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Immunohistology and remodeling in fatal pediatric and adolescent asthma

BACKGROUND: Thickening of reticular basement membrane, increased airway smooth muscle mass and eosinophilic inflammation are found in adult fatal asthma. At the present study the histopathology of fatal paediatric and adolescent asthma is evaluated. METHODS: Post-mortem lung autopsies from 12 fatal...

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Autores principales: Malmström, Kristiina, Lohi, Jouko, Sajantila, Antti, Jahnsen, Frode L., Kajosaari, Merja, Sarna, Seppo, Mäkelä, Mika J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434550/
https://www.ncbi.nlm.nih.gov/pubmed/28511697
http://dx.doi.org/10.1186/s12931-017-0575-0
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author Malmström, Kristiina
Lohi, Jouko
Sajantila, Antti
Jahnsen, Frode L.
Kajosaari, Merja
Sarna, Seppo
Mäkelä, Mika J.
author_facet Malmström, Kristiina
Lohi, Jouko
Sajantila, Antti
Jahnsen, Frode L.
Kajosaari, Merja
Sarna, Seppo
Mäkelä, Mika J.
author_sort Malmström, Kristiina
collection PubMed
description BACKGROUND: Thickening of reticular basement membrane, increased airway smooth muscle mass and eosinophilic inflammation are found in adult fatal asthma. At the present study the histopathology of fatal paediatric and adolescent asthma is evaluated. METHODS: Post-mortem lung autopsies from 12 fatal asthma cases and 8 non-asthmatic control subjects were examined. Thickness of reticular basement membrane (RBM) and percentage of airway smooth muscle (ASM%) mass area were measured and inflammatory cells were counted. Patient records were reviewed for clinical history. RESULTS: The age range of the cases was from 0.9 to 19.5 years, eight were males and five had received inhaled corticosteroids. Thickened RBM was detected in majority of the cases without any correlation to treatment delay, age at onset of symptoms or diagnosis. In the large airways ASM was clearly increased in one third of the cases whereas the median ASM% did not differ from that in healthy controls (14.0% vs. 14.0%). In small airways no increase of ASM was found, instead mucous plugs were seen in fatal asthma. The number of eosinophils, plasmacytoid dendritic cells, macrophages, and B-cells were significantly increased in fatal asthma cases compared with controls and the two latter correlated with the length of the fatal exacerbation. CONCLUSIONS: The findings highlight the strong presence of eosinophils and mucous plugs even in small airways in children and adolescents with fatal asthma. Thickened RBM was obvious in majority of the patients. Contrary to our hypothesis, increased ASM% was detected in only one third of the patients.
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spelling pubmed-54345502017-05-18 Immunohistology and remodeling in fatal pediatric and adolescent asthma Malmström, Kristiina Lohi, Jouko Sajantila, Antti Jahnsen, Frode L. Kajosaari, Merja Sarna, Seppo Mäkelä, Mika J. Respir Res Research BACKGROUND: Thickening of reticular basement membrane, increased airway smooth muscle mass and eosinophilic inflammation are found in adult fatal asthma. At the present study the histopathology of fatal paediatric and adolescent asthma is evaluated. METHODS: Post-mortem lung autopsies from 12 fatal asthma cases and 8 non-asthmatic control subjects were examined. Thickness of reticular basement membrane (RBM) and percentage of airway smooth muscle (ASM%) mass area were measured and inflammatory cells were counted. Patient records were reviewed for clinical history. RESULTS: The age range of the cases was from 0.9 to 19.5 years, eight were males and five had received inhaled corticosteroids. Thickened RBM was detected in majority of the cases without any correlation to treatment delay, age at onset of symptoms or diagnosis. In the large airways ASM was clearly increased in one third of the cases whereas the median ASM% did not differ from that in healthy controls (14.0% vs. 14.0%). In small airways no increase of ASM was found, instead mucous plugs were seen in fatal asthma. The number of eosinophils, plasmacytoid dendritic cells, macrophages, and B-cells were significantly increased in fatal asthma cases compared with controls and the two latter correlated with the length of the fatal exacerbation. CONCLUSIONS: The findings highlight the strong presence of eosinophils and mucous plugs even in small airways in children and adolescents with fatal asthma. Thickened RBM was obvious in majority of the patients. Contrary to our hypothesis, increased ASM% was detected in only one third of the patients. BioMed Central 2017-05-16 2017 /pmc/articles/PMC5434550/ /pubmed/28511697 http://dx.doi.org/10.1186/s12931-017-0575-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Malmström, Kristiina
Lohi, Jouko
Sajantila, Antti
Jahnsen, Frode L.
Kajosaari, Merja
Sarna, Seppo
Mäkelä, Mika J.
Immunohistology and remodeling in fatal pediatric and adolescent asthma
title Immunohistology and remodeling in fatal pediatric and adolescent asthma
title_full Immunohistology and remodeling in fatal pediatric and adolescent asthma
title_fullStr Immunohistology and remodeling in fatal pediatric and adolescent asthma
title_full_unstemmed Immunohistology and remodeling in fatal pediatric and adolescent asthma
title_short Immunohistology and remodeling in fatal pediatric and adolescent asthma
title_sort immunohistology and remodeling in fatal pediatric and adolescent asthma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434550/
https://www.ncbi.nlm.nih.gov/pubmed/28511697
http://dx.doi.org/10.1186/s12931-017-0575-0
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