GLP-1s Therapy and Sleep Apnea: What the SURMOUNT-OSA Trial Showed
The SURMOUNT-OSA trial demonstrated that tirzepatide significantly reduces sleep apnea severity. Here is what the data shows and what it means for prescribers.
GLP-1 Therapy and Sleep Apnea: What the SURMOUNT-OSA Trial Showed
Obstructive sleep apnea (OSA) affects approximately 30% of adults in the United States and is strongly associated with obesity. The SURMOUNT-OSA trial, published in The New England Journal of Medicine in 2024, demonstrated that tirzepatide significantly reduces sleep apnea severity β a finding with important implications for prescribers.
The SURMOUNT-OSA Trial
Design
SURMOUNT-OSA enrolled 469 adults with moderate-to-severe OSA and obesity (BMI β₯30). Participants were randomized to tirzepatide (up to 15 mg weekly) or placebo for 52 weeks.
The trial had two cohorts:
- Cohort 1: Patients not using positive airway pressure (PAP) therapy
- Cohort 2: Patients using PAP therapy who agreed to discontinue it for the trial
Primary Endpoint
The primary endpoint was change in the apnea-hypopnea index (AHI) β the number of breathing interruptions per hour of sleep. A higher AHI indicates more severe sleep apnea.
Results
Cohort 1 (no PAP therapy):
- Tirzepatide: AHI reduced by 25.3 events/hour (55% reduction)
- Placebo: AHI reduced by 5.3 events/hour (5% reduction)
- Difference: 20.1 events/hour (p<0.001)
Cohort 2 (PAP therapy discontinued):
- Tirzepatide: AHI reduced by 29.3 events/hour (63% reduction)
- Placebo: AHI reduced by 5.5 events/hour (6% reduction)
- Difference: 23.8 events/hour (p<0.001)
Secondary outcomes:
- 42% of tirzepatide patients in Cohort 1 achieved OSA resolution (AHI <5)
- Significant improvements in hypoxia, sleep quality, and patient-reported outcomes
- Average weight loss: 18.1% in tirzepatide group vs. 1.0% in placebo group
FDA Approval
Based on the SURMOUNT-OSA data, the FDA approved tirzepatide (Zepbound) for the treatment of moderate-to-severe OSA in adults with obesity in 2024 β the first pharmacological treatment approved specifically for OSA.
What This Means for Prescribers
A New Indication for GLP-1 Therapy
The OSA indication expands the clinical rationale for GLP-1 prescribing. Patients with obesity and OSA now have a strong evidence-based reason to consider GLP-1 therapy beyond weight loss alone.
Screening for OSA
Prescribers offering GLP-1 programs should screen patients for OSA:
- Ask about snoring, witnessed apneas, daytime sleepiness
- Use validated screening tools (STOP-BANG questionnaire)
- Refer for sleep study if OSA is suspected
Identifying OSA in GLP-1 patients strengthens the clinical rationale for therapy and may support insurance coverage.
Counseling Patients
Patients with OSA should be counseled about the potential for GLP-1 therapy to improve their sleep apnea:
- "Weight loss is one of the most effective treatments for sleep apnea, and GLP-1 therapy produces significant weight loss."
- "The SURMOUNT-OSA trial showed that tirzepatide reduced sleep apnea severity by more than 50% on average."
- "Some patients may be able to reduce or discontinue CPAP therapy as their sleep apnea improves."
Monitoring
For patients with OSA on GLP-1 therapy:
- Repeat sleep study after significant weight loss (20%+ of body weight)
- Assess CPAP pressure requirements β may need adjustment as OSA improves
- Monitor for OSA resolution
Semaglutide and OSA
The SURMOUNT-OSA trial used tirzepatide. What about semaglutide?
The SELECT trial (semaglutide for cardiovascular risk reduction) included patients with OSA and showed improvements in OSA-related outcomes as a secondary endpoint. A dedicated OSA trial for semaglutide is ongoing.
Given the strong relationship between weight loss and OSA improvement, it is likely that semaglutide also improves OSA β but the tirzepatide data is more robust.
Compounded Tirzepatide for OSA
For patients with OSA who cannot access branded tirzepatide (Zepbound), compounded tirzepatide offers an access pathway. The clinical rationale for compounded tirzepatide in OSA patients is strong given the SURMOUNT-OSA data.
This content is for informational and educational purposes only. It does not constitute medical advice. Prescribers should review current prescribing information and use clinical judgment.
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Written by
Shannon B.
Director of Provider Relations β GLP-1 & Compounding Specialist
Shannon leads provider relations at MedClinic Partners, working directly with licensed medical practices across all 50 states to onboard them onto the 503A/503B and peptide portal. She specializes in GLP-1 therapy protocols, NPI verification workflows, cGMP facility compliance, and cold-chain logistics for refrigerated compounded medications.
Editorial standards: All content on medclinicpartners.com is reviewed by licensed medical operators and compounding compliance specialists before publication. Articles are updated when regulatory guidance changes. This content is for licensed healthcare providers only and does not constitute medical advice.