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Human Molecular Genetics Advance Access published online on June 25, 2008

Human Molecular Genetics, doi:10.1093/hmg/ddn184
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© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

A common STAT4 risk haplotype for Systemic Lupus Erythematosus is over-expressed, correlates with anti-dsDNA production and shows additive effects with two IRF5 risk alleles

Snaevar Sigurdsson1, Gunnel Nordmark2, Sophie Garnier1, Elin Grundberg3, Tony Kwan3, Olof Nilsson4, Maija-Leena Eloranta2, Iva Gunnarsson5, Elisabet Svenungsson5, Gunnar Sturfelt6, Anders A. Bengtsson6, Andreas Jönsen6, Lennart Truedsson7, Solbritt Rantapää-Dahlqvist8, Catharina Eriksson9, Gunnar Alm10, Harald H.H. Göring11, Tomi Pastinen3,12, Ann-Christine Syvänen1,* and Lars Rönnblom2

1 Molecular Medicine, Department of Medical Sciences, Uppsala University, SE-75185 Uppsala, Sweden 2 Section of Rheumatology, Department of Medical Sciences, Uppsala University, SE-75185 Uppsala, Sweden 3 McGill University and Genome Quebec Innovation Centre, Montreal, Quebec, H3A 1A4, Canada 4 Department of Surgical Sciences, Uppsala University SE-7518 Uppsala, Sweden 5 Department of Medicine, Rheumatology Unit, Karolinska Institutet/Karolinska University Hospital, SE-77176 Stockholm, Sweden 6 Department of Rheumatology, Lund University, SE-22100, Lund 7 Institute of Laboratory Medicine Section of MIG, Lund University, SE-22100, Lund, Sweden 8 Department of Rheumatology, University Hospital, SE-901 85 Umeå, Sweden 9 Department of Clinical Immunology, University Hospital, SE-901 85 Umeå, Sweden 10 Department of Biomedical Sciences and Veterinary Public Health, Swedish University of Agricultural Sciences, Uppsala, Sweden 11 Department of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Texas, USA 12 Department of Human Genetics, McGill University, Montreal, Quebec, Canada

* Corresponding author: Ann-Christine Syvänen, Department of Medical Sciences, Uppsala University, Molecular Medicine, Entrance 70, Research Department 2, 3rd floor, Uppsala University Hospital, 75185 Uppsala, Sweden. Phone: +46-18-6112959, Fax +46-18-55 36 01, E-mail: Ann-Christine.Syvanen{at}medsci.uu.se

Received March 16, 2008; Revised June 14, 2008; Accepted June 23, 2008

Systemic Lupus Erythematosus (SLE) is the prototype autoimmune disease where genes regulated by type I interferon (IFN) are over-expressed and contribute to the disease pathogenesis. Because STAT4 plays a key role in the type I IFN receptor signaling, we performed a candidate gene study of a comprehensive set of single nucleotide polymorphism (SNPs) in STAT4 in Swedish patients with SLE. We found that ten out of 53 analyzed SNPs in STAT4 were associated with SLE, with the strongest signal of association (p=7.1 x 10–8) for two perfectly linked SNPs rs10181656 and rs7582694. The risk alleles of these ten SNPs form a common risk haplotype for SLE (p=1.7 x 10–5; OR=1.71). According to conditional logistic regression analysis the SNP rs10181656 or rs7582694 accounts for all of the observed association signal. By quantitative analysis of the allelic expression of STAT4 we found that the risk allele of STAT4 was over-expressed in primary human cells of mesenchymal origin, but not in B-cells, and that the risk allele of STAT4 was over-expressed (p=8.4 x 10–5; OR=1.59) in cells carrying the risk haplotype for SLE compared to cells with a non-risk haplotype. The risk allele of the SNP rs7582694 in STAT4 correlated to production of anti-dsDNA antibodies and displayed a multiplicatively increased, 1.82-fold risk of SLE with two independent risk alleles of the IRF5 gene.


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