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Lack of association between mannose-binding lectin gene polymorphisms and juvenile idiopathic arthritis in a Han population from the Hubei province of China

机译:湖北省汉族人群中甘露糖结合凝集素基因多态性与青少年特发性关节炎之间缺乏关联

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Many studies have reported that polymorphisms of the mannose-binding lectin (MBL) gene are associated with autoimmune disease. Here, we investigate the relationship between MBL gene polymorphisms and susceptibility to juvenile idiopathic arthritis (JIA) in a Han-nationality population from the Hubei province of China. PCR-restriction fragment length polymorphism was used to investigate polymorphisms of codons 54 and 57 in exon 1 of the MBL gene in 93 patients with JIA and 48 control children. Neither group showed codon 57 polymorphisms. There was no significant difference in the genotypic frequencies of codon 54 between patients with JIA and healthy controls (wild type, 71.0% versus 75.0%, respectively; heterozygous type, 25.8% versus 25.0%, respectively; and homozygous type, 3.2% versus 0.0%, respectively). In addition, no association was found between the subgroups of patients with JIA and control individuals. Our results provide no evidence for a relationship between MBL gene mutation and susceptibility to JIA.
机译:许多研究报告说,甘露糖结合凝集素(MBL)基因的多态性与自身免疫性疾病有关。在这里,我们调查了中国湖北省汉族人群MBL基因多态性与青少年特发性关节炎(JIA)易感性之间的关系。应用PCR-限制性片段长度多态性研究93例JIA患者和48例对照儿童MBL基因第1外显子的54和57位密码子多态性。两组均未显示密码子57多态性。 JIA患者和健康对照者之间54密码子的基因型频率无显着差异(野生型分别为71.0%和75.0%;杂合型分别为25.8%和25.0%;纯合型分别为3.2%和0.0。 %, 分别)。此外,在JIA患者亚组和对照组之间未发现关联。我们的结果没有证据表明MBL基因突变与对JIA的易感性之间的关系。

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