Suppr超能文献

司美格鲁肽用于体重管理的疗效和安全性:STEP 计划的证据。

Efficacy and safety of semaglutide for weight management: evidence from the STEP program.

机构信息

Penn Metabolic Medicine, Division of Endocrinology, University of Pennsylvania, Philadelphia, PA, USA.

Cedar Crosse Research Center, Chicago, IL, USA.

出版信息

Postgrad Med. 2022 Jan;134(sup1):5-17. doi: 10.1080/00325481.2022.2147326.

Abstract

Obesity is a global health challenge. It is a multifactorial, complex, and progressive disease associated with various health complications and increased mortality. Lifestyle modifications are central to weight management but may be insufficient to maintain clinically meaningful weight loss. Pharmacotherapies are recommended as an adjunct to lifestyle interventions to induce and sustain clinically meaningful weight loss and reduce the risk of comorbidities in appropriate patients. Glucagon-like peptide-1 is an incretin metabolic hormone responsible for a range of physiological effects, including glucose and appetite regulation. Several glucagon-like peptide-1 receptor agonists (GLP-1RAs) have been approved for the treatment of type 2 diabetes since 2005 including exenatide (short- and extended-release), lixisenatide, liraglutide, dulaglutide, albiglutide, and semaglutide. Of these, semaglutide (subcutaneous) and liraglutide are currently US Food and Drug Administration (FDA)-approved for chronic weight management in patients with or without diabetes. The phase 3 Semaglutide Treatment Effect in People with obesity (STEP) program was designed to investigate the effect of semaglutide versus placebo on weight loss, safety, and tolerability in adults with overweight or obesity. Following the submission of the results of the STEP 1-4 trials, the FDA approved once-weekly subcutaneous semaglutide 2.4 mg for chronic weight management in people with overweight or obesity in April 2021. Data from the program demonstrated that semaglutide (2.4 mg once weekly) achieved significant and sustained weight loss, together with improvements in cardiometabolic risk factors compared with placebo, and was generally well tolerated, with a safety profile consistent with other GLP-1RAs. The most common adverse events reported in STEP 1-5 were gastrointestinal events, which were transient, mild-to-moderate in severity, and typically resolved without permanent treatment discontinuation. This article reviews the data from STEP 1-5 and highlights clinically relevant findings for primary care providers.

摘要

肥胖是一个全球性的健康挑战。它是一种多因素、复杂和进行性的疾病,与各种健康并发症和死亡率增加有关。生活方式的改变是体重管理的核心,但可能不足以维持有临床意义的体重减轻。在适当的患者中,药物治疗被推荐作为生活方式干预的辅助手段,以诱导和维持有临床意义的体重减轻,并降低合并症的风险。胰高血糖素样肽-1 是一种肠促胰岛素代谢激素,负责一系列生理效应,包括葡萄糖和食欲调节。自 2005 年以来,已有几种胰高血糖素样肽-1 受体激动剂 (GLP-1RA) 被批准用于治疗 2 型糖尿病,包括艾塞那肽(短效和长效)、利西那肽、利拉鲁肽、度拉糖肽、阿必鲁肽和司美格鲁肽。其中,司美格鲁肽(皮下注射)和利拉鲁肽目前已获得美国食品和药物管理局 (FDA) 的批准,可用于有或无糖尿病的超重或肥胖患者的慢性体重管理。Semaglutide Treatment Effect in People with obesity (STEP) 项目的 3 期研究旨在研究司美格鲁肽与安慰剂相比在超重或肥胖成年人中对体重减轻、安全性和耐受性的影响。在 STEP 1-4 试验结果提交后,FDA 于 2021 年 4 月批准每周皮下注射 2.4 毫克司美格鲁肽用于超重或肥胖人群的慢性体重管理。该项目的数据表明,与安慰剂相比,司美格鲁肽(每周一次 2.4 毫克)可显著且持续地减轻体重,并改善心血管代谢风险因素,且总体耐受性良好,安全性与其他 GLP-1RA 一致。STEP 1-5 中报告的最常见不良事件是胃肠道事件,这些事件是短暂的、轻度至中度的,通常无需永久停药即可缓解。本文回顾了 STEP 1-5 的数据,并强调了对初级保健提供者具有临床意义的发现。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验