Li He, Hou Xiaodan, Liang Yan, Xu Fang, Zhang Xiyue, Cui Pan, Xing Gebeili, Wang Xuejiao, Jiang Wei
Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Tianjin, China.
Department of Neurology, Inner Mongolia People's Hospital, Hohhot, China.
Front Neurosci. 2021 May 11;15:614528. doi: 10.3389/fnins.2021.614528. eCollection 2021.
Multiple sclerosis (MS) is an autoimmune disorder influenced by genetic and environmental factors. Many studies have provided insights into genetic factors' contribution to MS via large-scale genome-wide association study (GWAS) datasets. However, genetic variants identified to date do not adequately explain genetic risks for MS. This study hypothesized that novel MS risk genes could be identified by analyzing the MS-GWAS dataset using gene-based tests. We analyzed a GWAS dataset consisting of 9,772 MS cases and 17,376 healthy controls of European descent. We performed gene-based tests of 464,357 autosomal single nucleotide polymorphisms (SNPs) using two methods (PLINK and VEGAS2) and identified 28 shared genes satisfied -value < 4.56 × 10. In further gene expression analysis, ten of the 28 genes were significantly differentially expressed in the MS case-control gene expression omnibus (GEO) database. GALC and HLA-DOB showed the most prominent differences in gene expression (two- and three-fold, respectively) between MS patients and healthy controls. In conclusion, our results reveal more information about MS hereditary characteristics and provide a basis for further studies.
多发性硬化症(MS)是一种受遗传和环境因素影响的自身免疫性疾病。许多研究通过大规模全基因组关联研究(GWAS)数据集,对遗传因素在MS中的作用提供了见解。然而,迄今为止鉴定出的基因变异并不能充分解释MS的遗传风险。本研究假设可以通过使用基于基因的测试分析MS-GWAS数据集来鉴定新的MS风险基因。我们分析了一个由9772例MS病例和17376例欧洲血统健康对照组成的GWAS数据集。我们使用两种方法(PLINK和VEGAS2)对464357个常染色体单核苷酸多态性(SNP)进行了基于基因的测试,并鉴定出28个共享基因,其满足值<4.56×10。在进一步的基因表达分析中,28个基因中的10个在MS病例对照基因表达综合数据库(GEO)中存在显著差异表达。GALC和HLA-DOB在MS患者和健康对照之间的基因表达差异最为显著(分别为两倍和三倍)。总之,我们的结果揭示了更多关于MS遗传特征的信息,并为进一步研究提供了基础。