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Influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate

INTRODUCTION: Familial combined hyperlipoproteinemia (FCHL) is a very common and aggressive genetic mixed hyperlipoproteinemia, with many features similar to that of the metabolic syndrome (MS). We aimed to evaluate whether the presence of the MS per se could account for a significant part of the el...

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Autores principales: Cicero, Arrigo F.G., Derosa, Giuseppe, Maffioli, Pamela, Reggi, Alessandra, Grandi, Elisa, Borghi, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648832/
https://www.ncbi.nlm.nih.gov/pubmed/23671433
http://dx.doi.org/10.5114/aoms.2013.34537
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author Cicero, Arrigo F.G.
Derosa, Giuseppe
Maffioli, Pamela
Reggi, Alessandra
Grandi, Elisa
Borghi, Claudio
author_facet Cicero, Arrigo F.G.
Derosa, Giuseppe
Maffioli, Pamela
Reggi, Alessandra
Grandi, Elisa
Borghi, Claudio
author_sort Cicero, Arrigo F.G.
collection PubMed
description INTRODUCTION: Familial combined hyperlipoproteinemia (FCHL) is a very common and aggressive genetic mixed hyperlipoproteinemia, with many features similar to that of the metabolic syndrome (MS). We aimed to evaluate whether the presence of the MS per se could account for a significant part of the elevated cardiovascular disease (CVD) risk associated with FCHL. MATERIAL AND METHODS: A retrospective cross-sectional evaluation of MS features’ influence on CVD prevalence in a large sample of adult Italian FCHL affected patients (64 familial clusters; 867 subjects) was carried out. RESULTS: Age is associated with early cardiovascular complications, both in men (OR 1.08, 95% CI: 1.05-1.11, p < 0.0001) and in women (OR 1.09, 95% CI: 1.04-1.13, p = 0.0001). No MS component appears to be related to cardiovascular complications in men, whilst only low plasma high-density lipoprotein cholesterol (HDL-C) shows such a relation in women. Among non-MS parameters, only low-density lipoprotein cholesterol (LDL-C) and lipoprotein(a) (Lp(a)) plasma levels are significantly associated with early cardiovascular complications in male FCHL patients (LDL-C: OR 2.24, 95% CI: 1.02-4.91, p = 0.04; Lp(a): OR 4.64, 95% CI: 1.85-11.62, p = 0.001), but not in women (LDL-C: OR 1.83, 95% CI 0.53-6.34, p = 0.34; Lp(a): OR 3.65, 95% CI: 0.89-14.97, p = 0.07). CONCLUSIONS: Our data support the hypothesis that MS is not associated with a higher prevalence of cardiovascular complications in FCHL affected subjects, probably because of the strongest risk increase associated with the FCHL itself.
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spelling pubmed-36488322013-05-13 Influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate Cicero, Arrigo F.G. Derosa, Giuseppe Maffioli, Pamela Reggi, Alessandra Grandi, Elisa Borghi, Claudio Arch Med Sci Clinical Research INTRODUCTION: Familial combined hyperlipoproteinemia (FCHL) is a very common and aggressive genetic mixed hyperlipoproteinemia, with many features similar to that of the metabolic syndrome (MS). We aimed to evaluate whether the presence of the MS per se could account for a significant part of the elevated cardiovascular disease (CVD) risk associated with FCHL. MATERIAL AND METHODS: A retrospective cross-sectional evaluation of MS features’ influence on CVD prevalence in a large sample of adult Italian FCHL affected patients (64 familial clusters; 867 subjects) was carried out. RESULTS: Age is associated with early cardiovascular complications, both in men (OR 1.08, 95% CI: 1.05-1.11, p < 0.0001) and in women (OR 1.09, 95% CI: 1.04-1.13, p = 0.0001). No MS component appears to be related to cardiovascular complications in men, whilst only low plasma high-density lipoprotein cholesterol (HDL-C) shows such a relation in women. Among non-MS parameters, only low-density lipoprotein cholesterol (LDL-C) and lipoprotein(a) (Lp(a)) plasma levels are significantly associated with early cardiovascular complications in male FCHL patients (LDL-C: OR 2.24, 95% CI: 1.02-4.91, p = 0.04; Lp(a): OR 4.64, 95% CI: 1.85-11.62, p = 0.001), but not in women (LDL-C: OR 1.83, 95% CI 0.53-6.34, p = 0.34; Lp(a): OR 3.65, 95% CI: 0.89-14.97, p = 0.07). CONCLUSIONS: Our data support the hypothesis that MS is not associated with a higher prevalence of cardiovascular complications in FCHL affected subjects, probably because of the strongest risk increase associated with the FCHL itself. Termedia Publishing House 2013-04-09 2013-04-20 /pmc/articles/PMC3648832/ /pubmed/23671433 http://dx.doi.org/10.5114/aoms.2013.34537 Text en Copyright © 2013 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
Cicero, Arrigo F.G.
Derosa, Giuseppe
Maffioli, Pamela
Reggi, Alessandra
Grandi, Elisa
Borghi, Claudio
Influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate
title Influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate
title_full Influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate
title_fullStr Influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate
title_full_unstemmed Influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate
title_short Influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate
title_sort influence of metabolic syndrome superposition on familial combined hyperlipoproteinemia cardiovascular complication rate
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648832/
https://www.ncbi.nlm.nih.gov/pubmed/23671433
http://dx.doi.org/10.5114/aoms.2013.34537
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