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Differences in systemic inflammation between cigarette and biomass smoke-induced COPD
BACKGROUND AND OBJECTIVE: It is known that biomarkers of systemic inflammation are raised in COPD caused by tobacco (T-COPD) compared with healthy controls, but there is less information on the inflammatory status of subjects with COPD caused by biomass smoke (B-COPD). In addition, the possible (if...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589102/ https://www.ncbi.nlm.nih.gov/pubmed/28979110 http://dx.doi.org/10.2147/COPD.S141068 |
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author | Golpe, Rafael Martín-Robles, Irene Sanjuán-López, Pilar Pérez-de-Llano, Luis González-Juanatey, Carlos López-Campos, José L Arellano-Orden, Elena |
author_facet | Golpe, Rafael Martín-Robles, Irene Sanjuán-López, Pilar Pérez-de-Llano, Luis González-Juanatey, Carlos López-Campos, José L Arellano-Orden, Elena |
author_sort | Golpe, Rafael |
collection | PubMed |
description | BACKGROUND AND OBJECTIVE: It is known that biomarkers of systemic inflammation are raised in COPD caused by tobacco (T-COPD) compared with healthy controls, but there is less information on the inflammatory status of subjects with COPD caused by biomass smoke (B-COPD). In addition, the possible (if any) differences in inflammation between both types of the disease are still not well known. The aim of this study was to assess the inflammatory profile in B-COPD and T-COPD. METHODS: A total of 20 subjects (15 men and five women) with T-COPD were matched one to one for sex, age and forced expiratory volume in 1 s (FEV(1)) to 20 B-COPD patients. In all, 20 sex-matched healthy subjects with normal lung function without smoking history or biomass exposure were included as controls. The following biomarkers were measured: exhaled nitric oxide, serum IL-6, IL-8, IL-5, IL-13, periostin, surfactant protein-P, TNF-α, IgE, erythrocyte sedimentation rate, C-reactive protein and fibrinogen. Complete blood count was also obtained. RESULTS: The age of the subjects was 70.2±7.9 years and FEV(1)% was 56.2%±14.6%. Most inflammatory biomarkers were higher in both types of COPD than in healthy controls. IL-6, IL-8 and IL-5 were significantly higher in T-COPD than in B-COPD, without other significant differences. CONCLUSION: Both types of COPD are associated with high levels of systemic inflammation biomarkers. T-COPD patients have a higher systemic inflammatory status than the patients with B-COPD. |
format | Online Article Text |
id | pubmed-5589102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55891022017-10-04 Differences in systemic inflammation between cigarette and biomass smoke-induced COPD Golpe, Rafael Martín-Robles, Irene Sanjuán-López, Pilar Pérez-de-Llano, Luis González-Juanatey, Carlos López-Campos, José L Arellano-Orden, Elena Int J Chron Obstruct Pulmon Dis Original Research BACKGROUND AND OBJECTIVE: It is known that biomarkers of systemic inflammation are raised in COPD caused by tobacco (T-COPD) compared with healthy controls, but there is less information on the inflammatory status of subjects with COPD caused by biomass smoke (B-COPD). In addition, the possible (if any) differences in inflammation between both types of the disease are still not well known. The aim of this study was to assess the inflammatory profile in B-COPD and T-COPD. METHODS: A total of 20 subjects (15 men and five women) with T-COPD were matched one to one for sex, age and forced expiratory volume in 1 s (FEV(1)) to 20 B-COPD patients. In all, 20 sex-matched healthy subjects with normal lung function without smoking history or biomass exposure were included as controls. The following biomarkers were measured: exhaled nitric oxide, serum IL-6, IL-8, IL-5, IL-13, periostin, surfactant protein-P, TNF-α, IgE, erythrocyte sedimentation rate, C-reactive protein and fibrinogen. Complete blood count was also obtained. RESULTS: The age of the subjects was 70.2±7.9 years and FEV(1)% was 56.2%±14.6%. Most inflammatory biomarkers were higher in both types of COPD than in healthy controls. IL-6, IL-8 and IL-5 were significantly higher in T-COPD than in B-COPD, without other significant differences. CONCLUSION: Both types of COPD are associated with high levels of systemic inflammation biomarkers. T-COPD patients have a higher systemic inflammatory status than the patients with B-COPD. Dove Medical Press 2017-09-01 /pmc/articles/PMC5589102/ /pubmed/28979110 http://dx.doi.org/10.2147/COPD.S141068 Text en © 2017 Golpe 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 Golpe, Rafael Martín-Robles, Irene Sanjuán-López, Pilar Pérez-de-Llano, Luis González-Juanatey, Carlos López-Campos, José L Arellano-Orden, Elena Differences in systemic inflammation between cigarette and biomass smoke-induced COPD |
title | Differences in systemic inflammation between cigarette and biomass smoke-induced COPD |
title_full | Differences in systemic inflammation between cigarette and biomass smoke-induced COPD |
title_fullStr | Differences in systemic inflammation between cigarette and biomass smoke-induced COPD |
title_full_unstemmed | Differences in systemic inflammation between cigarette and biomass smoke-induced COPD |
title_short | Differences in systemic inflammation between cigarette and biomass smoke-induced COPD |
title_sort | differences in systemic inflammation between cigarette and biomass smoke-induced copd |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589102/ https://www.ncbi.nlm.nih.gov/pubmed/28979110 http://dx.doi.org/10.2147/COPD.S141068 |
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