articleNew England Journal of MedicineSep 5, 2007BRONZE OA

TRAF1–C5 as a Risk Locus for Rheumatoid Arthritis — A Genomewide Study

Broad Institute · Massachusetts Institute of Technology

PubMed
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Abstract

Background

Rheumatoid arthritis has a complex mode of inheritance. Although HLA-DRB1 and PTPN22 are well-established susceptibility loci, other genes that confer a modest level of risk have been identified recently. We carried out a genomewide association analysis to identify additional genetic loci associated with an increased risk of rheumatoid arthritis.

Methods

We genotyped 317,503 single-nucleotide polymorphisms (SNPs) in a combined case-control study of 1522 case subjects with rheumatoid arthritis and 1850 matched control subjects. The patients were seropositive for autoantibodies against cyclic citrullinated peptide (CCP). We obtained samples from two data sets, the North American Rheumatoid Arthritis Consortium (NARAC) and the Swedish Epidemiological Investigation of Rheumatoid Arthritis (EIRA). Results from NARAC and EIRA for 297,086 SNPs that passed quality-control filters were combined with the use of Cochran-Mantel-Haenszel stratified analysis. SNPs showing a significant association with disease (P

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830
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Authors

29

Topics & keywords

Keywords
  • PTPN22
  • Single-nucleotide polymorphism
  • Rheumatoid arthritis
  • Medicine
  • Linkage disequilibrium
  • Odds ratio
  • Arthritis
  • SNP
UN Sustainable Development Goals
  • Good health and well-being
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