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Meta-analysis finds obstructive sleep apnea associated with sarcopenia in adults

Meta-analysis finds obstructive sleep apnea associated with sarcopenia in adults
Photo by Alexander Grey / Unsplash
Key Takeaway
Consider the observed association between obstructive sleep apnea and sarcopenia, noting the evidence is cross-sectional and not causal.

This is a meta-analysis of observational studies examining the association between obstructive sleep apnea syndrome (OSAS) and sarcopenia in adults. The analysis included 13,331 participants, of whom 3,572 had OSAS. The primary finding was a significant association between OSAS and sarcopenia, with an overall odds ratio of 1.85 (95% CI 1.30 to 2.63).

The authors synthesized subgroup analyses showing a stronger association in Asian populations (OR 2.92) compared to non-Asian populations (OR 1.33). The association was also stronger in older participants with a mean age of 64 years or more (OR 2.36) versus younger participants (OR 1.37). Furthermore, studies using objective sleep assessment showed a stronger association (OR 2.78) than those using questionnaires or medical records (OR 1.33).

Key limitations noted by the authors include that all included studies were cross-sectional, diagnostic criteria for both OSAS and sarcopenia varied across studies, and statistical power was limited for meta-regression analyses due to a small number of studies. The authors state that findings should be interpreted cautiously and do not imply causality.

The practice relevance is that OSAS is associated with increased odds of sarcopenia in adults, particularly in older and Asian populations and in studies using objective sleep assessment. However, the evidence is observational and cannot establish a causal relationship.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
Obstructive sleep apnea syndrome (OSAS) and sarcopenia are prevalent conditions associated with aging and metabolic disorders. Emerging evidence suggests a potential link between intermittent hypoxia and skeletal muscle impairment, but findings remain inconsistent. We conducted a meta-analysis to clarify the association between OSAS and sarcopenia in adults. PubMed, Embase, Web of Science, Wanfang, and CNKI were searched for observational studies evaluating the association between OSAS and sarcopenia in adults. Odds ratios (ORs) with 95% confidence intervals (CIs) were pooled using random-effects models by incorporating the influence of potential heterogeneity. Subgroup and sensitivity analyses were performed to explore heterogeneity. Eight cross-sectional studies comprising 13,331 participants (3,572 with OSAS) were included. Overall, OSAS was significantly associated with sarcopenia (OR 1.85, 95% CI 1.30–2.63; I2 = 62%). The association was stronger in Asian populations (OR 2.92) than in non-Asian populations (OR 1.33; p for subgroup difference < 0.001), and in older participants (mean age ≥ 64 years; OR 2.36 vs. 1.37; p for subgroup difference = 0.04). Studies using objective sleep assessment showed stronger associations than those using questionnaires or medical records (OR 2.78 vs. 1.33; p for subgroup difference < 0.001). Results were consistent in studies with NOS ≥ 8 (OR 1.82, 95% CI 1.23–2.70). Meta-regression analyses did not identify significant effect modifiers, although statistical power was limited by the small number of studies. No significant publication bias was detected (Egger’s p = 0.49). OSAS is associated with increased odds of sarcopenia in adults, particularly in older and Asian populations and in studies using objective sleep assessment. However, given that all included studies were cross-sectional and that diagnostic criteria for both OSAS and sarcopenia varied across studies, these findings should be interpreted cautiously and do not imply causality. https://www.crd.york.ac.uk/prospero/, identifier CRD420261324247.
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