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Variants within STAT genes reveal association with anticitrullinated protein antibody-negative rheumatoid arthritis in 2 European populations

Seddighzadeh, M; González Martínez-Pedrayo, Antonio; Ding, B; Ferreiro Iglesias, Aida; Gómez-Reino Carnota, Juan Jesús; Klareskog, L; Alfredsson, L; Dunussi-Joannopoulos, K; Clark, J D; Padyukov, L
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URI: http://hdl.handle.net/20.500.11940/4961
PMID: 22753649
DOI: 10.3899/jrheum.111284
ISSN: 0315-162X
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J Rheumatol . 2012 Aug;39(8):1509-16. (248.5Kb)
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Fecha de publicación
2012
Título de revista
JOURNAL OF RHEUMATOLOGY
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Artigo
Resumen
Objective. STAT3 and 4 are, among other factors, critical for the interleukin 12 (IL-12)-mediated Th1 response, for transfer of IL-23 signals, and for survival and expansion of Th17 cells. We investigated the association of STAT3 and STAT4 polymorphisms with serologically distinct subgroups of rheumatoid arthritis (RA). Methods. A total of 41 single-nucleotide polymorphisms (SNP) within STAT3 and STAT1-STAT4 loci were investigated in a Swedish cohort of 2043 RA cases and 1115 controls. Nine of the associated SNP were tested in a Spanish cohort of 1223 RA cases and 1090 controls. Results. Fourteen SNP in the STAT3 and STAT1-STAT4 loci were associated with anticitrullinated protein antibody (ACPA)-negative RA in the Swedish cohort. Three of the SNP in STAT4 and 2 SNP in STAT3 remained associated with ACPA-negative RA after considering the Spanish results. In addition, rs7574865 and rs10181656, in STAT4, were associated with ACPA-positive RA in the Swedish study. One of these SNP, rs7574865, showed a similar pattern of the association in serologically distinct subgroups of RA in a metaanalysis of all 7 published studies. Conclusion. Our findings suggest that variants in STAT genes may contribute differentially to susceptibility to RA in seropositive and in seronegative patients.

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