Metabolites related to purine catabolism and risk of type 2 diabetes incidence; modifying effects of the TCF7L2-rs7903146 polymorphism.

dc.contributor.authorPapandreou, Christopher
dc.contributor.authorLi, Jun
dc.contributor.authorLiang, Liming
dc.contributor.authorBulló, Mònica
dc.contributor.authorZheng, Yan
dc.contributor.authorRuiz Canela, Miguel
dc.contributor.authorYu, Edward
dc.contributor.authorGuasch-Ferré, Marta
dc.contributor.authorRazquin, Clary
dc.contributor.authorClish, Clary B.
dc.contributor.authorCorella Piquer, Dolores
dc.contributor.authorEstruch Riba, Ramon
dc.contributor.authorRos Rahola, Emilio
dc.contributor.authorFitó Colomer, Montserrat
dc.contributor.authorArós, Fernando
dc.contributor.authorSerra Majem, Lluís
dc.contributor.authorRosique Esteban, Núria
dc.contributor.authorMartínez-González, Miguel Ángel, 1957-
dc.contributor.authorHu, Frank B.
dc.contributor.authorSalas Salvadó, Jordi
dc.date.accessioned2020-05-26T21:31:27Z
dc.date.available2020-05-26T21:31:27Z
dc.date.issued2019-02-27
dc.date.updated2020-05-26T21:31:27Z
dc.description.abstractStudies examining associations between purine metabolites and type 2 diabetes (T2D) are limited. We prospectively examined associations between plasma levels of purine metabolites with T2D risk and the modifying effects of transcription factor-7-like-2 (TCF7L2) rs7903146 polymorphism on these associations. This is a case-cohort design study within the PREDIMED study, with 251 incident T2D cases and a random sample of 694 participants (641 non-cases and 53 overlapping cases) without T2D at baseline (median follow-up: 3.8 years). Metabolites were semi-quantitatively profiled with LC-MS/MS. Cox regression analysis revealed that high plasma allantoin levels, including allantoin-to-uric acid ratio and high xanthine-to-hypoxanthine ratio were inversely and positively associated with T2D risk, respectively, independently of classical risk factors. Elevated plasma xanthine and inosine levels were associated with a higher T2D risk in homozygous carriers of the TCF7L2-rs7903146 T-allele. The potential mechanisms linking the aforementioned purine metabolites and T2D risk must be also further investigated.
dc.format.extent11 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec687759
dc.identifier.issn2045-2322
dc.identifier.pmid30814579
dc.identifier.urihttps://hdl.handle.net/2445/162521
dc.language.isoeng
dc.publisherNature Publishing Group
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/s41598-019-39441-6
dc.relation.ispartofScientific Reports, 2019, vol. 9, p. 2892
dc.relation.urihttps://doi.org/10.1038/s41598-019-39441-6
dc.rightscc-by (c) Papandreou, Christopher et al., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationMetabòlits
dc.subject.classificationDiabetis no-insulinodependent
dc.subject.classificationPolimorfisme (Cristal·lografia)
dc.subject.otherMetabolites
dc.subject.otherNon-insulin-dependent diabetes
dc.subject.otherPolymorphism (Crystallography)
dc.titleMetabolites related to purine catabolism and risk of type 2 diabetes incidence; modifying effects of the TCF7L2-rs7903146 polymorphism.
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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