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Airway wall thickness is increased in COPD patients with bronchodilator responsiveness

RATIONALE: Bronchodilator responsiveness (BDR) is a common but variable phenomenon in COPD. The CT characteristics of airway dimensions that differentiate COPD subjects with BDR from those without BDR have not been well described. We aimed to assess airway dimensions in COPD subjects with and withou...

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Autores principales: Kim, Victor, Desai, Parag, Newell, John D, Make, Barry J, Washko, George R, Silverman, Edwin K, Crapo, James D, Bhatt, Surya P, Criner, Gerard J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198908/
https://www.ncbi.nlm.nih.gov/pubmed/25248436
http://dx.doi.org/10.1186/s12931-014-0084-3
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author Kim, Victor
Desai, Parag
Newell, John D
Make, Barry J
Washko, George R
Silverman, Edwin K
Crapo, James D
Bhatt, Surya P
Criner, Gerard J
author_facet Kim, Victor
Desai, Parag
Newell, John D
Make, Barry J
Washko, George R
Silverman, Edwin K
Crapo, James D
Bhatt, Surya P
Criner, Gerard J
author_sort Kim, Victor
collection PubMed
description RATIONALE: Bronchodilator responsiveness (BDR) is a common but variable phenomenon in COPD. The CT characteristics of airway dimensions that differentiate COPD subjects with BDR from those without BDR have not been well described. We aimed to assess airway dimensions in COPD subjects with and without BDR. METHODS: We analyzed subjects with GOLD 1–4 disease in the COPDGene® study who had CT airway analysis. We divided patients into two groups: BDR + (post bronchodilator ΔFEV(1) ≥ 10%) and BDR-(post bronchodilator ΔFEV(1) < 10%). The mean wall area percent (WA%) of six segmental bronchi in each subject was quantified using VIDA. Using 3D SLICER, airway wall thickness was also expressed as the square root wall area of an airway of 10 mm (Pi10) and 15 mm (Pi15) diameter. %Emphysema and %gas trapping were also calculated. RESULTS: 2355 subjects in the BDR-group and 1306 in the BDR + group formed our analysis. The BDR + group had a greater Pi10, Pi15, and mean segmental WA% compared to the BDR-group. In multivariate logistic regression using gender, race, current smoking, history of asthma, %emphysema, %gas trapping, %predicted FEV(1), and %predicted FVC, airway wall measures remained independent predictors of BDR. Using a threshold change in FEV(1) ≥ 15% and FEV(1) ≥ 12% and 200 mL to divide patients into groups, the results were similar. CONCLUSION: BDR in COPD is independently associated with CT evidence of airway pathology. This study provides us with greater evidence of changes in lung structure that correlate with physiologic manifestations of airflow obstruction in COPD.
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spelling pubmed-41989082014-10-17 Airway wall thickness is increased in COPD patients with bronchodilator responsiveness Kim, Victor Desai, Parag Newell, John D Make, Barry J Washko, George R Silverman, Edwin K Crapo, James D Bhatt, Surya P Criner, Gerard J Respir Res Research RATIONALE: Bronchodilator responsiveness (BDR) is a common but variable phenomenon in COPD. The CT characteristics of airway dimensions that differentiate COPD subjects with BDR from those without BDR have not been well described. We aimed to assess airway dimensions in COPD subjects with and without BDR. METHODS: We analyzed subjects with GOLD 1–4 disease in the COPDGene® study who had CT airway analysis. We divided patients into two groups: BDR + (post bronchodilator ΔFEV(1) ≥ 10%) and BDR-(post bronchodilator ΔFEV(1) < 10%). The mean wall area percent (WA%) of six segmental bronchi in each subject was quantified using VIDA. Using 3D SLICER, airway wall thickness was also expressed as the square root wall area of an airway of 10 mm (Pi10) and 15 mm (Pi15) diameter. %Emphysema and %gas trapping were also calculated. RESULTS: 2355 subjects in the BDR-group and 1306 in the BDR + group formed our analysis. The BDR + group had a greater Pi10, Pi15, and mean segmental WA% compared to the BDR-group. In multivariate logistic regression using gender, race, current smoking, history of asthma, %emphysema, %gas trapping, %predicted FEV(1), and %predicted FVC, airway wall measures remained independent predictors of BDR. Using a threshold change in FEV(1) ≥ 15% and FEV(1) ≥ 12% and 200 mL to divide patients into groups, the results were similar. CONCLUSION: BDR in COPD is independently associated with CT evidence of airway pathology. This study provides us with greater evidence of changes in lung structure that correlate with physiologic manifestations of airflow obstruction in COPD. BioMed Central 2014 2014-08-08 /pmc/articles/PMC4198908/ /pubmed/25248436 http://dx.doi.org/10.1186/s12931-014-0084-3 Text en Copyright © 2014 Kim et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Kim, Victor
Desai, Parag
Newell, John D
Make, Barry J
Washko, George R
Silverman, Edwin K
Crapo, James D
Bhatt, Surya P
Criner, Gerard J
Airway wall thickness is increased in COPD patients with bronchodilator responsiveness
title Airway wall thickness is increased in COPD patients with bronchodilator responsiveness
title_full Airway wall thickness is increased in COPD patients with bronchodilator responsiveness
title_fullStr Airway wall thickness is increased in COPD patients with bronchodilator responsiveness
title_full_unstemmed Airway wall thickness is increased in COPD patients with bronchodilator responsiveness
title_short Airway wall thickness is increased in COPD patients with bronchodilator responsiveness
title_sort airway wall thickness is increased in copd patients with bronchodilator responsiveness
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198908/
https://www.ncbi.nlm.nih.gov/pubmed/25248436
http://dx.doi.org/10.1186/s12931-014-0084-3
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