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遏制肥胖流行:GLP-1 受体激动剂是否应该成为肥胖治疗的标准?

Curbing the Obesity Epidemic: Should GLP-1 Receptor Agonists Be the Standard of Care for Obesity?

机构信息

Department of Internal Medicine, Section of Endocrinology, Diabetes, and Metabolism, Baylor College of Medicine, One Baylor Plaza, R618, Houston, TX, 77030, USA.

Department of Internal Medicine. Division of Endocrinology, Diabetes and Metabolism School of Medicine and Dentistry, University of Rochester, Box 693, 601 Elmwood Avenue, Rochester, NY, 14620, USA.

出版信息

Curr Cardiol Rep. 2024 Sep;26(9):1011-1019. doi: 10.1007/s11886-024-02097-4. Epub 2024 Jul 20.

Abstract

PURPOSE OF REVIEW

This article summarizes the medical management of obesity with an emphasis on incretin-based therapeutics that target the neuro-hormonal basis of obesity.

RECENT FINDINGS

Medications that mimic the effect of incretins, a group of peptide hormones released in response to nutrient intake that regulate appetite, result in potent and durable weight loss. Glucagon-like peptide 1 (GLP-1) agonists and glucose-dependent insulinotropic polypeptide (GIP) agonists such as semaglutide and tirzepatide are approved by the United States Food and Drug Administration (FDA) for the management of obesity. The SELECT trial demonstrated that semaglutide led to a reduction in major adverse cardiovascular events in patients without diabetes who were either overweight and had preexisting cardiovascular disease or obese.

SUMMARY

The treatment of obesity is critical to prevent the progression of cardiovascular-kidney-metabolic syndrome. Incretin-based therapies offer remarkable weight loss and reduce major cardiovascular adverse events.

摘要

目的综述

本文总结了肥胖的医学管理方法,重点介绍了基于肠促胰岛素的治疗方法,这些方法针对肥胖的神经激素基础。

最新发现

模仿肠促胰岛素(一种对营养摄入作出反应、调节食欲的肽类激素)作用的药物可导致强效且持久的体重减轻。美国食品和药物管理局(FDA)已批准胰高血糖素样肽 1(GLP-1)激动剂和葡萄糖依赖性胰岛素促泌多肽(GIP)激动剂,如司美格鲁肽和替西帕肽,用于肥胖症的治疗。SELECT 试验表明,对于无糖尿病但超重且有心血管疾病病史或肥胖的患者,司美格鲁肽可减少主要不良心血管事件。

总结

肥胖的治疗对于预防心血管-肾脏-代谢综合征的进展至关重要。基于肠促胰岛素的治疗方法可显著减轻体重并减少主要心血管不良事件。

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