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Pathway-based association analysis of two genome-wide screening data identifies rheumatoid arthritis-related pathways

机译:基于通路的两种全基因组筛选数据的关联分析可确定类风湿关节炎相关通路

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摘要

The pathways can explain molecular mechanisms of complex diseases from the perspective of biology function. We carried out a genome-wide pathway-based association analysis to identify the risk pathways of rheumatoid arthritis (RA). First, we performed two genome-wide association studies using two RA data sets from GAW16 (Genetic Analysis Workshop 16) and the Wellcome Trust Case Control Consortium, and obtained risk P-value for each single-nucleotide polymorphism (SNP). Next, we mapped all the SNPs to genome-wide autosomal genes and calculated gene-wise risk values by minimum P-value method. We calculated the KEGG (Kyoto Encyclopedia of Gene and Genomes) pathway risk scores according to Fisher combination method and identified the significant pathways by permutation test. At last, we merged the results from the two pathway-based genome-wide association analyses to identify the high-risk pathways, which were found in both the data sets. The results showed that there were nine pathways, focal adhesion pathway, extracellular matrix-receptor interaction pathway, calcium signaling pathway, dopaminergic synapse pathway, long-term potentiation pathway, retrograde endocannabinoid signaling pathway, glutamatergic synapse pathway, cholinergic synapse pathway and morphine addiction pathway, associated with susceptibility to RA. Among these pathways, four pathways were reported as RA-risk pathways in the previous literatures. We also inferred that other five pathways may be related to RA. Further researches of these pathways will help us to understand the molecular mechanisms of RA.
机译:这些途径可以从生物学功能的角度解释复杂疾病的分子机制。我们进行了基于全基因组途径的关联分析,以识别类风湿关节炎(RA)的危险途径。首先,我们使用来自GAW16(遗传分析研讨会16)和惠康信托案例对照协会的两个RA数据集进行了两个全基因组关联研究,并获得了每个单核苷酸多态性(SNP)的风险P值。接下来,我们将所有SNP映射到全基因组常染色体基因,并通过最小P值方法计算了基因方式的风险值。我们根据Fisher组合方法计算了KEGG(基因和基因组京都百科全书)途径风险评分,并通过置换测试确定了重要途径。最后,我们合并了两个基于通路的全基因组关联分析的结果,以识别在两个数据集中都发现的高风险通路。结果表明,共存在九种途径,即粘着途径,细胞外基质受体相互作用途径,钙信号传导途径,多巴胺能突触途径,长期增强途径,逆行内源性大麻素信号传导途径,谷氨酸能突触途径,胆碱能突触途径和吗啡成瘾途径。 ,与RA的易感性有关。在这些途径中,在先前的文献中报道了四种途径作为RA风险途径。我们还推断出其他五种途径可能与RA相关。这些途径的进一步研究将有助于我们了解RA的分子机制。

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