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A New Approach to Define and Diagnose Cardiometabolic Disorder in Children
The aim of the study was to test the performance of a new definition of metabolic syndrome (MetS), which better describes metabolic dysfunction in children. Methods. 15,794 youths aged 6–18 years participated. Mean z-score for CVD risk factors was calculated. Sensitivity analyses were performed to e...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402570/ https://www.ncbi.nlm.nih.gov/pubmed/25945355 http://dx.doi.org/10.1155/2015/539835 |
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author | Andersen, Lars Bo Lauersen, Jeppe Bo Brønd, Jan Christian Anderssen, Sigmund Alfred Sardinha, Luis B. Steene-Johannessen, Jostein McMurray, Robert G. Barros, Mauro V. G. Kriemler, Susi Møller, Niels Christian Bugge, Anna Kristensen, Peter Lund Ried-Larsen, Mathias Grøntved, Anders Ekelund, Ulf |
author_facet | Andersen, Lars Bo Lauersen, Jeppe Bo Brønd, Jan Christian Anderssen, Sigmund Alfred Sardinha, Luis B. Steene-Johannessen, Jostein McMurray, Robert G. Barros, Mauro V. G. Kriemler, Susi Møller, Niels Christian Bugge, Anna Kristensen, Peter Lund Ried-Larsen, Mathias Grøntved, Anders Ekelund, Ulf |
author_sort | Andersen, Lars Bo |
collection | PubMed |
description | The aim of the study was to test the performance of a new definition of metabolic syndrome (MetS), which better describes metabolic dysfunction in children. Methods. 15,794 youths aged 6–18 years participated. Mean z-score for CVD risk factors was calculated. Sensitivity analyses were performed to evaluate which parameters best described the metabolic dysfunction by analysing the score against independent variables not included in the score. Results. More youth had clustering of CVD risk factors (>6.2%) compared to the number selected by existing MetS definitions (International Diabetes Federation (IDF) < 1%). Waist circumference and BMI were interchangeable, but using insulin resistance homeostasis model assessment (HOMA) instead of fasting glucose increased the score. The continuous MetS score was increased when cardiorespiratory fitness (CRF) and leptin were included. A mean z-score of 0.40–0.85 indicated borderline and above 0.85 indicated clustering of risk factors. A noninvasive risk score based on adiposity and CRF showed sensitivity and specificity of 0.85 and an area under the curve of 0.92 against IDF definition of MetS. Conclusions. Diagnosis for MetS in youth can be improved by using continuous variables for risk factors and by including CRF and leptin. |
format | Online Article Text |
id | pubmed-4402570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-44025702015-05-05 A New Approach to Define and Diagnose Cardiometabolic Disorder in Children Andersen, Lars Bo Lauersen, Jeppe Bo Brønd, Jan Christian Anderssen, Sigmund Alfred Sardinha, Luis B. Steene-Johannessen, Jostein McMurray, Robert G. Barros, Mauro V. G. Kriemler, Susi Møller, Niels Christian Bugge, Anna Kristensen, Peter Lund Ried-Larsen, Mathias Grøntved, Anders Ekelund, Ulf J Diabetes Res Research Article The aim of the study was to test the performance of a new definition of metabolic syndrome (MetS), which better describes metabolic dysfunction in children. Methods. 15,794 youths aged 6–18 years participated. Mean z-score for CVD risk factors was calculated. Sensitivity analyses were performed to evaluate which parameters best described the metabolic dysfunction by analysing the score against independent variables not included in the score. Results. More youth had clustering of CVD risk factors (>6.2%) compared to the number selected by existing MetS definitions (International Diabetes Federation (IDF) < 1%). Waist circumference and BMI were interchangeable, but using insulin resistance homeostasis model assessment (HOMA) instead of fasting glucose increased the score. The continuous MetS score was increased when cardiorespiratory fitness (CRF) and leptin were included. A mean z-score of 0.40–0.85 indicated borderline and above 0.85 indicated clustering of risk factors. A noninvasive risk score based on adiposity and CRF showed sensitivity and specificity of 0.85 and an area under the curve of 0.92 against IDF definition of MetS. Conclusions. Diagnosis for MetS in youth can be improved by using continuous variables for risk factors and by including CRF and leptin. Hindawi Publishing Corporation 2015 2015-04-06 /pmc/articles/PMC4402570/ /pubmed/25945355 http://dx.doi.org/10.1155/2015/539835 Text en Copyright © 2015 Lars Bo Andersen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Andersen, Lars Bo Lauersen, Jeppe Bo Brønd, Jan Christian Anderssen, Sigmund Alfred Sardinha, Luis B. Steene-Johannessen, Jostein McMurray, Robert G. Barros, Mauro V. G. Kriemler, Susi Møller, Niels Christian Bugge, Anna Kristensen, Peter Lund Ried-Larsen, Mathias Grøntved, Anders Ekelund, Ulf A New Approach to Define and Diagnose Cardiometabolic Disorder in Children |
title | A New Approach to Define and Diagnose Cardiometabolic Disorder in Children |
title_full | A New Approach to Define and Diagnose Cardiometabolic Disorder in Children |
title_fullStr | A New Approach to Define and Diagnose Cardiometabolic Disorder in Children |
title_full_unstemmed | A New Approach to Define and Diagnose Cardiometabolic Disorder in Children |
title_short | A New Approach to Define and Diagnose Cardiometabolic Disorder in Children |
title_sort | new approach to define and diagnose cardiometabolic disorder in children |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4402570/ https://www.ncbi.nlm.nih.gov/pubmed/25945355 http://dx.doi.org/10.1155/2015/539835 |
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