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dc.contributor.authorDe Lamas Pérez, Carmela
dc.contributor.authorKalén, A.
dc.contributor.authorAnguita-Ruiz, A.
dc.contributor.authorPérez Ferreirós, Alexandra
dc.contributor.authorPicans Leis, Rosaura
dc.contributor.authorFlores, K.
dc.contributor.authorMoreno, L.A.
dc.contributor.authorBueno, G.
dc.contributor.authorGil, Á.
dc.contributor.authorGil-Campos, M.
dc.contributor.authorAguilera, C.M.
dc.contributor.authorLeis Trabazo, María Rosaura 
dc.date.accessioned2025-08-26T11:00:50Z
dc.date.available2025-08-26T11:00:50Z
dc.date.issued2022
dc.identifier.citationde Lamas C, Kalén A, Anguita-Ruiz A, Pérez-Ferreirós A, Picáns-Leis R, Flores K, et al. Progression of metabolic syndrome and associated cardiometabolic risk factors from prepuberty to puberty in children: The PUBMEP study. Frontiers in Endocrinology. 2022;13.
dc.identifier.issn1664-2392
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/63c39170b0644813d9027578*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20791
dc.description.abstractIntroduction: Metabolic syndrome (MetS) is a cluster of clinical and metabolic alterations related to the risk of cardiovascular diseases (CVD). Metabolic changes occurring during puberty, especially in children with overweight and obesity, can influence the risk of developing chronic diseases, especially CVD. Methods: Longitudinal study based on the follow-up until puberty of a cohort of 191 prepubertal Spanish boys and girls without congenital, chronic, or inflammatory diseases: undernutrition: or intake of any drug that could alter blood glucose, blood pressure, or lipid metabolism. The following parameters were used to determine the presence of MetS: obesity, hypertension, hyperglycemia, hypertriglyceridemia, and low HDL-c. Results: A total of 75·5% of participants stayed in the same BMI category from prepuberty to puberty, whereas 6·3% increased by at least one category. The prevalence of MetS was 9·1% (prepubertal stage) and 11·9% (pubertal stage). The risk of presenting alterations in puberty for systolic blood pressure (SBP), plasma triacylglycerols, HDL cholesterol (HDL-c), and HOMA-IR was significantly higher in those participants who had the same alterations in prepuberty. MetS prevalence in puberty was predicted by sex and levels of HOMA-IR, BMI-z, and waist circumference in the prepubertal stage, in the whole sample: in puberty, the predictors were levels of HOMA-IR, BMI-z, and diastolic blood pressure in participants with obesity. Two fast-and-frugal decision trees were built to predict the risk of MetS in puberty based on prepuberty HOMA-IR (cutoff 2·5), SBP (cutoff 106 mm of Hg), and TAG (cutoff 53 mg/dl). Discussion: Controlling obesity and cardiometabolic risk factors, especially HOMA-IR and blood pressure, in children during the prepubertal stage appears critical to preventing pubertal MetS effectively.en
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleProgression of metabolic syndrome and associated cardiometabolic risk factors from prepuberty to puberty in children: The PUBMEP study*
dc.typeArticleen
dc.authorsophosde Lamas, R. C.
dc.authorsophosKalén, A.
dc.authorsophosAnguita-Ruiz, A.
dc.authorsophosPérez-Ferreirós, A.
dc.authorsophosPicáns-Leis, R.
dc.authorsophosFlores, K.
dc.authorsophosMoreno, L. A.
dc.authorsophosBueno, G.
dc.authorsophosGil, Á
dc.authorsophosGil-Campos, M.
dc.authorsophosAguilera, C. M.
dc.authorsophosLeis
dc.identifier.doi10.3389/fendo.2022.1082684
dc.identifier.sophos63c39170b0644813d9027578
dc.journal.titleFrontiers in Endocrinology*
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fendo.2022.1082684/pdf;https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2022.1082684/pdfes
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Coruña APes
dc.subject.keywordIDISes
dc.subject.keywordAS Santiago APes
dc.subject.keywordCHUSes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number13


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