Publication: Genetic polymorphisms located in genes related to immune and inflammatory processes are associated with end-stage renal disease: a preliminary study
| dc.contributor.author | Jimenez-Sousa, Maria Angeles | |
| dc.contributor.author | López, Elisabeth | |
| dc.contributor.author | Fernandez-Rodriguez, Amanda | |
| dc.contributor.author | Tamayo, Eduardo | |
| dc.contributor.author | Fernandez-Navarro, Pablo L | |
| dc.contributor.author | Segura-Roda, Laura | |
| dc.contributor.author | Heredia, María | |
| dc.contributor.author | Gómez-Herreras, José I | |
| dc.contributor.author | Bustamante, Jesús | |
| dc.contributor.author | García-Gómez, Juan Miguel | |
| dc.contributor.author | Bermejo-Martin, Jesús F | |
| dc.contributor.author | Resino, Salvador | |
| dc.contributor.funder | Instituto de Salud Carlos III | |
| dc.contributor.funder | Junta de Castilla y León (España) | |
| dc.date.accessioned | 2019-02-01T14:57:30Z | |
| dc.date.available | 2019-02-01T14:57:30Z | |
| dc.date.issued | 2012-07-20 | |
| 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_ES |
| dc.description.peerreviewed | Sí | es_ES |
| dc.description.sponsorship | This work was supported by grants from Instituto de Salud Carlos III (Ref: PI08/0738 and PI11/00245) to SR and Junta de Castilla y León (Ref: GRS 234/A/08) to ET. MAJS is supported by a grant from Instituto de Salud Carlos III (CM10/00105). | es_ES |
| dc.format.number | 1 | es_ES |
| dc.format.page | 58 | es_ES |
| dc.format.volume | 13 | es_ES |
| dc.identifier.citation | BMC Med Genet. 2012 Jul 20;13:58. | es_ES |
| dc.identifier.doi | 10.1186/1471-2350-13-58 | es_ES |
| dc.identifier.issn | 1471-2350 | es_ES |
| dc.identifier.journal | BMC medical genetics | es_ES |
| dc.identifier.pubmedID | 22817530 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/7065 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | BioMed Central (BMC) | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/PI08/0738 | es_ES |
| dc.relation.projectID | info:eu-repo/grantAgreement/ES/PI11/00245 | es_ES |
| dc.relation.publisherversion | https://doi.org/10.1186/1471-2350-13-58 | es_ES |
| dc.repisalud.centro | ISCIII::Centro Nacional de Microbiología | es_ES |
| dc.repisalud.centro | ISCIII::Centro Nacional de Epidemiología | es_ES |
| dc.repisalud.institucion | ISCIII | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Atribución 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject.mesh | Aged | es_ES |
| dc.subject.mesh | Case-Control Studies | es_ES |
| dc.subject.mesh | Chemokine CCL2 | es_ES |
| dc.subject.mesh | Female | es_ES |
| dc.subject.mesh | Genetic Predisposition to Disease | es_ES |
| dc.subject.mesh | Genotype | es_ES |
| dc.subject.mesh | Humans | es_ES |
| dc.subject.mesh | Immune System | es_ES |
| dc.subject.mesh | Inflammation | es_ES |
| dc.subject.mesh | Kidney Failure, Chronic | es_ES |
| dc.subject.mesh | Male | es_ES |
| dc.subject.mesh | Middle Aged | es_ES |
| dc.subject.mesh | Models, Genetic | es_ES |
| dc.subject.mesh | Nitric Oxide Synthase Type III | es_ES |
| dc.subject.mesh | Receptors, Interleukin-4 | es_ES |
| dc.subject.mesh | Regression Analysis | es_ES |
| dc.subject.mesh | Retrospective Studies | es_ES |
| dc.subject.mesh | STAT4 Transcription Factor | es_ES |
| dc.subject.mesh | Polymorphism, Genetic | es_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_ES |
| dc.type | research article | es_ES |
| dc.type.hasVersion | VoR | es_ES |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 2bf7faec-7f00-44ba-9494-efb396305551 | |
| relation.isAuthorOfPublication | 6a32a4a3-2d81-43c5-8295-48346efbf498 | |
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| relation.isAuthorOfPublication | 89b17350-14e3-4dfd-b797-6ee6ca5363b8 | |
| relation.isAuthorOfPublication.latestForDiscovery | 2bf7faec-7f00-44ba-9494-efb396305551 |
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