نویسندگان | نفیسه خلیلی,روح اله نخعی سیستانی,هادی شیرزاد |
---|---|
نشریه | Biomacromolecular Journal |
شماره صفحات | 56 |
شماره مجلد | 8 |
ضریب تاثیر (IF) | ثبت نشده |
نوع مقاله | Full Paper |
تاریخ انتشار | 2024-05-08 |
رتبه نشریه | علمی - پژوهشی |
نوع نشریه | الکترونیکی |
کشور محل چاپ | ایران |
نمایه نشریه | ISC |
چکیده مقاله
Background: Multiple sclerosis (MS) is a chronic disease of the central nervous system that leads to the disability of the affected people. The etiology of the disease is not clear, but it is believed that it has an autoimmune nature. Several studies suggested that the major histocompatibility complex (MHC) class II loci are the most prominent genetic risk factor for MS susceptibility. The Human leukocyte antigen (HLA) DQB1*06 allele was introduced in numerous studies as the MS genetic predisposition factor, but there is a debate about it in different regions. Objective: This study aims to analyze the association of the HLA-DQB1*06 allele in Tehran. Method: Blood samples were collected from 117 MS and 114 healthy people. DNA was extracted, and genotyping was performed using allele-specific primers. Results: Our results showed that the HLA-DQB1*06 allele is significantly associated with MS (p-value < 0.000, odds ratio = 0.059, 95% CI = 0.02 to 0.14). The homozygous genotype was also more prevalent in the MS group compared with the control (p-value < 0.000, odds ratio = 0.2, 95% CI = 0.1-0.39). Our results show there is no difference in allelic distribution of this gene between men and women. Conclusion: Our data suggest that the HLA-DQB1*06 could be considered as an important genetic risk factor for MS in Tehran.
tags: Multiple sclerosis, HLA-DQB1, Association, Disease susceptibility, Genetic predisposition