APOE ε2-Carriers Are Associated with an Increased Risk of Primary Angle-Closure Glaucoma in Patients of Saudi Origin

Author:

Kondkar Altaf A.123ORCID,Azad Taif A.1,Sultan Tahira1,Khatlani Tanvir4,Alshehri Abdulaziz A.5,Radhakrishnan Rakesh6,Lobo Glenn P.6,Alsirhy Ehab1ORCID,Almobarak Faisal A.1ORCID,Osman Essam A.1,Al-Obeidan Saleh A.12ORCID

Affiliation:

1. Department of Ophthalmology, College of Medicine, King Saud University, Riyadh 11411, Saudi Arabia

2. Glaucoma Research Chair in Ophthalmology, College of Medicine, King Saud University, Riyadh 11411, Saudi Arabia

3. King Saud University Medical City, King Saud University, Riyadh 11411, Saudi Arabia

4. Department of Blood and Cancer Research, King Abdullah International Medical Research Center, King Saud Bin Abdulaziz University of Health Sciences, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia

5. Department of Ophthalmology, Imam Abdulrahman Alfaisal Hospital, Riyadh 14723, Saudi Arabia

6. Department of Ophthalmology and Visual Neurosciences, University of Minnesota, Minneapolis, MN 55347, USA

Abstract

This study investigated the association between apolipoprotein E (APOE) gene polymorphisms (rs429358 and rs7412) and primary angle-closure glaucoma (PACG) and pseudoexfoliation glaucoma (PXG) in a Saudi cohort. Genotyping of 437 DNA samples (251 controls, 92 PACG, 94 PXG) was conducted using PCR-based Sanger sequencing. The results showed no significant differences in the allele and genotype frequencies of rs429358 and rs7412 between the PACG/PXG cases and controls. Haplotype analysis revealed ε3 as predominant, followed by ε4 and ε2 alleles, with no significant variance in PACG/PXG. However, APOE genotype analysis indicated a significant association between ε2-carriers and PACG (odds ratio = 4.82, 95% CI 1.52–15.26, p = 0.007), whereas no notable association was observed with PXG. Logistic regression confirmed ε2-carriers as a significant predictor for PACG (p = 0.008), while age emerged as significant for PXG (p < 0.001). These findings suggest a potential role of ε2-carriers in PACG risk within the Saudi cohort. Further validation and larger-scale investigations are essential to elucidate the precise role of APOE in PACG pathogenesis and progression.

Funder

King Saud University

Publisher

MDPI AG

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