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Subclinical Cardiovascular System Changes in Obese Patients with Juvenile Idiopathic Arthritis
Objective. We aimed to determine the prevalence of excess body mass in juvenile idiopathic arthritis (JIA) children and to investigate the influence of obesity into the early, subclinical changes in cardiovascular system in these patients. Methods. Fifty-eight JIA patients, aged median 13 years, wer...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608356/ https://www.ncbi.nlm.nih.gov/pubmed/23554546 http://dx.doi.org/10.1155/2013/436702 |
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author | Głowińska-Olszewska, Barbara Bossowski, Artur Dobreńko, Elżbieta Hryniewicz, Andrzej Konstantynowicz, Jerzy Milewski, Robert Łuczyński, Włodzimierz Piotrowska-Jastrzębska, Janina Kowal-Bielecka, Otylia |
author_facet | Głowińska-Olszewska, Barbara Bossowski, Artur Dobreńko, Elżbieta Hryniewicz, Andrzej Konstantynowicz, Jerzy Milewski, Robert Łuczyński, Włodzimierz Piotrowska-Jastrzębska, Janina Kowal-Bielecka, Otylia |
author_sort | Głowińska-Olszewska, Barbara |
collection | PubMed |
description | Objective. We aimed to determine the prevalence of excess body mass in juvenile idiopathic arthritis (JIA) children and to investigate the influence of obesity into the early, subclinical changes in cardiovascular system in these patients. Methods. Fifty-eight JIA patients, aged median 13 years, were compared to 36 healthy controls. Traditional cardiovascular risk factors and inflammatory markers (hsCRP, IL-6, TNFα, adiponectin) were studied together with IMT (intima-media thickness), FMD (flow mediated dilation), and LVMi (left ventricle mass index) as surrogate markers of subclinical atherosclerosis. Results. Thirteen JIA children (22%) were obese and had increased systolic blood pressure, cholesterol, triglycerides, insulin, HOMA, hsCRP, and IL-6 compared to nonobese JIA and controls. FMD was decreased compared to nonobese JIA and controls, whereas IMT and LVMi were increased. In multivariate regression analysis, TNFα, SDS-BMI, and systolic blood pressure were independent predictors of early CV changes in JIA. Conclusions. Coincident obesity is common in JIA children and is associated with insulin resistance, dyslipidemia, and increased levels of inflammatory markers leading to early changes in cardiovascular system. Thus, medical care of children with JIA should include strategies preventing cardiovascular disease by maintenance of adequate body weight. |
format | Online Article Text |
id | pubmed-3608356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36083562013-04-02 Subclinical Cardiovascular System Changes in Obese Patients with Juvenile Idiopathic Arthritis Głowińska-Olszewska, Barbara Bossowski, Artur Dobreńko, Elżbieta Hryniewicz, Andrzej Konstantynowicz, Jerzy Milewski, Robert Łuczyński, Włodzimierz Piotrowska-Jastrzębska, Janina Kowal-Bielecka, Otylia Mediators Inflamm Clinical Study Objective. We aimed to determine the prevalence of excess body mass in juvenile idiopathic arthritis (JIA) children and to investigate the influence of obesity into the early, subclinical changes in cardiovascular system in these patients. Methods. Fifty-eight JIA patients, aged median 13 years, were compared to 36 healthy controls. Traditional cardiovascular risk factors and inflammatory markers (hsCRP, IL-6, TNFα, adiponectin) were studied together with IMT (intima-media thickness), FMD (flow mediated dilation), and LVMi (left ventricle mass index) as surrogate markers of subclinical atherosclerosis. Results. Thirteen JIA children (22%) were obese and had increased systolic blood pressure, cholesterol, triglycerides, insulin, HOMA, hsCRP, and IL-6 compared to nonobese JIA and controls. FMD was decreased compared to nonobese JIA and controls, whereas IMT and LVMi were increased. In multivariate regression analysis, TNFα, SDS-BMI, and systolic blood pressure were independent predictors of early CV changes in JIA. Conclusions. Coincident obesity is common in JIA children and is associated with insulin resistance, dyslipidemia, and increased levels of inflammatory markers leading to early changes in cardiovascular system. Thus, medical care of children with JIA should include strategies preventing cardiovascular disease by maintenance of adequate body weight. Hindawi Publishing Corporation 2013 2013-03-11 /pmc/articles/PMC3608356/ /pubmed/23554546 http://dx.doi.org/10.1155/2013/436702 Text en Copyright © 2013 Barbara Głowińska-Olszewska 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 | Clinical Study Głowińska-Olszewska, Barbara Bossowski, Artur Dobreńko, Elżbieta Hryniewicz, Andrzej Konstantynowicz, Jerzy Milewski, Robert Łuczyński, Włodzimierz Piotrowska-Jastrzębska, Janina Kowal-Bielecka, Otylia Subclinical Cardiovascular System Changes in Obese Patients with Juvenile Idiopathic Arthritis |
title | Subclinical Cardiovascular System Changes in Obese Patients with Juvenile Idiopathic Arthritis |
title_full | Subclinical Cardiovascular System Changes in Obese Patients with Juvenile Idiopathic Arthritis |
title_fullStr | Subclinical Cardiovascular System Changes in Obese Patients with Juvenile Idiopathic Arthritis |
title_full_unstemmed | Subclinical Cardiovascular System Changes in Obese Patients with Juvenile Idiopathic Arthritis |
title_short | Subclinical Cardiovascular System Changes in Obese Patients with Juvenile Idiopathic Arthritis |
title_sort | subclinical cardiovascular system changes in obese patients with juvenile idiopathic arthritis |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608356/ https://www.ncbi.nlm.nih.gov/pubmed/23554546 http://dx.doi.org/10.1155/2013/436702 |
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