# Ocular Glymphatic Dysfunction as a Potential Link Between Obstructive Sleep Apnea and Retinal Structural Changes. Comment on Pusic Sesar et al. Multimodal Assessment of Ocular Parameters in Patients with Severe Obstructive Sleep Apnea with Emphasis on Retinal Structural Changes. Life 2025, 15, 1307

**Authors:** Peter Wostyn, Maiken Nedergaard

PMC · DOI: 10.3390/life16020214 · 2026-01-28

## Full-text entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** normal (MESH:C537354), hypoxia (MESH:D000860), glaucomatous damage (MESH:D020263), venous congestion (MESH:D006940), insomnia (MESH:D007319), tension glaucoma (MESH:D057066), injury to (MESH:D014947), glaucomatous neurodegeneration (MESH:D019636), Impaired sleep (MESH:D012893), sleep apnea syndrome (MESH:D012891), Ocular Glymphatic Dysfunction (MESH:D005128), elevated ICP (MESH:D019586), OSA (MESH:D020181), glaucoma (MESH:D005901), apnea (MESH:D001049)
- **Species:** Homo sapiens (human, species) [taxon 9606]

---
Source: https://tomesphere.com/paper/PMC12941420