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Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent

PURPOSE: To evaluate how the HLA genotype is associated to the polypoidal choroidal vasculopathy (PCV) in a population of patients of Afro-Caribbean descent. METHODS: Forty-seven patients were diagnosed with PCV. The number of control patients was 457. All affected patients and control patients were...

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Autores principales: Merle, Harold, Béral, Laurence, Rocher, Maxime, Pierre, Mitta, Jean-Charles, Albert, Béra, Odile, Rosamont, Laurie-Anne, Robert, Pierre-Yves, Lézin, Agnes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995864/
https://www.ncbi.nlm.nih.gov/pubmed/35418742
http://dx.doi.org/10.2147/OPTH.S337084
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author Merle, Harold
Béral, Laurence
Rocher, Maxime
Pierre, Mitta
Jean-Charles, Albert
Béra, Odile
Rosamont, Laurie-Anne
Robert, Pierre-Yves
Lézin, Agnes
author_facet Merle, Harold
Béral, Laurence
Rocher, Maxime
Pierre, Mitta
Jean-Charles, Albert
Béra, Odile
Rosamont, Laurie-Anne
Robert, Pierre-Yves
Lézin, Agnes
author_sort Merle, Harold
collection PubMed
description PURPOSE: To evaluate how the HLA genotype is associated to the polypoidal choroidal vasculopathy (PCV) in a population of patients of Afro-Caribbean descent. METHODS: Forty-seven patients were diagnosed with PCV. The number of control patients was 457. All affected patients and control patients were of Afro-Caribbean descent and natives to Martinique. HLA typing was based on blood sample, using the polymerase chain reaction technique. Comparison of HLA alleles between the 2 groups was done using chi-2 test, odds ratio (OR) and confidence interval using Woolf’s method. The Bonferroni correction was considered significant when p-value ≤0.05. Alleles frequency was analyzed for DRB1 and DQB1 locus. RESULTS: HLA-DRB1*13 allele was significantly associated to PCV (OR = 2.02, CI = [1.3; 3.13], p = 0.003). In group DRB1, the Bonferroni correction significance threshold was <0.004. HLA-DQB1*04 allele was significantly associated to PCV (OR = 3.5, CI = [1.48; 8.3], p = 0.006). In group DQB1, the Bonferroni correction significance threshold was <0.006. CONCLUSION: Two HLA alleles are positively associated to PCV. The possible association between PCV and certain alleles suggest HLA implication in PCV pathogeny, most likely by modeling the immune system response.
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spelling pubmed-89958642022-04-12 Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent Merle, Harold Béral, Laurence Rocher, Maxime Pierre, Mitta Jean-Charles, Albert Béra, Odile Rosamont, Laurie-Anne Robert, Pierre-Yves Lézin, Agnes Clin Ophthalmol Original Research PURPOSE: To evaluate how the HLA genotype is associated to the polypoidal choroidal vasculopathy (PCV) in a population of patients of Afro-Caribbean descent. METHODS: Forty-seven patients were diagnosed with PCV. The number of control patients was 457. All affected patients and control patients were of Afro-Caribbean descent and natives to Martinique. HLA typing was based on blood sample, using the polymerase chain reaction technique. Comparison of HLA alleles between the 2 groups was done using chi-2 test, odds ratio (OR) and confidence interval using Woolf’s method. The Bonferroni correction was considered significant when p-value ≤0.05. Alleles frequency was analyzed for DRB1 and DQB1 locus. RESULTS: HLA-DRB1*13 allele was significantly associated to PCV (OR = 2.02, CI = [1.3; 3.13], p = 0.003). In group DRB1, the Bonferroni correction significance threshold was <0.004. HLA-DQB1*04 allele was significantly associated to PCV (OR = 3.5, CI = [1.48; 8.3], p = 0.006). In group DQB1, the Bonferroni correction significance threshold was <0.006. CONCLUSION: Two HLA alleles are positively associated to PCV. The possible association between PCV and certain alleles suggest HLA implication in PCV pathogeny, most likely by modeling the immune system response. Dove 2022-04-06 /pmc/articles/PMC8995864/ /pubmed/35418742 http://dx.doi.org/10.2147/OPTH.S337084 Text en © 2022 Merle et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Merle, Harold
Béral, Laurence
Rocher, Maxime
Pierre, Mitta
Jean-Charles, Albert
Béra, Odile
Rosamont, Laurie-Anne
Robert, Pierre-Yves
Lézin, Agnes
Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent
title Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent
title_full Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent
title_fullStr Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent
title_full_unstemmed Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent
title_short Class II Human Leukocyte Antigen (HLA) and Susceptibility to Polypoidal Choroidal Vasculopathy in Afro-Caribbean Descent
title_sort class ii human leukocyte antigen (hla) and susceptibility to polypoidal choroidal vasculopathy in afro-caribbean descent
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995864/
https://www.ncbi.nlm.nih.gov/pubmed/35418742
http://dx.doi.org/10.2147/OPTH.S337084
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