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Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran

Background: One of the demyelinating and inflammatory diseases of the central nervous system (CNS) is multiple sclerosis (MS). Though pathogenesis of MS is still unknown, both genetic and environmental factors are involved. The human leukocyte antigen (HLA) class-II alleles including HLA-DRB5*01, DQ...

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Autores principales: Delfan, Nooshin, Galehdari, Hamid, Shafiei, Mohammad, Ghanbari-Mardasi, Farideh, Latifi, Tahereh, Majdinasab, Nastaran, Seifi, Tahereh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555884/
https://www.ncbi.nlm.nih.gov/pubmed/31210899
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author Delfan, Nooshin
Galehdari, Hamid
Shafiei, Mohammad
Ghanbari-Mardasi, Farideh
Latifi, Tahereh
Majdinasab, Nastaran
Seifi, Tahereh
author_facet Delfan, Nooshin
Galehdari, Hamid
Shafiei, Mohammad
Ghanbari-Mardasi, Farideh
Latifi, Tahereh
Majdinasab, Nastaran
Seifi, Tahereh
author_sort Delfan, Nooshin
collection PubMed
description Background: One of the demyelinating and inflammatory diseases of the central nervous system (CNS) is multiple sclerosis (MS). Though pathogenesis of MS is still unknown, both genetic and environmental factors are involved. The human leukocyte antigen (HLA) class-II alleles including HLA-DRB5*01, DQB1*0602, DRB1*1501, and DQA1*0102 may have remarkable effect in MS risk although it is controversial in studies. As there is no data with respect to the HLA-DRB1*1501-DRB5*01 correlation with MS in Khuzestan Province, Iran, the goal of the survey was to investigate the association of this haplotype with MS in this population. Methods: The study focused on DRB5*01-DRB1*1501 haplotype association with MS in 200 patients and 200 healthy individuals. Typing of HLA was carried out by polymerase chain reaction (PCR) amplification with sequence-specific primers (SSP) method. SPSS software was used for the statistical analyses. Results: No association between DRB5*01(+)-DRB1*1501(+) and MS was found (P = 0.156). Distribution of DRB1*1501(+)-DRB5*01(-) (carrying DRB1*1501(+) but not DRB5*01(-)) and DRB1*1501(-)-DRB5*01(-) haplotypes was statistically different between patients and controls (29.73% vs. 11.81%, P < 0.001) and (42.16% vs. 68.50%, P < 0.001), respectively. However, DRB1*1501(-)-DRB5*01(+) revealed no association with MS (15.13% vs. 11.81%, P = 0.403). HLA-DRB1*1501(-)-DRB5*01(+) was significantly more frequent among female patients with MS (16.19% vs. 6.12%, P = 0.019) and Persian group (17.11% vs. 5.79%, P = 0.027). Positive correlation of HLA-DRB1*1501(+)-DRB5*01(-) haplotype with the expanded disability status scale (EDSS) steps from 5 to 10 was observed (62.50% vs. 25.76%, P = 0.026). Moreover, no meaningful association was shown among the haplotypes with EDSS, course of MS, ethnicity, and gender. Conclusion: Our findings suggest that DRB1*1501(+)-DRB5*01(-) and DRB1*1501(-)-DRB5*01(-) haplotypes may have positive association with MS risk. Also, this survey indicates that HLA-DRB1*1501(-)-DRB5*01(+) is involved in susceptibility of the disease among women and Persians. DRB1*1501(+)-DRB5*01(-) genotype frequency may have a key role in MS developing.
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spelling pubmed-65558842019-06-17 Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran Delfan, Nooshin Galehdari, Hamid Shafiei, Mohammad Ghanbari-Mardasi, Farideh Latifi, Tahereh Majdinasab, Nastaran Seifi, Tahereh Iran J Neurol Original Article Background: One of the demyelinating and inflammatory diseases of the central nervous system (CNS) is multiple sclerosis (MS). Though pathogenesis of MS is still unknown, both genetic and environmental factors are involved. The human leukocyte antigen (HLA) class-II alleles including HLA-DRB5*01, DQB1*0602, DRB1*1501, and DQA1*0102 may have remarkable effect in MS risk although it is controversial in studies. As there is no data with respect to the HLA-DRB1*1501-DRB5*01 correlation with MS in Khuzestan Province, Iran, the goal of the survey was to investigate the association of this haplotype with MS in this population. Methods: The study focused on DRB5*01-DRB1*1501 haplotype association with MS in 200 patients and 200 healthy individuals. Typing of HLA was carried out by polymerase chain reaction (PCR) amplification with sequence-specific primers (SSP) method. SPSS software was used for the statistical analyses. Results: No association between DRB5*01(+)-DRB1*1501(+) and MS was found (P = 0.156). Distribution of DRB1*1501(+)-DRB5*01(-) (carrying DRB1*1501(+) but not DRB5*01(-)) and DRB1*1501(-)-DRB5*01(-) haplotypes was statistically different between patients and controls (29.73% vs. 11.81%, P < 0.001) and (42.16% vs. 68.50%, P < 0.001), respectively. However, DRB1*1501(-)-DRB5*01(+) revealed no association with MS (15.13% vs. 11.81%, P = 0.403). HLA-DRB1*1501(-)-DRB5*01(+) was significantly more frequent among female patients with MS (16.19% vs. 6.12%, P = 0.019) and Persian group (17.11% vs. 5.79%, P = 0.027). Positive correlation of HLA-DRB1*1501(+)-DRB5*01(-) haplotype with the expanded disability status scale (EDSS) steps from 5 to 10 was observed (62.50% vs. 25.76%, P = 0.026). Moreover, no meaningful association was shown among the haplotypes with EDSS, course of MS, ethnicity, and gender. Conclusion: Our findings suggest that DRB1*1501(+)-DRB5*01(-) and DRB1*1501(-)-DRB5*01(-) haplotypes may have positive association with MS risk. Also, this survey indicates that HLA-DRB1*1501(-)-DRB5*01(+) is involved in susceptibility of the disease among women and Persians. DRB1*1501(+)-DRB5*01(-) genotype frequency may have a key role in MS developing. Tehran University of Medical Sciences 2018-10-07 /pmc/articles/PMC6555884/ /pubmed/31210899 Text en Copyright © 2015 Iranian Neurological Association, and Tehran University of Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Delfan, Nooshin
Galehdari, Hamid
Shafiei, Mohammad
Ghanbari-Mardasi, Farideh
Latifi, Tahereh
Majdinasab, Nastaran
Seifi, Tahereh
Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran
title Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran
title_full Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran
title_fullStr Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran
title_full_unstemmed Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran
title_short Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran
title_sort association of human leukocyte antigen-drb haplotype in multiple sclerosis population of khuzestan, iran
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555884/
https://www.ncbi.nlm.nih.gov/pubmed/31210899
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