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Small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue
INTRODUCTION: Airway dysfunction in patients with the Acute Respiratory Distress Syndrome (ARDS) is evidenced by expiratory flow limitation and dynamic hyperinflation. These functional alterations have been attributed to closure/obstruction of small airways. Airway morphological changes have been re...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3222031/ https://www.ncbi.nlm.nih.gov/pubmed/21211006 http://dx.doi.org/10.1186/cc9401 |
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author | Morales, Maina MB Pires-Neto, Ruy C Inforsato, Nicole Lanças, Tatiana da Silva, Luiz FF Saldiva, Paulo HN Mauad, Thais Carvalho, Carlos RR Amato, Marcelo BP Dolhnikoff, Marisa |
author_facet | Morales, Maina MB Pires-Neto, Ruy C Inforsato, Nicole Lanças, Tatiana da Silva, Luiz FF Saldiva, Paulo HN Mauad, Thais Carvalho, Carlos RR Amato, Marcelo BP Dolhnikoff, Marisa |
author_sort | Morales, Maina MB |
collection | PubMed |
description | INTRODUCTION: Airway dysfunction in patients with the Acute Respiratory Distress Syndrome (ARDS) is evidenced by expiratory flow limitation and dynamic hyperinflation. These functional alterations have been attributed to closure/obstruction of small airways. Airway morphological changes have been reported in experimental models of acute lung injury, characterized by epithelial necrosis and denudation in distal airways. To date, however, no study has focused on the morphological airway changes in lungs from human subjects with ARDS. The aim of this study is to evaluate structural and inflammatory changes in distal airways in ARDS patients. METHODS: We retrospectively studied autopsy lung tissue from subjects who died with ARDS and from control subjects who died of non pulmonary causes. Using image analysis, we quantified the extension of epithelial changes (normal, abnormal and denudated epithelium expressed as percentages of the total epithelium length), bronchiolar inflammation, airway wall thickness, and extracellular matrix (ECM) protein content in distal airways. The Student's t-test or the Mann-Whitney test was used to compare data between the ARDS and control groups. Bonferroni adjustments were used for multiple tests. The association between morphological and clinical data was analyzed by Pearson rank test. RESULTS: Thirty-one ARDS patients (A: PaO(2)/FiO(2 )≤200, 45 ± 14 years, 16 males) and 11 controls (C: 52 ± 16 years, 7 males) were included in the study. ARDS airways showed a shorter extension of normal epithelium (A:32.9 ± 27.2%, C:76.7 ± 32.7%, P < 0.001), a larger extension of epithelium denudation (A:52.6 ± 35.2%, C:21.8 ± 32.1%, P < 0.01), increased airway inflammation (A:1(3), C:0(1), P = 0.03), higher airway wall thickness (A:138.7 ± 54.3 μm, C:86.4 ± 33.3 μm, P < 0.01), and higher airway content of collagen I, fibronectin, versican and matrix metalloproteinase-9 (MMP-9) compared to controls (P ≤0.03). The extension of normal epithelium showed a positive correlation with PaO(2)/FiO(2 )(r(2 )= 0.34; P = 0.02) and a negative correlation with plateau pressure (r(2 )= 0.27; P = 0.04). The extension of denuded epithelium showed a negative correlation with PaO(2)/FiO(2 )(r(2 )= 0.27; P = 0.04). CONCLUSIONS: Structural changes in small airways of patients with ARDS were characterized by epithelial denudation, inflammation and airway wall thickening with ECM remodeling. These changes are likely to contribute to functional airway changes in patients with ARDS. |
format | Online Article Text |
id | pubmed-3222031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32220312011-11-22 Small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue Morales, Maina MB Pires-Neto, Ruy C Inforsato, Nicole Lanças, Tatiana da Silva, Luiz FF Saldiva, Paulo HN Mauad, Thais Carvalho, Carlos RR Amato, Marcelo BP Dolhnikoff, Marisa Crit Care Research INTRODUCTION: Airway dysfunction in patients with the Acute Respiratory Distress Syndrome (ARDS) is evidenced by expiratory flow limitation and dynamic hyperinflation. These functional alterations have been attributed to closure/obstruction of small airways. Airway morphological changes have been reported in experimental models of acute lung injury, characterized by epithelial necrosis and denudation in distal airways. To date, however, no study has focused on the morphological airway changes in lungs from human subjects with ARDS. The aim of this study is to evaluate structural and inflammatory changes in distal airways in ARDS patients. METHODS: We retrospectively studied autopsy lung tissue from subjects who died with ARDS and from control subjects who died of non pulmonary causes. Using image analysis, we quantified the extension of epithelial changes (normal, abnormal and denudated epithelium expressed as percentages of the total epithelium length), bronchiolar inflammation, airway wall thickness, and extracellular matrix (ECM) protein content in distal airways. The Student's t-test or the Mann-Whitney test was used to compare data between the ARDS and control groups. Bonferroni adjustments were used for multiple tests. The association between morphological and clinical data was analyzed by Pearson rank test. RESULTS: Thirty-one ARDS patients (A: PaO(2)/FiO(2 )≤200, 45 ± 14 years, 16 males) and 11 controls (C: 52 ± 16 years, 7 males) were included in the study. ARDS airways showed a shorter extension of normal epithelium (A:32.9 ± 27.2%, C:76.7 ± 32.7%, P < 0.001), a larger extension of epithelium denudation (A:52.6 ± 35.2%, C:21.8 ± 32.1%, P < 0.01), increased airway inflammation (A:1(3), C:0(1), P = 0.03), higher airway wall thickness (A:138.7 ± 54.3 μm, C:86.4 ± 33.3 μm, P < 0.01), and higher airway content of collagen I, fibronectin, versican and matrix metalloproteinase-9 (MMP-9) compared to controls (P ≤0.03). The extension of normal epithelium showed a positive correlation with PaO(2)/FiO(2 )(r(2 )= 0.34; P = 0.02) and a negative correlation with plateau pressure (r(2 )= 0.27; P = 0.04). The extension of denuded epithelium showed a negative correlation with PaO(2)/FiO(2 )(r(2 )= 0.27; P = 0.04). CONCLUSIONS: Structural changes in small airways of patients with ARDS were characterized by epithelial denudation, inflammation and airway wall thickening with ECM remodeling. These changes are likely to contribute to functional airway changes in patients with ARDS. BioMed Central 2011 2011-01-06 /pmc/articles/PMC3222031/ /pubmed/21211006 http://dx.doi.org/10.1186/cc9401 Text en Copyright ©2011 Morales et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Morales, Maina MB Pires-Neto, Ruy C Inforsato, Nicole Lanças, Tatiana da Silva, Luiz FF Saldiva, Paulo HN Mauad, Thais Carvalho, Carlos RR Amato, Marcelo BP Dolhnikoff, Marisa Small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue |
title | Small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue |
title_full | Small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue |
title_fullStr | Small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue |
title_full_unstemmed | Small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue |
title_short | Small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue |
title_sort | small airway remodeling in acute respiratory distress syndrome: a study in autopsy lung tissue |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3222031/ https://www.ncbi.nlm.nih.gov/pubmed/21211006 http://dx.doi.org/10.1186/cc9401 |
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