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Small airway dysfunction in patients with cough variant asthma: a retrospective cohort study
BACKGROUND: Cough variant asthma (CVA) is one of the special populations of asthma. The aim of the study was to compare small airways, the degree of bronchial hyperresponsiveness (BHR) and airway inflammatory subtypes between CVA and classic asthma (CA), and investigate the relationship between thes...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860218/ https://www.ncbi.nlm.nih.gov/pubmed/33536015 http://dx.doi.org/10.1186/s12890-021-01419-4 |
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author | Gao, Jie Wu, Haigui Wu, Feng |
author_facet | Gao, Jie Wu, Haigui Wu, Feng |
author_sort | Gao, Jie |
collection | PubMed |
description | BACKGROUND: Cough variant asthma (CVA) is one of the special populations of asthma. The aim of the study was to compare small airways, the degree of bronchial hyperresponsiveness (BHR) and airway inflammatory subtypes between CVA and classic asthma (CA), and investigate the relationship between these markers to determine the accuracy as indicators of CVA. METHODS: A total of 825 asthmatic patients participated in the study and 614 were included. 614 patients underwent spirometry and a bronchial challenge with methacholine and 459 patients performed induction sputum cell test. RESULTS: The number of CVA patients showed less small airway dysfunction than those of CA patients (p < 0.005). The degree of small airways dysfunction was higher in the CA group compared with the CVA group (p < 0.001). Small airways dysfunction was severer in the eosinophilic airway inflammatory subtype compared with other subtypes (p < 0.05).The area under curve of MMEF, FEF(50) and FEF(75) (% predicted) was 0.615, 0.621, 0.606, respectively. 0.17mcg of PD(20) and 4.7% of sputum eosinophils was the best diagnostic value for CVA with an AUC of 0.582 and 0.575 (p = 0.001 and p = 0.005, respectively). CONCLUSIONS: The eosinophilic airway inflammatory subtype may be increased small airway dysfunction. The value of small airways, BHR and induction sputum cells in CVA prediction, which reflected significant, but not enough to be clinically useful. |
format | Online Article Text |
id | pubmed-7860218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78602182021-02-05 Small airway dysfunction in patients with cough variant asthma: a retrospective cohort study Gao, Jie Wu, Haigui Wu, Feng BMC Pulm Med Research Article BACKGROUND: Cough variant asthma (CVA) is one of the special populations of asthma. The aim of the study was to compare small airways, the degree of bronchial hyperresponsiveness (BHR) and airway inflammatory subtypes between CVA and classic asthma (CA), and investigate the relationship between these markers to determine the accuracy as indicators of CVA. METHODS: A total of 825 asthmatic patients participated in the study and 614 were included. 614 patients underwent spirometry and a bronchial challenge with methacholine and 459 patients performed induction sputum cell test. RESULTS: The number of CVA patients showed less small airway dysfunction than those of CA patients (p < 0.005). The degree of small airways dysfunction was higher in the CA group compared with the CVA group (p < 0.001). Small airways dysfunction was severer in the eosinophilic airway inflammatory subtype compared with other subtypes (p < 0.05).The area under curve of MMEF, FEF(50) and FEF(75) (% predicted) was 0.615, 0.621, 0.606, respectively. 0.17mcg of PD(20) and 4.7% of sputum eosinophils was the best diagnostic value for CVA with an AUC of 0.582 and 0.575 (p = 0.001 and p = 0.005, respectively). CONCLUSIONS: The eosinophilic airway inflammatory subtype may be increased small airway dysfunction. The value of small airways, BHR and induction sputum cells in CVA prediction, which reflected significant, but not enough to be clinically useful. BioMed Central 2021-02-03 /pmc/articles/PMC7860218/ /pubmed/33536015 http://dx.doi.org/10.1186/s12890-021-01419-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Gao, Jie Wu, Haigui Wu, Feng Small airway dysfunction in patients with cough variant asthma: a retrospective cohort study |
title | Small airway dysfunction in patients with cough variant asthma: a retrospective cohort study |
title_full | Small airway dysfunction in patients with cough variant asthma: a retrospective cohort study |
title_fullStr | Small airway dysfunction in patients with cough variant asthma: a retrospective cohort study |
title_full_unstemmed | Small airway dysfunction in patients with cough variant asthma: a retrospective cohort study |
title_short | Small airway dysfunction in patients with cough variant asthma: a retrospective cohort study |
title_sort | small airway dysfunction in patients with cough variant asthma: a retrospective cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7860218/ https://www.ncbi.nlm.nih.gov/pubmed/33536015 http://dx.doi.org/10.1186/s12890-021-01419-4 |
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