Chavoshi Tarzjani Seyedeh Parisa, Shahzadeh Fazeli Seyed Abol Hassan, Sanati Mohammad Hossein, Nabavi Seyed Massood
Department of Biological Sciences, Tehran North Branch, Islamic Azad University, Tehran, Iran.
Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Cell J. 2019 Jan;20(4):599-603. doi: 10.22074/cellj.2019.5620. Epub 2018 Aug 1.
Multiple sclerosis (MS) is a chronic disease of the central nervous system and one of the most common causes of neurological disability among those aged 20-40 years, particularly in women. Major histocompatibility complex (MHC) Class II genes are known to be involved in the development of MS. One of the important groups of this complex is the HSP gene family, especially HSP70, which is induced under stress conditions. The aim of the present case-control study was to determine the association between the heat shock protein 70 (HSP70) and risk of MS in Iranian patients by genotyping the rs1061581 gene polymorphism. A total of 50 relapsing-remitting MS (RRMS) patients and 50 healthy control subjects were considered for this study. Genotyping was performed by the polymerase chain reaction-restriction fragment length polymorphism (PCRRFLP) method. PCR-RFLP results of twenty-five randomly selected samples were confirmed by DNA sequencing. Genotypic and allelic distributions were compared between the case and control groups. We observed no significant difference in the distribution of rs1061581 genotype and allele frequencies between RRMS patients and controls. In addition, there was no association between the HSP70 gene polymorphism and the clinical variables in the case group. Our data indicate that HSP70, in particular rs1061581, is unlikely to be involved in the susceptibility to or the severity of RRMS in Iranian patients. Further large prospective studies are required to confirm these findings.
多发性硬化症(MS)是一种中枢神经系统的慢性疾病,是20至40岁人群中神经功能障碍最常见的病因之一,在女性中尤为常见。已知主要组织相容性复合体(MHC)II类基因参与MS的发病过程。该复合体的重要基因群之一是热休克蛋白(HSP)基因家族,尤其是在应激条件下被诱导产生的HSP70。本病例对照研究的目的是通过对rs1061581基因多态性进行基因分型,确定伊朗患者中热休克蛋白70(HSP70)与MS风险之间的关联。本研究共纳入50例复发缓解型多发性硬化症(RRMS)患者和50名健康对照者。采用聚合酶链反应-限制性片段长度多态性(PCRRFLP)方法进行基因分型。随机选取25个样本的PCRRFLP结果通过DNA测序进行验证。比较病例组和对照组的基因型和等位基因分布。我们观察到RRMS患者与对照组之间rs1061581基因型和等位基因频率分布无显著差异。此外,病例组中HSP70基因多态性与临床变量之间也无关联。我们的数据表明,HSP70,特别是rs1061581,不太可能参与伊朗患者RRMS的易感性或严重程度。需要进一步开展大型前瞻性研究来证实这些发现。