胰高血糖素样肽-1受体激动剂在阻塞性睡眠呼吸暂停患者中的安全性和有效性:随机对照试验的系统回顾和荟萃分析

IF 1.8 Q3 RESPIRATORY SYSTEM
European Clinical Respiratory Journal Pub Date : 2025-03-24 eCollection Date: 2025-01-01 DOI:10.1080/20018525.2025.2484048
Obieda Altobaishat, Ahmed Farid Gadelmawla, Elsayed Balbaa, Mustafa Turkmani, Mohamed Abouzid
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引用次数: 0

摘要

背景:阻塞性睡眠呼吸暂停(OSA)是一种常见疾病,影响全球约10亿人。最近研究的新证据表明胰高血糖素样肽1受体(GLP-1)激动剂可能降低OSA严重程度。因此,本荟萃分析旨在评估GLP-1激动剂在OSA患者中的疗效和安全性。方法:根据PRISMA(系统评价和荟萃分析的首选报告项目)指南,我们检索了四个电子数据库(PubMed, EMBASE, Cochrane Library, Scopus和Web of Science),以确定截至2024年6月24日报道的符合条件的研究。使用Review Manager软件,我们以风险比(rr)或平均差异(MD)和置信区间(CIs)报告结果。本综述的方案已在PROSPERO上注册并发布,编号为CRD42024562853。结果:meta分析纳入3项随机对照试验,共纳入828例患者。合并分析显示,给予GLP-1激动剂或替西帕肽的患者呼吸暂停/低通气指数(MD -16.57事件/小时,95% CI [-27.41, -5.73], p = 0.003)、体重减轻(MD -12.71%, 95% CI [-21.38, -4.03], p = 0.004)和收缩压(MD -4.93 mmHg,95% CI [-7.67, -2.19], p = 0.0004)均有改善。替西帕肽显示高敏c反应蛋白降低(MD -0.89 mg/dl, 95% CI [-1.25, -0.54], p p p = 0.07)。GLP-1激动剂/替西肽未观察到明显的严重不良事件,但与胃肠道不良事件发生率较高相关。结论:GLP-1激动剂,包括替西肽,可改善中度至重度OSA成人的呼吸暂停/低呼吸指数、体重和收缩压。然而,证据仍然局限于两项已发表的研究,包括三个使用不同药理学药物的随机对照试验。因此,在得出确定的结论之前,需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and efficacy of glucagon-like peptide-1 receptor agonists in patients with obstructive sleep apnea: a systematic review and meta-analysis of randomized controlled trials.

Background: Obstructive sleep apnea (OSA) is a common condition affecting around one billion people worldwide. Emerging evidence from recent studies suggests that Glucagon-like peptide 1 receptor (GLP-1) agonists may reduce OSA severity. Hence, this meta-analysis aims to evaluate the efficacy and safety of GLP-1 agonists in patients with OSA.

Methods: Following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines, we searched four electronic databases (PubMed, EMBASE, Cochrane Library, Scopus, and Web of Science) to identify eligible studies reported up to 24 June 2024. Using Review Manager software, we reported outcomes as risk ratios (RRs) or mean difference (MD) and confidence intervals (CIs). The protocol for this review has been registered and published in PROSPERO with the ID (CRD42024562853).

Results: The meta-analysis included three randomized controlled trials with 828 patients. Pooled analysis of patients administered GLP-1 agonists or tirzepatide showed improvement in Apnea/Hypopnea Index (MD -16.57 events per hour, 95% CI [-27.41, -5.73], p = 0.003), weight reduction (MD -12.71%, 95% CI [-21.38, -4.03], p = 0.004), and systolic blood pressure (MD -4.93 mmHg,95% CI [-7.67, -2.19], p = 0.0004). Tirzepatide showed a reduction in high-sensitivity C-reactive protein (MD -0.89 mg/dl, 95% CI [-1.25, -0.54], p < 0.0001) and sleep apnea-specific hypoxic burden (MD -66.21%/min, 95% CI [-81.75, -50.67], p < 0.0001). Despite the heterogeneity observed in the AHI and weight, it was resolved, and the results were consistent. GLP-1 agonists/tirzepatide showed comparable outcomes concerning diastolic blood pressure (MD -1.34 mmHg, 95% CI [-2.80, 0.12], p = 0.07). No significant serious adverse events were observed for GLP-1 agonists/tirzepatide, but it was associated with a higher incidence of gastrointestinal adverse events.

Conclusion: GLP-1 agonists, including tirzepatide, improved Apnea/Hypopnea Index, weight, and systolic blood pressure in adults with moderate-to-severe OSA. However, the evidence remains limited to two published studies comprising three randomized controlled trials using different pharmacological agents. Consequently, further research is needed before firm conclusions can be drawn.

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来源期刊
CiteScore
3.80
自引率
0.00%
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