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Insulin Resistance, Dyslipidemia and Cardiovascular Changes in a Group of Obese Children

INTRODUCTION: Obesity-related comorbidities are present in young obese children, providing a platform for early adult cardiovascular disorders. OBJECTIVES: To compare and correlate markers of adiposity to metabolic disturbances, vascular and cardiac morphology in a European pediatric obese cohort. M...

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Autores principales: Pires, António, Martins, Paula, Pereira, Ana Margarida, Silva, Patricia Vaz, Marinho, Joana, Marques, Margarida, Castela, Eduardo, Sena, Cristina, Seiça, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415862/
https://www.ncbi.nlm.nih.gov/pubmed/25993589
http://dx.doi.org/10.5935/abc.20140206
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author Pires, António
Martins, Paula
Pereira, Ana Margarida
Silva, Patricia Vaz
Marinho, Joana
Marques, Margarida
Castela, Eduardo
Sena, Cristina
Seiça, Raquel
author_facet Pires, António
Martins, Paula
Pereira, Ana Margarida
Silva, Patricia Vaz
Marinho, Joana
Marques, Margarida
Castela, Eduardo
Sena, Cristina
Seiça, Raquel
author_sort Pires, António
collection PubMed
description INTRODUCTION: Obesity-related comorbidities are present in young obese children, providing a platform for early adult cardiovascular disorders. OBJECTIVES: To compare and correlate markers of adiposity to metabolic disturbances, vascular and cardiac morphology in a European pediatric obese cohort. METHODS: We carried out an observational and transversal analysis in a cohort consisting of 121 obese children of both sexes, between the ages of 6 and 17 years. The control group consisted of 40 children with normal body mass index within the same age range. Markers of adiposity, plasma lipids and lipoproteins, homeostasis model assessment-insulin resistance, common carotid artery intima-media thickness and left ventricular diameters were analyzed. RESULTS: There were statistically significant differences between the control and obese groups for the variables analyzed, all higher in the obese group, except for age, high-density lipoprotein cholesterol and adiponectin, higher in the control group. In the obese group, body mass index was directly correlated to left ventricular mass (r=0.542; p=0.001), the homeostasis model assessment-insulin resistance (r=0.378; p=<0.001) and mean common carotid artery intima-media thickness (r=0.378; p=<0.001). In that same group, insulin resistance was present in 38.1%, 12.5% had a combined dyslipidemic pattern, and eccentric hypertrophy was the most common left ventricular geometric pattern. CONCLUSIONS: These results suggest that these markers may be used in clinical practice to stratify cardiovascular risk, as well as to assess the impact of weight control programs.
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spelling pubmed-44158622015-05-04 Insulin Resistance, Dyslipidemia and Cardiovascular Changes in a Group of Obese Children Pires, António Martins, Paula Pereira, Ana Margarida Silva, Patricia Vaz Marinho, Joana Marques, Margarida Castela, Eduardo Sena, Cristina Seiça, Raquel Arq Bras Cardiol Original Articles INTRODUCTION: Obesity-related comorbidities are present in young obese children, providing a platform for early adult cardiovascular disorders. OBJECTIVES: To compare and correlate markers of adiposity to metabolic disturbances, vascular and cardiac morphology in a European pediatric obese cohort. METHODS: We carried out an observational and transversal analysis in a cohort consisting of 121 obese children of both sexes, between the ages of 6 and 17 years. The control group consisted of 40 children with normal body mass index within the same age range. Markers of adiposity, plasma lipids and lipoproteins, homeostasis model assessment-insulin resistance, common carotid artery intima-media thickness and left ventricular diameters were analyzed. RESULTS: There were statistically significant differences between the control and obese groups for the variables analyzed, all higher in the obese group, except for age, high-density lipoprotein cholesterol and adiponectin, higher in the control group. In the obese group, body mass index was directly correlated to left ventricular mass (r=0.542; p=0.001), the homeostasis model assessment-insulin resistance (r=0.378; p=<0.001) and mean common carotid artery intima-media thickness (r=0.378; p=<0.001). In that same group, insulin resistance was present in 38.1%, 12.5% had a combined dyslipidemic pattern, and eccentric hypertrophy was the most common left ventricular geometric pattern. CONCLUSIONS: These results suggest that these markers may be used in clinical practice to stratify cardiovascular risk, as well as to assess the impact of weight control programs. Sociedade Brasileira de Cardiologia 2015-04 /pmc/articles/PMC4415862/ /pubmed/25993589 http://dx.doi.org/10.5935/abc.20140206 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Pires, António
Martins, Paula
Pereira, Ana Margarida
Silva, Patricia Vaz
Marinho, Joana
Marques, Margarida
Castela, Eduardo
Sena, Cristina
Seiça, Raquel
Insulin Resistance, Dyslipidemia and Cardiovascular Changes in a Group of Obese Children
title Insulin Resistance, Dyslipidemia and Cardiovascular Changes in a Group of Obese Children
title_full Insulin Resistance, Dyslipidemia and Cardiovascular Changes in a Group of Obese Children
title_fullStr Insulin Resistance, Dyslipidemia and Cardiovascular Changes in a Group of Obese Children
title_full_unstemmed Insulin Resistance, Dyslipidemia and Cardiovascular Changes in a Group of Obese Children
title_short Insulin Resistance, Dyslipidemia and Cardiovascular Changes in a Group of Obese Children
title_sort insulin resistance, dyslipidemia and cardiovascular changes in a group of obese children
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415862/
https://www.ncbi.nlm.nih.gov/pubmed/25993589
http://dx.doi.org/10.5935/abc.20140206
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