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dc.contributor.authorAnguita-Ruiz, A.
dc.contributor.authorGonzalez-Gil, E. M.
dc.contributor.authorRuperez, A. I.
dc.contributor.authorLlorente-Cantarero, F. J.
dc.contributor.authorPastor-Villaescusa, B.
dc.contributor.authorAlcala-Fdez, J.
dc.contributor.authorMoreno, L. A.
dc.contributor.authorGil, A.
dc.contributor.authorGil-Campos, M.
dc.contributor.authorBueno, G.
dc.contributor.authorLeis Trabazo, María Rosaura 
dc.contributor.authorAguilera, C. M.
dc.date.accessioned2022-04-29T10:25:28Z
dc.date.available2022-04-29T10:25:28Z
dc.date.issued2020
dc.identifier.issn2077-0383
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/32498346es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16589
dc.description.abstractPolygenetic risk scores (pGRSs) consisting of adult body mass index (BMI) genetic variants have been widely associated with obesity in children populations. The implication of such obesity pGRSs in the development of cardio-metabolic alterations during childhood as well as their utility for the clinical prediction of pubertal obesity outcomes has been barely investigated otherwise. In the present study, we evaluated the utility of an adult BMI predisposing pGRS for the prediction and pharmacological management of obesity in Spanish children, further investigating its implication in the appearance of cardio-metabolic alterations. For that purpose, we counted on genetics data from three well-characterized children populations (composed of 574, 96 and 124 individuals), following both cross-sectional and longitudinal designs, expanding childhood and puberty. As a result, we demonstrated that the pGRS is strongly associated with childhood BMI Z-Score (B = 1.56, SE = 0.27 and p-value = 1.90 x 10(-8)), and that could be used as a good predictor of obesity longitudinal trajectories during puberty. On the other hand, we showed that the pGRS is not associated with cardio-metabolic comorbidities in children and that certain environmental factors interact with the genetic predisposition to the disease. Finally, according to the results derived from a weight-reduction metformin intervention in children with obesity, we discarded the utility of the pGRS as a pharmacogenetics marker of metformin response.en
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleEvaluation of the Predictive Ability, Environmental Regulation and Pharmacogenetics Utility of a BMI-Predisposing Genetic Risk Score during Childhood and Pubertyen
dc.typeJournal Articlees
dc.authorsophosAnguita-Ruiz, A.;Gonzalez-Gil, E. M.;Ruperez, A. I.;Llorente-Cantarero, F. J.;Pastor-Villaescusa, B.;Alcala-Fdez, J.;Moreno, L. A.;Gil, A.;Gil-Campos, M.;Bueno, G.;Leis, R.;Aguilera, C. M.
dc.identifier.doi10.3390/jcm9061705
dc.identifier.pmid32498346
dc.identifier.sophos39488
dc.issue.number6es
dc.journal.titleJournal of Clinical Medicinees
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Pediatríaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)es
dc.rights.accessRightsopenAccess
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number9es


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