Influence of the IL17A locus in giant cell arteritis susceptibility

dc.contributor.authorMárquez, A.
dc.contributor.authorHernández Rodríguez, J.
dc.contributor.authorCid, M.C.
dc.contributor.authorSolans, R.
dc.contributor.authorCastañeda, S.
dc.contributor.authorFernández Contreras, María Encarnación
dc.contributor.authorRamentol, M.
dc.contributor.authorMorado, I.C.
dc.contributor.authorNarváez, J.
dc.contributor.authorGómez Vaquero, C.
dc.contributor.authorMartínez Taboada, V.M.
dc.contributor.authorOrtego Centeno, N.
dc.contributor.authorSopeña, B.
dc.contributor.authorMonfort, J.
dc.contributor.authorGarcía Villanueva, M.J.
dc.contributor.authorCaminal Montero, L.
dc.contributor.authorDe Miguel, E.
dc.contributor.authorBlanco, R.
dc.contributor.authorPalm, O.
dc.contributor.authorMolberg, O.
dc.contributor.authorLatus, J.
dc.contributor.authorBraun, N.
dc.contributor.authorMoosig, F.
dc.contributor.authorWitte, T.
dc.contributor.authorBeretta, L.
dc.contributor.authorSantaniello, A.
dc.contributor.authorPazzola, G.
dc.contributor.authorBoiardi, L.
dc.contributor.authorSalvarani, C.
dc.contributor.authorGonzález Gay, M.A
dc.contributor.authorMartín, J.
dc.date.accessioned2025-01-09T14:49:47Z
dc.date.available2025-01-09T14:49:47Z
dc.date.created2014
dc.date.issued2014
dc.description.abstractObjective: Different lines of evidence have highlighted the role of IL-17A in the inflammatory process occurring in giant cell arteritis (GCA). The aim of the present study was to assess whether the IL17A locus in fluences GCA susceptibility and its clinical subphenotypes. Methods: We carried out a large meta-analysis including a total of 1266 biopsy-proven GCA patients and 3779 healthy controls from four European populations (Spain, Italy, Germany and Norway). Five IL17A polymorphisms (rs4711998, rs8193036, rs3819024, rs2275913 and rs7747909) were selected by tagging and genotyped using TaqMan assays. Allelic combination and dependency tests were also performed. Results: In the pooled analysis, two of the five analysed polymorphisms showed evidence of association with GCA (rs2275913: PMH=1.85E-03, OR=1.17 (1.06-1.29); rs7747909: PMH=8.49E -03, OR=1.15 (1.04-1.27)). A clear trend of association was also found for the rs4711998 variant (PMH=0.059, OR=1.11 (1.00-1.23)). An independent effect of rs2275913 and rs4711998 was evident by conditional regression analysis. In addition, the haplotype harbouring the risk alleles better explained the observed association than the polymorphisms independently (likelihood p value <10-05). Conclusions: Polymorphisms within the IL17A locus show a novel association with GCA. This finding supports the relevant role of the Th17 cells in this vasculitis pathophysiology.es_ES
dc.formatapplication/pdfes_ES
dc.identifier.locationN/Aes_ES
dc.identifier.urihttps://hdl.handle.net/20.500.12080/45055
dc.languageenges_ES
dc.relation.ispartofAnnals of the Rheumatic Diseaseses_ES
dc.rightsCC-BYes_ES
dc.rights.accessrightsinfo:eu-repo/semantics/restrictedAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.eses_ES
dc.titleInfluence of the IL17A locus in giant cell arteritis susceptibilityes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES

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