Literature DB >> 24532676

High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci.

Kwangwoo Kim1, So-Young Bang2, Hye-Soon Lee2, Soo-Kyung Cho2, Chan-Bum Choi2, Yoon-Kyoung Sung2, Tae-Hwan Kim2, Jae-Bum Jun2, Dae Hyun Yoo2, Young Mo Kang3, Seong-Kyu Kim4, Chang-Hee Suh5, Seung-Cheol Shim6, Shin-Seok Lee7, Jisoo Lee8, Won Tae Chung9, Jung-Yoon Choe4, Hyoung Doo Shin10, Jong-Young Lee11, Bok-Ghee Han11, Swapan K Nath12, Steve Eyre13, John Bowes13, Dimitrios A Pappas14, Joel M Kremer15, Miguel A Gonzalez-Gay16, Luis Rodriguez-Rodriguez17, Lisbeth Ärlestig18, Yukinori Okada19, Dorothée Diogo20, Katherine P Liao21, Elizabeth W Karlson21, Soumya Raychaudhuri22, Solbritt Rantapää-Dahlqvist18, Javier Martin23, Lars Klareskog24, Leonid Padyukov24, Peter K Gregersen25, Jane Worthington12, Jeffrey D Greenberg26, Robert M Plenge20, Sang-Cheol Bae2.   

Abstract

OBJECTIVE: A highly polygenic aetiology and high degree of allele-sharing between ancestries have been well elucidated in genetic studies of rheumatoid arthritis. Recently, the high-density genotyping array Immunochip for immune disease loci identified 14 new rheumatoid arthritis risk loci among individuals of European ancestry. Here, we aimed to identify new rheumatoid arthritis risk loci using Korean-specific Immunochip data.
METHODS: We analysed Korean rheumatoid arthritis case-control samples using the Immunochip and genome-wide association studies (GWAS) array to search for new risk alleles of rheumatoid arthritis with anticitrullinated peptide antibodies. To increase power, we performed a meta-analysis of Korean data with previously published European Immunochip and GWAS data for a total sample size of 9299 Korean and 45,790 European case-control samples.
RESULTS: We identified eight new rheumatoid arthritis susceptibility loci (TNFSF4, LBH, EOMES, ETS1-FLI1, COG6, RAD51B, UBASH3A and SYNGR1) that passed a genome-wide significance threshold (p<5×10(-8)), with evidence for three independent risk alleles at 1q25/TNFSF4. The risk alleles from the seven new loci except for the TNFSF4 locus (monomorphic in Koreans), together with risk alleles from previously established RA risk loci, exhibited a high correlation of effect sizes between ancestries. Further, we refined the number of single nucleotide polymorphisms (SNPs) that represent potentially causal variants through a trans-ethnic comparison of densely genotyped SNPs.
CONCLUSIONS: This study demonstrates the advantage of dense-mapping and trans-ancestral analysis for identification of potentially causal SNPs. In addition, our findings support the importance of T cells in the pathogenesis and the fact of frequent overlap of risk loci among diverse autoimmune diseases. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Ant-CCP; Gene Polymorphism; Rheumatoid Arthritis

Mesh:

Year:  2014        PMID: 24532676      PMCID: PMC4467986          DOI: 10.1136/annrheumdis-2013-204749

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  44 in total

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Journal:  PLoS Genet       Date:  2010-02-12       Impact factor: 5.917

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Journal:  Nat Genet       Date:  2010-02-28       Impact factor: 38.330

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10.  Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.

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Journal:  Diabetes       Date:  2008-10-07       Impact factor: 9.461

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  52 in total

1.  Decreased UBASH3A mRNA Expression Levels in Peripheral Blood Mononuclear Cells from Patients with Systemic Lupus Erythematosus.

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3.  Regulation of the Cell Cycle and Inflammatory Arthritis by the Transcription Cofactor LBH Gene.

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4.  The Role of the Transcription Factor Ets1 in Lupus and Other Autoimmune Diseases.

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Review 5.  Advancing stroke genomic research in the age of Trans-Omics big data science: Emerging priorities and opportunities.

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6.  LBH Gene Transcription Regulation by the Interplay of an Enhancer Risk Allele and DNA Methylation in Rheumatoid Arthritis.

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7.  Molecular-genetic characterization of common, noncoding UBASH3A variants associated with type 1 diabetes.

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Review 8.  Update on the genetic architecture of rheumatoid arthritis.

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9.  OX40 Ligand Contributes to Human Lupus Pathogenesis by Promoting T Follicular Helper Response.

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10.  Association of UBASH3A gene polymorphism and atopic dermatitis in the Chinese Han population.

Authors:  Y Li; H Cheng; F-L Xiao; B Liang; F-S Zhou; P Li; X-D Zheng; L-D Sun; S Yang; X-J Zhang
Journal:  Genes Immun       Date:  2017-07-27       Impact factor: 2.676

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