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Skeletal Myosteatosis is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD

BACKGROUND: Common features among patients with more advanced chronic obstructive pulmonary disease (COPD) are systemic inflammation and a loss of both muscle mass and normal muscle composition. In the present study, we investigated COPD subjects to better understand how thigh muscle fat infiltratio...

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Autores principales: Persson, Hans Lennart, Sioutas, Apostolos, Kentson, Magnus, Jacobson, Petra, Lundberg, Peter, Dahlqvist Leinhard, Olof, Forsgren, Mikael Fredrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9355337/
https://www.ncbi.nlm.nih.gov/pubmed/35937916
http://dx.doi.org/10.2147/JIR.S366204
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author Persson, Hans Lennart
Sioutas, Apostolos
Kentson, Magnus
Jacobson, Petra
Lundberg, Peter
Dahlqvist Leinhard, Olof
Forsgren, Mikael Fredrik
author_facet Persson, Hans Lennart
Sioutas, Apostolos
Kentson, Magnus
Jacobson, Petra
Lundberg, Peter
Dahlqvist Leinhard, Olof
Forsgren, Mikael Fredrik
author_sort Persson, Hans Lennart
collection PubMed
description BACKGROUND: Common features among patients with more advanced chronic obstructive pulmonary disease (COPD) are systemic inflammation and a loss of both muscle mass and normal muscle composition. In the present study, we investigated COPD subjects to better understand how thigh muscle fat infiltration (MFI) and energy metabolism relate to each other and to clinical features of COPD with emphasis on systemic inflammation. METHODS: Thirty-two Caucasians with stable COPD were investigated using questionnaires, lung function tests, blood analysis and magnetic resonance imaging (MRI) for analysis of body- and thigh muscle composition. Bioenergetics in the resting thigh muscle, expressed as the PCr/Pi ratio, were analysed using (31)phosphorus magnetic resonance spectroscopy ((31)P-MRS). RESULTS: Based on the combination of the MFI adjusted for sex (MFI(a)) and the thigh fat-tissue free muscle volume, expressed as the deviation from the expected muscle volume of a matched virtual control group (FFMV(vcg)), all COPD subjects displayed abnormally composed thigh muscles. Clinical features of increased COPD severity, including a decrease of blood oxygenation (r = −0.44, p < 0.05) and FEV(1)/FVC ratio, reflecting airway obstruction (r = −0.53, p < 0.01) and an increase of COPD symptoms (r = 0.37, p < 0.05) and breathing frequency at rest (r = 0.41, p < 0.05), were all associated with a raise of the PCr/Pi ratio in the thigh muscle. Increased MFI(a) of the thigh muscle correlated positively with markers of systemic inflammation (white blood cell count, r = 0.41, p < 0.05; fibrinogen, r = 0.44, p < 0.05), and negatively with weekly physical activity (r = −0.40, p < 0.05) and the PCr/Pi ratio in the resting thigh muscle (r = −0.41, p < 0.05). CONCLUSION: The present study implies a link between systemic inflammation, excessive MFI and a loss of bioenergetics in subjects with stable COPD.
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spelling pubmed-93553372022-08-06 Skeletal Myosteatosis is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD Persson, Hans Lennart Sioutas, Apostolos Kentson, Magnus Jacobson, Petra Lundberg, Peter Dahlqvist Leinhard, Olof Forsgren, Mikael Fredrik J Inflamm Res Original Research BACKGROUND: Common features among patients with more advanced chronic obstructive pulmonary disease (COPD) are systemic inflammation and a loss of both muscle mass and normal muscle composition. In the present study, we investigated COPD subjects to better understand how thigh muscle fat infiltration (MFI) and energy metabolism relate to each other and to clinical features of COPD with emphasis on systemic inflammation. METHODS: Thirty-two Caucasians with stable COPD were investigated using questionnaires, lung function tests, blood analysis and magnetic resonance imaging (MRI) for analysis of body- and thigh muscle composition. Bioenergetics in the resting thigh muscle, expressed as the PCr/Pi ratio, were analysed using (31)phosphorus magnetic resonance spectroscopy ((31)P-MRS). RESULTS: Based on the combination of the MFI adjusted for sex (MFI(a)) and the thigh fat-tissue free muscle volume, expressed as the deviation from the expected muscle volume of a matched virtual control group (FFMV(vcg)), all COPD subjects displayed abnormally composed thigh muscles. Clinical features of increased COPD severity, including a decrease of blood oxygenation (r = −0.44, p < 0.05) and FEV(1)/FVC ratio, reflecting airway obstruction (r = −0.53, p < 0.01) and an increase of COPD symptoms (r = 0.37, p < 0.05) and breathing frequency at rest (r = 0.41, p < 0.05), were all associated with a raise of the PCr/Pi ratio in the thigh muscle. Increased MFI(a) of the thigh muscle correlated positively with markers of systemic inflammation (white blood cell count, r = 0.41, p < 0.05; fibrinogen, r = 0.44, p < 0.05), and negatively with weekly physical activity (r = −0.40, p < 0.05) and the PCr/Pi ratio in the resting thigh muscle (r = −0.41, p < 0.05). CONCLUSION: The present study implies a link between systemic inflammation, excessive MFI and a loss of bioenergetics in subjects with stable COPD. Dove 2022-08-01 /pmc/articles/PMC9355337/ /pubmed/35937916 http://dx.doi.org/10.2147/JIR.S366204 Text en © 2022 Persson et al. https://creativecommons.org/licenses/by-nc/3.0/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/ (https://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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Persson, Hans Lennart
Sioutas, Apostolos
Kentson, Magnus
Jacobson, Petra
Lundberg, Peter
Dahlqvist Leinhard, Olof
Forsgren, Mikael Fredrik
Skeletal Myosteatosis is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD
title Skeletal Myosteatosis is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD
title_full Skeletal Myosteatosis is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD
title_fullStr Skeletal Myosteatosis is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD
title_full_unstemmed Skeletal Myosteatosis is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD
title_short Skeletal Myosteatosis is Associated with Systemic Inflammation and a Loss of Muscle Bioenergetics in Stable COPD
title_sort skeletal myosteatosis is associated with systemic inflammation and a loss of muscle bioenergetics in stable copd
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9355337/
https://www.ncbi.nlm.nih.gov/pubmed/35937916
http://dx.doi.org/10.2147/JIR.S366204
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