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Airway inflammation and mannitol challenge test in COPD
BACKGROUND: Eosinophilic airway inflammation has successfully been used to tailor anti-inflammatory therapy in chronic obstructive pulmonary disease (COPD). Airway hyperresponsiveness (AHR) by indirect challenges is associated with airway inflammation. We hypothesized that AHR to inhaled mannitol ca...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3036630/ https://www.ncbi.nlm.nih.gov/pubmed/21241520 http://dx.doi.org/10.1186/1465-9921-12-11 |
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author | de Nijs, Selma B Fens, Niki Lutter, Rene Dijkers, Erica Krouwels, Frans H Smids-Dierdorp, Barbara S van Steenwijk, Reindert P Sterk, Peter J |
author_facet | de Nijs, Selma B Fens, Niki Lutter, Rene Dijkers, Erica Krouwels, Frans H Smids-Dierdorp, Barbara S van Steenwijk, Reindert P Sterk, Peter J |
author_sort | de Nijs, Selma B |
collection | PubMed |
description | BACKGROUND: Eosinophilic airway inflammation has successfully been used to tailor anti-inflammatory therapy in chronic obstructive pulmonary disease (COPD). Airway hyperresponsiveness (AHR) by indirect challenges is associated with airway inflammation. We hypothesized that AHR to inhaled mannitol captures eosinophilia in induced sputum in COPD. METHODS: Twenty-eight patients (age 58 ± 7.8 yr, packyears 40 ± 15.5, post-bronchodilator FEV(1 )77 ± 14.0%predicted, no inhaled steroids ≥4 wks) with mild-moderate COPD (GOLD I-II) completed two randomized visits with hypertonic saline-induced sputum and mannitol challenge (including sputum collection). AHR to mannitol was expressed as response-dose-ratio (RDR) and related to cell counts, ECP, MPO and IL-8 levels in sputum. RESULTS: There was a positive correlation between RDR to mannitol and eosinophil numbers (r = 0.47, p = 0.03) and level of IL-8 (r = 0.46, p = 0.04) in hypertonic saline-induced sputum. Furthermore, significant correlations were found between RDR and eosinophil numbers (r = 0.71, p = 0.001), level of ECP (r = 0.72, p = 0.001), IL-8 (r = 0.57, p = 0.015) and MPO (r = 0.64, p = 0.007) in sputum collected after mannitol challenge. ROC-curves showed 60% sensitivity and 100% specificity of RDR for >2.5% eosinophils in mannitol-induced sputum. CONCLUSIONS: In mild-moderate COPD mannitol hyperresponsiveness is associated with biomarkers of airway inflammation. The high specificity of mannitol challenge suggests that the test is particularly suitable to exclude eosinophilic airways inflammation, which may facilitate individualized treatment in COPD. TRIAL REGISTRATION: Netherlands Trial Register (NTR): NTR1283 |
format | Text |
id | pubmed-3036630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30366302011-02-10 Airway inflammation and mannitol challenge test in COPD de Nijs, Selma B Fens, Niki Lutter, Rene Dijkers, Erica Krouwels, Frans H Smids-Dierdorp, Barbara S van Steenwijk, Reindert P Sterk, Peter J Respir Res Research BACKGROUND: Eosinophilic airway inflammation has successfully been used to tailor anti-inflammatory therapy in chronic obstructive pulmonary disease (COPD). Airway hyperresponsiveness (AHR) by indirect challenges is associated with airway inflammation. We hypothesized that AHR to inhaled mannitol captures eosinophilia in induced sputum in COPD. METHODS: Twenty-eight patients (age 58 ± 7.8 yr, packyears 40 ± 15.5, post-bronchodilator FEV(1 )77 ± 14.0%predicted, no inhaled steroids ≥4 wks) with mild-moderate COPD (GOLD I-II) completed two randomized visits with hypertonic saline-induced sputum and mannitol challenge (including sputum collection). AHR to mannitol was expressed as response-dose-ratio (RDR) and related to cell counts, ECP, MPO and IL-8 levels in sputum. RESULTS: There was a positive correlation between RDR to mannitol and eosinophil numbers (r = 0.47, p = 0.03) and level of IL-8 (r = 0.46, p = 0.04) in hypertonic saline-induced sputum. Furthermore, significant correlations were found between RDR and eosinophil numbers (r = 0.71, p = 0.001), level of ECP (r = 0.72, p = 0.001), IL-8 (r = 0.57, p = 0.015) and MPO (r = 0.64, p = 0.007) in sputum collected after mannitol challenge. ROC-curves showed 60% sensitivity and 100% specificity of RDR for >2.5% eosinophils in mannitol-induced sputum. CONCLUSIONS: In mild-moderate COPD mannitol hyperresponsiveness is associated with biomarkers of airway inflammation. The high specificity of mannitol challenge suggests that the test is particularly suitable to exclude eosinophilic airways inflammation, which may facilitate individualized treatment in COPD. TRIAL REGISTRATION: Netherlands Trial Register (NTR): NTR1283 BioMed Central 2011 2011-01-18 /pmc/articles/PMC3036630/ /pubmed/21241520 http://dx.doi.org/10.1186/1465-9921-12-11 Text en Copyright ©2011 de Nijs et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research de Nijs, Selma B Fens, Niki Lutter, Rene Dijkers, Erica Krouwels, Frans H Smids-Dierdorp, Barbara S van Steenwijk, Reindert P Sterk, Peter J Airway inflammation and mannitol challenge test in COPD |
title | Airway inflammation and mannitol challenge test in COPD |
title_full | Airway inflammation and mannitol challenge test in COPD |
title_fullStr | Airway inflammation and mannitol challenge test in COPD |
title_full_unstemmed | Airway inflammation and mannitol challenge test in COPD |
title_short | Airway inflammation and mannitol challenge test in COPD |
title_sort | airway inflammation and mannitol challenge test in copd |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3036630/ https://www.ncbi.nlm.nih.gov/pubmed/21241520 http://dx.doi.org/10.1186/1465-9921-12-11 |
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