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dc.contributor.authorGonzález-Gil, E.M.*
dc.contributor.authorAnguita-Ruiz, A.*
dc.contributor.authorKalén, A.*
dc.contributor.authorDe las Lamas Perez, C.*
dc.contributor.authorRupérez, A.I.*
dc.contributor.authorVázquez-Cobela, R.*
dc.contributor.authorFlores, K.*
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.accessioned2025-09-10T08:39:40Z
dc.date.available2025-09-10T08:39:40Z
dc.date.issued2023
dc.identifier.citationGonzález-Gil EM, Anguita-Ruiz A, Kalén A, De las Lamas Perez C, Rupérez AI, Vázquez-Cobela R, et al. Longitudinal associations between cardiovascular biomarkers and metabolic syndrome during puberty: the PUBMEP study. European Journal of Pediatrics. 2023;182(1):419-29.
dc.identifier.issn1432-1076
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/63824bd78a8e8f4672203b9e
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21690
dc.description.abstractPuberty has been described as a life stage of considerable metabolic risk specially for those with obesity. The low-grade systemic inflammatory status associated with obesity could be one of the connections with metabolic syndrome (MetS). Thus, we aimed to assess the relationship between inflammatory and cardiovascular biomarkers and the development of MetS during puberty. Seventy-five children from the PUBMEP study (33 females), aged 4-18 years, were included. Cardiovascular and inflammatory biomarkers were measured in the prepubertal and pubertal stage, including high-sensitivity C-reactive protein (CRP), leptin, tumor necrosis factor-alpha (TNF?), interleukin 8 (IL8), monocyte chemoattractant protein 1 (MCP-1), total plasminogen activator inhibitor-1 (tPAI), resistin, adiponectin, myeloperoxidase (MPO), and soluble intercellular adhesion molecule-1 (sICAM-1). MetS was diagnosed at each measurement point. Mixed-effects and logistic regressions were performed. Those children with MetS in puberty presented higher prepubertal values of several cardiometabolic biomarkers in comparison to those without MetS (z-score body mass index (zBMI), waist circumference, insulin, HOMA-IR, leptin, and tPAI (p < 0.05)). For prepubertal children with obesity, the odds of developing MetS in puberty were significantly higher in those having high zBMI (OR = 4.27; CI: 1.39-22.59) or high concentrations of tPAI (OR = 1.19; CI: 1.06-1.43). Conclusion: Those with obesity with higher prepubertal tPAI plasma levels had 19% higher odds of having MetS at puberty highlighting the existence of association between MetS, obesity, and inflammation already in puberty. Thus, assessing cardiometabolic and inflammatory status in children with obesity already at prepuberty is key to avoiding future comorbidities.What is Known:- Inflammation, metabolic syndrome, and obesity may have their onset in childhood.- Puberty is a life stage characterized for an increased cardiovascular risk.What is New:- Prepuberty state could be an early indicator of future cardiometabolic risk.- Children with obesity and high total plasminogen have higher odds of future metabolic syndrome.
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshChild *
dc.subject.meshFemale *
dc.subject.meshHumans *
dc.subject.meshAdiponectin *
dc.subject.meshBiomarkers*
dc.subject.meshBody Mass Index *
dc.subject.meshCardiovascular Diseases *
dc.subject.meshInflammation *
dc.subject.meshInsulin Resistance *
dc.subject.meshLeptin *
dc.subject.meshMetabolic Syndrome*
dc.subject.meshObesity *
dc.subject.meshPuberty *
dc.subject.meshMale *
dc.subject.meshChild, Preschool *
dc.subject.meshAdolescent *
dc.titleLongitudinal associations between cardiovascular biomarkers and metabolic syndrome during puberty: the PUBMEP study
dc.typeArtigo
dc.authorsophosGonzález-Gil, E.M.; Anguita-Ruiz, A.; Kalén, A.; De las Lamas Perez, C.; Rupérez, A.I.; Vázquez-Cobela, R.; Flores, K.; Gil, A.; Gil-Campos, M.; Bueno, G.; Leis, R.; Aguilera, C.M.
dc.identifier.doi10.1007/s00431-022-04702-6
dc.identifier.sophos63824bd78a8e8f4672203b9e
dc.issue.number1
dc.journal.titleEuropean Journal of Pediatrics*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Santiago::Pediatría
dc.page.initial419
dc.page.final429
dc.relation.publisherversionhttps://doi.org/10.1007/s00431-022-04702-6
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Santiago
dc.subject.keywordCHUS
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number182


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)