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.
Eur Clin Respir J · 2025
Last updated 2026-09-07A review of three small studies with 828 patients found that GLP-1 drugs, including tirzepatide, reduced the number of breathing interruptions per hour by 16.57, lowered body weight by 12.71%, and decreased systolic blood pressure by 4.93 mmHg in people with obstructive sleep apnea. The drugs also reduced sleep apnea-specific hypoxic burden by 66.21% per minute and a marker of inflammation by 0.89 mg/dl, but they increased the risk of gastrointestinal side effects.
AI summary of the abstract below.
| Journal | Eur Clin Respir J, 2025 |
|---|---|
| Citations | 16 |
| Relative citation ratio | 5.32 |
| Molecules | — |
Abstract
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], = 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.
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.
Verbatim abstract via PubMed 40144943 ↗