight gain, and hypoglycemia are the main pitfalls of previous treatments for T2DM. New therapies have been designed with the aim of improving the results in efficacy and quality of life. Glucagon-like peptide 1 (GLP-1) receptor agonists (GLP-1 RA) increase glucose-dependent insulin secretion, decrease gastric emptying, and reduce postprandial glucagon secretion. The last GLP-1 RA approved by the US Food and Drug Administration and European Medicines Agency was semaglutide. This review describes its pharmacology, core clinical data coming from the randomized controlled trials included in the development program, proven cardiovascular benefits, safety issues, and precautions for the use of semaglutide in special populations. Additionally, an overview of the positioning of semaglutide in T2DM therapy and practical issues regarding semaglutide initiation are offered.
2型糖尿病(T2DM)已成为发达国家发病和死亡的主要原因之一。疗效不佳、体重增加和低血糖是既往T2DM治疗的主要缺陷。已设计出新的疗法,旨在提高疗效和生活质量。胰高血糖素样肽1(GLP-1)受体激动剂(GLP-1 RA)可增加葡萄糖依赖性胰岛素分泌,减少胃排空,并降低餐后胰高血糖素分泌。美国食品药品监督管理局和欧洲药品管理局批准的最新GLP-1 RA是司美格鲁肽。本综述描述了其药理学、来自开发项目中纳入的随机对照试验的核心临床数据、已证实的心血管益处、安全性问题以及司美格鲁肽在特殊人群中使用的注意事项。此外,还概述了司美格鲁肽在T2DM治疗中的定位以及司美格鲁肽起始治疗的实际问题。