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Am J Hum Genet DOI:10.1086/498651

Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4.

Publication TypeJournal Article
Year of Publication2005
AuthorsPlenge, RM, Padyukov, L, Remmers, EF, Purcell, S, Lee, AT, Karlson, EW, Wolfe, F, Kastner, DL, Alfredsson, L, Altshuler, D, Gregersen, PK, Klareskog, L, Rioux, JD
JournalAm J Hum Genet
Volume77
Issue6
Pages1044-60
Date Published2005 Dec
ISSN0002-9297
KeywordsAdult, Age of Onset, Alleles, Antigens, CD, Antigens, Differentiation, Arthritis, Rheumatoid, Case-Control Studies, Cohort Studies, CTLA-4 Antigen, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Genetic Variation, Humans, Hydrolases, Male, Middle Aged, North America, Odds Ratio, Protein Tyrosine Phosphatase, Non-Receptor Type 22, Protein Tyrosine Phosphatases, Retrospective Studies, Review Literature as Topic, Sex Factors, Sweden
Abstract

Candidate-gene association studies in rheumatoid arthritis (RA) have lead to encouraging yet apparently inconsistent results. One explanation for the inconsistency is insufficient power to detect modest effects in the context of a low prior probability of a true effect. To overcome this limitation, we selected alleles with an increased probability of a disease association, on the basis of a review of the literature on RA and other autoimmune diseases, and tested them for association with RA susceptibility in a sample collection powered to detect modest genetic effects. We tested 17 alleles from 14 genes in 2,370 RA cases and 1,757 controls from the North American Rheumatoid Arthritis Consortium (NARAC) and the Swedish Epidemiological Investigation of Rheumatoid Arthritis (EIRA) collections. We found strong evidence of an association of PTPN22 with the development of anti-citrulline antibody-positive RA (odds ratio [OR] 1.49; P=.00002), using previously untested EIRA samples. We provide support for an association of CTLA4 (CT60 allele, OR 1.23; P=.001) and PADI4 (PADI4_94, OR 1.24; P=.001) with the development of RA, but only in the NARAC cohort. The CTLA4 association is stronger in patients with RA from both cohorts who are seropositive for anti-citrulline antibodies (P=.0006). Exploration of our data set with clinically relevant subsets of RA reveals that PTPN22 is associated with an earlier age at disease onset (P=.004) and that PTPN22 has a stronger effect in males than in females (P=.03). A meta-analysis failed to demonstrate an association of the remaining alleles with RA susceptibility, suggesting that the previously published associations may represent false-positive results. Given the strong statistical power to replicate a true-positive association in this study, our results provide support for PTPN22, CTLA4, and PADI4 as RA susceptibility genes and demonstrate novel associations with clinically relevant subsets of RA.

URLhttp://linkinghub.elsevier.com/retrieve/pii/S0002-9297(07)63388-6
DOI10.1086/498651
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/16380915?dopt=Abstract

Alternate JournalAm. J. Hum. Genet.
PubMed ID16380915
PubMed Central IDPMC1285162
Grant ListP60 AR47782-05 / AR / NIAMS NIH HHS / United States
K24 AR0524-01 / AR / NIAMS NIH HHS / United States
K08 AI 55314 / AI / NIAID NIH HHS / United States
P60 AR047782 / AR / NIAMS NIH HHS / United States
/ / Intramural NIH HHS / United States
R01 AR49880-01 / AR / NIAMS NIH HHS / United States
R01 AR049880 / AR / NIAMS NIH HHS / United States
R01-AR44222 / AR / NIAMS NIH HHS / United States
N01-AR-2-2263 / AR / NIAMS NIH HHS / United States
K08 AI055314 / AI / NIAID NIH HHS / United States