Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/104289
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dc.contributor.authorAbulí, Anna-
dc.contributor.authorCastells Garangou, Antoni-
dc.contributor.authorBujanda, Luis-
dc.contributor.authorLozano Salvatella, Juan José-
dc.contributor.authorBessa i Caserras, Xavier-
dc.contributor.authorHernández-Munain, Cristina-
dc.contributor.authorÁlvarez Urturi, Cristina-
dc.contributor.authorPellisé Urquiza, Maria-
dc.contributor.authorEsteban-Jurado, Clara-
dc.contributor.authorHijona, Elizabeth-
dc.contributor.authorBurón, Andrea-
dc.contributor.authorMacià, Francesc-
dc.contributor.authorGrau Cano, J. (Jaume)-
dc.contributor.authorGuayta, Rafael (Guayta Escolies)-
dc.contributor.authorCastellví Bel, Sergi-
dc.contributor.authorAndreu, Montserrat-
dc.contributor.authorTrilla García, Antoni-
dc.contributor.authorPROCOLON Research Group-
dc.date.accessioned2016-11-30T09:34:27Z-
dc.date.available2016-11-30T09:34:27Z-
dc.date.issued2016-04-14-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/2445/104289-
dc.description.abstractBackground Common low-penetrance genetic variants have been consistently associated with colorec- tal cancer risk. Aim To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with increased risk for advanced adenomas and/or multi- plicity ( 3 adenomas). Methods We selected 1,326 patients with increased risk for advanced adenomas and/or multiplicity and 1,252 controls with normal colonoscopy from population-based colorectal cancer screening programs. We conducted a case-control association study analyzing 30 colorec- tal cancer susceptibility variants in order to investigate the contribution of these variants to the development of subsequent advanced neoplasia and/or multiplicity. Results We found that 14 of the analyzed genetic variants showed a statistically significant associa- tion with advanced adenomas and/or multiplicity: the probability of developing these lesions increased with the number of risk alleles reaching a 2.3-fold risk increment in individuals with 17 risk alleles. Conclusions Nearly half of the genetic variants associated with colorectal cancer risk are also related to advanced adenoma and/or multiplicity predisposition. Assessing the number of risk alleles in individuals within colorectal cancer screening programs may help to identify better a sub- group with increased risk for advanced neoplasia and/or multiplicity in the general population.-
dc.format.extent12 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherPublic Library of Science (PLoS)-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1371/journal.pone.0153084-
dc.relation.ispartofPLoS One, 2016, vol. 11, num. 4, p. e0153084-
dc.relation.urihttps://doi.org/10.1371/journal.pone.0153084-
dc.rightscc-by (c) Abulí, Anna et al., 2016-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.sourceArticles publicats en revistes (Medicina)-
dc.subject.classificationCàncer colorectal-
dc.subject.classificationGenètica humana-
dc.subject.classificationEstudi de casos-
dc.subject.classificationMutació (Biologia)-
dc.subject.classificationColonoscòpia-
dc.subject.otherColorectal cancer-
dc.subject.otherHuman genetics-
dc.subject.otherCase studies-
dc.subject.otherMutation (Biology)-
dc.subject.otherColonoscopy-
dc.titleGenetic Variants Associated with Colorectal Adenoma Susceptibility-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec664539-
dc.date.updated2016-11-30T09:34:32Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid27078840-
Appears in Collections:Articles publicats en revistes (Medicina)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

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