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Optic disc morphology in "age-related atrophic glaucoma"
1University Eye Hospital, Erlangen, Germany.
Summary
Fundus tessellation in primary open-angle glaucoma (POAG) is linked to specific optic disc changes. Patients with more tessellation show lower intraocular pressure and distinct optic nerve atrophy patterns.
Area of Science:
- Ophthalmology
- Glaucoma Research
- Optic Nerve Imaging
Background:
- Primary open-angle glaucoma (POAG) is a leading cause of irreversible blindness.
- Fundus tessellation, a pattern of choroidal visibility, is common in myopic eyes.
- The relationship between fundus tessellation and optic disc morphology in POAG remains unclear.
Purpose of the Study:
- To investigate if varying degrees of fundus tessellation correlate with optic disc morphology and intraocular pressure (IOP) in POAG patients.
- To identify potential subtypes of POAG based on fundus tessellation patterns.
Main Methods:
- Morphometric analysis of optic disc photographs from 562 POAG patients with myopia < -8 diopters.
- Classification into tessellated (n=256) and nontessellated (n=306) subgroups, matched for neuroretinal rim area and refractive error.
- Comparison of IOP, optic disc parameters, and visual field defects between subgroups.
Main Results:
- The tessellated subgroup exhibited significantly lower mean maximal IOP, larger parapapillary atrophy, shallower optic cups, and higher patient age compared to the nontessellated subgroup.
- Fundus tessellation degree positively correlated with parapapillary atrophy and negatively with mean maximal IOP and optic cup depth.
- Higher degrees of tessellation were associated with the greatest parapapillary atrophy and lowest mean maximal IOP.
Conclusions:
- Marked fundus tessellation in low-pressure POAG is associated with significant parapapillary atrophy, shallow optic cupping, and older patient age.
- Findings suggest a distinct POAG subtype in older individuals with relatively low IOP, characterized by diffuse optic nerve atrophy.
- Fundus tessellation may serve as a clinical indicator for specific POAG phenotypes.