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Genetic Contributions to Glaucoma: Heritability of Intraocular Pressure, Retinal Nerve Fiber Layer Thickness, and Optic Disc Morphology

¹From the Glaucoma Service, The Rotterdam Eye Hospital, Rotterdam, The Netherlands; the ⁴Department of Ophthalmology and the ²Departments of Epidemiology and Biostatistics and ³Clinical Genetics, Genetic Epidemiology Unit, Erasmus Medical Center, Rotterdam, The Netherlands; and the ⁵Department of Molecular and Clinical Ophthalmogenetics, The Netherlands Institute for Neuroscience, Amsterdam, The Netherlands.

PURPOSE. The genetic etiology of primary open-angle glaucoma (POAG) is still largely unknown, because of its complexity and disparities in its classification. This study was undertaken to determine the genetic contribution to various early, continuous markers of POAG by assessing the heritability of intraocular pressure (IOP), retinal nerve fiber layer (RNFL) thickness, and neuroretinal rim and optic disc parameters in a genetically isolated population.

METHODS. A total of 2620 subjects (mean age, 48 years; range 18–86) from extended pedigrees living in a small town in The Netherlands underwent an extensive ophthalmic examination. Their IOP was measured by Goldmann applanation tonometry, their RNFL thickness by scanning laser polarimetry (GDx VCC), and their optic disc parameters by confocal scanning laser ophthalmoscopy (HRT II). Risk associations were explored by linear regression analyses and heritability estimates by variance component methods.

RESULTS. Inbreeding was present in 2042 (81%) participants, and was significantly associated with a higher IOP (P < 0.001). The heritability estimate for IOP was 0.35 (95% confidence interval [CI], 0.27–0.43); for RNFL thickness, 0.48 (95% CI, 0.35–0.60); and for neuroretinal rim area, 0.39 (95% CI, 0.20–0.58). Nongenetic factors accounted for only a small proportion (0.13) of the variance in all three traits.

CONCLUSIONS. Early, continuous markers of POAG are strongly determined by additive genetic effects. The results support a quantitative trait linkage strategy to discover new genes for POAG.

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