Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk

Soumya Raychaudhuri, Brian P. Thomson, Elaine F. Remmers, Stephen Eyre, Anne Hinks, Candace Guiducci, Joseph J. Catanese, Gang Xie, Eli A. Stahl, Robert Chen, Lars Alfredsson, Christopher I. Amos, Kristin G. Ardlie, Anne Barton, John Bowes, Noel P. Burtt, Monica Chang, Jonathan Coblyn, Karen H. Costenbader, Lindsey A. CriswellJ. Bart A Crusius, Jing Cui, Phillip L. De Jager, Bo Ding, Paul Emery, Edward Flynn, Pille Harrison, Lynne J. Hocking, Tom W J Huizinga, Daniel L. Kastner, Xiayi Ke, Fina A S Kurreeman, Annette T. Lee, Xiangdong Liu, Yonghong Li, Paul Martin, Ann W. Morgan, Leonid Padyukov, David M. Reid, Mark Seielstad, Michael F. Seldin, Nancy A. Shadick, Sophia Steer, Paul P. Tak, Wendy Thomson, Annette H M Van Der Helm-Van Mil, Irene E. Van Der Horst-Bruinsma, Michael E. Weinblatt, Anthony G. Wilson, Gert Jan Wolbink, Paul Wordsworth, David Altshuler, Elizabeth W. Karlson, Rene E M Toes, Niek De Vries, Ann B. Begovich, Katherine A. Siminovitch, Jane Worthington, Lars Klareskog, Peter K. Gregersen, Mark J. Daly, Robert M. Plenge

    Research output: Contribution to journalArticlepeer-review

    Abstract

    To discover new rheumatoid arthritis (RA) risk loci, we systematically examined 370 SNPs from 179 independent loci with P 0.001 in a published meta-analysis of RA genome-wide association studies (GWAS) of 3,393 cases and 12,462 controls. We used Gene Relationships Across Implicated Loci (GRAIL), a computational method that applies statistical text mining to PubMed abstracts, to score these 179 loci for functional relationships to genes in 16 established RA disease loci. We identified 22 loci with a significant degree of functional connectivity. We genotyped 22 representative SNPs in an independent set of 7,957 cases and 11,958 matched controls. Three were convincingly validated: CD2-CD58 (rs11586238, P = 1 × 10 6 replication, P = 1 × 10 9 overall), CD28 (rs1980422, P = 5 × 10 6 replication, P = 1 × 10 9 overall) and PRDM1 (rs548234, P = 1 × 10 5 replication, P = 2 × 10 8 overall). An additional four were replicated (P 0.0023): TAGAP (rs394581, P = 0.0002 replication, P = 4 × 10 7 overall), PTPRC (rs10919563, P = 0.0003 replication, P = 7 × 10 7 overall), TRAF6-RAG1 (rs540386, P = 0.0008 replication, P = 4 × 10 6 overall) and FCGR2A (rs12746613, P = 0.0022 replication, P = 2 × 10 5 overall). Many of these loci are also associated to other immunologic diseases. © 2009 Nature America, Inc. All rights reserved.
    Original languageEnglish
    Pages (from-to)1313-1318
    Number of pages5
    JournalNature Genetics
    Volume41
    Issue number12
    DOIs
    Publication statusPublished - Dec 2009

    Fingerprint

    Dive into the research topics of 'Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk'. Together they form a unique fingerprint.

    Cite this