Quantitative computed tomography–derived clusters: Redefining airway remodeling in asthmatic patients

Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)–assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms. The aim of this study was to explore no...

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Published inJournal of allergy and clinical immunology Vol. 133; no. 3; pp. 729 - 738.e18
Main Authors Gupta, Sumit, Hartley, Ruth, Khan, Umair T., Singapuri, Amisha, Hargadon, Beverly, Monteiro, William, Pavord, Ian D., Sousa, Ana R., Marshall, Richard P., Subramanian, Deepak, Parr, David, Entwisle, James J., Siddiqui, Salman, Raj, Vimal, Brightling, Christopher E.
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Inc 01.03.2014
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Abstract Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)–assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms. The aim of this study was to explore novel, quantitative, CT-determined asthma phenotypes. Sixty-five asthmatic patients and 30 healthy subjects underwent detailed clinical, physiologic characterization and quantitative CT analysis. Factor and cluster analysis techniques were used to determine 3 novel, quantitative, CT-based asthma phenotypes. Patients with severe and mild-to-moderate asthma demonstrated smaller mean right upper lobe apical segmental bronchus (RB1) lumen volume (LV) in comparison with healthy control subjects (272.3 mm3 [SD, 112.6 mm3], 259.0 mm3 [SD, 53.3 mm3], 366.4 mm3 [SD, 195.3 mm3], respectively; P = .007) but no difference in RB1 wall volume (WV). Air trapping measured based on mean lung density expiratory/inspiratory ratio was greater in patients with severe and mild-to-moderate asthma compared with that seen in healthy control subjects (0.861 [SD, 0.05)], 0.866 [SD, 0.07], and 0.830 [SD, 0.06], respectively; P = .04). The fractal dimension of the segmented airway tree was less in asthmatic patients compared with that seen in control subjects (P = .007). Three novel, quantitative, CT-based asthma clusters were identified, all of which demonstrated air trapping. Cluster 1 demonstrates increased RB1 WV and RB1 LV but decreased RB1 percentage WV. On the contrary, cluster 3 subjects have the smallest RB1 WV and LV values but the highest RB1 percentage WV values. There is a lack of proximal airway remodeling in cluster 2 subjects. Quantitative CT analysis provides a new perspective in asthma phenotyping, which might prove useful in patient selection for novel therapies.
AbstractList Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)-assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms.BACKGROUNDAsthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)-assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms.The aim of this study was to explore novel, quantitative, CT-determined asthma phenotypes.OBJECTIVESThe aim of this study was to explore novel, quantitative, CT-determined asthma phenotypes.Sixty-five asthmatic patients and 30 healthy subjects underwent detailed clinical, physiologic characterization and quantitative CT analysis. Factor and cluster analysis techniques were used to determine 3 novel, quantitative, CT-based asthma phenotypes.METHODSSixty-five asthmatic patients and 30 healthy subjects underwent detailed clinical, physiologic characterization and quantitative CT analysis. Factor and cluster analysis techniques were used to determine 3 novel, quantitative, CT-based asthma phenotypes.Patients with severe and mild-to-moderate asthma demonstrated smaller mean right upper lobe apical segmental bronchus (RB1) lumen volume (LV) in comparison with healthy control subjects (272.3 mm(3) [SD, 112.6 mm(3)], 259.0 mm(3) [SD, 53.3 mm(3)], 366.4 mm(3) [SD, 195.3 mm(3)], respectively; P = .007) but no difference in RB1 wall volume (WV). Air trapping measured based on mean lung density expiratory/inspiratory ratio was greater in patients with severe and mild-to-moderate asthma compared with that seen in healthy control subjects (0.861 [SD, 0.05)], 0.866 [SD, 0.07], and 0.830 [SD, 0.06], respectively; P = .04). The fractal dimension of the segmented airway tree was less in asthmatic patients compared with that seen in control subjects (P = .007). Three novel, quantitative, CT-based asthma clusters were identified, all of which demonstrated air trapping. Cluster 1 demonstrates increased RB1 WV and RB1 LV but decreased RB1 percentage WV. On the contrary, cluster 3 subjects have the smallest RB1 WV and LV values but the highest RB1 percentage WV values. There is a lack of proximal airway remodeling in cluster 2 subjects.RESULTSPatients with severe and mild-to-moderate asthma demonstrated smaller mean right upper lobe apical segmental bronchus (RB1) lumen volume (LV) in comparison with healthy control subjects (272.3 mm(3) [SD, 112.6 mm(3)], 259.0 mm(3) [SD, 53.3 mm(3)], 366.4 mm(3) [SD, 195.3 mm(3)], respectively; P = .007) but no difference in RB1 wall volume (WV). Air trapping measured based on mean lung density expiratory/inspiratory ratio was greater in patients with severe and mild-to-moderate asthma compared with that seen in healthy control subjects (0.861 [SD, 0.05)], 0.866 [SD, 0.07], and 0.830 [SD, 0.06], respectively; P = .04). The fractal dimension of the segmented airway tree was less in asthmatic patients compared with that seen in control subjects (P = .007). Three novel, quantitative, CT-based asthma clusters were identified, all of which demonstrated air trapping. Cluster 1 demonstrates increased RB1 WV and RB1 LV but decreased RB1 percentage WV. On the contrary, cluster 3 subjects have the smallest RB1 WV and LV values but the highest RB1 percentage WV values. There is a lack of proximal airway remodeling in cluster 2 subjects.Quantitative CT analysis provides a new perspective in asthma phenotyping, which might prove useful in patient selection for novel therapies.CONCLUSIONSQuantitative CT analysis provides a new perspective in asthma phenotyping, which might prove useful in patient selection for novel therapies.
Background Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)–assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms. Objectives The aim of this study was to explore novel, quantitative, CT-determined asthma phenotypes. Methods Sixty-five asthmatic patients and 30 healthy subjects underwent detailed clinical, physiologic characterization and quantitative CT analysis. Factor and cluster analysis techniques were used to determine 3 novel, quantitative, CT-based asthma phenotypes. Results Patients with severe and mild-to-moderate asthma demonstrated smaller mean right upper lobe apical segmental bronchus (RB1) lumen volume (LV) in comparison with healthy control subjects (272.3 mm3 [SD, 112.6 mm3 ], 259.0 mm3 [SD, 53.3 mm3 ], 366.4 mm3 [SD, 195.3 mm3 ], respectively; P  = .007) but no difference in RB1 wall volume (WV). Air trapping measured based on mean lung density expiratory/inspiratory ratio was greater in patients with severe and mild-to-moderate asthma compared with that seen in healthy control subjects (0.861 [SD, 0.05)], 0.866 [SD, 0.07], and 0.830 [SD, 0.06], respectively; P  = .04). The fractal dimension of the segmented airway tree was less in asthmatic patients compared with that seen in control subjects ( P  = .007). Three novel, quantitative, CT-based asthma clusters were identified, all of which demonstrated air trapping. Cluster 1 demonstrates increased RB1 WV and RB1 LV but decreased RB1 percentage WV. On the contrary, cluster 3 subjects have the smallest RB1 WV and LV values but the highest RB1 percentage WV values. There is a lack of proximal airway remodeling in cluster 2 subjects. Conclusions Quantitative CT analysis provides a new perspective in asthma phenotyping, which might prove useful in patient selection for novel therapies.
Background: Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)-assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms.
Background Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)-assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms. Objectives The aim of this study was to explore novel, quantitative, CT-determined asthma phenotypes. Methods Sixty-five asthmatic patients and 30 healthy subjects underwent detailed clinical, physiologic characterization and quantitative CT analysis. Factor and cluster analysis techniques were used to determine 3 novel, quantitative, CT-based asthma phenotypes. Results Patients with severe and mild-to-moderate asthma demonstrated smaller mean right upper lobe apical segmental bronchus (RB1) lumen volume (LV) in comparison with healthy control subjects (272.3 mm3[SD, 112.6 mm3], 259.0 mm3[SD, 53.3 mm3], 366.4 mm3[SD, 195.3 mm3], respectively;P = .007) but no difference in RB1 wall volume (WV). Air trapping measured based on mean lung density expiratory/inspiratory ratio was greater in patients with severe and mild-to-moderate asthma compared with that seen in healthy control subjects (0.861 [SD, 0.05)], 0.866 [SD, 0.07], and 0.830 [SD, 0.06], respectively;P = .04). The fractal dimension of the segmented airway tree was less in asthmatic patients compared with that seen in control subjects (P = .007). Three novel, quantitative, CT-based asthma clusters were identified, all of which demonstrated air trapping. Cluster 1 demonstrates increased RB1 WV and RB1 LV but decreased RB1 percentage WV. On the contrary, cluster 3 subjects have the smallest RB1 WV and LV values but the highest RB1 percentage WV values. There is a lack of proximal airway remodeling in cluster 2 subjects. Conclusions Quantitative CT analysis provides a new perspective in asthma phenotyping, which might prove useful in patient selection for novel therapies.
Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)–assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms. The aim of this study was to explore novel, quantitative, CT-determined asthma phenotypes. Sixty-five asthmatic patients and 30 healthy subjects underwent detailed clinical, physiologic characterization and quantitative CT analysis. Factor and cluster analysis techniques were used to determine 3 novel, quantitative, CT-based asthma phenotypes. Patients with severe and mild-to-moderate asthma demonstrated smaller mean right upper lobe apical segmental bronchus (RB1) lumen volume (LV) in comparison with healthy control subjects (272.3 mm3 [SD, 112.6 mm3], 259.0 mm3 [SD, 53.3 mm3], 366.4 mm3 [SD, 195.3 mm3], respectively; P = .007) but no difference in RB1 wall volume (WV). Air trapping measured based on mean lung density expiratory/inspiratory ratio was greater in patients with severe and mild-to-moderate asthma compared with that seen in healthy control subjects (0.861 [SD, 0.05)], 0.866 [SD, 0.07], and 0.830 [SD, 0.06], respectively; P = .04). The fractal dimension of the segmented airway tree was less in asthmatic patients compared with that seen in control subjects (P = .007). Three novel, quantitative, CT-based asthma clusters were identified, all of which demonstrated air trapping. Cluster 1 demonstrates increased RB1 WV and RB1 LV but decreased RB1 percentage WV. On the contrary, cluster 3 subjects have the smallest RB1 WV and LV values but the highest RB1 percentage WV values. There is a lack of proximal airway remodeling in cluster 2 subjects. Quantitative CT analysis provides a new perspective in asthma phenotyping, which might prove useful in patient selection for novel therapies.
Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)-assessed proximal airway remodeling and air trapping in asthmatic patients might provide new insights into underlying disease mechanisms. The aim of this study was to explore novel, quantitative, CT-determined asthma phenotypes. Sixty-five asthmatic patients and 30 healthy subjects underwent detailed clinical, physiologic characterization and quantitative CT analysis. Factor and cluster analysis techniques were used to determine 3 novel, quantitative, CT-based asthma phenotypes. Patients with severe and mild-to-moderate asthma demonstrated smaller mean right upper lobe apical segmental bronchus (RB1) lumen volume (LV) in comparison with healthy control subjects (272.3 mm(3) [SD, 112.6 mm(3)], 259.0 mm(3) [SD, 53.3 mm(3)], 366.4 mm(3) [SD, 195.3 mm(3)], respectively; P = .007) but no difference in RB1 wall volume (WV). Air trapping measured based on mean lung density expiratory/inspiratory ratio was greater in patients with severe and mild-to-moderate asthma compared with that seen in healthy control subjects (0.861 [SD, 0.05)], 0.866 [SD, 0.07], and 0.830 [SD, 0.06], respectively; P = .04). The fractal dimension of the segmented airway tree was less in asthmatic patients compared with that seen in control subjects (P = .007). Three novel, quantitative, CT-based asthma clusters were identified, all of which demonstrated air trapping. Cluster 1 demonstrates increased RB1 WV and RB1 LV but decreased RB1 percentage WV. On the contrary, cluster 3 subjects have the smallest RB1 WV and LV values but the highest RB1 percentage WV values. There is a lack of proximal airway remodeling in cluster 2 subjects. Quantitative CT analysis provides a new perspective in asthma phenotyping, which might prove useful in patient selection for novel therapies.
Author Hargadon, Beverly
Pavord, Ian D.
Gupta, Sumit
Khan, Umair T.
Marshall, Richard P.
Entwisle, James J.
Subramanian, Deepak
Parr, David
Brightling, Christopher E.
Siddiqui, Salman
Monteiro, William
Sousa, Ana R.
Singapuri, Amisha
Raj, Vimal
Hartley, Ruth
AuthorAffiliation c Respiratory Therapy Unit, GlaxoSmithKline, Stockley Park, Uxbridge, United Kingdom
e Radiology Department, Wellington Hospital, Capital and Coast District Health Board, Wellington, New Zealand
a Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
d Department of Respiratory Medicine, University Hospitals Coventry and Warwickshire, Coventry, United Kingdom
b Radiology Department, Glenfield Hospital, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom
AuthorAffiliation_xml – name: c Respiratory Therapy Unit, GlaxoSmithKline, Stockley Park, Uxbridge, United Kingdom
– name: a Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– name: e Radiology Department, Wellington Hospital, Capital and Coast District Health Board, Wellington, New Zealand
– name: d Department of Respiratory Medicine, University Hospitals Coventry and Warwickshire, Coventry, United Kingdom
– name: b Radiology Department, Glenfield Hospital, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom
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  givenname: Sumit
  surname: Gupta
  fullname: Gupta, Sumit
  email: drsumitgupta@yahoo.com
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– sequence: 2
  givenname: Ruth
  surname: Hartley
  fullname: Hartley, Ruth
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– sequence: 3
  givenname: Umair T.
  surname: Khan
  fullname: Khan, Umair T.
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– sequence: 4
  givenname: Amisha
  surname: Singapuri
  fullname: Singapuri, Amisha
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– sequence: 5
  givenname: Beverly
  surname: Hargadon
  fullname: Hargadon, Beverly
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– sequence: 6
  givenname: William
  surname: Monteiro
  fullname: Monteiro, William
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– sequence: 7
  givenname: Ian D.
  surname: Pavord
  fullname: Pavord, Ian D.
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– sequence: 8
  givenname: Ana R.
  surname: Sousa
  fullname: Sousa, Ana R.
  organization: Respiratory Therapy Unit, GlaxoSmithKline, Stockley Park, Uxbridge, United Kingdom
– sequence: 9
  givenname: Richard P.
  surname: Marshall
  fullname: Marshall, Richard P.
  organization: Respiratory Therapy Unit, GlaxoSmithKline, Stockley Park, Uxbridge, United Kingdom
– sequence: 10
  givenname: Deepak
  surname: Subramanian
  fullname: Subramanian, Deepak
  organization: Department of Respiratory Medicine, University Hospitals Coventry and Warwickshire, Coventry, United Kingdom
– sequence: 11
  givenname: David
  surname: Parr
  fullname: Parr, David
  organization: Department of Respiratory Medicine, University Hospitals Coventry and Warwickshire, Coventry, United Kingdom
– sequence: 12
  givenname: James J.
  surname: Entwisle
  fullname: Entwisle, James J.
  organization: Radiology Department, Wellington Hospital, Capital and Coast District Health Board, Wellington, New Zealand
– sequence: 13
  givenname: Salman
  surname: Siddiqui
  fullname: Siddiqui, Salman
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
– sequence: 14
  givenname: Vimal
  surname: Raj
  fullname: Raj, Vimal
  organization: Radiology Department, Glenfield Hospital, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom
– sequence: 15
  givenname: Christopher E.
  surname: Brightling
  fullname: Brightling, Christopher E.
  organization: Department of Infection, Inflammation and Immunity, Institute for Lung Health, University of Leicester, Leicester, United Kingdom
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28383878$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/24238646$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright 2013 The Authors
The Authors
2015 INIST-CNRS
Copyright © 2013 The Authors. Published by Mosby, Inc. All rights reserved.
Copyright Elsevier Limited Mar 2014
2013 The Authors 2013
Copyright_xml – notice: 2013 The Authors
– notice: The Authors
– notice: 2015 INIST-CNRS
– notice: Copyright © 2013 The Authors. Published by Mosby, Inc. All rights reserved.
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Issue 3
Keywords quantitative imaging
ATS
RB1
fractal analysis
RV
LV
TLC
WA
HU
BSA
distal airway
Dsc
MLD E/I
VI−850/−950 E-I
cluster analysis
Pi10
WV
De
airway remodeling
ICC
VI−850 E-I
ROI
Asthma
CT
Dsce
phenotypes
VI
LA
FRC
Dav
Po20
Averaged fractal dimension
Hypothetical airways with outer airway perimeter of 20 mm
D e
D av
Computed tomography
Voxel index
VI −850/−950 E-I
Mean lung density expiratory/inspiratory ratio
VI−850 change on paired inspiratory and expiratory CT scan
Right upper lobe apical segmental bronchus
Intraclass correlation coefficient
Lumen area
D sc
Lumen volume
Wall volume
Functional residual capacity
Hypothetical airway with internal perimeter of 10 mm
Region of interest
Body surface area
Total lung capacity
Voxel index change of percent voxels between −950 and −850 HU on paired inspiratory and expiratory CT scan
American Thoracic Society
VI −850 E-I
Residual volume
Slope-corrected fractal dimension
Wall area
D sce
Hounsfield units
Most efficient cover fractal dimension
Slope-corrected most-efficient covering fractal dimension
Human
Lung disease
Immunopathology
Radiodiagnosis
Respiratory disease
Remodeling
Respiratory system
Respiratory tract
Phenotype
Immunology
Distal
Bronchus disease
Medical imagery
Computerized axial tomography
Obstructive pulmonary disease
Quantitative analysis
Language English
License http://creativecommons.org/licenses/by/3.0
CC BY 4.0
Copyright © 2013 The Authors. Published by Mosby, Inc. All rights reserved.
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Snippet Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)–assessed proximal airway remodeling...
Background Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)–assessed proximal airway...
Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)-assessed proximal airway remodeling...
Background Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)-assessed proximal airway...
Background: Asthma heterogeneity is multidimensional and requires additional tools to unravel its complexity. Computed tomography (CT)-assessed proximal airway...
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StartPage 729
SubjectTerms Adult
Aged
Airway Remodeling
Allergy and Immunology
Asthma
Asthma - diagnostic imaging
Asthma - pathology
Asthma - physiopathology
Asthma and Lower Airway Disease
Biological and medical sciences
Chronic obstructive pulmonary disease, asthma
Cluster Analysis
distal airway
Drug therapy
Female
fractal analysis
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Humans
Immunopathology
Lung - physiopathology
Male
Medical sciences
Methods
Middle Aged
Phenotype
phenotypes
Pneumology
Quality of life
quantitative imaging
Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis
Software
Statistical analysis
Tomography
Tomography, X-Ray Computed - methods
Variables
Title Quantitative computed tomography–derived clusters: Redefining airway remodeling in asthmatic patients
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https://dx.doi.org/10.1016/j.jaci.2013.09.039
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Volume 133
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