In a 59-year-old Han Chinese man with unilateral NAION, OSAHS was identified after other etiologies were excluded, and the authors conclude this highlights the clinical importance of screening for and managing OSAHS in patients with NAION.
Key Findings
Results
A 59-year-old Han Chinese man presented with unilateral nonarteritic anterior ischemic optic neuropathy (NAION) associated with obstructive sleep apnea-hypopnea syndrome (OSAHS).
He had a 6-day history of blurred vision and visual field defects in the left eye.
NAION is characterized by painless vision loss, visual field defects, and optic disc edema.
The diagnosis was confirmed after excluding other potential etiologies.
Results
The patient improved moderately after combined ophthalmic treatment and respiratory management of OSAHS.
He received 80 mg oral methylprednisolone, gradually tapered, plus neuroprotective and circulation-improving therapies.
After consultation with the Department of Respiratory and Sleep Medicine, he started noninvasive ventilation (NIV) to correct systemic hypoxia and received bronchodilators.
The abstract reports that symptoms showed 'moderate improvement'; the abstract gives no quantitative visual outcomes.
Discussion
An association between OSAHS and NAION was observed in this case after other confounding etiologies were excluded.
This is a single case report, so the observation cannot establish causation.
The authors describe OSAHS as a significant and independent risk factor for NAION.
Background
NAION is described as arising from hypoperfusion of the short posterior ciliary arteries and is commonly associated with systemic vascular risk factors.
Hypoperfusion causes acute ischemia and structural and functional impairment of the optic nerve, manifesting as blurred vision or blindness.
Associated risk factors include hypertension, diabetes mellitus, dyslipidemia, ischemic heart disease, and cerebrovascular disease.
These conditions compromise microvascular supply to the optic nerve head, leading to ischemia, necrosis, and optic atrophy.
Background
OSAHS is a syndrome of recurrent apnea and hypopnea during sleep that is a recognized risk factor for systemic vascular comorbidities.
It causes intermittent hypoxia, hypercapnia, and sleep fragmentation.
It is a well-established risk factor for cardiovascular disease and diabetes mellitus.
Conclusions
The authors conclude that screening for and managing OSAHS in NAION patients is clinically important and may support optimized treatment strategies.
The recommendation is based on the observed association in this case and the recognized role of OSAHS as a NAION risk factor.
What This Means
This case report describes a 59-year-old man who developed blurred vision and a missing area of vision in his left eye over about six days. Doctors diagnosed nonarteritic anterior ischemic optic neuropathy (NAION), a condition in which reduced blood flow damages the optic nerve at the back of the eye. After other possible causes were ruled out, obstructive sleep apnea-hypopnea syndrome (OSAHS) was identified as a likely contributing factor. OSAHS is a condition in which breathing repeatedly pauses during sleep, lowering oxygen levels.
He was treated with steroid tablets that were gradually reduced, along with medicines to protect nerves and improve circulation. He also began noninvasive ventilation to correct low oxygen levels and received bronchodilators. His symptoms improved moderately, though the report gives no detailed measurements of how much his vision recovered.
This research suggests that sleep apnea may be worth looking for in people who develop NAION, and that treating it may be considered as part of their care. Because this is a single case, it cannot prove that sleep apnea caused the eye problem or that treating it improved his vision. Larger studies would be needed to confirm these ideas.
Zhang C, Lei Q, Song X, Fan Y, Wang X. (2026). Unilateral nonarteritic anterior ischemic optic neuropathy associated with obstructive sleep apnea-hypopnea syndrome: a case report.. Journal of medical case reports. https://doi.org/10.1186/s13256-026-06598-4