Altobaishat Obieda, Farid Gadelmawla Ahmed, Balbaa Elsayed, Turkmani Mustafa, Abouzid Mohamed
Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
Faculty of Medicine, Menoufia University, Menoufia, Egypt.
Eur Clin Respir J. 2025 Mar 24;12(1):2484048. doi: 10.1080/20018525.2025.2484048. eCollection 2025.
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.
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).
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], = 0.003), weight reduction (MD -12.71%, 95% CI [-21.38, -4.03], = 0.004), and systolic blood pressure (MD -4.93 mmHg,95% CI [-7.67, -2.19], = 0.0004). Tirzepatide showed a reduction in high-sensitivity C-reactive protein (MD -0.89 mg/dl, 95% CI [-1.25, -0.54], < 0.0001) and sleep apnea-specific hypoxic burden (MD -66.21%/min, 95% CI [-81.75, -50.67], < 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], = 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.
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.
阻塞性睡眠呼吸暂停(OSA)是一种常见病症,全球约有10亿人受其影响。近期研究的新证据表明,胰高血糖素样肽1受体(GLP-1)激动剂可能会降低OSA的严重程度。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。
按照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图书馆、Scopus和科学网),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,我们将结果报告为风险比(RRs)或平均差(MD)以及置信区间(CIs)。本综述的方案已在PROSPERO中注册并发表,注册号为(CRD42024562853)。
该荟萃分析纳入了三项随机对照试验,共828名患者。对接受GLP-1激动剂或替尔泊肽治疗的患者进行的汇总分析显示,呼吸暂停/低通气指数有所改善(MD -16.57次/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),收缩压降低(MD -4.93 mmHg,95% CI [-7.67, -2.19],P = 0.0004)。替尔泊肽使高敏C反应蛋白降低(MD -0.89 mg/dl,95% CI [-1.25, -0.54]),睡眠呼吸暂停特异性低氧负荷降低(MD -66.21%/分钟,95% CI [-81.75, -50.67])。尽管在呼吸暂停低通气指数和体重方面观察到异质性,但已得到解决,结果是一致的。GLP-1激动剂/替尔泊肽在舒张压方面显示出类似结果(MD -1.34 mmHg,95% CI [-2.80, 0.12],P = 0.07)。未观察到GLP-1激动剂/替尔泊肽有显著的严重不良事件,但它与胃肠道不良事件的较高发生率相关。
包括替尔泊肽在内的GLP-1激动剂改善了中度至重度OSA成人的呼吸暂停/低通气指数、体重和收缩压。然而,证据仍然限于两项已发表的研究,包括三项使用不同药物的随机对照试验。因此,在得出确切结论之前还需要进一步研究。