肠促胰岛素药物对超重或肥胖伴/不伴2型糖尿病成人血糖控制、体重和血压的比较疗效:一项系统综述和网络meta分析

IF 4.6 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Frontiers in Endocrinology Pub Date : 2025-02-04 eCollection Date: 2025-01-01 DOI:10.3389/fendo.2025.1513641
Song Liu, Jiaqiang Hu, Chen Zhao, Hang Liu, Chunyang He
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引用次数: 0

摘要

背景:靶向胰高血糖素样肽-1受体(GLP-1R)的多受体药物的快速发展推动了2型糖尿病和肥胖患者治疗的重大进展。本系统综述和网络荟萃分析旨在比较多受体药物对超重或肥胖成人伴或不伴2型糖尿病患者的疗效和安全性。方法:系统检索PubMed、Cochrane、Web of Science、Embase、CNKI、万方等数据库,检索时间截止到2024年5月12日。随机对照试验(rct)干预时间至少为12周。感兴趣的人群包括超重或肥胖的个体,有或没有2型糖尿病。符合条件的研究将多受体药物与安慰剂或其他多受体药物进行了比较。主要结局是体重减轻、糖化血红蛋白(HbA1c)、空腹血糖(FPG)、血压变化和不良事件。使用Cochrane风险偏倚工具(ROB2)评估偏倚风险,并使用频率分析方法进行随机效应网络荟萃分析。使用网络元分析(CINeMA)框架评估效果估计的置信度。结果:共纳入24项试验,9165名受试者。利特鲁肽(平均差值(MD): -11.91 kg, 95% CI: -19.00至-4.82,p -评分:0.80,p: 0.0003)和替西帕肽(MD: -12.78 kg, 95% CI: -16.10至-9.46,p -评分:0.89,p < 0.0001)在减轻体重方面表现出卓越的疗效,除玛度肽(MD: -5.31 kg, 95% CI: -9.78至-0.84,p -评分:0.37,p: 0.0189)外,所有其他药物的减轻体重均超过8 kg。在2型糖尿病患者中,所有药物均可使HbA1c降低1%以上,其中替西帕肽(MD: -1.87%, 95% CI: -2.15至-1.59,p -评分:0.87,p < 0.0001)和马度肽(MD: -1.89%, 95% CI: -2.43至-1.35,p -评分:0.88,p < 0.0001)对血糖控制的影响最大。对于血压管理,替西帕肽显著降低收缩压(MD: -6.69 mmHg, 95% CI: -7.62至-5.75,p -评分:0.84,p < 0.0001)和舒张压(MD: -3.73 mmHg, 95% CI: -4.75至-2.71,p -评分:0.92,p < 0.0001),几乎所有药物降低收缩压均超过5 mmHg。非糖尿病参与者在体重和血压方面都有更明显的改善。安全性分析显示,替西帕肽具有良好的安全性,与安慰剂相比,所有药物对严重不良事件没有显着影响。结论:多受体药物在超重或肥胖成人(伴或不伴糖尿病)的体重管理、血糖控制和血压调节方面显示出巨大的治疗潜力,具有良好的安全性。系统综述注册:https://www.crd.york.ac.uk/prospero/,标识符CRD42024554005。
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Comparative efficacy of incretin drugs on glycemic control, body weight, and blood pressure in adults with overweight or obesity and with/without type 2 diabetes: a systematic review and network meta-analysis.

Background: The rapid development of multi-receptor drugs targeting glucagon-like peptide-1 receptor (GLP-1R) is driving significant advancements in the treatment of individuals with type 2 diabetes and obesity. This systematic review and network meta-analysis aims to compare the efficacy and safety of multi-receptor drugs in adults with overweight or obesity, with or without type 2 diabetes.

Methods: A systematic search was conducted in PubMed, Cochrane, Web of Science, Embase, CNKI, and WanFang databases up to May 12, 2024. Randomized controlled trials (RCTs) with an intervention duration of at least 12 weeks were included. The population of interest consisted of individuals with overweight or obesity, with or without type 2 diabetes. Eligible studies compared multi-receptor drugs with placebo or other multi-receptor drugs. The primary outcomes were weight reduction, glycated hemoglobin (HbA1c), fasting plasma glucose (FPG), blood pressure changes, and adverse events. Risk of bias was assessed using the version 2 of the Cochrane risk-of-bias tool (ROB2), and a random-effects network meta-analysis was performed using the frequentist approach. Confidence in effect estimates was evaluated using the Confidence In Network Meta-Analysis (CINeMA) framework.

Results: A total of 24 trials, involving 9165 participants, were included. Retatrutide (mean difference (MD): -11.91 kg, 95% CI: -19.00 to -4.82, P-score: 0.80, p: 0.0003) and Tirzepatide (MD: -12.78 kg, 95% CI: -16.10 to -9.46, P-score: 0.89, p < 0.0001) exhibited superior efficacy in reducing body weight, with all other agents except Mazdutide (MD: -5.31 kg, 95% CI: -9.78 to -0.84, P-score: 0.37, p: 0.0189) achieving reductions of over 8 kg. In patients with type 2 diabetes, all agents reduced HbA1c by over 1%, with Tirzepatide (MD: -1.87%, 95% CI: -2.15 to -1.59, P-score: 0.87, p < 0.0001) and Mazdutide (MD: -1.89%, 95% CI: -2.43 to -1.35, P-score: 0.88, p < 0.0001) showing the greatest effects on glycemic control. For blood pressure management, Tirzepatide significantly reduced systolic blood pressure (MD: -6.69 mmHg, 95% CI: -7.62 to -5.75, P-score: 0.84, p < 0.0001) and diastolic blood pressure (MD: -3.73 mmHg, 95% CI: -4.75 to -2.71, P-score: 0.92, p < 0.0001), with nearly all agents lowering systolic blood pressure by more than 5 mmHg. Non-diabetic participants showed more pronounced improvements in both weight and blood pressure. Safety analysis revealed that Tirzepatide had a favorable safety profile and all agents showed no significant impact on serious adverse events compared to placebo.

Conclusions: Multi-receptor drugs demonstrated substantial therapeutic potential in weight management, glycemic control, and blood pressure regulation in adults with overweight or obesity, with or without diabetes, with a generally favorable safety profile.

Systematic review registration: https://www.crd.york.ac.uk/prospero/, identifier CRD42024554005.

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来源期刊
Frontiers in Endocrinology
Frontiers in Endocrinology Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.70
自引率
9.60%
发文量
3023
审稿时长
14 weeks
期刊介绍: Frontiers in Endocrinology is a field journal of the "Frontiers in" journal series. In today’s world, endocrinology is becoming increasingly important as it underlies many of the challenges societies face - from obesity and diabetes to reproduction, population control and aging. Endocrinology covers a broad field from basic molecular and cellular communication through to clinical care and some of the most crucial public health issues. The journal, thus, welcomes outstanding contributions in any domain of endocrinology. Frontiers in Endocrinology publishes articles on the most outstanding discoveries across a wide research spectrum of Endocrinology. The mission of Frontiers in Endocrinology is to bring all relevant Endocrinology areas together on a single platform.
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