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HLA-DRB and HLA-DQB loci in the genetic susceptibility to develop glaucoma in Mexicans

PURPOSE: Glaucoma is a clinically heterogeneous disease with a pathophysiology that may include genetic susceptibility, possibly associated with an immunologic disorder. The aim of this study was to determine whether the DNA polymorphisms located in the HLA-DRB1 and HLA-DQB1 genes show a specific as...

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Published in:American journal of ophthalmology 1999-09, Vol.128 (3), p.297-300
Main Authors: Gil-Carrasco, Felix, Vargas-Alarcón, Gilberto, Zúñiga, Joaquín, Tinajero-Castañeda, Olga, Hernández-Martinez, Betina, Hernández-Pacheco, Guadalupe, Rodríguez-Reyna, Tatiana Sofía, Hesiquio, Ramiro, Gamboa, Ricardo, Granados, Julio
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cited_by cdi_FETCH-LOGICAL-c390t-9b20c328ffd81b4a730257e88c70e11ecb233989f2cdd420b6f84d01a860f9b53
cites cdi_FETCH-LOGICAL-c390t-9b20c328ffd81b4a730257e88c70e11ecb233989f2cdd420b6f84d01a860f9b53
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container_title American journal of ophthalmology
container_volume 128
creator Gil-Carrasco, Felix
Vargas-Alarcón, Gilberto
Zúñiga, Joaquín
Tinajero-Castañeda, Olga
Hernández-Martinez, Betina
Hernández-Pacheco, Guadalupe
Rodríguez-Reyna, Tatiana Sofía
Hesiquio, Ramiro
Gamboa, Ricardo
Granados, Julio
description PURPOSE: Glaucoma is a clinically heterogeneous disease with a pathophysiology that may include genetic susceptibility, possibly associated with an immunologic disorder. The aim of this study was to determine whether the DNA polymorphisms located in the HLA-DRB1 and HLA-DQB1 genes show a specific association pattern in Mexican mestizo patients with primary open-angle glaucoma. METHODS: This was a cross-sectional, case-control, multicenter study. We analyzed the HLA-DRB1 and DQB1 loci of 81 Mexican mestizo nonrelated patients with primary open-angle glaucoma and 98 healthy ethnic matched control subjects. Patients were diagnosed clinically and by visual fields examination. HLA typing was performed by PCR-SSO reverse dot blot. RESULTS: We documented increased frequencies of HLA-DRB1∗0301, DRB1∗1101, DRB1∗0701, DRB1∗1402, DQB1∗0302, and DQB1∗0301; however, none of them were significantly different from normal control subjects. Haplotype analysis showed that the HLA-DRB1∗0407-DQB1∗0302 haplotype is significantly increased in patients compared with control subjects ( P = .0001). CONCLUSIONS: The haplotype HLA-DRB1∗0407-DQB1∗0302 is common among Mexican mestizo (haplotype frequency = 0.102), and it was increased in our patients (haplotype frequency = 0.259, P = .0001). This may reflect an independent association of this haplotype with the disease as the result of linkage disequilibrium or the influence of a neighboring gene. The pathophysiology of this illness is uncertain, and further studies are needed regarding the genetic susceptibility to develop primary open-angle glaucoma.
doi_str_mv 10.1016/S0002-9394(99)00180-4
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The aim of this study was to determine whether the DNA polymorphisms located in the HLA-DRB1 and HLA-DQB1 genes show a specific association pattern in Mexican mestizo patients with primary open-angle glaucoma. METHODS: This was a cross-sectional, case-control, multicenter study. We analyzed the HLA-DRB1 and DQB1 loci of 81 Mexican mestizo nonrelated patients with primary open-angle glaucoma and 98 healthy ethnic matched control subjects. Patients were diagnosed clinically and by visual fields examination. HLA typing was performed by PCR-SSO reverse dot blot. RESULTS: We documented increased frequencies of HLA-DRB1∗0301, DRB1∗1101, DRB1∗0701, DRB1∗1402, DQB1∗0302, and DQB1∗0301; however, none of them were significantly different from normal control subjects. Haplotype analysis showed that the HLA-DRB1∗0407-DQB1∗0302 haplotype is significantly increased in patients compared with control subjects ( P = .0001). CONCLUSIONS: The haplotype HLA-DRB1∗0407-DQB1∗0302 is common among Mexican mestizo (haplotype frequency = 0.102), and it was increased in our patients (haplotype frequency = 0.259, P = .0001). This may reflect an independent association of this haplotype with the disease as the result of linkage disequilibrium or the influence of a neighboring gene. 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The aim of this study was to determine whether the DNA polymorphisms located in the HLA-DRB1 and HLA-DQB1 genes show a specific association pattern in Mexican mestizo patients with primary open-angle glaucoma. METHODS: This was a cross-sectional, case-control, multicenter study. We analyzed the HLA-DRB1 and DQB1 loci of 81 Mexican mestizo nonrelated patients with primary open-angle glaucoma and 98 healthy ethnic matched control subjects. Patients were diagnosed clinically and by visual fields examination. HLA typing was performed by PCR-SSO reverse dot blot. RESULTS: We documented increased frequencies of HLA-DRB1∗0301, DRB1∗1101, DRB1∗0701, DRB1∗1402, DQB1∗0302, and DQB1∗0301; however, none of them were significantly different from normal control subjects. Haplotype analysis showed that the HLA-DRB1∗0407-DQB1∗0302 haplotype is significantly increased in patients compared with control subjects ( P = .0001). 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The aim of this study was to determine whether the DNA polymorphisms located in the HLA-DRB1 and HLA-DQB1 genes show a specific association pattern in Mexican mestizo patients with primary open-angle glaucoma. METHODS: This was a cross-sectional, case-control, multicenter study. We analyzed the HLA-DRB1 and DQB1 loci of 81 Mexican mestizo nonrelated patients with primary open-angle glaucoma and 98 healthy ethnic matched control subjects. Patients were diagnosed clinically and by visual fields examination. HLA typing was performed by PCR-SSO reverse dot blot. RESULTS: We documented increased frequencies of HLA-DRB1∗0301, DRB1∗1101, DRB1∗0701, DRB1∗1402, DQB1∗0302, and DQB1∗0301; however, none of them were significantly different from normal control subjects. Haplotype analysis showed that the HLA-DRB1∗0407-DQB1∗0302 haplotype is significantly increased in patients compared with control subjects ( P = .0001). CONCLUSIONS: The haplotype HLA-DRB1∗0407-DQB1∗0302 is common among Mexican mestizo (haplotype frequency = 0.102), and it was increased in our patients (haplotype frequency = 0.259, P = .0001). This may reflect an independent association of this haplotype with the disease as the result of linkage disequilibrium or the influence of a neighboring gene. The pathophysiology of this illness is uncertain, and further studies are needed regarding the genetic susceptibility to develop primary open-angle glaucoma.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10511023</pmid><doi>10.1016/S0002-9394(99)00180-4</doi><tpages>4</tpages></addata></record>
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ispartof American journal of ophthalmology, 1999-09, Vol.128 (3), p.297-300
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source Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list)
subjects Alleles
Biological and medical sciences
Case-Control Studies
Cross-Sectional Studies
DNA - analysis
Gene Frequency
Genetic Predisposition to Disease
Glaucoma and intraocular pressure
Glaucoma, Open-Angle - ethnology
Glaucoma, Open-Angle - genetics
Haplotypes
HLA-DQ Antigens - genetics
HLA-DQ beta-Chains
HLA-DR Antigens - genetics
HLA-DRB1 Chains
Humans
Medical sciences
Mexico - ethnology
Ophthalmology
Polymorphism, Genetic
title HLA-DRB and HLA-DQB loci in the genetic susceptibility to develop glaucoma in Mexicans
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