Structural changes in the bronchial mucosa of young children at risk of developing asthma
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24028346
DOI
10.1111/pai.12119
Knihovny.cz E-resources
- Keywords
- basement membrane, bronchial asthma, collagen IV, laminin, remodelling, tenascin,
- MeSH
- Basement Membrane chemistry pathology MeSH
- Biopsy MeSH
- Asthma etiology metabolism pathology MeSH
- Bronchoscopy MeSH
- Bronchi chemistry pathology MeSH
- Early Diagnosis MeSH
- Immunohistochemistry MeSH
- Infant MeSH
- Collagen Type IV analysis MeSH
- Laminin analysis MeSH
- Humans MeSH
- Predictive Value of Tests MeSH
- Child, Preschool MeSH
- Airway Remodeling * MeSH
- Respiratory Mucosa chemistry pathology MeSH
- Risk Factors MeSH
- Case-Control Studies MeSH
- Tenascin analysis MeSH
- Age Factors MeSH
- Check Tag
- Infant MeSH
- Humans MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Collagen Type IV MeSH
- Laminin MeSH
- Tenascin MeSH
BACKGROUND: Bronchial asthma often starts in early childhood. Clinical manifestation of the disease is likely due to inflammatory processes in the airways initiated by various stimuli. Developed remodelling is regularly observed in the bronchial mucosa of adult asthmatics but we still lack information about its onset and latter development with the natural course of the disease. In this study, we analysed histological findings in bronchial biopsies obtained from very young children (under 4 yr of age). We hypothesized that initial undetectable changes in the airway epithelium of children predisposed to asthma may be one of the first mechanisms leading to morphological changes in the bronchial mucosa. METHODS: We measured the thickness of the basement membrane using a light microscope and analysed the presence of its three basic structural glycoproteins: laminin, tenascin and collagen IV, using immunohistochemical techniques. We compared these findings in children predisposed to asthma according to the selected clinical criteria of the Asthma Predictive Index and in a control group of children. RESULTS: We found a significant difference in the thickness of the basement membrane between the two groups. We also found a difference in the subepithelial deposition of laminin and collagen IV in the basement membrane but no difference in the deposition of tenascin. CONCLUSIONS: We conclude that initial changes leading to further remodelling may start at a very early age even before clinical manifestation of the disease.
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