Association of HLA rs3135388 and rs9271366 Single-Nucleotide Polymorphisms With Multiple Sclerosis in the Chaharmahal and Bakhtiari Province, Iran

Background and aims: Genetics and environment are synergistic in multiple sclerosis (MS). Human leukocyte antigen (HLA) class II has a strong genetic association with MS. The aim of this study was to determine the association of HLA rs3135388 and rs9271366 single-nucleotide polymorphisms (SNPs) with...

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Main Authors: Shahrbanou Parchami Barjui, Zahra Forouzandeh Shahrakei, Nahid Jivad
Format: Article
Language:English
Published: Shahrekord University of Medical Sciences 2023-12-01
Series:Epidemiology and Health System Journal
Subjects:
Online Access:https://ehsj.skums.ac.ir/PDF/ehsj-26068.pdf
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author Shahrbanou Parchami Barjui
Zahra Forouzandeh Shahrakei
Nahid Jivad
author_facet Shahrbanou Parchami Barjui
Zahra Forouzandeh Shahrakei
Nahid Jivad
author_sort Shahrbanou Parchami Barjui
collection DOAJ
description Background and aims: Genetics and environment are synergistic in multiple sclerosis (MS). Human leukocyte antigen (HLA) class II has a strong genetic association with MS. The aim of this study was to determine the association of HLA rs3135388 and rs9271366 single-nucleotide polymorphisms (SNPs) with MS. Methods: The rs3135388, rs9271366, and rs422951 SNPs were genotyped in 173 Iranian relapsing-remitting MS (RRMS) patients and 200 matched healthy controls, using the polymerase chain reaction-restriction fragment length polymorphism method. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using statistical software to estimate the risk factor for disease. The allele and genotype frequencies of SNPs were determined based on data analysis using SPSS, version 20. Results: Our results identified a strong association in the allele distribution for both rs3135388 and rs9271366 SNP, such that the A allele of rs3135388 (OR=1.765; 95% CI: 1.071–2.909) and the G allele of rs9271366 were found to be more frequent in MS patients than in healthy controls (OR=1.861; 95% CI: 1.025–3.3378). The mutated G allele for rs422951 SNP was relatively frequent (OR=1.128; 95% CI: 0.745–1.707). Conclusion: Our findings revealed the critical role of the rs3135388 and rs9271366 SNPs in MS disease progression. Genotyping MS patients could facilitate personalized medical management.
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spelling doaj.art-971ecd32d145458aae98b6234ad868ec2024-01-23T08:29:13ZengShahrekord University of Medical SciencesEpidemiology and Health System Journal2980-78912023-12-0110417017410.34172/ehsj.26068ehsj-26068Association of HLA rs3135388 and rs9271366 Single-Nucleotide Polymorphisms With Multiple Sclerosis in the Chaharmahal and Bakhtiari Province, IranShahrbanou Parchami Barjui0Zahra Forouzandeh Shahrakei1Nahid Jivad2Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, IranDeputy of Research and Technology, Shahrekord University of Medical Science, Shahrekord, IranCellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, IranBackground and aims: Genetics and environment are synergistic in multiple sclerosis (MS). Human leukocyte antigen (HLA) class II has a strong genetic association with MS. The aim of this study was to determine the association of HLA rs3135388 and rs9271366 single-nucleotide polymorphisms (SNPs) with MS. Methods: The rs3135388, rs9271366, and rs422951 SNPs were genotyped in 173 Iranian relapsing-remitting MS (RRMS) patients and 200 matched healthy controls, using the polymerase chain reaction-restriction fragment length polymorphism method. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using statistical software to estimate the risk factor for disease. The allele and genotype frequencies of SNPs were determined based on data analysis using SPSS, version 20. Results: Our results identified a strong association in the allele distribution for both rs3135388 and rs9271366 SNP, such that the A allele of rs3135388 (OR=1.765; 95% CI: 1.071–2.909) and the G allele of rs9271366 were found to be more frequent in MS patients than in healthy controls (OR=1.861; 95% CI: 1.025–3.3378). The mutated G allele for rs422951 SNP was relatively frequent (OR=1.128; 95% CI: 0.745–1.707). Conclusion: Our findings revealed the critical role of the rs3135388 and rs9271366 SNPs in MS disease progression. Genotyping MS patients could facilitate personalized medical management.https://ehsj.skums.ac.ir/PDF/ehsj-26068.pdfmultiple sclerosissingle-nucleotide polymorphismshlars3135388rs9271366
spellingShingle Shahrbanou Parchami Barjui
Zahra Forouzandeh Shahrakei
Nahid Jivad
Association of HLA rs3135388 and rs9271366 Single-Nucleotide Polymorphisms With Multiple Sclerosis in the Chaharmahal and Bakhtiari Province, Iran
Epidemiology and Health System Journal
multiple sclerosis
single-nucleotide polymorphisms
hla
rs3135388
rs9271366
title Association of HLA rs3135388 and rs9271366 Single-Nucleotide Polymorphisms With Multiple Sclerosis in the Chaharmahal and Bakhtiari Province, Iran
title_full Association of HLA rs3135388 and rs9271366 Single-Nucleotide Polymorphisms With Multiple Sclerosis in the Chaharmahal and Bakhtiari Province, Iran
title_fullStr Association of HLA rs3135388 and rs9271366 Single-Nucleotide Polymorphisms With Multiple Sclerosis in the Chaharmahal and Bakhtiari Province, Iran
title_full_unstemmed Association of HLA rs3135388 and rs9271366 Single-Nucleotide Polymorphisms With Multiple Sclerosis in the Chaharmahal and Bakhtiari Province, Iran
title_short Association of HLA rs3135388 and rs9271366 Single-Nucleotide Polymorphisms With Multiple Sclerosis in the Chaharmahal and Bakhtiari Province, Iran
title_sort association of hla rs3135388 and rs9271366 single nucleotide polymorphisms with multiple sclerosis in the chaharmahal and bakhtiari province iran
topic multiple sclerosis
single-nucleotide polymorphisms
hla
rs3135388
rs9271366
url https://ehsj.skums.ac.ir/PDF/ehsj-26068.pdf
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