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The Link between Obstructive Sleep Apnea and Dry Eye Disease: Pathophysiology and Current Updates
Hung-Liang Pai1,2, Ting-Chi Pan3, Chien-Han Tsao4
1Department of Medical Education, Chung Shan Medical University Hospital, Taichung, Taiwan.
Ophthalmic Research
|July 7, 2026
Summary
Obstructive Sleep Apnea (OSA) causes Dry Eye Disease (DED) through inflammation and oxidative stress. While CPAP therapy helps OSA, it can worsen DED, necessitating integrated care.
Area of Science:
- Ophthalmology
- Sleep Medicine
- Ocular Surface Disease
Background:
- Obstructive Sleep Apnea (OSA) and Dry Eye Disease (DED) are increasingly recognized as interrelated conditions.
- Intermittent hypoxia and oxidative stress in OSA disrupt tear film stability, leading to DED.
- Continuous Positive Airway Pressure (CPAP) therapy, while standard for OSA, can have detrimental effects on DED.
Purpose of the Study:
- To review the multifactorial etiology of OSA-related DED.
- To highlight the roles of inflammation, lipid metabolism dysfunction, and mechanical stress.
- To emphasize the need for interdisciplinary management of OSA patients with ocular surface disorders.
Main Methods:
- Literature review focusing on the relationship between OSA and DED.
- Analysis of the impact of OSA pathophysiology on ocular surface health.
- Examination of CPAP therapy's effects on DED.
Main Results:
- OSA-induced inflammation, hypoxia, and oxidative stress contribute to both aqueous-deficient and evaporative DED.
- CPAP therapy may exacerbate DED through airflow leakage or retrograde air movement.
- Mechanical factors like sleeping position and eye rubbing worsen meibomian gland dysfunction in OSA patients.
Conclusions:
- OSA-related DED has a multifactorial etiology involving systemic/ocular inflammation, lipid dysfunction, and mechanical stress.
- Interdisciplinary management combining sleep medicine and ophthalmology is crucial for optimizing patient outcomes.
- Future research should focus on targeted therapies and improved CPAP designs to mitigate OSA-induced ocular complications.
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