Novel Association in Chromosome 4q27 Region with Rheumatoid Arthritis and Confirmation of Type 1 Diabetes Point to a General Risk Locus for Autoimmune Diseases

Recently, association of celiac disease with common single-nucleotide polymorphism (SNP) variants in an extensive linkage-disequilibrium block of 480 kb containing the KIAA1109, Tenr, IL2, and IL21 genes has been demonstrated in three independent populations ( rs6822844 P combined=1.3×10 −14). The K...

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Veröffentlicht in:American journal of human genetics 2007-12, Vol.81 (6), p.1284-1288
Hauptverfasser: Zhernakova, Alexandra, Alizadeh, Behrooz Z., Bevova, Marianna, van Leeuwen, Miek A., Coenen, Marieke J.H., Franke, Barbara, Franke, Lude, Posthumus, Marcel D., van Heel, David A., van der Steege, Gerrit, Radstake, Timothy R.D.J., Barrera, Pilar, Roep, Bart O., Koeleman, Bobby P.C., Wijmenga, Cisca
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Sprache:eng
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Zusammenfassung:Recently, association of celiac disease with common single-nucleotide polymorphism (SNP) variants in an extensive linkage-disequilibrium block of 480 kb containing the KIAA1109, Tenr, IL2, and IL21 genes has been demonstrated in three independent populations ( rs6822844 P combined=1.3×10 −14). The KIAA1109/Tenr/IL2/IL21 block corresponds to the Idd3 locus in the nonobese diabetic mouse model of type 1 diabetes (T1D). This block was recently found to be associated with T1D in a genomewide association study, although this finding lacks unequivocal confirmation. We therefore aimed to investigate whether the KIAA1109/Tenr/IL2/IL21 region is involved in susceptibility to multiple autoimmune diseases. We tested SNP rs6822844 for association with disease in 350 T1D-affected and 1,047 rheumatoid arthritis (RA)–affected Dutch patients and in 929 controls. We replicated the association with T1D ( P=.0006; OR 0.64 [95% CI 0.50–0.83]), and revealed a similar novel association with RA ( P=.0002; OR 0.72 [95% CI 0.61–0.86]). Our results replicate and extend the association found in the KIAA1109/Tenr/IL2/IL21 gene region with autoimmune diseases, implying that this locus is a general risk factor for multiple autoimmune diseases.
ISSN:0002-9297
1537-6605
DOI:10.1086/522037