Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting

Detalhes bibliográficos
Autor(a) principal: Zhou, Guanghui
Data de Publicação: 2019
Outros Autores: Gui, Xianhua, Chen, Ruhua, Fu, Xingli, Ji, Xiuhai, Ding, Hui
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/159503
Resumo: OBJECTIVE: Muscle wasting contributes to the reduced quality of life and increased mortality in chronic obstructive pulmonary disease (COPD). Muscle atrophy in mice with cachexia was caused by Activin A binding to ActRIIB. The role of circulating Activin A leading to muscle atrophy in COPD remains elusive. METHODS: In the present study, we evaluated the relationship between serum levels of Activin A and skeletal muscle wasting in COPD patients. The expression levels of serum Activin A were measured in 78 stable COPD patients and in 60 healthy controls via ELISA, which was also used to determine the expression of circulating TNF-a levels. Total skeletal muscle mass (SMM) was calculated according to a validated formula by age and anthropometric measurements. The fat-free mass index (FFMI) was determined as the fat-free mass (FFM) corrected for body surface area. RESULTS: Compared to the healthy controls, COPD patients had upregulated Activin A expression. The elevated levels of Activin A were correlated with TNF-a expression, while total SMM and FFMI were significantly decreased in COPD patients. Furthermore, serum Activin A expression in COPD patients was negatively associated with both FFMI and BMI. CONCLUSION: The above results showed an association between increased circulating Activin A in COPD patients and the presence of muscle atrophy. Given our previous knowledge, we speculate that Activin A contributes to skeletal muscle wasting in COPD.
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spelling Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wastingCOPDSkeletal MuscleActivin AOBJECTIVE: Muscle wasting contributes to the reduced quality of life and increased mortality in chronic obstructive pulmonary disease (COPD). Muscle atrophy in mice with cachexia was caused by Activin A binding to ActRIIB. The role of circulating Activin A leading to muscle atrophy in COPD remains elusive. METHODS: In the present study, we evaluated the relationship between serum levels of Activin A and skeletal muscle wasting in COPD patients. The expression levels of serum Activin A were measured in 78 stable COPD patients and in 60 healthy controls via ELISA, which was also used to determine the expression of circulating TNF-a levels. Total skeletal muscle mass (SMM) was calculated according to a validated formula by age and anthropometric measurements. The fat-free mass index (FFMI) was determined as the fat-free mass (FFM) corrected for body surface area. RESULTS: Compared to the healthy controls, COPD patients had upregulated Activin A expression. The elevated levels of Activin A were correlated with TNF-a expression, while total SMM and FFMI were significantly decreased in COPD patients. Furthermore, serum Activin A expression in COPD patients was negatively associated with both FFMI and BMI. CONCLUSION: The above results showed an association between increased circulating Activin A in COPD patients and the presence of muscle atrophy. Given our previous knowledge, we speculate that Activin A contributes to skeletal muscle wasting in COPD.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2019-06-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/xmlhttps://www.revistas.usp.br/clinics/article/view/15950310.6061/clinics/2019/e981Clinics; Vol. 74 (2019); e981Clinics; v. 74 (2019); e981Clinics; Vol. 74 (2019); e9811980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/159503/154276https://www.revistas.usp.br/clinics/article/view/159503/154277Copyright (c) 2019 Clinicsinfo:eu-repo/semantics/openAccessZhou, GuanghuiGui, XianhuaChen, RuhuaFu, XingliJi, XiuhaiDing, Hui2019-06-28T19:30:14Zoai:revistas.usp.br:article/159503Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2019-06-28T19:30:14Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting
title Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting
spellingShingle Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting
Zhou, Guanghui
COPD
Skeletal Muscle
Activin A
title_short Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting
title_full Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting
title_fullStr Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting
title_full_unstemmed Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting
title_sort Elevated serum Activin A in chronic obstructive pulmonary disease with skeletal muscle wasting
author Zhou, Guanghui
author_facet Zhou, Guanghui
Gui, Xianhua
Chen, Ruhua
Fu, Xingli
Ji, Xiuhai
Ding, Hui
author_role author
author2 Gui, Xianhua
Chen, Ruhua
Fu, Xingli
Ji, Xiuhai
Ding, Hui
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Zhou, Guanghui
Gui, Xianhua
Chen, Ruhua
Fu, Xingli
Ji, Xiuhai
Ding, Hui
dc.subject.por.fl_str_mv COPD
Skeletal Muscle
Activin A
topic COPD
Skeletal Muscle
Activin A
description OBJECTIVE: Muscle wasting contributes to the reduced quality of life and increased mortality in chronic obstructive pulmonary disease (COPD). Muscle atrophy in mice with cachexia was caused by Activin A binding to ActRIIB. The role of circulating Activin A leading to muscle atrophy in COPD remains elusive. METHODS: In the present study, we evaluated the relationship between serum levels of Activin A and skeletal muscle wasting in COPD patients. The expression levels of serum Activin A were measured in 78 stable COPD patients and in 60 healthy controls via ELISA, which was also used to determine the expression of circulating TNF-a levels. Total skeletal muscle mass (SMM) was calculated according to a validated formula by age and anthropometric measurements. The fat-free mass index (FFMI) was determined as the fat-free mass (FFM) corrected for body surface area. RESULTS: Compared to the healthy controls, COPD patients had upregulated Activin A expression. The elevated levels of Activin A were correlated with TNF-a expression, while total SMM and FFMI were significantly decreased in COPD patients. Furthermore, serum Activin A expression in COPD patients was negatively associated with both FFMI and BMI. CONCLUSION: The above results showed an association between increased circulating Activin A in COPD patients and the presence of muscle atrophy. Given our previous knowledge, we speculate that Activin A contributes to skeletal muscle wasting in COPD.
publishDate 2019
dc.date.none.fl_str_mv 2019-06-28
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/159503
10.6061/clinics/2019/e981
url https://www.revistas.usp.br/clinics/article/view/159503
identifier_str_mv 10.6061/clinics/2019/e981
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/159503/154276
https://www.revistas.usp.br/clinics/article/view/159503/154277
dc.rights.driver.fl_str_mv Copyright (c) 2019 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2019 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/xml
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 74 (2019); e981
Clinics; v. 74 (2019); e981
Clinics; Vol. 74 (2019); e981
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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