Department of Internal Medicine, Lampang Hospital, Lampang, Thailand.
Division of Endocrinology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
PLoS One. 2024 Feb 26;19(2):e0297488. doi: 10.1371/journal.pone.0297488. eCollection 2024.
To date, no studies have addressed the comparative efficacy of glucagon-like peptide-1 receptor agonists (GLP1-RAs) therapy on body composition and anthropometric indices among adult overweight or obese patients with or without type 2 diabetes. To provide evidence-based recommendations, we will conduct a traditional pairwise and network meta-analysis of all available randomized clinical trials that evaluated the effects of GLP1-RAs interventions for adult overweight or obese patients with or without type 2 diabetes.
Electronic databases, including Medline, Embase, PubMed, Cochrane Library (CENTRAL), Scopus, and CINAHL, will be searched from inception without language restriction. Grey literature will be searched, including Google Scholar, ongoing clinical trial registries, and preprint reports. Reference lists of included trials, relevant major endocrinology scientific meetings, and manual hand searches from key general medicine and obesity and endocrinology journals will also be browsed. Two authors will screen, select, extract, appraise the risk of bias, and rate the evidence findings. Any disagreement will be resolved through team discussion. Based on a random-effects model, we will employ a two-step approach of traditional pairwise meta-analysis and network meta-analysis for quantitative synthesis. The pooled effect estimates using a frequentist approach with 95% confidence intervals for continuous endpoints will be expressed as the standardized mean difference, whereas odds ratios will be used for categorical endpoints. The quality of included trials will be evaluated using the Cochrane risk-of-bias version 2 assessment tool. Certainty of evidence for each outcome will be assessed using the modified confidence in network meta-analysis approach and the Grading of Recommended Assessment, Development, and Evaluation approach. The magnitude of the effect size, prediction intervals, surface under the cumulative ranking curve values, and certainty of evidence will be incorporated to draw evidence-based conclusions.
This systematic review and network meta-analysis will summarize the comparative efficacy of GLP1-RAs therapy on body composition and anthropometric indices. Evidence identified from this review will promote the rational use of interventions for adult overweight or obese patients with or without type 2 diabetes and will serve as an important step for evidence-based practice within this area.
PROSPERO registration number: CRD42023458228.
迄今为止,尚无研究探讨胰高血糖素样肽-1 受体激动剂 (GLP1-RAs) 治疗在伴有或不伴有 2 型糖尿病的超重或肥胖成年患者中的身体成分和人体测量学指标的比较疗效。为了提供循证推荐意见,我们将对所有评估 GLP1-RAs 干预对伴有或不伴有 2 型糖尿病的超重或肥胖成年患者的影响的现有随机临床试验进行传统的两两和网络荟萃分析。
电子数据库,包括 Medline、Embase、PubMed、Cochrane 图书馆 (CENTRAL)、Scopus 和 CINAHL,将从无语言限制的初始状态进行搜索。灰色文献也将被搜索,包括 Google Scholar、正在进行的临床试验注册处和预印本报告。还将浏览纳入试验的参考文献、相关主要内分泌学科学会议以及来自主要普通医学和肥胖与内分泌学杂志的手动检索。两名作者将筛选、选择、提取、评估偏倚风险,并对证据发现进行评级。任何分歧都将通过团队讨论解决。基于随机效应模型,我们将采用传统的两两荟萃分析和网络荟萃分析的两步方法进行定量综合。使用具有 95%置信区间的连续终点的频率论方法汇总的效应估计将表示为标准化均数差,而分类终点将使用优势比表示。使用 Cochrane 风险偏倚版本 2 评估工具评估纳入试验的质量。使用修改后的网络荟萃分析置信度评估方法和推荐评估、制定和评估方法对每个结局的证据确定性进行评估。将效应大小的大小、预测区间、累积排序曲线下面积值和证据确定性纳入其中,以得出基于证据的结论。
本系统评价和网络荟萃分析将总结 GLP1-RAs 治疗对身体成分和人体测量学指标的比较疗效。从本综述中确定的证据将促进对伴有或不伴有 2 型糖尿病的超重或肥胖成年患者干预措施的合理使用,并为该领域的循证实践提供重要步骤。
PROSPERO 注册号:CRD42023458228。