Abstract

Rheumatoid arthritis (RA) is a complex and systematic autoimmune disease, which is usually influenced by both genetic and environmental factors. Pathway analyses based on a single data type such as microarray data or SNP data have successfully revealed some biology pathways associated with RA. However, we found that the pathway analysis based on a single data type only provide limited understanding about the pathogenesis of RA. Gene-disease association is usually caused by many ways, such as genotype, gene expression and so on. Therefore, the integrative analysis method combining multiple levels of evidence can more precisely and comprehensively identify the pathway associations. In this study, we performed a pathway analysis by integrating GWAS and gene expression analysis to detect the RA-related pathways. The integrative analysis identified 28 pathways associated with RA. Among these pathways, 18 pathways were also found by both GWAS and gene expression analysis, 7 pathways are novel RA-related pathways, such as B cell receptor signaling pathway, Toll-like receptor signaling pathway, Fc gamma R-mediated phagocytosis and so on. Compared with pathway analyses using only one type genomic data, we found integrative analysis can increase the power to identify the real associations and provided more stable and accurate results. We believe these results will contribute to perform future genetic studies in RA pathogenesis and may promote the development of new therapeutic strategies by targeting these pathways.

Highlights

  • Rheumatoid arthritis (RA) is a common, chronic autoimmune disease, which characterized by nonspecific inflammation of the peripheral joints

  • The 28 pathways (FDR< 0.05) after FDR correction were identified as RA-related pathways based on integration Genome-wide association studies (GWAS) and gene expression data

  • We found that pathways which were identified by pathway analyses based on GWAS and gene expression analysis were not entirely consistent

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Summary

Introduction

Rheumatoid arthritis (RA) is a common, chronic autoimmune disease, which characterized by nonspecific inflammation of the peripheral joints It affects 1% of the world’s population, and it occurs more frequently in women than in men [1, 2]. Many GWAS have been successfully applied to RA and have identified large number of single nucleotide polymorphisms (SNPs) related to RA [3,4,5,6,7,8]. These loci account for a small proportion of genetic variants and can not dissect and explain the complex molecular mechanisms of RA.

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