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The association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the Ewha Birth and Growth Cohort Study

We assessed the association between metabolic health and markers of inflammation and of endothelial dysfunction using data from the Ewha Birth and Growth Cohort Study. The data of 195 subjects aged 13–15 years were analyzed. To assess metabolic syndrome, continuous metabolic syndrome (cMets) scores...

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Autores principales: Lee, Hye Ah, Choi, Eun Jeong, Park, Bohyun, Lee, Hwayoung, Hong, Young Sun, Kim, Hae Soon, Shin, Moon-Kyung, Park, Hyesook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239476/
https://www.ncbi.nlm.nih.gov/pubmed/32433661
http://dx.doi.org/10.1371/journal.pone.0233469
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author Lee, Hye Ah
Choi, Eun Jeong
Park, Bohyun
Lee, Hwayoung
Hong, Young Sun
Kim, Hae Soon
Shin, Moon-Kyung
Park, Hyesook
author_facet Lee, Hye Ah
Choi, Eun Jeong
Park, Bohyun
Lee, Hwayoung
Hong, Young Sun
Kim, Hae Soon
Shin, Moon-Kyung
Park, Hyesook
author_sort Lee, Hye Ah
collection PubMed
description We assessed the association between metabolic health and markers of inflammation and of endothelial dysfunction using data from the Ewha Birth and Growth Cohort Study. The data of 195 subjects aged 13–15 years were analyzed. To assess metabolic syndrome, continuous metabolic syndrome (cMets) scores were calculated. We measured the levels of high-sensitivity C-reactive protein (hs-CRP), intercellular adhesion molecule 1 (ICAM-1), and vascular cell adhesion molecule 1 (VCAM-1) as markers of inflammation and endothelial dysfunction. An increase of one SD in the cMets score resulted in a 1.25-fold (95% CI 1.10–1.42) increase in the risk of acute inflammatory status and a 1.26-fold (95% CI 1.11–1.43) increase in the risk of endothelial dysfunction as defined by ICAM-1, while VCAM-1 showed a meaningless trend. Of the metabolic components, body mass index (BMI) was positively associated with elevated hs-CRP levels and high-density lipoprotein cholesterol (HDL-c) levels were negatively associated with elevated ICAM-1 levels. Additionally, a mediation analysis showed that a high BMI was directly related to elevated hs-CRP levels and indirectly related to elevated ICAM-1 levels via HDL-c. Our findings show that poor metabolic health was related to an unfavorable inflammatory status and endothelial dysfunction in adolescents.
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spelling pubmed-72394762020-06-08 The association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the Ewha Birth and Growth Cohort Study Lee, Hye Ah Choi, Eun Jeong Park, Bohyun Lee, Hwayoung Hong, Young Sun Kim, Hae Soon Shin, Moon-Kyung Park, Hyesook PLoS One Research Article We assessed the association between metabolic health and markers of inflammation and of endothelial dysfunction using data from the Ewha Birth and Growth Cohort Study. The data of 195 subjects aged 13–15 years were analyzed. To assess metabolic syndrome, continuous metabolic syndrome (cMets) scores were calculated. We measured the levels of high-sensitivity C-reactive protein (hs-CRP), intercellular adhesion molecule 1 (ICAM-1), and vascular cell adhesion molecule 1 (VCAM-1) as markers of inflammation and endothelial dysfunction. An increase of one SD in the cMets score resulted in a 1.25-fold (95% CI 1.10–1.42) increase in the risk of acute inflammatory status and a 1.26-fold (95% CI 1.11–1.43) increase in the risk of endothelial dysfunction as defined by ICAM-1, while VCAM-1 showed a meaningless trend. Of the metabolic components, body mass index (BMI) was positively associated with elevated hs-CRP levels and high-density lipoprotein cholesterol (HDL-c) levels were negatively associated with elevated ICAM-1 levels. Additionally, a mediation analysis showed that a high BMI was directly related to elevated hs-CRP levels and indirectly related to elevated ICAM-1 levels via HDL-c. Our findings show that poor metabolic health was related to an unfavorable inflammatory status and endothelial dysfunction in adolescents. Public Library of Science 2020-05-20 /pmc/articles/PMC7239476/ /pubmed/32433661 http://dx.doi.org/10.1371/journal.pone.0233469 Text en © 2020 Lee 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lee, Hye Ah
Choi, Eun Jeong
Park, Bohyun
Lee, Hwayoung
Hong, Young Sun
Kim, Hae Soon
Shin, Moon-Kyung
Park, Hyesook
The association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the Ewha Birth and Growth Cohort Study
title The association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the Ewha Birth and Growth Cohort Study
title_full The association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the Ewha Birth and Growth Cohort Study
title_fullStr The association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the Ewha Birth and Growth Cohort Study
title_full_unstemmed The association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the Ewha Birth and Growth Cohort Study
title_short The association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the Ewha Birth and Growth Cohort Study
title_sort association between metabolic components and markers of inflammatory and endothelial dysfunction in adolescents, based on the ewha birth and growth cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239476/
https://www.ncbi.nlm.nih.gov/pubmed/32433661
http://dx.doi.org/10.1371/journal.pone.0233469
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