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Linkage of Epidemiologic Evidence With the Clinical Aspects of Metabolic Syndrome
Metabolic syndrome (MetS) is characterized by a cluster of cardiovascular risk factors, such as hypertension, glucose intolerance, high triglycerides, and a low high density lipoprotein-cholesterol level. MetS is known to be associated with cardiovascular diseases. In order to diagnose MetS, definit...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Cardiology
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390421/ https://www.ncbi.nlm.nih.gov/pubmed/22787466 http://dx.doi.org/10.4070/kcj.2012.42.6.371 |
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author | Jee, Sun Ha Jo, Jaeseong |
author_facet | Jee, Sun Ha Jo, Jaeseong |
author_sort | Jee, Sun Ha |
collection | PubMed |
description | Metabolic syndrome (MetS) is characterized by a cluster of cardiovascular risk factors, such as hypertension, glucose intolerance, high triglycerides, and a low high density lipoprotein-cholesterol level. MetS is known to be associated with cardiovascular diseases. In order to diagnose MetS, definitions such as National Cholesterol Education Program Adult Treatment Panel III, American Heart Association/National Heart Lung and Blood Institute, International Diabetes Federation, World Health Organization, European Group for the Study of Insulin Resistance and American College of Endocrinology are widely used. However, using different criteria may lead to confusion regarding the diagnosis and treatment of patients with MetS in the primary care setting. Our objected was to review 3 aspects concerning MetS using the Metabolic Syndrome Research Initiatives study of 123892 healthy Koreans (1994-2001) that had a maximum follow-up of 12 years. The 3 aspects were reviewed by determination of the association of MetS with the development of atherosclerotic cardiovascular disease (ASCVD) and ischemic heart disease (IHD). Based on our findings, each metabolic factor associated with MetS was not weighted equally. The hazard ratio (HR) was higher in individuals with higher glucose compared with the HR in individuals with higher body mass index. Individuals with pre-MetS (having 1 or 2 metabolic factors) had 1.5-2.3 fold higher risk of developing ASCVD and IHD in both genders. In the presence of MetS, both singly and in combination, precede the development of ASCVD and IHD and individuals with pre-MetS must not be ignored as there is no apparent threshold in defining MetS. Furthermore, MetS may complement the Framingham Risk Score and can be used as the first line approach to treat the ASCVD or IHD. |
format | Online Article Text |
id | pubmed-3390421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Society of Cardiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-33904212012-07-11 Linkage of Epidemiologic Evidence With the Clinical Aspects of Metabolic Syndrome Jee, Sun Ha Jo, Jaeseong Korean Circ J Review Metabolic syndrome (MetS) is characterized by a cluster of cardiovascular risk factors, such as hypertension, glucose intolerance, high triglycerides, and a low high density lipoprotein-cholesterol level. MetS is known to be associated with cardiovascular diseases. In order to diagnose MetS, definitions such as National Cholesterol Education Program Adult Treatment Panel III, American Heart Association/National Heart Lung and Blood Institute, International Diabetes Federation, World Health Organization, European Group for the Study of Insulin Resistance and American College of Endocrinology are widely used. However, using different criteria may lead to confusion regarding the diagnosis and treatment of patients with MetS in the primary care setting. Our objected was to review 3 aspects concerning MetS using the Metabolic Syndrome Research Initiatives study of 123892 healthy Koreans (1994-2001) that had a maximum follow-up of 12 years. The 3 aspects were reviewed by determination of the association of MetS with the development of atherosclerotic cardiovascular disease (ASCVD) and ischemic heart disease (IHD). Based on our findings, each metabolic factor associated with MetS was not weighted equally. The hazard ratio (HR) was higher in individuals with higher glucose compared with the HR in individuals with higher body mass index. Individuals with pre-MetS (having 1 or 2 metabolic factors) had 1.5-2.3 fold higher risk of developing ASCVD and IHD in both genders. In the presence of MetS, both singly and in combination, precede the development of ASCVD and IHD and individuals with pre-MetS must not be ignored as there is no apparent threshold in defining MetS. Furthermore, MetS may complement the Framingham Risk Score and can be used as the first line approach to treat the ASCVD or IHD. The Korean Society of Cardiology 2012-06 2012-06-28 /pmc/articles/PMC3390421/ /pubmed/22787466 http://dx.doi.org/10.4070/kcj.2012.42.6.371 Text en Copyright © 2012 The Korean Society of Cardiology 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 non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Jee, Sun Ha Jo, Jaeseong Linkage of Epidemiologic Evidence With the Clinical Aspects of Metabolic Syndrome |
title | Linkage of Epidemiologic Evidence With the Clinical Aspects of Metabolic Syndrome |
title_full | Linkage of Epidemiologic Evidence With the Clinical Aspects of Metabolic Syndrome |
title_fullStr | Linkage of Epidemiologic Evidence With the Clinical Aspects of Metabolic Syndrome |
title_full_unstemmed | Linkage of Epidemiologic Evidence With the Clinical Aspects of Metabolic Syndrome |
title_short | Linkage of Epidemiologic Evidence With the Clinical Aspects of Metabolic Syndrome |
title_sort | linkage of epidemiologic evidence with the clinical aspects of metabolic syndrome |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3390421/ https://www.ncbi.nlm.nih.gov/pubmed/22787466 http://dx.doi.org/10.4070/kcj.2012.42.6.371 |
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