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Atopy May Be an Important Determinant of Subepithelial Fibrosis in Subjects with Asymptomatic Airway Hyperresponsiveness

The bronchial pathology of asymptomatic airway hyperreponsiveness (AHR) subjects is not well understood, and the role of atopy in the development of airway remodeling is unclear. The aim of this study was to evaluate whether atopy is associated with airway remodeling in asymptomatic AHR subjects. Fi...

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Autores principales: Sohn, Seong-Wook, Chang, Yoon-Seok, Lee, Hye-Seung, Chung, Doo-Hyun, Lee, Choon-Taek, Kim, Young-Hwan, Kim, Yoon-Keun, Min, Kyung-Up, Kim, You-Young, Cho, Sang-Heon
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526529/
https://www.ncbi.nlm.nih.gov/pubmed/18583872
http://dx.doi.org/10.3346/jkms.2008.23.3.390
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author Sohn, Seong-Wook
Chang, Yoon-Seok
Lee, Hye-Seung
Chung, Doo-Hyun
Lee, Choon-Taek
Kim, Young-Hwan
Kim, Yoon-Keun
Min, Kyung-Up
Kim, You-Young
Cho, Sang-Heon
author_facet Sohn, Seong-Wook
Chang, Yoon-Seok
Lee, Hye-Seung
Chung, Doo-Hyun
Lee, Choon-Taek
Kim, Young-Hwan
Kim, Yoon-Keun
Min, Kyung-Up
Kim, You-Young
Cho, Sang-Heon
author_sort Sohn, Seong-Wook
collection PubMed
description The bronchial pathology of asymptomatic airway hyperreponsiveness (AHR) subjects is not well understood, and the role of atopy in the development of airway remodeling is unclear. The aim of this study was to evaluate whether atopy is associated with airway remodeling in asymptomatic AHR subjects. Five groups, i.e., atopic or non-atopic subjects with asymptomatic AHR, atopic or non-atopic healthy controls, and subjects with mild atopic asthma, were evaluated by bronchoscopic biopsy. By electron microscopy, mean reticular basement membrane (RBM) thicknesses were 4.3±1.7 µm, 3.4±1.8 µm, 2.5±1.5 µm, 2.6±1.1 µm, and 2.3±1.2 µm in the mild atopic asthma, atopic and non-atopic asymptomatic AHR, atopic and non-atopic control groups, respectively (p=0.002). RBM thicknesses were significantly higher in the mild atopic asthma group and in the atopic asymptomatic AHR group than in the other three groups (p=0.048). No significant difference in RBM thickness was observed between the atopic asymptomatic AHR group and the mild atopic asthma group (p>0.05), nor between non-atopic asymptomatic AHR group and the two control groups (p>0.05). By light microscopy, subepithelial layer thicknesses between the groups showed the same results. These findings suggest that RBM thickening occurs in subjects with atopic asymptomatic AHR, and that atopy plays an important role in airway remodeling.
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spelling pubmed-25265292008-11-07 Atopy May Be an Important Determinant of Subepithelial Fibrosis in Subjects with Asymptomatic Airway Hyperresponsiveness Sohn, Seong-Wook Chang, Yoon-Seok Lee, Hye-Seung Chung, Doo-Hyun Lee, Choon-Taek Kim, Young-Hwan Kim, Yoon-Keun Min, Kyung-Up Kim, You-Young Cho, Sang-Heon J Korean Med Sci Original Article The bronchial pathology of asymptomatic airway hyperreponsiveness (AHR) subjects is not well understood, and the role of atopy in the development of airway remodeling is unclear. The aim of this study was to evaluate whether atopy is associated with airway remodeling in asymptomatic AHR subjects. Five groups, i.e., atopic or non-atopic subjects with asymptomatic AHR, atopic or non-atopic healthy controls, and subjects with mild atopic asthma, were evaluated by bronchoscopic biopsy. By electron microscopy, mean reticular basement membrane (RBM) thicknesses were 4.3±1.7 µm, 3.4±1.8 µm, 2.5±1.5 µm, 2.6±1.1 µm, and 2.3±1.2 µm in the mild atopic asthma, atopic and non-atopic asymptomatic AHR, atopic and non-atopic control groups, respectively (p=0.002). RBM thicknesses were significantly higher in the mild atopic asthma group and in the atopic asymptomatic AHR group than in the other three groups (p=0.048). No significant difference in RBM thickness was observed between the atopic asymptomatic AHR group and the mild atopic asthma group (p>0.05), nor between non-atopic asymptomatic AHR group and the two control groups (p>0.05). By light microscopy, subepithelial layer thicknesses between the groups showed the same results. These findings suggest that RBM thickening occurs in subjects with atopic asymptomatic AHR, and that atopy plays an important role in airway remodeling. The Korean Academy of Medical Sciences 2008-06 2008-06-20 /pmc/articles/PMC2526529/ /pubmed/18583872 http://dx.doi.org/10.3346/jkms.2008.23.3.390 Text en Copyright © 2008 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sohn, Seong-Wook
Chang, Yoon-Seok
Lee, Hye-Seung
Chung, Doo-Hyun
Lee, Choon-Taek
Kim, Young-Hwan
Kim, Yoon-Keun
Min, Kyung-Up
Kim, You-Young
Cho, Sang-Heon
Atopy May Be an Important Determinant of Subepithelial Fibrosis in Subjects with Asymptomatic Airway Hyperresponsiveness
title Atopy May Be an Important Determinant of Subepithelial Fibrosis in Subjects with Asymptomatic Airway Hyperresponsiveness
title_full Atopy May Be an Important Determinant of Subepithelial Fibrosis in Subjects with Asymptomatic Airway Hyperresponsiveness
title_fullStr Atopy May Be an Important Determinant of Subepithelial Fibrosis in Subjects with Asymptomatic Airway Hyperresponsiveness
title_full_unstemmed Atopy May Be an Important Determinant of Subepithelial Fibrosis in Subjects with Asymptomatic Airway Hyperresponsiveness
title_short Atopy May Be an Important Determinant of Subepithelial Fibrosis in Subjects with Asymptomatic Airway Hyperresponsiveness
title_sort atopy may be an important determinant of subepithelial fibrosis in subjects with asymptomatic airway hyperresponsiveness
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526529/
https://www.ncbi.nlm.nih.gov/pubmed/18583872
http://dx.doi.org/10.3346/jkms.2008.23.3.390
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