Cargando…

Annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample

BACKGROUND: Few studies have examined the relationships between sputum inflammatory markers and subsequent annual decline in forced expiratory volume in 1 s (dFEV(1)). This study investigated whether indices of airway inflammation are predictors of dFEV(1) in a general population-based sample. METHO...

Descripción completa

Detalles Bibliográficos
Autores principales: Kononova, Natalia, Sikkeland, Liv Ingunn Bjoner, Mahmood, Faiza, Vistnes, Maria, Kongerud, Johny, Einvik, Gunnar, Søyseth, Vidar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509765/
https://www.ncbi.nlm.nih.gov/pubmed/31072364
http://dx.doi.org/10.1186/s12890-018-0765-7
_version_ 1783417310923456512
author Kononova, Natalia
Sikkeland, Liv Ingunn Bjoner
Mahmood, Faiza
Vistnes, Maria
Kongerud, Johny
Einvik, Gunnar
Søyseth, Vidar
author_facet Kononova, Natalia
Sikkeland, Liv Ingunn Bjoner
Mahmood, Faiza
Vistnes, Maria
Kongerud, Johny
Einvik, Gunnar
Søyseth, Vidar
author_sort Kononova, Natalia
collection PubMed
description BACKGROUND: Few studies have examined the relationships between sputum inflammatory markers and subsequent annual decline in forced expiratory volume in 1 s (dFEV(1)). This study investigated whether indices of airway inflammation are predictors of dFEV(1) in a general population-based sample. METHODS: The study, conducted from 2003 to 2005, included 120 healthy Norwegian subjects aged 40 to 70 years old. At baseline, the participants completed a self-administered respiratory questionnaire and underwent a clinical examination that included spirometry, venous blood sampling, and induced sputum examination. From 2015 to 2016, 62 (52%) participants agreed to a follow-up examination that did not include induced sputum examination. Those with a FEV(1)/forced vital capacity (FVC) ratio <  0.70 underwent a bronchial reversibility test. The levels of cytokines, pro-inflammatory M1 macrophage phenotypes were measured in induced sputum using bead-based multiplex analysis. The associations between cytokine levels and dFEV(1) were then analysed. RESULTS: The mean dFEV(1) was 32.9 ml/year (standard deviation 26.3). We found no associations between dFEV(1) and the baseline indices of sputum inflammation. Seven participants had irreversible airflow limitation at follow-up. They had lower FEV1 and gas diffusion at baseline compared with the remaining subjects. Moreover, two of these individuals had a positive reversibility test and sputum eosinophilia at baseline. CONCLUSIONS: In this cohort of presumably healthy subjects, we found no associations between sputum inflammatory cells or mediators and dFEV(1) during 10 years of follow-up. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12890-018-0765-7) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6509765
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-65097652019-06-05 Annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample Kononova, Natalia Sikkeland, Liv Ingunn Bjoner Mahmood, Faiza Vistnes, Maria Kongerud, Johny Einvik, Gunnar Søyseth, Vidar BMC Pulm Med Research Article BACKGROUND: Few studies have examined the relationships between sputum inflammatory markers and subsequent annual decline in forced expiratory volume in 1 s (dFEV(1)). This study investigated whether indices of airway inflammation are predictors of dFEV(1) in a general population-based sample. METHODS: The study, conducted from 2003 to 2005, included 120 healthy Norwegian subjects aged 40 to 70 years old. At baseline, the participants completed a self-administered respiratory questionnaire and underwent a clinical examination that included spirometry, venous blood sampling, and induced sputum examination. From 2015 to 2016, 62 (52%) participants agreed to a follow-up examination that did not include induced sputum examination. Those with a FEV(1)/forced vital capacity (FVC) ratio <  0.70 underwent a bronchial reversibility test. The levels of cytokines, pro-inflammatory M1 macrophage phenotypes were measured in induced sputum using bead-based multiplex analysis. The associations between cytokine levels and dFEV(1) were then analysed. RESULTS: The mean dFEV(1) was 32.9 ml/year (standard deviation 26.3). We found no associations between dFEV(1) and the baseline indices of sputum inflammation. Seven participants had irreversible airflow limitation at follow-up. They had lower FEV1 and gas diffusion at baseline compared with the remaining subjects. Moreover, two of these individuals had a positive reversibility test and sputum eosinophilia at baseline. CONCLUSIONS: In this cohort of presumably healthy subjects, we found no associations between sputum inflammatory cells or mediators and dFEV(1) during 10 years of follow-up. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12890-018-0765-7) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-09 /pmc/articles/PMC6509765/ /pubmed/31072364 http://dx.doi.org/10.1186/s12890-018-0765-7 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 Article
Kononova, Natalia
Sikkeland, Liv Ingunn Bjoner
Mahmood, Faiza
Vistnes, Maria
Kongerud, Johny
Einvik, Gunnar
Søyseth, Vidar
Annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample
title Annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample
title_full Annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample
title_fullStr Annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample
title_full_unstemmed Annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample
title_short Annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample
title_sort annual decline in forced expiratory volume and airway inflammatory cells and mediators in a general population-based sample
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509765/
https://www.ncbi.nlm.nih.gov/pubmed/31072364
http://dx.doi.org/10.1186/s12890-018-0765-7
work_keys_str_mv AT kononovanatalia annualdeclineinforcedexpiratoryvolumeandairwayinflammatorycellsandmediatorsinageneralpopulationbasedsample
AT sikkelandlivingunnbjoner annualdeclineinforcedexpiratoryvolumeandairwayinflammatorycellsandmediatorsinageneralpopulationbasedsample
AT mahmoodfaiza annualdeclineinforcedexpiratoryvolumeandairwayinflammatorycellsandmediatorsinageneralpopulationbasedsample
AT vistnesmaria annualdeclineinforcedexpiratoryvolumeandairwayinflammatorycellsandmediatorsinageneralpopulationbasedsample
AT kongerudjohny annualdeclineinforcedexpiratoryvolumeandairwayinflammatorycellsandmediatorsinageneralpopulationbasedsample
AT einvikgunnar annualdeclineinforcedexpiratoryvolumeandairwayinflammatorycellsandmediatorsinageneralpopulationbasedsample
AT søysethvidar annualdeclineinforcedexpiratoryvolumeandairwayinflammatorycellsandmediatorsinageneralpopulationbasedsample