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Cardiac steatosis and left ventricular function in men with metabolic syndrome
BACKGROUND: Ectopic accumulation of fat accompanies visceral obesity with detrimental effects. Lipid oversupply to cardiomyocytes leads to cardiac steatosis, and in animal studies lipotoxicity has been associated with impaired left ventricular (LV) function. In humans, studies have yielded inconclus...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842676/ https://www.ncbi.nlm.nih.gov/pubmed/24228979 http://dx.doi.org/10.1186/1532-429X-15-103 |
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author | Nyman, Kristofer Granér, Marit Pentikäinen, Markku O Lundbom, Jesper Hakkarainen, Antti Sirén, Reijo Nieminen, Markku S Taskinen, Marja-Riitta Lundbom, Nina Lauerma, Kirsi |
author_facet | Nyman, Kristofer Granér, Marit Pentikäinen, Markku O Lundbom, Jesper Hakkarainen, Antti Sirén, Reijo Nieminen, Markku S Taskinen, Marja-Riitta Lundbom, Nina Lauerma, Kirsi |
author_sort | Nyman, Kristofer |
collection | PubMed |
description | BACKGROUND: Ectopic accumulation of fat accompanies visceral obesity with detrimental effects. Lipid oversupply to cardiomyocytes leads to cardiac steatosis, and in animal studies lipotoxicity has been associated with impaired left ventricular (LV) function. In humans, studies have yielded inconclusive results. The aim of the study was to evaluate the role of epicardial, pericardial and myocardial fat depots on LV structure and function in male subjects with metabolic syndrome (MetS). METHODS: A study population of 37 men with MetS and 38 men without MetS underwent cardiovascular magnetic resonance and proton magnetic spectroscopy at 1.5 T to assess LV function, epicardial and pericardial fat area and myocardial triglyceride (TG) content. RESULTS: All three fat deposits were greater in the MetS than in the control group (p <0.001). LV diastolic dysfunction was associated with MetS as measured by absolute (471 mL/s vs. 667 mL/s, p = 0.002) and normalized (3.37 s(-1) vs. 3.75 s(-1), p = 0.02) LV early diastolic peak filling rate and the ratio of early diastole (68% vs. 78%, p = 0.001). The amount of epicardial and pericardial fat correlated inversely with LV diastolic function. However, myocardial TG content was not independently associated with LV diastolic dysfunction. CONCLUSIONS: In MetS, accumulation of epicardial and pericardial fat is linked to the severity of structural and functional alterations of the heart. The role of increased intramyocardial TG in MetS is more complex and merits further study. |
format | Online Article Text |
id | pubmed-3842676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38426762013-11-29 Cardiac steatosis and left ventricular function in men with metabolic syndrome Nyman, Kristofer Granér, Marit Pentikäinen, Markku O Lundbom, Jesper Hakkarainen, Antti Sirén, Reijo Nieminen, Markku S Taskinen, Marja-Riitta Lundbom, Nina Lauerma, Kirsi J Cardiovasc Magn Reson Research BACKGROUND: Ectopic accumulation of fat accompanies visceral obesity with detrimental effects. Lipid oversupply to cardiomyocytes leads to cardiac steatosis, and in animal studies lipotoxicity has been associated with impaired left ventricular (LV) function. In humans, studies have yielded inconclusive results. The aim of the study was to evaluate the role of epicardial, pericardial and myocardial fat depots on LV structure and function in male subjects with metabolic syndrome (MetS). METHODS: A study population of 37 men with MetS and 38 men without MetS underwent cardiovascular magnetic resonance and proton magnetic spectroscopy at 1.5 T to assess LV function, epicardial and pericardial fat area and myocardial triglyceride (TG) content. RESULTS: All three fat deposits were greater in the MetS than in the control group (p <0.001). LV diastolic dysfunction was associated with MetS as measured by absolute (471 mL/s vs. 667 mL/s, p = 0.002) and normalized (3.37 s(-1) vs. 3.75 s(-1), p = 0.02) LV early diastolic peak filling rate and the ratio of early diastole (68% vs. 78%, p = 0.001). The amount of epicardial and pericardial fat correlated inversely with LV diastolic function. However, myocardial TG content was not independently associated with LV diastolic dysfunction. CONCLUSIONS: In MetS, accumulation of epicardial and pericardial fat is linked to the severity of structural and functional alterations of the heart. The role of increased intramyocardial TG in MetS is more complex and merits further study. BioMed Central 2013-11-14 /pmc/articles/PMC3842676/ /pubmed/24228979 http://dx.doi.org/10.1186/1532-429X-15-103 Text en Copyright © 2013 Nyman et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Nyman, Kristofer Granér, Marit Pentikäinen, Markku O Lundbom, Jesper Hakkarainen, Antti Sirén, Reijo Nieminen, Markku S Taskinen, Marja-Riitta Lundbom, Nina Lauerma, Kirsi Cardiac steatosis and left ventricular function in men with metabolic syndrome |
title | Cardiac steatosis and left ventricular function in men with metabolic syndrome |
title_full | Cardiac steatosis and left ventricular function in men with metabolic syndrome |
title_fullStr | Cardiac steatosis and left ventricular function in men with metabolic syndrome |
title_full_unstemmed | Cardiac steatosis and left ventricular function in men with metabolic syndrome |
title_short | Cardiac steatosis and left ventricular function in men with metabolic syndrome |
title_sort | cardiac steatosis and left ventricular function in men with metabolic syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842676/ https://www.ncbi.nlm.nih.gov/pubmed/24228979 http://dx.doi.org/10.1186/1532-429X-15-103 |
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