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Association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease

BACKGROUND: This is an observational study undertaken in aim to evaluate the association between metabolic syndrome (MS) and high homocysteinemia (HHcy) in relation with cardiovascular disease (CVD). METHODS: The study involved 126 subjects with angiographically documented CVD and 65 healthy subject...

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Detalles Bibliográficos
Autores principales: Bellia, Chiara, Bivona, Giulia, Scazzone, Concetta, Ciaccio, Marcello
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2387296/
https://www.ncbi.nlm.nih.gov/pubmed/18516267
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author Bellia, Chiara
Bivona, Giulia
Scazzone, Concetta
Ciaccio, Marcello
author_facet Bellia, Chiara
Bivona, Giulia
Scazzone, Concetta
Ciaccio, Marcello
author_sort Bellia, Chiara
collection PubMed
description BACKGROUND: This is an observational study undertaken in aim to evaluate the association between metabolic syndrome (MS) and high homocysteinemia (HHcy) in relation with cardiovascular disease (CVD). METHODS: The study involved 126 subjects with angiographically documented CVD and 65 healthy subjects. MS has been diagnosed according to the ATP III criteria and plasma homocysteine concentration has been evaluated. RESULTS: In patients with CVD the prevalence of MS and HHcy is 17.4% and 25.4% respectively; MS coexists with HHcy in 67.2% of patients; analogous results can be observed among men and women. HHcy and MS are associated with CVD (OR 2.53, 95% CI 1.95–12.43 and OR 5.74, 95% CI 2.67–12.34 respectively) but the presence of the two conditions gives rise to a stronger increase in CVD risk (OR 13.11, 95% CI 5.27–32.06). CONCLUSIONS: Our data suggest that HHcy and MS could work together in increasing CVD risk.
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spelling pubmed-23872962008-05-30 Association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease Bellia, Chiara Bivona, Giulia Scazzone, Concetta Ciaccio, Marcello Ther Clin Risk Manag Original Research BACKGROUND: This is an observational study undertaken in aim to evaluate the association between metabolic syndrome (MS) and high homocysteinemia (HHcy) in relation with cardiovascular disease (CVD). METHODS: The study involved 126 subjects with angiographically documented CVD and 65 healthy subjects. MS has been diagnosed according to the ATP III criteria and plasma homocysteine concentration has been evaluated. RESULTS: In patients with CVD the prevalence of MS and HHcy is 17.4% and 25.4% respectively; MS coexists with HHcy in 67.2% of patients; analogous results can be observed among men and women. HHcy and MS are associated with CVD (OR 2.53, 95% CI 1.95–12.43 and OR 5.74, 95% CI 2.67–12.34 respectively) but the presence of the two conditions gives rise to a stronger increase in CVD risk (OR 13.11, 95% CI 5.27–32.06). CONCLUSIONS: Our data suggest that HHcy and MS could work together in increasing CVD risk. Dove Medical Press 2007-12 2007-12 /pmc/articles/PMC2387296/ /pubmed/18516267 Text en © 2007 Dove Medical Press Limited. All rights reserved
spellingShingle Original Research
Bellia, Chiara
Bivona, Giulia
Scazzone, Concetta
Ciaccio, Marcello
Association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease
title Association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease
title_full Association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease
title_fullStr Association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease
title_full_unstemmed Association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease
title_short Association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease
title_sort association between homocysteinemia and metabolic syndrome in patients with cardiovascular disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2387296/
https://www.ncbi.nlm.nih.gov/pubmed/18516267
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