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Abstract #108227 Published in IGR 23-4
Lack of Association of Polymorphism Located Upstream of (rs2472493), in (rs7636836), and Near - Genes (rs61275591) in Primary Open-Angle Glaucoma Patients of Saudi Origin
Kondkar AA; Sultan T; Azad TA; Osman EA; Almobarak FA; Lobo GP; Lobo GP; Al-Obeidan SAGenes 2023; 14:
Polymorphisms rs2472493 near , rs7636836 in , and rs61275591 near the genes were previously reported to exhibit genome-wide significance in primary open-angle glaucoma (POAG). Since these polymorphisms have not been investigated in the Arab population of Saudi Arabia, we examined their association with POAG in a Saudi cohort. Genotyping was performed in 152 POAG cases and 246 controls using Taqman real-time assays and their associations with POAG and clinical markers, such as intraocular pressure, cup/disc ratio, and the number of antiglaucoma medications, were tested by statistical methods. There was no association observed between POAG and the minor allele frequencies of rs2472493[G], rs7636836[T], or rs61275591[A]. None of the genetic models such as co-dominant, dominant, recessive, over-dominant, and log-additive demonstrated any genotype link. The Rs2472493 genotype showed a modest association ( = 0.044) with the number of antiglaucoma medications in the POAG group, but no significant genotype effect on post hoc analysis. In addition, a G-T allelic haplotype of rs2472493 () and rs7636836 () did show an over two-fold increased risk of POAG (odds ratio = 2.18), albeit non-significantly ( = 0.092). Similarly, no other allelic haplotype of the three variants showed any significant association with POAG. Our study did not replicate the genetic association of rs2472493 (), rs763683 (), and rs61275591 (-) in POAG and related clinical phenotypes, suggesting that these polymorphisms are not associated with POAG in a Saudi cohort of Arab ethnicity. However, large population-based multicenter studies are needed to validate these results.
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