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The clinical implication of serum cyclophilin A in patients with chronic obstructive pulmonary disease
BACKGROUND: Cyclophilin A (CyPA) is a secreted molecule that is regulated by inflammatory stimuli. Although inflammation has an important role in the pathogenesis of chronic obstructive pulmonary disease (COPD), little is known regarding the relationship between serum CyPA and COPD. METHODS: Ninety-...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783015/ https://www.ncbi.nlm.nih.gov/pubmed/29403273 http://dx.doi.org/10.2147/COPD.S152898 |
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author | Zhang, Ming Tang, Jingjing Yin, Jiafeng Wang, Xiaoying Feng, Xiangli Yang, Xia Shan, Hu Zhang, Qiuhong Zhang, Jie Li, Yali |
author_facet | Zhang, Ming Tang, Jingjing Yin, Jiafeng Wang, Xiaoying Feng, Xiangli Yang, Xia Shan, Hu Zhang, Qiuhong Zhang, Jie Li, Yali |
author_sort | Zhang, Ming |
collection | PubMed |
description | BACKGROUND: Cyclophilin A (CyPA) is a secreted molecule that is regulated by inflammatory stimuli. Although inflammation has an important role in the pathogenesis of chronic obstructive pulmonary disease (COPD), little is known regarding the relationship between serum CyPA and COPD. METHODS: Ninety-three COPD patients with acute exacerbation were enrolled in the study and were reassessed during the convalescence phase. Eighty-eight controls were matched for age, gender, body mass index, smoking index and comorbidity. The basic clinical information and pulmonary function of all participants were collected. Serum levels of CyPA and other inflammation indexes were further measured. RESULTS: Serum CyPA was significantly increased in convalescent COPD patients compared to healthy controls, and further elevated in COPD patients with acute exacerbation. Serum CyPA positively correlated with serum interleukin-6, matrix metalloproteinase-9 and high-sensitivity C-reactive protein in both the exacerbation and convalescence phases of COPD. Furthermore, it negatively correlated with percent value of forced expiratory volume in 1 second (FEV(1)%) predicted and FEV(1)/forced vital capacity in convalescent COPD patients. CONCLUSION: These results suggest that serum CyPA can be used as a potential inflammatory biomarker for COPD and assessment of serum CyPA may reflect the severity of inflammation in COPD. |
format | Online Article Text |
id | pubmed-5783015 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57830152018-02-05 The clinical implication of serum cyclophilin A in patients with chronic obstructive pulmonary disease Zhang, Ming Tang, Jingjing Yin, Jiafeng Wang, Xiaoying Feng, Xiangli Yang, Xia Shan, Hu Zhang, Qiuhong Zhang, Jie Li, Yali Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND: Cyclophilin A (CyPA) is a secreted molecule that is regulated by inflammatory stimuli. Although inflammation has an important role in the pathogenesis of chronic obstructive pulmonary disease (COPD), little is known regarding the relationship between serum CyPA and COPD. METHODS: Ninety-three COPD patients with acute exacerbation were enrolled in the study and were reassessed during the convalescence phase. Eighty-eight controls were matched for age, gender, body mass index, smoking index and comorbidity. The basic clinical information and pulmonary function of all participants were collected. Serum levels of CyPA and other inflammation indexes were further measured. RESULTS: Serum CyPA was significantly increased in convalescent COPD patients compared to healthy controls, and further elevated in COPD patients with acute exacerbation. Serum CyPA positively correlated with serum interleukin-6, matrix metalloproteinase-9 and high-sensitivity C-reactive protein in both the exacerbation and convalescence phases of COPD. Furthermore, it negatively correlated with percent value of forced expiratory volume in 1 second (FEV(1)%) predicted and FEV(1)/forced vital capacity in convalescent COPD patients. CONCLUSION: These results suggest that serum CyPA can be used as a potential inflammatory biomarker for COPD and assessment of serum CyPA may reflect the severity of inflammation in COPD. Dove Medical Press 2018-01-19 /pmc/articles/PMC5783015/ /pubmed/29403273 http://dx.doi.org/10.2147/COPD.S152898 Text en © 2018 Zhang 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 Zhang, Ming Tang, Jingjing Yin, Jiafeng Wang, Xiaoying Feng, Xiangli Yang, Xia Shan, Hu Zhang, Qiuhong Zhang, Jie Li, Yali The clinical implication of serum cyclophilin A in patients with chronic obstructive pulmonary disease |
title | The clinical implication of serum cyclophilin A in patients with chronic obstructive pulmonary disease |
title_full | The clinical implication of serum cyclophilin A in patients with chronic obstructive pulmonary disease |
title_fullStr | The clinical implication of serum cyclophilin A in patients with chronic obstructive pulmonary disease |
title_full_unstemmed | The clinical implication of serum cyclophilin A in patients with chronic obstructive pulmonary disease |
title_short | The clinical implication of serum cyclophilin A in patients with chronic obstructive pulmonary disease |
title_sort | clinical implication of serum cyclophilin a in patients with chronic obstructive pulmonary disease |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783015/ https://www.ncbi.nlm.nih.gov/pubmed/29403273 http://dx.doi.org/10.2147/COPD.S152898 |
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