25
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

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

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          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.

          Related collections

          Most cited references38

          • Record: found
          • Abstract: found
          • Article: not found

          Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.

          Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene result in defective epithelial cAMP-dependent Cl(-) secretion and increased airway Na(+) absorption. The mechanistic links between these altered ion transport processes and the pathogenesis of cystic fibrosis lung disease, however, are unclear. To test the hypothesis that accelerated Na(+) transport alone can produce cystic fibrosis-like lung disease, we generated mice with airway-specific overexpression of epithelial Na(+) channels (ENaC). Here we show that increased airway Na(+) absorption in vivo caused airway surface liquid (ASL) volume depletion, increased mucus concentration, delayed mucus transport and mucus adhesion to airway surfaces. Defective mucus transport caused a severe spontaneous lung disease sharing features with cystic fibrosis, including mucus obstruction, goblet cell metaplasia, neutrophilic inflammation and poor bacterial clearance. We conclude that increasing airway Na(+) absorption initiates cystic fibrosis-like lung disease and produces a model for the study of the pathogenesis and therapy of this disease.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            The forced oscillation technique in clinical practice: methodology, recommendations and future developments

              Bookmark
              • Record: found
              • Abstract: not found
              • Book Chapter: not found

              Multiscale vessel enhancement filtering

                Bookmark

                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                27 July 2016
                2016
                : 6
                : 29438
                Affiliations
                [1 ]Department of Mechanical & Aerospace Engineering, Monash University , Melbourne, VIC, Australia
                [2 ]4Dx Limited , Melbourne, VIC, Australia
                [3 ]Robinson Research Institute, University of Adelaide , SA, Australia
                [4 ]Women’s and Children’s Hospital, North Adelaide , SA, Australia
                [5 ]School of Physics and Astronomy, Monash University , Melbourne, VIC, Australia
                [6 ]School of Medicine, University of Tasmania , Hobart, TAS, Australia
                [7 ]Department of Medicine, University of North Carolina at Chapel Hill , Chapel Hill, NC, USA
                [8 ]Department of Translational Pulmonology Translational Lung Research Center (TLRC), Member of the German Center for Lung Research (DZL), University of Heidelberg , Heidelberg, Germany
                Author notes
                [*]

                These authors contributed equally to this work.

                Article
                srep29438
                10.1038/srep29438
                4962033
                27461961
                357e0d98-2f47-4ddd-b721-30f782c40fd0
                Copyright © 2016, Macmillan Publishers Limited

                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/

                History
                : 04 March 2016
                : 17 June 2016
                Categories
                Article

                Uncategorized
                Uncategorized

                Comments

                Comment on this article