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dc.contributor.authorMc Manus, Rossen
dc.contributor.authorKane, Daviden
dc.date.accessioned2020-03-03T15:54:43Z
dc.date.available2020-03-03T15:54:43Z
dc.date.issued2012en
dc.date.submitted2012en
dc.identifier.citationBowes J, Ho P, Flynn E, Marzo-Ortega H, UKRAG Consortium, Coates L, McManus R, Ryan A, Kane D, Korendowych E, McHugh N, FitzGerald O, Packham J, Morgan AW, Bruce IN, Barton A, Comprehensive assessment of rheumatoid arthritis susceptibility loci in a large psoriatic arthritis cohort, Annals of Rheumatic Diseases, 71, 8, 2012, 1350-1354en
dc.identifier.otherYen
dc.identifier.urihttps://ard.bmj.com/content/71/8/1350
dc.identifier.urihttp://hdl.handle.net/2262/91681
dc.descriptionACCEPTEDen
dc.description.abstractObjective: A number of rheumatoid arthritis (RA) susceptibility genes have been identified in recent years. Given the overlap in phenotypic expression of synovial joint inflammation between RA and psoriatic arthritis (PsA), the authors explored whether RA susceptibility genes are also associated with PsA. Methods: 56 single nucleotide polymorphisms (SNPs) mapping to 41 genes previously reported as RA susceptibility loci were selected for investigation. PsA was defined as an inflammatory arthritis associated with psoriasis and subjects were recruited from the UK and Ireland. Genotyping was performed using the Sequenom MassArray platform and frequencies compared with data derived from large UK control collections. Results: Significant evidence for association with susceptibility to PsA was found to a SNP mapping to the REL (rs13017599, p trend =5.2?10 4 ) gene, while nominal evidence for association (p trend <0.05) was found to seven other loci including PLCL2 (rs4535211, p=1.7?10 ?3 ); STAT4 (rs10181656, p=3.0?10 ?3 ) and the AFF3 , CD28 , CCL21 , IL2 and KIF5A loci. Interestingly, three SNPs demonstrated opposite effects to those reported for RA. Conclusions: The REL gene, a key modulator of the NF ? B pathway, is associated with PsA but the allele conferring risk to RA is protective in PsA suggesting that there are fundamental differences in the aetiological mechanisms underlying these two types of inflammatory arthritisen
dc.description.sponsorshipThe authors acknowledge the support of the NIHR Manchester Biomedical Research Centre and NIHR Leeds Musculoskeletal Biomedical Research Unit. John Bowes, Ian Bruce and Anne Barton are funded by Arthritis Research UK (arc grant; 17552). Edward Flynn is supported by the European Community?s Sixth Framework Programme AutoCure funding. This study makes use of data generated by the Wellcome Trust Case-Control Consortium. A full list of the investigators who contributed to the generation of the data is available from www. wtccc.org.uk. Funding for the project was provided by the Wellcome Trust under award 076113 and 085475.en
dc.format.extent1350-1354en
dc.language.isoenen
dc.relation.ispartofseriesAnnals of Rheumatic Diseasesen
dc.relation.ispartofseries71en
dc.relation.ispartofseries8en
dc.rightsYen
dc.subjectRheumatoid arthritis (RA)en
dc.subjectSingle nucleotide polymorphismsen
dc.subjectPsoriatic arthritisen
dc.subject.lcshrheumatoid arthritis (RA)en
dc.titleComprehensive assessment of rheumatoid arthritis susceptibility loci in a large psoriatic arthritis cohorten
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/rmcmanusen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/kanedjen
dc.identifier.rssinternalid77042en
dc.identifier.doihttp://dx.doi.org/10.1136/annrheumdis-2011-20080en
dc.subject.TCDThemeGenes & Societyen
dc.subject.TCDThemeImmunology, Inflammation & Infectionen


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