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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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). |
format | Online Article Text |
id | pubmed-6668103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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