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No association of primary Sjogren's syndrome with Fc gamma receptor gene variants
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2013 (English)In: Genes and Immunity, ISSN 1466-4879, E-ISSN 1476-5470, Vol. 14, no 4, 234-237 p.Article in journal (Refereed) Published
Abstract [en]

The genetic background of primary Sjögren's syndrome (pSS) is partly shared with systemic lupus erythematosus (SLE). Immunoglobulin G Fc receptors are important for clearance of immune complexes. Fcγ receptor variants and gene deletion have been found to confer SLE risk. In this study, four Fcγ receptor single-nucleotide polymorphisms (SNPs) and one copy number variation (CNV) were studied. Swedish and Norwegian pSS patients (N=527) and controls (N=528) were genotyped for the Fcγ receptor gene variant FCGR2A H131R (rs1801274) by the Illumina GoldenGate assay. FCGR3A F158V (rs396991) was analysed in 488 patients and 485 controls, FCGR3B rs447536 was analysed in 471 patients and 467 controls, and FCGR3B rs448740 was analysed in 478 cases and 455 controls, using TaqMan SNP genotyping assays. FCGR3B CNV was analysed in 124 patients and 139 controls using a TaqMan copy number assay. None of the SNPs showed any association with pSS. Also, no FCGR3B CNV association was detected. The lack of association of pSS with Fcγ receptor gene variants indicates that defective immune complex clearance may not be as important in pSS pathogenesis as in SLE, and may point to important differences between SLE and pSS.

Place, publisher, year, edition, pages
2013. Vol. 14, no 4, 234-237 p.
Keyword [en]
Sjögrens syndrome
National Category
Rheumatology and Autoimmunity
Identifiers
URN: urn:nbn:se:uu:diva-201485DOI: 10.1038/gene.2013.12ISI: 000320029300005PubMedID: 23552400OAI: oai:DiVA.org:uu-201485DiVA: diva2:627563
Available from: 2013-06-12 Created: 2013-06-12 Last updated: 2017-12-06Bibliographically approved

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Rönnblom, LarsNordmark, Gunnel
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