Title of article :
Association of HLA-DR2-Related Haplotype (HLA-DRB5*01-DRB1*1501-DQB1*0602) in Patients with Multiple Sclerosis in Khuzestan Province
Author/Authors :
delfan, nooshin shahid chamran university of ahvaz - faculty of sciences - department of genetics, Ahvaz, Iran , galehdari, hamid shahid chamran university of ahvaz - faculty of sciences - department of genetics, Ahvaz, Iran , ghanbari mardasi, farideh shahid chamran university of ahvaz - faculty of sciences - department of genetics, Ahvaz, Iran , zabihi, rezvan shahid chamran university of ahvaz - faculty of sciences - department of genetics, Ahvaz, Iran , latifi pakdehi, tahereh shahid chamran university of ahvaz - faculty of sciences - department of genetics, Ahvaz, Iran , seifi, tahereh shahid chamran university of ahvaz - faculty of sciences - department of genetics, Ahvaz, Iran , majdinasab, nastaran jondishapour university of medical sciences - musculoskeletal rehabilitation research center - department of neurology, Ahvaz, Iran
From page :
35
To page :
46
Abstract :
Objective: Multiple sclerosis (MS) is a partially heritable autoimmune disease. HLA-DR2 is the largest identified genetic risk factor for MS. The largest identified genetic risk factor is haplotype from the MHC class II HLA-DR2, which increases the disease risk. The HLA-DR2 distribution in MS patients has been confirmed, but contradictory outcomes have been found. Moreover, the HLA-DR2 effect on ethnicity and gender is unclear. There are no data regarding the HLADR2 (HLA-DRB1*1501-DRB5*01-DQB1*0602) association with MS in Khuzestan Province, Iran. This study aimed to investigate the association of HLA-DR2 with MS regarding both sex and ethnicity in this province. Materials Methods: A total of 399 individuals were recruited. HLA typing was conducted using the polymerase chain reaction amplification with sequence specific primers technology. The HLA-DR2 association with MS was analyzed, and also its probable association with gender, ethnicity, the expanded disability status scale (EDSS), and MS clinical course was examined using the Chi-square test. Results: HLA-DRB5*01--DQB1*0602- as the most common HLA haplo type was found in both patient and control groups. In contrast, the DRB5*01+-DRB1*1501+-DQB1*0602- frequency was very low in the groups. It was observed that haplotypes had no association with MS susceptibility. Most of the haplotypes showed no association with ethnicity, sex, EDSS, and MS course except for the HLA-DRB5*01+- DRB1*1501+-DQB1*0602- haplotype that was positively associated with EDSS steps 5 to 10 (p=0.014) and non-RRMS (p=0.023). Conclusion: There was no association between HLA-DR2 and MS susceptibility. However, the higher HLA-DRB5*01+-DRB1*1501+-DQB1*0602-frequency may play a role in MS development. Also, HLA-DR2 did not increase significantly concerning clinical course, ethnicity, sex, and EDSS. This study further supports the importance of replication studies as susceptible loci that might differ in various ethnicities. Therefore, it is concluded that the association between HLA-DR2 and MS is more allelic than haplotypic in Khuzestan.
Keywords :
Multiple sclerosis , HLA , DRB1*1501 , HLA , DR2 , PCRSSP , Iran
Journal title :
Iranian Journal of Child Neurology (IJCN)
Journal title :
Iranian Journal of Child Neurology (IJCN)
Record number :
2669305
Link To Document :
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