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Clustering of the Metabolic Syndrome Components in Adolescence: Role of Visceral Fat
Visceral fat (VF) promotes the development of metabolic syndrome (MetS), which emerges as early as in adolescence. The clustering of MetS components suggests shared etiologies, but these are largely unknown and may vary between males and females. Here, we investigated the latent structure of pre-cli...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869691/ https://www.ncbi.nlm.nih.gov/pubmed/24376531 http://dx.doi.org/10.1371/journal.pone.0082368 |
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author | Melka, Melkaye G. Abrahamowicz, Michal Leonard, Gabriel T. Perron, Michel Richer, Louis Veillette, Suzanne Gaudet, Daniel Paus, Tomáš Pausova, Zdenka |
author_facet | Melka, Melkaye G. Abrahamowicz, Michal Leonard, Gabriel T. Perron, Michel Richer, Louis Veillette, Suzanne Gaudet, Daniel Paus, Tomáš Pausova, Zdenka |
author_sort | Melka, Melkaye G. |
collection | PubMed |
description | Visceral fat (VF) promotes the development of metabolic syndrome (MetS), which emerges as early as in adolescence. The clustering of MetS components suggests shared etiologies, but these are largely unknown and may vary between males and females. Here, we investigated the latent structure of pre-clinical MetS in a community-based sample of 286 male and 312 female adolescents, assessing their abdominal adiposity (VF) directly with magnetic resonance imaging. Principal component analysis of the five MetS-defining variables (VF, blood pressure [BP], fasting serum triglycerides, HDL-cholesterol and glucose) identified two independent components in both males and females. The first component was sex-similar; it explained >30% of variance and was loaded by all but BP variables. The second component explained >20% of variance; it was loaded by BP similarly in both sexes but additional loading by metabolic variables was sex-specific. This sex-specificity was not detected in analyses that used waist circumference instead of VF. In adolescence, MetS-defining variables cluster into at least two sub-syndromes: (1) sex-similar metabolic abnormalities of obesity-induced insulin resistance and (2) sex-specific metabolic abnormalities associated with BP elevation. These results suggest that the etiology of MetS may involve more than one pathway and that some of the pathways may differ between males and females. Further, the sex-specific metabolic abnormalities associated with BP elevation suggest the need for sex-specific prevention and treatment strategies of MetS. |
format | Online Article Text |
id | pubmed-3869691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38696912013-12-27 Clustering of the Metabolic Syndrome Components in Adolescence: Role of Visceral Fat Melka, Melkaye G. Abrahamowicz, Michal Leonard, Gabriel T. Perron, Michel Richer, Louis Veillette, Suzanne Gaudet, Daniel Paus, Tomáš Pausova, Zdenka PLoS One Research Article Visceral fat (VF) promotes the development of metabolic syndrome (MetS), which emerges as early as in adolescence. The clustering of MetS components suggests shared etiologies, but these are largely unknown and may vary between males and females. Here, we investigated the latent structure of pre-clinical MetS in a community-based sample of 286 male and 312 female adolescents, assessing their abdominal adiposity (VF) directly with magnetic resonance imaging. Principal component analysis of the five MetS-defining variables (VF, blood pressure [BP], fasting serum triglycerides, HDL-cholesterol and glucose) identified two independent components in both males and females. The first component was sex-similar; it explained >30% of variance and was loaded by all but BP variables. The second component explained >20% of variance; it was loaded by BP similarly in both sexes but additional loading by metabolic variables was sex-specific. This sex-specificity was not detected in analyses that used waist circumference instead of VF. In adolescence, MetS-defining variables cluster into at least two sub-syndromes: (1) sex-similar metabolic abnormalities of obesity-induced insulin resistance and (2) sex-specific metabolic abnormalities associated with BP elevation. These results suggest that the etiology of MetS may involve more than one pathway and that some of the pathways may differ between males and females. Further, the sex-specific metabolic abnormalities associated with BP elevation suggest the need for sex-specific prevention and treatment strategies of MetS. Public Library of Science 2013-12-20 /pmc/articles/PMC3869691/ /pubmed/24376531 http://dx.doi.org/10.1371/journal.pone.0082368 Text en © 2013 Melka et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Melka, Melkaye G. Abrahamowicz, Michal Leonard, Gabriel T. Perron, Michel Richer, Louis Veillette, Suzanne Gaudet, Daniel Paus, Tomáš Pausova, Zdenka Clustering of the Metabolic Syndrome Components in Adolescence: Role of Visceral Fat |
title | Clustering of the Metabolic Syndrome Components in Adolescence: Role of Visceral Fat |
title_full | Clustering of the Metabolic Syndrome Components in Adolescence: Role of Visceral Fat |
title_fullStr | Clustering of the Metabolic Syndrome Components in Adolescence: Role of Visceral Fat |
title_full_unstemmed | Clustering of the Metabolic Syndrome Components in Adolescence: Role of Visceral Fat |
title_short | Clustering of the Metabolic Syndrome Components in Adolescence: Role of Visceral Fat |
title_sort | clustering of the metabolic syndrome components in adolescence: role of visceral fat |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869691/ https://www.ncbi.nlm.nih.gov/pubmed/24376531 http://dx.doi.org/10.1371/journal.pone.0082368 |
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