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The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study
BACKGROUND: To evaluate the clinical value of metabolic syndrome based on different definitions [American Heart Association/National Heart, Lung and Blood Institute (AHA/NHLBI), International Diabetes Federation (IDF) and European Group for the Study of Insulin Resistance (EGIR)] in middle-aged and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847340/ https://www.ncbi.nlm.nih.gov/pubmed/27117940 http://dx.doi.org/10.1186/s12933-016-0387-4 |
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author | van Herpt, Thijs T. W. Dehghan, Abbas van Hoek, Mandy Ikram, M. Arfan Hofman, Albert Sijbrands, Eric J. G. Franco, Oscar H. |
author_facet | van Herpt, Thijs T. W. Dehghan, Abbas van Hoek, Mandy Ikram, M. Arfan Hofman, Albert Sijbrands, Eric J. G. Franco, Oscar H. |
author_sort | van Herpt, Thijs T. W. |
collection | PubMed |
description | BACKGROUND: To evaluate the clinical value of metabolic syndrome based on different definitions [American Heart Association/National Heart, Lung and Blood Institute (AHA/NHLBI), International Diabetes Federation (IDF) and European Group for the Study of Insulin Resistance (EGIR)] in middle-aged and elderly populations. METHODS: We studied 8643 participants from the Rotterdam study (1990–2012; mean age 62.7; 57.6 % female), a large prospective population-based study with predominantly elderly participants. We performed cox-proportional hazards models for different definitions, triads within definitions and each separate component for the risk of incident type 2 diabetes mellitus, coronary heart disease, stroke, cardiovascular- and all-cause mortality. RESULTS: In our population of 8643 subjects, metabolic syndrome was highly prevalent (prevalence between 19.4 and 42.4 %). Metabolic syndrome in general was associated with incident type 2 diabetes mellitus (median follow-up of 6.8 years, hazard ratios 3.13–3.78). The associations with coronary heart disease (median follow-up of 7.2 years, hazard ratios 1.08–1.32), stroke (median follow-up of 7.7 years, hazard ratios 0.98–1.32), cardiovascular mortality (median follow-up of 8.2 years, ratios 0.95–1.29) and all-cause mortality (median follow-up of 8.7 years, hazard ratios 1.05–1.10) were weaker. AHA/NHLBI- and IDF-definitions showed similar associations with clinical endpoints compared to the EGIR, which was only significantly associated with incident type 2 diabetes mellitus. All significant associations disappeared after correcting metabolic syndrome for its individual components. CONCLUSIONS: Large variability exists between and within definitions of the metabolic syndrome with respect to risk of clinical events and mortality. In a relatively old population the metabolic syndrome did not show an additional predictive value on top of its individual components. So, besides as a manner of easy identification of high risk patients, the metabolic syndrome does not seem to add any predictive value for clinical practice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12933-016-0387-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4847340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48473402016-04-28 The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study van Herpt, Thijs T. W. Dehghan, Abbas van Hoek, Mandy Ikram, M. Arfan Hofman, Albert Sijbrands, Eric J. G. Franco, Oscar H. Cardiovasc Diabetol Original Investigation BACKGROUND: To evaluate the clinical value of metabolic syndrome based on different definitions [American Heart Association/National Heart, Lung and Blood Institute (AHA/NHLBI), International Diabetes Federation (IDF) and European Group for the Study of Insulin Resistance (EGIR)] in middle-aged and elderly populations. METHODS: We studied 8643 participants from the Rotterdam study (1990–2012; mean age 62.7; 57.6 % female), a large prospective population-based study with predominantly elderly participants. We performed cox-proportional hazards models for different definitions, triads within definitions and each separate component for the risk of incident type 2 diabetes mellitus, coronary heart disease, stroke, cardiovascular- and all-cause mortality. RESULTS: In our population of 8643 subjects, metabolic syndrome was highly prevalent (prevalence between 19.4 and 42.4 %). Metabolic syndrome in general was associated with incident type 2 diabetes mellitus (median follow-up of 6.8 years, hazard ratios 3.13–3.78). The associations with coronary heart disease (median follow-up of 7.2 years, hazard ratios 1.08–1.32), stroke (median follow-up of 7.7 years, hazard ratios 0.98–1.32), cardiovascular mortality (median follow-up of 8.2 years, ratios 0.95–1.29) and all-cause mortality (median follow-up of 8.7 years, hazard ratios 1.05–1.10) were weaker. AHA/NHLBI- and IDF-definitions showed similar associations with clinical endpoints compared to the EGIR, which was only significantly associated with incident type 2 diabetes mellitus. All significant associations disappeared after correcting metabolic syndrome for its individual components. CONCLUSIONS: Large variability exists between and within definitions of the metabolic syndrome with respect to risk of clinical events and mortality. In a relatively old population the metabolic syndrome did not show an additional predictive value on top of its individual components. So, besides as a manner of easy identification of high risk patients, the metabolic syndrome does not seem to add any predictive value for clinical practice. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12933-016-0387-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-27 /pmc/articles/PMC4847340/ /pubmed/27117940 http://dx.doi.org/10.1186/s12933-016-0387-4 Text en © van Herpt et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Original Investigation van Herpt, Thijs T. W. Dehghan, Abbas van Hoek, Mandy Ikram, M. Arfan Hofman, Albert Sijbrands, Eric J. G. Franco, Oscar H. The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study |
title | The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study |
title_full | The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study |
title_fullStr | The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study |
title_full_unstemmed | The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study |
title_short | The clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the Rotterdam study |
title_sort | clinical value of metabolic syndrome and risks of cardiometabolic events and mortality in the elderly: the rotterdam study |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847340/ https://www.ncbi.nlm.nih.gov/pubmed/27117940 http://dx.doi.org/10.1186/s12933-016-0387-4 |
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