Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/190284
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dc.contributor.authorBatista Liz, Joao Carlos-
dc.contributor.authorGenre, Fernanda-
dc.contributor.authorPulito Cueto, Verónica-
dc.contributor.authorRemuzgo Martínez, Sara-
dc.contributor.authorPrieto Peña, Diana-
dc.contributor.authorMárquez, Ana-
dc.contributor.authorOrtego Centeno, Norberto-
dc.contributor.authorLeonardo, María Teresa-
dc.contributor.authorPeñalba, Ana-
dc.contributor.authorNarváez, Javier-
dc.contributor.authorMartín Penagos, Luis-
dc.contributor.authorBelmar Vega, Lara-
dc.contributor.authorGómez Fernández, Cristina-
dc.contributor.authorMiranda Filloy, José A.-
dc.contributor.authorCaminal Montero, Luis-
dc.contributor.authorCollado, Paz-
dc.contributor.authorDe Árgila, Diego-
dc.contributor.authorQuiroga Colina, Patricia-
dc.contributor.authorVicente Rabaneda, Esther F.-
dc.contributor.authorTriguero Martínez, Ana-
dc.contributor.authorRubio, Esteban-
dc.contributor.authorLeón Luque, Manuel-
dc.contributor.authorBlanco Madrigal, Juan María-
dc.contributor.authorGalíndez Agirregoikoa, Eva-
dc.contributor.authorMartín, Javier-
dc.contributor.authorGualillo, Oreste-
dc.contributor.authorBlanco, Ricardo-
dc.contributor.authorCastañeda, Santos-
dc.contributor.authorGonzález Gay, Miguel A.-
dc.contributor.authorLópez Mejías, Raquel-
dc.date.accessioned2022-10-27T20:38:58Z-
dc.date.available2022-10-27T20:38:58Z-
dc.date.issued2022-09-22-
dc.identifier.issn2077-0383-
dc.identifier.urihttp://hdl.handle.net/2445/190284-
dc.description.abstractCD40, BLK and BANK1 genes involved in the development and signaling of B-cells are identified as susceptibility loci for numerous inflammatory diseases. Accordingly, we assessed the potential influence of CD40, BLK and BANK1 on the pathogenesis of immunoglobulin-A vasculitis (IgAV), predominantly a B-lymphocyte inflammatory condition. Three genetic variants within CD40 (rs1883832, rs1535045, rs4813003) and BLK (rs2254546, rs2736340, rs2618476) as well as two BANK1 polymorphisms (rs10516487, rs3733197), previously associated with inflammatory diseases, were genotyped in 382 Caucasian patients with IgAV and 955 sex- and ethnically matched healthy controls. No statistically significant differences were observed in the genotype and allele frequencies of CD40, BLK and BANK1 when IgAV patients and healthy controls were compared. Similar results were found when CD40, BLK and BANK1 genotypes or alleles frequencies were compared between patients with IgAV stratified according to the age at disease onset or to the presence/absence of gastrointestinal or renal manifestations. Moreover, no CD40, BLK and BANK1 haplotype differences were disclosed between patients with IgAV and healthy controls and between patients with IgAV stratified according to the clinical characteristics mentioned above. Our findings indicate that CD40, BLK and BANK1 do not contribute to the genetic background of IgAV.-
dc.format.extent11 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherMDPI AG-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/jcm11195577-
dc.relation.ispartofJournal of Clinical Medicine, 2022, vol. 11, issue. 19, p. 5577-
dc.relation.urihttps://doi.org/10.3390/jcm11195577-
dc.rightscc by (c) Batista Liz, Joao Carlos et al., 2022-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.subject.classificationPolimorfisme genètic-
dc.subject.classificationVasculitis-
dc.subject.otherGenetic polymorphisms-
dc.subject.otherVasculitis-
dc.titleIgA Vasculitis: Influence of CD40, BLK and BANK1 Gene Polymorphisms-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.date.updated2022-10-27T10:49:48Z-
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/734899/EU//Olive-Net-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid36233442-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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