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dc.contributor.authorNúñez, Concepción-
dc.contributor.authorOliver, Javier-
dc.contributor.authorMendoza, Juan Luis-
dc.contributor.authorGómez García, María-
dc.contributor.authorTaxonera, Carlos-
dc.contributor.authorGómez Osorio, Luis Miguel-
dc.contributor.authorLópez Nevot, Miguel A-
dc.contributor.authorde la Concha, Emilio G-
dc.contributor.authorUrcelay, Elena-
dc.contributor.authorMartínez, Alfonso-
dc.contributor.authorMartín, Javier-
dc.date.accessioned2022-02-02T21:50:23Z-
dc.date.available2022-02-02T21:50:23Z-
dc.date.issued2007-
dc.identifier.urihttp://hdl.handle.net/10495/25769-
dc.description.abstractABSTRACT: Background The etiology of Ulcerative Colitis (UC) and Crohn's Disease (CD), considered together as Inflammatory Bowel Diseases (IBD), involves environmental and genetic factors. Although some genes are already known, the genetics underlying these diseases is complex and new candidates are continuously emerging. The CD209 gene is located in a region linked previously to IBD and a CD209 functional polymorphism (rs4804803) has been associated to other inflammatory conditions. Our aim was to study the potential involvement of this CD209 variant in IBD susceptibility. Methods We performed a case-control study with 515 CD patients, 497 UC patients and 731 healthy controls, all of them white Spaniards. Samples were typed for the CD209 single nucleotide polymorphism (SNP) rs4804803 by TaqMan technology. Frequency comparisons were performed using χ2 tests. Results No association between CD209 and UC or CD was observed initially. However, stratification of UC patients by HLA-DR3 status, a strong protective allele, showed that carriage of the CD209_G allele could increase susceptibility in the subgroup of HLA-DR3-positive individuals (p = 0.03 OR = 1.77 95% CI 1.04–3.02, vs. controls). Conclusion A functional variant in the CD209 gene, rs4804803, does not seem to be influencing Crohn's disease susceptibility. However, it could be involved in the etiology or pathology of Ulcerative Colitis in HLA-DR3-positive individuals but further studies are necessary.spa
dc.format.extent4spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherBMCspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleCD209 in inflammatory bowel disease: a case-control study in the Spanish populationspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupBiología Celular y Molecular CIB U. de A. U. del Rosariospa
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1471-2350-
oaire.citationtitleBMC Medical Geneticsspa
oaire.citationstartpage1spa
oaire.citationendpage4spa
oaire.citationvolume8spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeLondres, Inglaterraspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsEnfermedades Intestinales-
dc.subject.decsIntestinal Diseases-
dc.description.researchgroupidCOL0000962spa
dc.relation.ispartofjournalabbrevBMC Med. Genet.spa
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