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Neutrophil elastase as a biomarker for bacterial infection in COPD

BACKGROUND: Chronic obstructive pulmonary disease (COPD) is predominantly associated with neutrophilic inflammation. Active neutrophil elastase (NE) is a serine proteinase, secreted by neutrophils, in response to inflammation and pathogen invasion. We sought to investigate if NE could be used as a b...

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Autores principales: Thulborn, Samantha J., Mistry, Vijay, Brightling, Christopher E., Moffitt, Kelly L., Ribeiro, David, Bafadhel, Mona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668103/
https://www.ncbi.nlm.nih.gov/pubmed/31362723
http://dx.doi.org/10.1186/s12931-019-1145-4
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author Thulborn, Samantha J.
Mistry, Vijay
Brightling, Christopher E.
Moffitt, Kelly L.
Ribeiro, David
Bafadhel, Mona
author_facet Thulborn, Samantha J.
Mistry, Vijay
Brightling, Christopher E.
Moffitt, Kelly L.
Ribeiro, David
Bafadhel, Mona
author_sort Thulborn, Samantha J.
collection PubMed
description BACKGROUND: Chronic obstructive pulmonary disease (COPD) is predominantly associated with neutrophilic inflammation. Active neutrophil elastase (NE) is a serine proteinase, secreted by neutrophils, in response to inflammation and pathogen invasion. We sought to investigate if NE could be used as a biomarker for bacterial infection in patients with COPD. METHODS: NE was quantified using ProteaseTag® Active NE Immunoassay (ProAxsis, Belfast) from the sputum of COPD subjects at stable state, exacerbation and 2 weeks post treatment visit. RESULTS: NE was measured in 90 samples from 30 COPD subjects (18 males) with a mean (range) age of 65 (45–81) years and mean (SD) FEV(1) of 47% (18). The geometric mean (95%CI) of NE at stable state was 2454 ng/mL (1460 to 4125 ng/mL). There was a significant increase in NE levels at an exacerbation (p = 0.003), and NE levels were higher in a bacterial-associated exacerbation (NE log difference 3.873, 95% CI of log difference 1.396 to 10.740, p = 0.011). NE was an accurate predictor of a bacteria-associated exacerbation (area (95%CI) under the receiver operator characteristic curve 0.812 (0.657 to 0.968). CONCLUSION: NE is elevated during exacerbations of COPD. NE may be a viable biomarker for distinguishing a bacterial exacerbation in patients with COPD. TRIAL REGISTRATION: Leicestershire, Northamptonshire and Rutland ethics committee (reference number: 07/H0406/157).
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spelling pubmed-66681032019-08-05 Neutrophil elastase as a biomarker for bacterial infection in COPD Thulborn, Samantha J. Mistry, Vijay Brightling, Christopher E. Moffitt, Kelly L. Ribeiro, David Bafadhel, Mona Respir Res Research BACKGROUND: Chronic obstructive pulmonary disease (COPD) is predominantly associated with neutrophilic inflammation. Active neutrophil elastase (NE) is a serine proteinase, secreted by neutrophils, in response to inflammation and pathogen invasion. We sought to investigate if NE could be used as a biomarker for bacterial infection in patients with COPD. METHODS: NE was quantified using ProteaseTag® Active NE Immunoassay (ProAxsis, Belfast) from the sputum of COPD subjects at stable state, exacerbation and 2 weeks post treatment visit. RESULTS: NE was measured in 90 samples from 30 COPD subjects (18 males) with a mean (range) age of 65 (45–81) years and mean (SD) FEV(1) of 47% (18). The geometric mean (95%CI) of NE at stable state was 2454 ng/mL (1460 to 4125 ng/mL). There was a significant increase in NE levels at an exacerbation (p = 0.003), and NE levels were higher in a bacterial-associated exacerbation (NE log difference 3.873, 95% CI of log difference 1.396 to 10.740, p = 0.011). NE was an accurate predictor of a bacteria-associated exacerbation (area (95%CI) under the receiver operator characteristic curve 0.812 (0.657 to 0.968). CONCLUSION: NE is elevated during exacerbations of COPD. NE may be a viable biomarker for distinguishing a bacterial exacerbation in patients with COPD. TRIAL REGISTRATION: Leicestershire, Northamptonshire and Rutland ethics committee (reference number: 07/H0406/157). BioMed Central 2019-07-30 2019 /pmc/articles/PMC6668103/ /pubmed/31362723 http://dx.doi.org/10.1186/s12931-019-1145-4 Text en © The Author(s). 2019 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
Thulborn, Samantha J.
Mistry, Vijay
Brightling, Christopher E.
Moffitt, Kelly L.
Ribeiro, David
Bafadhel, Mona
Neutrophil elastase as a biomarker for bacterial infection in COPD
title Neutrophil elastase as a biomarker for bacterial infection in COPD
title_full Neutrophil elastase as a biomarker for bacterial infection in COPD
title_fullStr Neutrophil elastase as a biomarker for bacterial infection in COPD
title_full_unstemmed Neutrophil elastase as a biomarker for bacterial infection in COPD
title_short Neutrophil elastase as a biomarker for bacterial infection in COPD
title_sort neutrophil elastase as a biomarker for bacterial infection in copd
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668103/
https://www.ncbi.nlm.nih.gov/pubmed/31362723
http://dx.doi.org/10.1186/s12931-019-1145-4
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