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Chest adipose tissue distribution in patients with morbid obesity
PURPOSE: Obesity is a well-known of risk factor for atherosclerosis and the amount of visceral adipose tissue is considered as an independent predictor of coronary artery disease (CAD). An aim of the study was to investigate the distribution of intrathoracic adipose tissue in morbidly obese patients...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047076/ https://www.ncbi.nlm.nih.gov/pubmed/30038681 http://dx.doi.org/10.5114/pjr.2018.73406 |
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author | Lemanowicz, Adam Leszczyński, Waldemar Rusak, Grażyna Białecki, Marcin Ratajczak, Przemysław |
author_facet | Lemanowicz, Adam Leszczyński, Waldemar Rusak, Grażyna Białecki, Marcin Ratajczak, Przemysław |
author_sort | Lemanowicz, Adam |
collection | PubMed |
description | PURPOSE: Obesity is a well-known of risk factor for atherosclerosis and the amount of visceral adipose tissue is considered as an independent predictor of coronary artery disease (CAD). An aim of the study was to investigate the distribution of intrathoracic adipose tissue in morbidly obese patients. MATERIAL AND METHODS: Fifty-one patients with morbid obesity (BMI ≥ 40 kg/m(2)) and thirty controls were scanned in a coronary calcium scoring protocol. Control group consisted of patients scanned due to a clinical suspicion of CAD, who did not fulfill obesity criteria. The amount of adipose tissue was measured as epicardial adipose tissue (EAT) thickness, pericoronary fat (PCF) thickness, total intra-pericardial fat (IPF) volume, and total intrathoracic fat (ITF) volume. RESULTS: Mean BMI of obese patients and controls was 47.3 and 26.5, respectively (p < 0.0001). Patients with obesity and controls did not differ with respect to mean EAT, mean PCF, and IPF. However, ITF was lower in obesity group than in control group (268 vs. 332 cm(3), respectively; p < 0.03). Moreover, ROC analysis presented relation between obesity and the superior EAT thickness, PCF at LCX, mean PCF, ITF, and chest soft tissue (CST) thickness (p < 0.03). CST thickness of > 60 mm was the parameter that presented the strongest association with morbid obesity (AUC 0.95; p < 0.0001). CONLCUSIONS: Increased chest soft tissue thickness but not the increased intrathoracic adipose tissue volume was associated with morbid obesity. Since the quantity of the pericardiac fat is not directly related to the obesity, its accumulation may be related to a mechanism different than that of subcutaneous adipose tissue growth. |
format | Online Article Text |
id | pubmed-6047076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-60470762018-07-23 Chest adipose tissue distribution in patients with morbid obesity Lemanowicz, Adam Leszczyński, Waldemar Rusak, Grażyna Białecki, Marcin Ratajczak, Przemysław Pol J Radiol Original Paper PURPOSE: Obesity is a well-known of risk factor for atherosclerosis and the amount of visceral adipose tissue is considered as an independent predictor of coronary artery disease (CAD). An aim of the study was to investigate the distribution of intrathoracic adipose tissue in morbidly obese patients. MATERIAL AND METHODS: Fifty-one patients with morbid obesity (BMI ≥ 40 kg/m(2)) and thirty controls were scanned in a coronary calcium scoring protocol. Control group consisted of patients scanned due to a clinical suspicion of CAD, who did not fulfill obesity criteria. The amount of adipose tissue was measured as epicardial adipose tissue (EAT) thickness, pericoronary fat (PCF) thickness, total intra-pericardial fat (IPF) volume, and total intrathoracic fat (ITF) volume. RESULTS: Mean BMI of obese patients and controls was 47.3 and 26.5, respectively (p < 0.0001). Patients with obesity and controls did not differ with respect to mean EAT, mean PCF, and IPF. However, ITF was lower in obesity group than in control group (268 vs. 332 cm(3), respectively; p < 0.03). Moreover, ROC analysis presented relation between obesity and the superior EAT thickness, PCF at LCX, mean PCF, ITF, and chest soft tissue (CST) thickness (p < 0.03). CST thickness of > 60 mm was the parameter that presented the strongest association with morbid obesity (AUC 0.95; p < 0.0001). CONLCUSIONS: Increased chest soft tissue thickness but not the increased intrathoracic adipose tissue volume was associated with morbid obesity. Since the quantity of the pericardiac fat is not directly related to the obesity, its accumulation may be related to a mechanism different than that of subcutaneous adipose tissue growth. Termedia Publishing House 2018-02-12 /pmc/articles/PMC6047076/ /pubmed/30038681 http://dx.doi.org/10.5114/pjr.2018.73406 Text en Copyright © Polish Medical Society of Radiology 2018 https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0). License allowing third parties to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially. |
spellingShingle | Original Paper Lemanowicz, Adam Leszczyński, Waldemar Rusak, Grażyna Białecki, Marcin Ratajczak, Przemysław Chest adipose tissue distribution in patients with morbid obesity |
title | Chest adipose tissue distribution in patients with morbid obesity |
title_full | Chest adipose tissue distribution in patients with morbid obesity |
title_fullStr | Chest adipose tissue distribution in patients with morbid obesity |
title_full_unstemmed | Chest adipose tissue distribution in patients with morbid obesity |
title_short | Chest adipose tissue distribution in patients with morbid obesity |
title_sort | chest adipose tissue distribution in patients with morbid obesity |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047076/ https://www.ncbi.nlm.nih.gov/pubmed/30038681 http://dx.doi.org/10.5114/pjr.2018.73406 |
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