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Association between Metabolic Components and Subclinical Atherosclerosis in Korean Adults
BACKGROUND: Many studies have attempted to develop relatively simple and easy noninvasive measurements of atherosclerosis (NIMA), and each NIMA assesses different atherosclerotic properties. We, therefore, investigated the association between metabolic syndrome (MetS) components and different NIMAs....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Academy of Family Medicine
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3418342/ https://www.ncbi.nlm.nih.gov/pubmed/22916325 http://dx.doi.org/10.4082/kjfm.2012.33.4.229 |
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author | Hwang, In Cheol Suh, Sang-Yeon Seo, Ah-Ram Ahn, Hong Yup Yim, Eunji |
author_facet | Hwang, In Cheol Suh, Sang-Yeon Seo, Ah-Ram Ahn, Hong Yup Yim, Eunji |
author_sort | Hwang, In Cheol |
collection | PubMed |
description | BACKGROUND: Many studies have attempted to develop relatively simple and easy noninvasive measurements of atherosclerosis (NIMA), and each NIMA assesses different atherosclerotic properties. We, therefore, investigated the association between metabolic syndrome (MetS) components and different NIMAs. METHODS: This study included 1,132 Korean subjects over 20 years of age who had visited a Health Promotion Center in Korea. Carotid injury (increased carotid intima-media thickness or plaques) was evaluated by ultrasonography and arterial stiffness by brachial-ankle pulse wave velocity. The MetS components were assessed according to the Asian criteria of the American Heart Association/National Heart, Lung, and Blood Institute. RESULTS: Both arterial stiffness and carotid injury gradually deteriorated with increase in the number of MetS components. Arterial stiffness and carotid injury were associated with different MetS components, each of which had varying impact. After adjustment for all possible confounders such as age, sex, and lifestyle, elevated blood pressure (BP) was found to have the strongest association with arterial stiffness, whereas central obesity, impaired fasting plasma glucose, and elevated BP had comparable connection with carotid atherosclerosis. CONCLUSION: Individual MetS components were related with subclinical atherosclerosis in different ways. Elevated BP showed the strongest association with arterial stiffness, while central obesity, impaired fasting plasma glucose, and elevated BP showed good correlation with carotid atherosclerosis. |
format | Online Article Text |
id | pubmed-3418342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Academy of Family Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-34183422012-08-22 Association between Metabolic Components and Subclinical Atherosclerosis in Korean Adults Hwang, In Cheol Suh, Sang-Yeon Seo, Ah-Ram Ahn, Hong Yup Yim, Eunji Korean J Fam Med Original Article BACKGROUND: Many studies have attempted to develop relatively simple and easy noninvasive measurements of atherosclerosis (NIMA), and each NIMA assesses different atherosclerotic properties. We, therefore, investigated the association between metabolic syndrome (MetS) components and different NIMAs. METHODS: This study included 1,132 Korean subjects over 20 years of age who had visited a Health Promotion Center in Korea. Carotid injury (increased carotid intima-media thickness or plaques) was evaluated by ultrasonography and arterial stiffness by brachial-ankle pulse wave velocity. The MetS components were assessed according to the Asian criteria of the American Heart Association/National Heart, Lung, and Blood Institute. RESULTS: Both arterial stiffness and carotid injury gradually deteriorated with increase in the number of MetS components. Arterial stiffness and carotid injury were associated with different MetS components, each of which had varying impact. After adjustment for all possible confounders such as age, sex, and lifestyle, elevated blood pressure (BP) was found to have the strongest association with arterial stiffness, whereas central obesity, impaired fasting plasma glucose, and elevated BP had comparable connection with carotid atherosclerosis. CONCLUSION: Individual MetS components were related with subclinical atherosclerosis in different ways. Elevated BP showed the strongest association with arterial stiffness, while central obesity, impaired fasting plasma glucose, and elevated BP showed good correlation with carotid atherosclerosis. The Korean Academy of Family Medicine 2012-07 2012-07-25 /pmc/articles/PMC3418342/ /pubmed/22916325 http://dx.doi.org/10.4082/kjfm.2012.33.4.229 Text en Copyright © 2012 The Korean Academy of Family Medicine 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 (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hwang, In Cheol Suh, Sang-Yeon Seo, Ah-Ram Ahn, Hong Yup Yim, Eunji Association between Metabolic Components and Subclinical Atherosclerosis in Korean Adults |
title | Association between Metabolic Components and Subclinical Atherosclerosis in Korean Adults |
title_full | Association between Metabolic Components and Subclinical Atherosclerosis in Korean Adults |
title_fullStr | Association between Metabolic Components and Subclinical Atherosclerosis in Korean Adults |
title_full_unstemmed | Association between Metabolic Components and Subclinical Atherosclerosis in Korean Adults |
title_short | Association between Metabolic Components and Subclinical Atherosclerosis in Korean Adults |
title_sort | association between metabolic components and subclinical atherosclerosis in korean adults |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3418342/ https://www.ncbi.nlm.nih.gov/pubmed/22916325 http://dx.doi.org/10.4082/kjfm.2012.33.4.229 |
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