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Ectopic adiposity and cardiometabolic health in COPD

RATIONALE: Obesity/overweight is the most prevalent body composition abnormality in COPD. However, little is known about the impact of fat distribution on cardiometabolic health in COPD. OBJECTIVE: To study the associations between ectopic adiposity, cardiometabolic health, and COPD. METHODS: A tota...

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Autores principales: Coats, Valérie, Després, Jean-Pierre, Alméras, Natalie, Martin, Mickaël, Sin, Don D, Rabasa-Lhoret, Rémi, Larose, Éric, Tan, Wan C, Bourbeau, Jean, Maltais, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197246/
https://www.ncbi.nlm.nih.gov/pubmed/30410322
http://dx.doi.org/10.2147/COPD.S168963
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author Coats, Valérie
Després, Jean-Pierre
Alméras, Natalie
Martin, Mickaël
Sin, Don D
Rabasa-Lhoret, Rémi
Larose, Éric
Tan, Wan C
Bourbeau, Jean
Maltais, François
author_facet Coats, Valérie
Després, Jean-Pierre
Alméras, Natalie
Martin, Mickaël
Sin, Don D
Rabasa-Lhoret, Rémi
Larose, Éric
Tan, Wan C
Bourbeau, Jean
Maltais, François
author_sort Coats, Valérie
collection PubMed
description RATIONALE: Obesity/overweight is the most prevalent body composition abnormality in COPD. However, little is known about the impact of fat distribution on cardiometabolic health in COPD. OBJECTIVE: To study the associations between ectopic adiposity, cardiometabolic health, and COPD. METHODS: A total of 263 subjects (166 males; age=65±9 years) were randomly selected from the general population. Subjects were classified as non-COPD controls and COPD, according to the Global initiative for chronic Obstructive Lung Disease (GOLD) classification, and the presence of cardiometabolic comorbidities was recorded. Ectopic fat accumulation was documented from computed tomography measurements of visceral adipose tissue cross-sectional areas and muscle mean attenuation, assessed at L4–L5. Blood glucose, lipid, and adipokine profiles were also evaluated. RESULTS: After correcting for age, sex, and tobacco exposure, visceral adipose tissue cross-sectional area was higher in GOLD 2+ compared to GOLD 1 individuals. Consistent with this, mean muscle tissue attenuation was lower in GOLD 2+ vs GOLD 1 and non-COPD controls (P<0.001). In multiple regression models, visceral adipose tissue cross-sectional area was strongly associated with hypertension (P<0.001) and diabetes (P<0.001), while muscle attenuation was associated with coronary artery disease (P<0.001). Blood glucose, lipid, and adipokine profiles were similar across groups with the exception of leptin level which was higher in GOLD 2+ subjects compared to GOLD 1 and controls. CONCLUSION: GOLD 2+ COPD was associated with ectopic fat accumulation which modulated cardiometabolic health.
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spelling pubmed-61972462018-11-08 Ectopic adiposity and cardiometabolic health in COPD Coats, Valérie Després, Jean-Pierre Alméras, Natalie Martin, Mickaël Sin, Don D Rabasa-Lhoret, Rémi Larose, Éric Tan, Wan C Bourbeau, Jean Maltais, François Int J Chron Obstruct Pulmon Dis Original Research RATIONALE: Obesity/overweight is the most prevalent body composition abnormality in COPD. However, little is known about the impact of fat distribution on cardiometabolic health in COPD. OBJECTIVE: To study the associations between ectopic adiposity, cardiometabolic health, and COPD. METHODS: A total of 263 subjects (166 males; age=65±9 years) were randomly selected from the general population. Subjects were classified as non-COPD controls and COPD, according to the Global initiative for chronic Obstructive Lung Disease (GOLD) classification, and the presence of cardiometabolic comorbidities was recorded. Ectopic fat accumulation was documented from computed tomography measurements of visceral adipose tissue cross-sectional areas and muscle mean attenuation, assessed at L4–L5. Blood glucose, lipid, and adipokine profiles were also evaluated. RESULTS: After correcting for age, sex, and tobacco exposure, visceral adipose tissue cross-sectional area was higher in GOLD 2+ compared to GOLD 1 individuals. Consistent with this, mean muscle tissue attenuation was lower in GOLD 2+ vs GOLD 1 and non-COPD controls (P<0.001). In multiple regression models, visceral adipose tissue cross-sectional area was strongly associated with hypertension (P<0.001) and diabetes (P<0.001), while muscle attenuation was associated with coronary artery disease (P<0.001). Blood glucose, lipid, and adipokine profiles were similar across groups with the exception of leptin level which was higher in GOLD 2+ subjects compared to GOLD 1 and controls. CONCLUSION: GOLD 2+ COPD was associated with ectopic fat accumulation which modulated cardiometabolic health. Dove Medical Press 2018-10-15 /pmc/articles/PMC6197246/ /pubmed/30410322 http://dx.doi.org/10.2147/COPD.S168963 Text en © 2018 Coats et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Coats, Valérie
Després, Jean-Pierre
Alméras, Natalie
Martin, Mickaël
Sin, Don D
Rabasa-Lhoret, Rémi
Larose, Éric
Tan, Wan C
Bourbeau, Jean
Maltais, François
Ectopic adiposity and cardiometabolic health in COPD
title Ectopic adiposity and cardiometabolic health in COPD
title_full Ectopic adiposity and cardiometabolic health in COPD
title_fullStr Ectopic adiposity and cardiometabolic health in COPD
title_full_unstemmed Ectopic adiposity and cardiometabolic health in COPD
title_short Ectopic adiposity and cardiometabolic health in COPD
title_sort ectopic adiposity and cardiometabolic health in copd
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197246/
https://www.ncbi.nlm.nih.gov/pubmed/30410322
http://dx.doi.org/10.2147/COPD.S168963
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