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dc.contributor.authorMicó, Víctor
dc.contributor.authorBueno Cavanillas, Aurora 
dc.date.accessioned2022-12-13T08:00:32Z
dc.date.available2022-12-13T08:00:32Z
dc.date.issued2022-09-06
dc.identifier.citationMicó V... [et al.]. (2022) Morbid liver manifestations are intrinsically bound to metabolic syndrome and nutrient intake based on a machine-learning cluster analysis. Front. Endocrinol. 13:936956. doi: [10.3389/fendo.2022.936956]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/78406
dc.description.abstractMetabolic syndrome (MetS) is one of the most important medical problems around the world. Identification of patient´s singular characteristic could help to reduce the clinical impact and facilitate individualized management. This study aimed to categorize MetS patients using phenotypical and clinical variables habitually collected during health check-ups of individuals considered to have high cardiovascular risk. The selected markers to categorize MetS participants included anthropometric variables as well as clinical data, biochemical parameters and prescribed pharmacological treatment. An exploratory factor analysis was carried out with a subsequent hierarchical cluster analysis using the z-scores from factor analysis. The first step identified three different factors. The first was determined by hypercholesterolemia and associated treatments, the second factor exhibited glycemic disorders and accompanying treatments and the third factor was characterized by hepatic enzymes. Subsequently four clusters of patients were identified, where cluster 1 was characterized by glucose disorders and treatments, cluster 2 presented mild MetS, cluster 3 presented exacerbated levels of hepatic enzymes and cluster 4 highlighted cholesterol and its associated treatments Interestingly, the liver status related cluster was characterized by higher protein consumption and cluster 4 with low polyunsaturated fatty acid intake. This research emphasized the potential clinical relevance of hepatic impairments in addition to MetS traditional characterization for precision and personalized management of MetS patients.es_ES
dc.description.sponsorshipEuropean Research Council (ERC) European Commission 340918es_ES
dc.description.sponsorshipofficial Spanish institutions for funding scientific biomedical researches_ES
dc.description.sponsorshipCIBER Fisiopatologia de la Obesidad y Nutricion (CIBEROBN)es_ES
dc.description.sponsorshipInstituto de Salud Carlos III (ISCIII) through the Fondo de Investigacio' n para la Salud (FIS) - European Regional Development Fund PI13/00673 PI13/00492 PI13/00272 PI13/01123 PI13/00462 PI13/00233 PI13/02184 PI13/00728 PI13/01090 PI13/01056 PI14/01722 PI14/00636 PI14/00618 PI14/00696 PI14/01206 PI14/01919 PI14/00853 PI14/01374 PI14/00972 PI14/00728es_ES
dc.description.sponsorshipThe Instituto de Salud Carlos III (ISCIII) through the Fondo de Investigacio' n para la Salud (FIS) - European Regional Development Fund PI14/01471 PI16/00473 PI16/00662 PI16/01873 PI16/01094 PI16/00501 PI16/00533 PI16/00381 PI16/00366 PI16/01522 PI16/01120 PI17/00764 PI17/01183 PI17/00855 PI17/01347 PI17/00525 PI17/01827 PI17/00532 PI17/00215 PI17/01441 PI17/00508es_ES
dc.description.sponsorshipEspecial Action Project "Implementacion y evaluacion de una intervencion intensiva sobre la actividad fisica Cohorte PREDIMED-Plus"es_ES
dc.description.sponsorshipLa Caixa Foundation 2013ACUP00194es_ES
dc.description.sponsorshipICREA under the ICREA Academia programes_ES
dc.description.sponsorshipSEMERGEN grantes_ES
dc.description.sponsorshipDepartment of Health of the Government of Navarra 61/ 2015es_ES
dc.description.sponsorshipFundacioLa Maratode TV 201630.10es_ES
dc.description.sponsorshipAstraZenecaes_ES
dc.description.sponsorshipJunta de Andalucia PI0458/2013 PS0358/2016 PI0137/2018es_ES
dc.description.sponsorshipCenter for Forestry Research & Experimentation (CIEF)es_ES
dc.description.sponsorshipEuropean Commission PROMETEO/ 2017/017es_ES
dc.description.sponsorshipBalearic Islands Government 35/2011es_ES
dc.description.sponsorshipEuropean Commission PI17/01732 PI17/00926 PI19/00957 PI19/00386 PI19/00309 PI19/01032 PI19/00576 PI19/00017 PI19/01226 PI19/00781 PI19/01560 PI19/01332 PI20/01802 PI20/00138 PI20/01532 PI20/00456 PI20/00339 PI20/00557 PI20/00886 PI20/01158es_ES
dc.language.isoenges_ES
dc.publisherFrontierses_ES
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHepatic enzymeses_ES
dc.subjectMetabolic syndromees_ES
dc.subjectClusteres_ES
dc.subjectBiomarkerses_ES
dc.subjectGlucose disorderses_ES
dc.subjectDyslipidemiaes_ES
dc.titleMorbid liver manifestations are intrinsically bound to metabolic syndrome and nutrient intake based on a machine-learning cluster analysises_ES
dc.typejournal articlees_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/FP7/340918es_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3389/fendo.2022.936956
dc.type.hasVersionVoRes_ES


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