Literature DB >> 19092840

Replication of the TNFSF4 (OX40L) promoter region association with systemic lupus erythematosus.

Javier Martin1, Marta E Alarcón-Riquelme2,3, Angélica M Delgado-Vega2, Anna-Karin Abelson2, Elena Sánchez1, Torsten Witte4, Sandra D'Alfonso5, Mauro Galeazzi6, Juan Jiménez-Alonso7, Bernardo A Pons-Estel8.   

Abstract

The tumor necrosis factor ligand superfamily member 4 gene (TNFSF4) encodes the OX40 ligand (OX40L), a costimulatory molecule involved in T-cell activation. A recent study demonstrated the association of TNFSF4 haplotypes located in the upstream region with risk for or protection from systemic lupus erythematosus (SLE). To replicate this association, five single nucleotide polymorphisms (SNPs) tagging the previously associated haplotypes and passing the proper quality-control filters were tested in 1312 cases and 1801 controls from Germany, Italy, Spain and Argentina. The association of TNFSF4 with SLE was replicated in all the sets except Spain. There was a unique risk haplotype tagged by the minor alleles of the SNPs rs1234317 (pooled odds ratio (OR)=1.39, P=0.0009) and rs12039904 (pooled OR=1.38, P=0.0012). We did not observe association to a single protective marker (rs844644) or haplotype as the first study reported; instead, we observed different protective haplotypes, all carrying the major alleles of both SNPs rs1234317 and rs12039904. Association analysis conditioning on the haplotypic background confirmed that these two SNPs explain the entire haplotype effect. This first replication study confirms the association of genetic variation in the upstream region of TNFSF4 with susceptibility to SLE.

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Year:  2008        PMID: 19092840      PMCID: PMC3867640          DOI: 10.1038/gene.2008.95

Source DB:  PubMed          Journal:  Genes Immun        ISSN: 1466-4879            Impact factor:   2.676


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