Suppr超能文献

基于通路的两个全基因组筛查数据关联分析确定类风湿性关节炎相关通路。

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

作者信息

Zhang M-M, Jiang Y-S, Lv H-C, Mu H-B, Li J, Shang Z-W, Zhang R-J

机构信息

College of Bioinformatics Science and Technology, Harbin Medical University, Harbin, China.

College of Science, Northeast Forestry University, Harbin, China.

出版信息

Genes Immun. 2014 Oct;15(7):487-94. doi: 10.1038/gene.2014.48. Epub 2014 Aug 7.

Abstract

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.

摘要

这些通路能够从生物学功能的角度解释复杂疾病的分子机制。我们开展了一项基于全基因组通路的关联分析,以确定类风湿关节炎(RA)的风险通路。首先,我们使用来自GAW16(遗传分析研讨会16)和威康信托病例对照协会的两个RA数据集进行了两项全基因组关联研究,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值法计算基因层面的风险值。我们根据Fisher组合法计算KEGG(京都基因与基因组百科全书)通路风险评分,并通过置换检验确定显著通路。最后,我们合并了两项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均发现的高风险通路。结果显示,有九条通路与RA易感性相关,分别是粘着斑通路、细胞外基质-受体相互作用通路、钙信号通路、多巴胺能突触通路、长时程增强通路、逆行性内源性大麻素信号通路、谷氨酸能突触通路、胆碱能突触通路和吗啡成瘾通路。在这些通路中,有四条通路在之前的文献中被报道为RA风险通路。我们还推断其他五条通路可能与RA有关。对这些通路的进一步研究将有助于我们理解RA的分子机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验