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dc.contributor.authorJiménez Sousa, María Ángeles
dc.contributor.authorEngel López, Elisabeth
dc.contributor.authorFernández Rodríguez, Amanda
dc.contributor.authorTamayo Gómez, Eduardo 
dc.contributor.authorFernández Navarro, Pablo
dc.contributor.authorSegura Roda, Laura
dc.contributor.authorHeredia Rodríguez, María 
dc.contributor.authorGómez Herreras, José Ignacio 
dc.contributor.authorBustamante, Jesús
dc.contributor.authorGarcía Gómez, Juan Miguel
dc.contributor.authorBermejo Martín, Jesús Francisco
dc.contributor.authorResino, Salvador
dc.date.accessioned2021-03-11T09:42:24Z
dc.date.available2021-03-11T09:42:24Z
dc.date.issued2012
dc.identifier.citationBMC Medical Genetics, 2012, vol. 13. 6 p.es
dc.identifier.issn1471-2350es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/45654
dc.descriptionProducción Científicaes
dc.description.abstractBackground: Chronic kidney disease progression has been linked to pro-inflammatory cytokines and markers of inflammation. These markers are also elevated in end-stage renal disease (ESRD), which constitutes a serious public health problem. Objective: To investigate whether single nucleotide polymorphisms (SNPs) located in genes related to immune and inflammatory processes, could be associated with ESRD development. Design and methods: A retrospective case-control study was carried out on 276 patients with ESRD and 288 control subjects. Forty-eight SNPs were genotyped via SNPlex platform. Logistic regression was used to assess the relationship between each sigle polymorphism and the development of ESRD. Results: Four polymorphisms showed association with ESRD: rs1801275 in the interleukin 4 receptor (IL4R) gene (OR: 0.66 (95%CI = 0.46-0.95); p = 0.025; overdominant model), rs4586 in chemokine (C-C motif) ligand 2 (CCL2) gene (OR: 0.70 (95%CI = 0.54-0.90); p = 0.005; additive model), rs301640 located in an intergenic binding site for signal transducer and activator of transcription 4 (STAT4) (OR: 1.82 (95%CI = 1.17-2.83); p = 0.006; additive model) and rs7830 in the nitric oxide synthase 3 (NOS3) gene (OR: 1.31 (95%CI = 1.01-1.71); p = 0.043; additive model). After adjusting for multiple testing, results lost significance. Conclusion: Our preliminary data suggest that four genetic polymorphisms located in genes related to inflammation and immune processes could help to predict the risk of developing ESRD.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherSpringer Naturees
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/*
dc.subject.classificationGenetic polymorphismes
dc.subject.classificationPolimorfismo genéticoes
dc.subject.classificationRenal disease:es
dc.subject.classificationEnfermedad renales
dc.titleGenetic polymorphisms located in genes related to immune and inflammatory processes are associated with end-stage renal disease: a preliminary studyes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2012 Springer Naturees
dc.identifier.doi10.1186/1471-2350-13-58es
dc.relation.publisherversionhttps://bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2350-13-58es
dc.peerreviewedSIes
dc.description.projectInstituto de Salud Carlos III (grants PI08/0738, PI11/00245 and CM10/00105)es
dc.description.projectJunta de Castilla y León (grant GRS 234/A/08)es
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Unported*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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