Eyes of Africa: The Genetics of Blindness. Baseline characteristics, ocular features, and associations with glaucoma in continental Africans

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Abstract

Importance: Glaucoma is the leading cause of irreversible blindness worldwide, with disproportionately high prevalence and severity in Africans. Objective: To characterise the baseline phenotypic findings and glaucoma-related ocular features of participants with primary open-angle glaucoma (POAG, cases) and non-glaucoma controls and to report sociodemographic and medical associations of POAG in the cohort. Design: Multicentre, cross-sectional study. Participants: 9418 adults (5189 POAG cases; 4229 controls) recruited from 16 centres in Nigeria, Ghana and Malawi. Methods: Standardised demographic, medical and ophthalmic data were collected, including visual acuity, intraocular pressure (IOP), optic disc evaluation, visual fields and central corneal thickness. Main outcome measures: Glaucoma severity, visual impairment (VI) and sociodemographic/medical associations of POAG. Results: Compared to controls, cases were older (mean age 63.9 years vs 61.4 years, P < 0.001) and more likely to be male (57.4% vs 45.2%, P < 0.001). Three-quarters of cases (76.8%) were classified as having severe glaucoma in at least one eye at recruitment, with a third (34.4%) suffering severe VI or blindness. The leading causes of VI in controls were cataract (65.0%) and uncorrected refractive error (13.8%). POAG was significantly associated with older age, male sex, higher level of education, unemployment, history of alcohol consumption, African trypanosomiasis, higher maximum IOP and a positive family history of glaucoma. Conclusion: There is a significant glaucoma disease burden in sub-Saharan Africa. Further analyses of the cohort will identify genetic determinants of these clinical findings and reinforce the urgent need for public health interventions in sub-Saharan Africa.

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Eye Basingstoke

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