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Quantification of heterogeneity in lung disease with image-based pulmonary function testing

Computed tomography (CT) and spirometry are the mainstays of clinical pulmonary assessment. Spirometry is effort dependent and only provides a single global measure that is insensitive for regional disease, and as such, poor for capturing the early onset of lung disease, especially patchy disease su...

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Autores principales: Stahr, Charlene S., Samarage, Chaminda R., Donnelley, Martin, Farrow, Nigel, Morgan, Kaye S., Zosky, Graeme, Boucher, Richard C., Siu, Karen K. W., Mall, Marcus A., Parsons, David W., Dubsky, Stephen, Fouras, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962033/
https://www.ncbi.nlm.nih.gov/pubmed/27461961
http://dx.doi.org/10.1038/srep29438
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author Stahr, Charlene S.
Samarage, Chaminda R.
Donnelley, Martin
Farrow, Nigel
Morgan, Kaye S.
Zosky, Graeme
Boucher, Richard C.
Siu, Karen K. W.
Mall, Marcus A.
Parsons, David W.
Dubsky, Stephen
Fouras, Andreas
author_facet Stahr, Charlene S.
Samarage, Chaminda R.
Donnelley, Martin
Farrow, Nigel
Morgan, Kaye S.
Zosky, Graeme
Boucher, Richard C.
Siu, Karen K. W.
Mall, Marcus A.
Parsons, David W.
Dubsky, Stephen
Fouras, Andreas
author_sort Stahr, Charlene S.
collection PubMed
description Computed tomography (CT) and spirometry are the mainstays of clinical pulmonary assessment. Spirometry is effort dependent and only provides a single global measure that is insensitive for regional disease, and as such, poor for capturing the early onset of lung disease, especially patchy disease such as cystic fibrosis lung disease. CT sensitively measures change in structure associated with advanced lung disease. However, obstructions in the peripheral airways and early onset of lung stiffening are often difficult to detect. Furthermore, CT imaging poses a radiation risk, particularly for young children, and dose reduction tends to result in reduced resolution. Here, we apply a series of lung tissue motion analyses, to achieve regional pulmonary function assessment in β-ENaC-overexpressing mice, a well-established model of lung disease. The expiratory time constants of regional airflows in the segmented airway tree were quantified as a measure of regional lung function. Our results showed marked heterogeneous lung function in β-ENaC-Tg mice compared to wild-type littermate controls; identified locations of airway obstruction, and quantified regions of bimodal airway resistance demonstrating lung compensation. These results demonstrate the applicability of regional lung function derived from lung motion as an effective alternative respiratory diagnostic tool.
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spelling pubmed-49620332016-08-08 Quantification of heterogeneity in lung disease with image-based pulmonary function testing Stahr, Charlene S. Samarage, Chaminda R. Donnelley, Martin Farrow, Nigel Morgan, Kaye S. Zosky, Graeme Boucher, Richard C. Siu, Karen K. W. Mall, Marcus A. Parsons, David W. Dubsky, Stephen Fouras, Andreas Sci Rep Article Computed tomography (CT) and spirometry are the mainstays of clinical pulmonary assessment. Spirometry is effort dependent and only provides a single global measure that is insensitive for regional disease, and as such, poor for capturing the early onset of lung disease, especially patchy disease such as cystic fibrosis lung disease. CT sensitively measures change in structure associated with advanced lung disease. However, obstructions in the peripheral airways and early onset of lung stiffening are often difficult to detect. Furthermore, CT imaging poses a radiation risk, particularly for young children, and dose reduction tends to result in reduced resolution. Here, we apply a series of lung tissue motion analyses, to achieve regional pulmonary function assessment in β-ENaC-overexpressing mice, a well-established model of lung disease. The expiratory time constants of regional airflows in the segmented airway tree were quantified as a measure of regional lung function. Our results showed marked heterogeneous lung function in β-ENaC-Tg mice compared to wild-type littermate controls; identified locations of airway obstruction, and quantified regions of bimodal airway resistance demonstrating lung compensation. These results demonstrate the applicability of regional lung function derived from lung motion as an effective alternative respiratory diagnostic tool. Nature Publishing Group 2016-07-27 /pmc/articles/PMC4962033/ /pubmed/27461961 http://dx.doi.org/10.1038/srep29438 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Stahr, Charlene S.
Samarage, Chaminda R.
Donnelley, Martin
Farrow, Nigel
Morgan, Kaye S.
Zosky, Graeme
Boucher, Richard C.
Siu, Karen K. W.
Mall, Marcus A.
Parsons, David W.
Dubsky, Stephen
Fouras, Andreas
Quantification of heterogeneity in lung disease with image-based pulmonary function testing
title Quantification of heterogeneity in lung disease with image-based pulmonary function testing
title_full Quantification of heterogeneity in lung disease with image-based pulmonary function testing
title_fullStr Quantification of heterogeneity in lung disease with image-based pulmonary function testing
title_full_unstemmed Quantification of heterogeneity in lung disease with image-based pulmonary function testing
title_short Quantification of heterogeneity in lung disease with image-based pulmonary function testing
title_sort quantification of heterogeneity in lung disease with image-based pulmonary function testing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962033/
https://www.ncbi.nlm.nih.gov/pubmed/27461961
http://dx.doi.org/10.1038/srep29438
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