N. Delfan, H. Galehdari, M. Shafiei, Farideh Ghanbari-Mardasi, Tahereh Latifi, N. Majdinasab, T. Seifi
{"title":"Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran","authors":"N. Delfan, H. Galehdari, M. Shafiei, Farideh Ghanbari-Mardasi, Tahereh Latifi, N. Majdinasab, T. Seifi","doi":"10.18502/IJNL.V17I4.586","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":45759,"journal":{"name":"Iranian Journal of Neurology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Journal of Neurology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18502/IJNL.V17I4.586","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.
背景:多发性硬化症(MS)是中枢神经系统(CNS)脱髓鞘和炎症性疾病之一。虽然MS的发病机制尚不清楚,但遗传和环境因素均有涉及。人类白细胞抗原(HLA)ⅱ类等位基因HLA- drb5 *01、DQB1*0602、DRB1*1501、DQA1*0102可能对MS风险有显著影响,但研究中存在争议。由于在伊朗Khuzestan省没有HLA-DRB1*1501-DRB5*01与MS相关性的数据,本次调查的目的是调查该人群中该单倍型与MS的相关性。方法:对200例患者和200例健康人的DRB5*01-DRB1*1501单倍型与MS的相关性进行研究。HLA分型采用序列特异性引物(SSP)扩增聚合酶链反应(PCR)法。采用SPSS软件进行统计分析。结果:DRB5*01+-DRB1*1501+与MS无相关性(P = 0.156)。DRB1*1501+-DRB5*01-(携带DRB1*1501+而不携带DRB5*01-)和DRB1*1501- DRB5*01-单倍型在患者和对照组之间的分布差异有统计学意义(分别为29.73% vs. 11.81%, P < 0.001)和(42.16% vs. 68.50%, P < 0.001)。然而,DRB1*1501—DRB5*01+与MS无相关性(15.13% vs. 11.81%, P = 0.403)。HLA-DRB1*1501—DRB5*01+在女性MS患者(16.19% vs. 6.12%, P = 0.019)和波斯组(17.11% vs. 5.79%, P = 0.027)中更为常见。HLA-DRB1*1501+- drb5 *01-单倍型与扩展残疾状态量表(EDSS) 5 ~ 10级呈正相关(62.50% vs. 25.76%, P = 0.026)。此外,单倍型与EDSS、病程、种族和性别之间没有明显的关联。结论:DRB1*1501+-DRB5*01-和DRB1*1501—DRB5*01-单倍型可能与MS风险呈正相关。此外,本调查表明HLA-DRB1*1501—DRB5*01+与女性和波斯人的疾病易感性有关。DRB1*1501+- drb5 *01-基因型频率可能在MS发生中起关键作用。