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Adipokine Imbalance in the Pericardial Cavity of Cardiac and Vascular Disease Patients

AIM: Obesity and especially hypertrophy of epicardial adipose tissue accelerate coronary atherogenesis. We aimed at comparing levels of inflammatory and atherogenic hormones from adipose tissue in the pericardial fluid and circulation of cardiovascular disease patients. METHODS AND RESULTS: Venous p...

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Autores principales: Elie, Atlanta G. I. M., Jensen, Pia S., Nissen, Katrine D., Geraets, Ilvy M. E., Xu, Aimin, Song, Erfei, Hansen, Maria L., Irmukhamedov, Akhmadjon, Rasmussen, Lars M., Wang, Yu, De Mey, Jo G. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854456/
https://www.ncbi.nlm.nih.gov/pubmed/27139713
http://dx.doi.org/10.1371/journal.pone.0154693
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author Elie, Atlanta G. I. M.
Jensen, Pia S.
Nissen, Katrine D.
Geraets, Ilvy M. E.
Xu, Aimin
Song, Erfei
Hansen, Maria L.
Irmukhamedov, Akhmadjon
Rasmussen, Lars M.
Wang, Yu
De Mey, Jo G. R.
author_facet Elie, Atlanta G. I. M.
Jensen, Pia S.
Nissen, Katrine D.
Geraets, Ilvy M. E.
Xu, Aimin
Song, Erfei
Hansen, Maria L.
Irmukhamedov, Akhmadjon
Rasmussen, Lars M.
Wang, Yu
De Mey, Jo G. R.
author_sort Elie, Atlanta G. I. M.
collection PubMed
description AIM: Obesity and especially hypertrophy of epicardial adipose tissue accelerate coronary atherogenesis. We aimed at comparing levels of inflammatory and atherogenic hormones from adipose tissue in the pericardial fluid and circulation of cardiovascular disease patients. METHODS AND RESULTS: Venous plasma (P) and pericardial fluid (PF) were obtained from elective cardiothoracic surgery patients (n = 37). Concentrations of leptin, adipocyte fatty acid-binding protein (A-FABP) and adiponectin (APN) were determined by enzyme-linked immunosorbent assays (ELISA). The median concentration of leptin in PF (4.3 (interquartile range: 2.8–9.1) μg/L) was comparable to that in P (5.9 (2.2–11) μg/L) and these were significantly correlated to most of the same patient characteristics. The concentration of A-FABP was markedly higher (73 (28–124) versus 8.4 (5.2–14) μg/L) and that of APN was markedly lower (2.8 (1.7–4.2) versus 13 (7.2–19) mg/L) in PF compared to P. APN in PF was unlike in P not significantly related to age, body mass index, plasma triglycerides or coronary artery disease. PF levels of APN, but not A-FABP, were related to the size of paracardial adipocytes. PF levels of APN and A-FABP were not related to the immunoreactivity of paracardial adipocytes for these proteins. CONCLUSION: In cardiac and vascular disease patients, PF is enriched in A-FABP and poor in APN. This adipokine microenvironment is more likely determined by the heart than by the circulation or paracardial adipose tissue.
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spelling pubmed-48544562016-05-07 Adipokine Imbalance in the Pericardial Cavity of Cardiac and Vascular Disease Patients Elie, Atlanta G. I. M. Jensen, Pia S. Nissen, Katrine D. Geraets, Ilvy M. E. Xu, Aimin Song, Erfei Hansen, Maria L. Irmukhamedov, Akhmadjon Rasmussen, Lars M. Wang, Yu De Mey, Jo G. R. PLoS One Research Article AIM: Obesity and especially hypertrophy of epicardial adipose tissue accelerate coronary atherogenesis. We aimed at comparing levels of inflammatory and atherogenic hormones from adipose tissue in the pericardial fluid and circulation of cardiovascular disease patients. METHODS AND RESULTS: Venous plasma (P) and pericardial fluid (PF) were obtained from elective cardiothoracic surgery patients (n = 37). Concentrations of leptin, adipocyte fatty acid-binding protein (A-FABP) and adiponectin (APN) were determined by enzyme-linked immunosorbent assays (ELISA). The median concentration of leptin in PF (4.3 (interquartile range: 2.8–9.1) μg/L) was comparable to that in P (5.9 (2.2–11) μg/L) and these were significantly correlated to most of the same patient characteristics. The concentration of A-FABP was markedly higher (73 (28–124) versus 8.4 (5.2–14) μg/L) and that of APN was markedly lower (2.8 (1.7–4.2) versus 13 (7.2–19) mg/L) in PF compared to P. APN in PF was unlike in P not significantly related to age, body mass index, plasma triglycerides or coronary artery disease. PF levels of APN, but not A-FABP, were related to the size of paracardial adipocytes. PF levels of APN and A-FABP were not related to the immunoreactivity of paracardial adipocytes for these proteins. CONCLUSION: In cardiac and vascular disease patients, PF is enriched in A-FABP and poor in APN. This adipokine microenvironment is more likely determined by the heart than by the circulation or paracardial adipose tissue. Public Library of Science 2016-05-03 /pmc/articles/PMC4854456/ /pubmed/27139713 http://dx.doi.org/10.1371/journal.pone.0154693 Text en © 2016 Elie et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Elie, Atlanta G. I. M.
Jensen, Pia S.
Nissen, Katrine D.
Geraets, Ilvy M. E.
Xu, Aimin
Song, Erfei
Hansen, Maria L.
Irmukhamedov, Akhmadjon
Rasmussen, Lars M.
Wang, Yu
De Mey, Jo G. R.
Adipokine Imbalance in the Pericardial Cavity of Cardiac and Vascular Disease Patients
title Adipokine Imbalance in the Pericardial Cavity of Cardiac and Vascular Disease Patients
title_full Adipokine Imbalance in the Pericardial Cavity of Cardiac and Vascular Disease Patients
title_fullStr Adipokine Imbalance in the Pericardial Cavity of Cardiac and Vascular Disease Patients
title_full_unstemmed Adipokine Imbalance in the Pericardial Cavity of Cardiac and Vascular Disease Patients
title_short Adipokine Imbalance in the Pericardial Cavity of Cardiac and Vascular Disease Patients
title_sort adipokine imbalance in the pericardial cavity of cardiac and vascular disease patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854456/
https://www.ncbi.nlm.nih.gov/pubmed/27139713
http://dx.doi.org/10.1371/journal.pone.0154693
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