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Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis

BACKGROUND: Cystic fibrosis (CF) is associated with bacterial pulmonary infections and neutrophil-dominated inflammation in the airways. The aim of this study was to evaluate the neutrophil-derived protein Heparin-binding protein (HBP) as a potential sputum marker of airway inflammation and bacteria...

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Autores principales: Hovold, Gisela, Palmcrantz, Victoria, Kahn, Fredrik, Egesten, Arne, Påhlman, Lisa I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011334/
https://www.ncbi.nlm.nih.gov/pubmed/29925362
http://dx.doi.org/10.1186/s12890-018-0668-7
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author Hovold, Gisela
Palmcrantz, Victoria
Kahn, Fredrik
Egesten, Arne
Påhlman, Lisa I.
author_facet Hovold, Gisela
Palmcrantz, Victoria
Kahn, Fredrik
Egesten, Arne
Påhlman, Lisa I.
author_sort Hovold, Gisela
collection PubMed
description BACKGROUND: Cystic fibrosis (CF) is associated with bacterial pulmonary infections and neutrophil-dominated inflammation in the airways. The aim of this study was to evaluate the neutrophil-derived protein Heparin-binding protein (HBP) as a potential sputum marker of airway inflammation and bacterial load. METHODS: Nineteen CF patients, aged 6–18 years, were prospectively followed for 6 months with sputum sampling at every visit to the CF clinic. A total of 41 sputum samples were collected. Sputum-HBP was analysed with ELISA, neutrophil elastase activity with a chromogenic assay, and total bacterial load with RT-PCR of the 16 s rDNA gene. Data were compared to lung function parameters and airway symptoms. RESULTS: HBP and elastase correlated to a decrease in FEV(1)%predicted compared to the patients´ individual baseline pulmonary function (∆FEV(1)), but not to bacterial load. Area under the receiver operating characteristic curve values for the detection of > 10% decrease in ∆FEV(1) were 0.80 for HBP, 0.78 for elastase, and 0.54 for bacterial load. CONCLUSIONS: Sputum HBP is a promising marker of airway inflammation and pulmonary function in children with CF.
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spelling pubmed-60113342018-06-27 Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis Hovold, Gisela Palmcrantz, Victoria Kahn, Fredrik Egesten, Arne Påhlman, Lisa I. BMC Pulm Med Research Article BACKGROUND: Cystic fibrosis (CF) is associated with bacterial pulmonary infections and neutrophil-dominated inflammation in the airways. The aim of this study was to evaluate the neutrophil-derived protein Heparin-binding protein (HBP) as a potential sputum marker of airway inflammation and bacterial load. METHODS: Nineteen CF patients, aged 6–18 years, were prospectively followed for 6 months with sputum sampling at every visit to the CF clinic. A total of 41 sputum samples were collected. Sputum-HBP was analysed with ELISA, neutrophil elastase activity with a chromogenic assay, and total bacterial load with RT-PCR of the 16 s rDNA gene. Data were compared to lung function parameters and airway symptoms. RESULTS: HBP and elastase correlated to a decrease in FEV(1)%predicted compared to the patients´ individual baseline pulmonary function (∆FEV(1)), but not to bacterial load. Area under the receiver operating characteristic curve values for the detection of > 10% decrease in ∆FEV(1) were 0.80 for HBP, 0.78 for elastase, and 0.54 for bacterial load. CONCLUSIONS: Sputum HBP is a promising marker of airway inflammation and pulmonary function in children with CF. BioMed Central 2018-06-20 /pmc/articles/PMC6011334/ /pubmed/29925362 http://dx.doi.org/10.1186/s12890-018-0668-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hovold, Gisela
Palmcrantz, Victoria
Kahn, Fredrik
Egesten, Arne
Påhlman, Lisa I.
Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis
title Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis
title_full Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis
title_fullStr Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis
title_full_unstemmed Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis
title_short Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis
title_sort heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011334/
https://www.ncbi.nlm.nih.gov/pubmed/29925362
http://dx.doi.org/10.1186/s12890-018-0668-7
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