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Airway Elastin is increased in severe asthma and relates to proximal wall area: histological and computed tomography findings from the U-BIOPRED severe asthma study

Airway Elastin is increased in severe asthma and relates to proximal wall area: histological and computed tomography findings from the U-BIOPRED severe asthma study
Airway Elastin is increased in severe asthma and relates to proximal wall area: histological and computed tomography findings from the U-BIOPRED severe asthma study
Background: Airway remodelling, which may include goblet cell hyperplasia / hypertrophy, changes in epithelial integrity, accumulation of extracellular matrix components, smooth muscle hypertrophy and thickening of the lamina reticularis, is a feature of severe asthma and contributes to the clinical phenotype.

Objective: Within the U-BIOPRED severe asthma study, we have assessed histological elements of airway remodelling and their relationship to computed tomography (CT) measures of proximal airway dimensions.

Methods: Bronchial biopsies were collected from two severe asthma groups, one non-smoker (SAns, n=28) and one current/ex-smoker (SAs/ex, n=13), and a mild-moderate asthma group (MMA, n=28) classified and treated according to GINA guidelines, plus a healthy control group (HC, n=33). A Movat’s pentachrome technique was used to identify mucin, elastin and total collagen in these biopsies. The number of goblet cells (mucin+) were counted as a percentage of the total number of epithelial cells and the percentage mucin epithelial area measured. The percentage area of elastic fibres and total collagen within the submucosa were also measured, and the morphology of the elastic fibres classified. Participants in the asthma groups also had a CT scan to assess large airway morphometry.

Results: The submucosal tissue elastin percentage was higher in both severe asthma groups (16.1% SAns, 18.9% SAs/ex) compared to the HC (9.7%) but did not differ between asthma groups. There was a positive relationship between elastin and airway wall area measured by CT (n= 18-20, rho=0.544, p=0.024), which also related to an increase in elastic fibres with a thickened lamellar morphological appearance. Mucin epithelial area and total collagen were not different between the four groups. Due to small numbers of suitable CT scans it was not feasible to compare airway morphometry between the asthma groups.

Conclusion: These findings identify a link between extent of elastin deposition and airway wall thickening in severe asthma.
0954-7894
Wilson, Susan
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Ward, Jonathan
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Pickett, Helen M
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Baldi, Simonetta
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Sousa, Ana R.
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Sterk, Peter J.
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Chung, Kian Fan
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Djukanovic, Ratko
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Dahlén, Barbro
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Billing, Bo
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Shaw, Dominick E.
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Krug, Norbert
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Sandström, Thomas
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Brightling, Christopher E.
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Howarth, Peter
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Wilson, Susan
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Ward, Jonathan
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Pickett, Helen M
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Baldi, Simonetta
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Sousa, Ana R.
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Sterk, Peter J.
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Chung, Kian Fan
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Djukanovic, Ratko
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Dahlén, Barbro
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Billing, Bo
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Shaw, Dominick E.
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Krug, Norbert
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Sandström, Thomas
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Brightling, Christopher E.
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Howarth, Peter
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Wilson, Susan, Ward, Jonathan, Pickett, Helen M, Baldi, Simonetta, Sousa, Ana R., Sterk, Peter J., Chung, Kian Fan, Djukanovic, Ratko, Dahlén, Barbro, Billing, Bo, Shaw, Dominick E., Krug, Norbert, Sandström, Thomas, Brightling, Christopher E. and Howarth, Peter (2020) Airway Elastin is increased in severe asthma and relates to proximal wall area: histological and computed tomography findings from the U-BIOPRED severe asthma study. Clinical & Experimental Allergy. (doi:10.1111/cea.13813).

Record type: Article

Abstract

Background: Airway remodelling, which may include goblet cell hyperplasia / hypertrophy, changes in epithelial integrity, accumulation of extracellular matrix components, smooth muscle hypertrophy and thickening of the lamina reticularis, is a feature of severe asthma and contributes to the clinical phenotype.

Objective: Within the U-BIOPRED severe asthma study, we have assessed histological elements of airway remodelling and their relationship to computed tomography (CT) measures of proximal airway dimensions.

Methods: Bronchial biopsies were collected from two severe asthma groups, one non-smoker (SAns, n=28) and one current/ex-smoker (SAs/ex, n=13), and a mild-moderate asthma group (MMA, n=28) classified and treated according to GINA guidelines, plus a healthy control group (HC, n=33). A Movat’s pentachrome technique was used to identify mucin, elastin and total collagen in these biopsies. The number of goblet cells (mucin+) were counted as a percentage of the total number of epithelial cells and the percentage mucin epithelial area measured. The percentage area of elastic fibres and total collagen within the submucosa were also measured, and the morphology of the elastic fibres classified. Participants in the asthma groups also had a CT scan to assess large airway morphometry.

Results: The submucosal tissue elastin percentage was higher in both severe asthma groups (16.1% SAns, 18.9% SAs/ex) compared to the HC (9.7%) but did not differ between asthma groups. There was a positive relationship between elastin and airway wall area measured by CT (n= 18-20, rho=0.544, p=0.024), which also related to an increase in elastic fibres with a thickened lamellar morphological appearance. Mucin epithelial area and total collagen were not different between the four groups. Due to small numbers of suitable CT scans it was not feasible to compare airway morphometry between the asthma groups.

Conclusion: These findings identify a link between extent of elastin deposition and airway wall thickening in severe asthma.

Text
Remodelling and CT in severe asthma_Wilson SJ for PURE - Accepted Manuscript
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More information

Submitted date: 4 September 2020
Accepted/In Press date: 15 December 2020
e-pub ahead of print date: 20 December 2020

Identifiers

Local EPrints ID: 445990
URI: http://eprints.soton.ac.uk/id/eprint/445990
ISSN: 0954-7894
PURE UUID: 989361e7-596a-4146-92a5-1e766e0f32cc
ORCID for Susan Wilson: ORCID iD orcid.org/0000-0003-1305-8271
ORCID for Jonathan Ward: ORCID iD orcid.org/0000-0002-9278-0002
ORCID for Ratko Djukanovic: ORCID iD orcid.org/0000-0001-6039-5612

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Date deposited: 18 Jan 2021 17:31
Last modified: 17 Mar 2024 06:11

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Contributors

Author: Susan Wilson ORCID iD
Author: Jonathan Ward ORCID iD
Author: Helen M Pickett
Author: Simonetta Baldi
Author: Ana R. Sousa
Author: Peter J. Sterk
Author: Kian Fan Chung
Author: Barbro Dahlén
Author: Bo Billing
Author: Dominick E. Shaw
Author: Norbert Krug
Author: Thomas Sandström
Author: Christopher E. Brightling
Author: Peter Howarth

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