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dc.contributor.author | Jiménez Sousa, María Ángeles | |
dc.contributor.author | Engel López, Elisabeth | |
dc.contributor.author | Fernández Rodríguez, Amanda | |
dc.contributor.author | Tamayo Gómez, Eduardo | |
dc.contributor.author | Fernández Navarro, Pablo | |
dc.contributor.author | Segura Roda, Laura | |
dc.contributor.author | Heredia Rodríguez, María | |
dc.contributor.author | Gómez Herreras, José Ignacio | |
dc.contributor.author | Bustamante, Jesús | |
dc.contributor.author | García Gómez, Juan Miguel | |
dc.contributor.author | Bermejo Martín, Jesús Francisco | |
dc.contributor.author | Resino, Salvador | |
dc.date.accessioned | 2021-03-11T09:42:24Z | |
dc.date.available | 2021-03-11T09:42:24Z | |
dc.date.issued | 2012 | |
dc.identifier.citation | BMC Medical Genetics, 2012, vol. 13. 6 p. | es |
dc.identifier.issn | 1471-2350 | es |
dc.identifier.uri | http://uvadoc.uva.es/handle/10324/45654 | |
dc.description | Producción Científica | es |
dc.description.abstract | Background: 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.mimetype | application/pdf | es |
dc.language.iso | eng | es |
dc.publisher | Springer Nature | es |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/ | * |
dc.subject.classification | Genetic polymorphism | es |
dc.subject.classification | Polimorfismo genético | es |
dc.subject.classification | Renal disease: | es |
dc.subject.classification | Enfermedad renal | es |
dc.title | Genetic polymorphisms located in genes related to immune and inflammatory processes are associated with end-stage renal disease: a preliminary study | es |
dc.type | info:eu-repo/semantics/article | es |
dc.rights.holder | © 2012 Springer Nature | es |
dc.identifier.doi | 10.1186/1471-2350-13-58 | es |
dc.relation.publisherversion | https://bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2350-13-58 | es |
dc.peerreviewed | SI | es |
dc.description.project | Instituto de Salud Carlos III (grants PI08/0738, PI11/00245 and CM10/00105) | es |
dc.description.project | Junta de Castilla y León (grant GRS 234/A/08) | es |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Unported | * |
dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es |
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