Discontinuing glucagon-like peptide-1 receptor agonists and body habitus: A systematic review and meta-analysis.

IF 8 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Obesity Reviews Pub Date : 2025-04-04 DOI:10.1111/obr.13929
Sara Berg, Hannah Stickle, Suzanne J Rose, Eric C Nemec
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引用次数: 0

Abstract

Research on Glucagon-like peptide 1 receptor agonist (GLP-1RA) has mainly focused on the efficacy of weight loss and not the long-term efficacy of weight loss maintenance. This systematic review and meta-analysis aims to evaluate the sustainability of weight loss of patients taking GLP-1RAs following the discontinuation of the drug. EBSCOhost was used to simultaneously search Academic Search Premier, CINHAL Ultimate, Cochrane Central Register of Controlled Trials, MEDLINE with full text, Cochrane Database of Systematic Reviews, and separate PubMed search was systematically investigated using a predetermined search strategy from inception to February 1st, 2024. The authors extracted data regarding body weight change from baseline on treatment and off treatment, change in waist circumference from baseline on and off treatment, and change in BMI from baseline on and off treatment. Meta-analysis was conducted using RevMan (version 5.4) to calculate pooled mean differences using a Der Simonian-Laird Random Effects model. ResultsThe initial search yielded 497 relevant articles and, after screening, retained 8 randomized controlled trials comprised of 2372 participants, all with a BMI ≥ 27 kg/m2. After discontinuing GLP-1RA therapy, weight regain was proportional to the original weight loss. Participants who took liraglutide regained 2.20 kg (95% CI 1.69 to 2.70, P < 0.00001), and participants taking semaglutide/tirzepatide regained 9.69 kg (95% CI 5.78 to 13.60, P < 0.00001). This systematic review and meta-analysis show that significant weight is regained after discontinuing GLP-1RA treatment, which should be discussed when stopping therapy. PRACTITIONER POINTS: Question: Does discontinuation of Glucagon-like peptide 1 receptor agonist (GLP-1RA) treatment lead to significant weight gain? Findings: In this systematic review and meta-analysis, discontinuing GLP-1RA treatment led to a pooled overall mean weight regain of 2.20 kg in participants taking liraglutide and 9.69 kg in those patients prescribed semaglutide/tirzepatide. The proportion of weight regained was proportional to the amount originally lost. Meaning: Discontinuation of GLP-1RA treatment leads to weight regain, regardless of lifestyle interventions, and should therefore be considered a chronic therapy to prevent weight regain and associated undesirable outcomes related to obesity.

有关胰高血糖素样肽 1 受体激动剂(GLP-1RA)的研究主要集中在减轻体重的疗效上,而非维持体重的长期疗效。本系统综述和荟萃分析旨在评估服用 GLP-1RA 的患者在停药后体重减轻的可持续性。作者使用 EBSCOhost 同时检索了 Academic Search Premier、CINHAL Ultimate、Cochrane Central Register of Controlled Trials、MEDLINE 全文、Cochrane Database of Systematic Reviews,并使用预先确定的检索策略对从开始到 2024 年 2 月 1 日的单独 PubMed 检索进行了系统研究。作者提取了治疗和非治疗时体重从基线开始的变化、治疗和非治疗时腰围从基线开始的变化以及治疗和非治疗时体重指数从基线开始的变化等数据。使用RevMan(5.4版)进行了Meta分析,利用Der Simonian-Laird随机效应模型计算了汇总的平均差异。结果最初的搜索结果显示有497篇相关文章,经过筛选,保留了8项随机对照试验,共有2372名参与者,所有参与者的体重指数均≥27 kg/m2。在停止GLP-1RA治疗后,体重的恢复与最初体重的下降成正比。服用利拉鲁肽的参与者体重增加了 2.20 千克(95% CI 1.69 至 2.70,P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Obesity Reviews
Obesity Reviews 医学-内分泌学与代谢
CiteScore
19.30
自引率
1.10%
发文量
130
审稿时长
1 months
期刊介绍: Obesity Reviews is a monthly journal publishing reviews on all disciplines related to obesity and its comorbidities. This includes basic and behavioral sciences, clinical treatment and outcomes, epidemiology, prevention and public health. The journal should, therefore, appeal to all professionals with an interest in obesity and its comorbidities. Review types may include systematic narrative reviews, quantitative meta-analyses and narrative reviews but all must offer new insights, critical or novel perspectives that will enhance the state of knowledge in the field. The editorial policy is to publish high quality peer-reviewed manuscripts that provide needed new insight into all aspects of obesity and its related comorbidities while minimizing the period between submission and publication.
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