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Rheumatology 2003; 42: 304-307
© 2003 British Society for Rheumatology

Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15

S. Steer, S. A. Fisher1, M. Fife, A. Cuthbert1, J. Newton2, P. Wordsworth2, C. M. Lewis1, C. G. Mathew1 and J. S. Lanchbury

Molecular Immunogenetics, Department of Rheumatology, Division of Medicine and
1 Division of Medical and Molecular Genetics, Guy's, King's and St Thomas' School of Medicine, Guy's Hospital Campus, King's College, London and
2 Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK

Introduction. It has been proposed that genetic susceptibility loci for rheumatoid arthritis (RA) may be shared with other autoimmune/inflammatory diseases. Recently, common variation in the CARD15 (NOD2) gene on chromosome 16q12 has been associated with Crohn's disease (CD) in several independent populations. CARD15 is an excellent functional and positional candidate gene for RA.

Methods. Genomic DNA was obtained from 392 RA cases and 471 ethnically matched healthy controls. All samples were genotyped for two polymorphisms in CARD15, 1007fs and R702W, using 5' nuclease reporter assays. Allele frequencies were compared between cases and controls using the {chi}2 test. Estimated haplotype frequencies across the two mutations were determined using the EH program.

Results. The allele frequency of the 1007fs variant in RA cases was 1.8% compared with 1.6% in normal controls (not significant). The frequency of the R702W variant was 4.0% in both cases and controls. Haplotypes carrying either of the two mutations accounted for 5.6% of possible haplotypes. A haplotype carrying both mutations was rare, with estimated frequency <0.01%. This study provided high power to detect an association of similar magnitude to that in Crohn's disease. These data therefore exclude the possibility that the contribution of these mutations to RA is comparable to that seen in CD.

Conclusion. Within defined statistical parameters, we excluded a role for the CARD15 1007fs and R702W variants in RA susceptibility. These data do not preclude a role for other polymorphisms in the CARD15 gene in RA susceptibility. Results from other autoimmune and inflammatory diseases will reveal whether the CARD15 gene is in fact a common autoimmune susceptibility locus.

Correspondence to: J. S. Lanchbury, Department of Rheumatology, 5th Floor, Thomas Guy House, Guy's, King's and St Thomas' School of Medicine, King's College, Guy's Hospital, London SE1 9RT, UK. E-mail: jerry.lanchbury{at}kcl.ac.uk


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