Unbound MEDLINE

Airway structural alterations selectively associated with severe asthma. American journal of respiratory and critical care medicine. [Am J Respir Crit Care Med] Journal article

 
TitleAirway structural alterations selectively associated with severe asthma.
Author(s)Benayoun L, Druilhe A, Dombret MC, Aubier M, Pretolani M 
InstitutionInstitut National de la Santé et de la Recherche Médicale Unité 408, Faculté de Médecine Xavier Bichat, Service de Pneumologie, Hôpital Bichat, Paris, France.
SourceAm J Respir Crit Care Med 2003 May 15; 167(10):1360-8.
MeSHAdult
Age Factors
Aged
Airway Resistance
Asthma
Biopsy, Needle
Bronchial Hyperreactivity
Bronchoalveolar Lavage Fluid
Case-Control Studies
Cohort Studies
Comparative Study
Female
Humans
Immunohistochemistry
Male
Middle Aged
Multivariate Analysis
Muscle, Smooth
Probability
Pulmonary Disease, Chronic Obstructive
Reference Values
Regression Analysis
Research Support, Non-U.S. Gov't
Respiratory Function Tests
Risk Assessment
Sensitivity and Specificity
Severity of Illness Index
Sex Factors
AbstractTo identify airway pathologic abnormalities selectively associated with severe asthma, we examined 10 control subjects, 10 patients with intermittent asthma, 15 patients with mild-to-moderate persistent asthma, 15 patients with severe persistent asthma, and 10 patients with chronic obstructive pulmonary disease. Bronchial biopsies were assessed for epithelial integrity; subepithelial basement membrane (SBM) thickness; collagen type III deposition; eosinophil, neutrophil, and fibroblast numbers; mucous gland and airway smooth muscle (ASM) areas; SBM-ASM distance; ASM hypertrophy (increased cell size); and the expression of the contractile proteins alpha-actin, smooth muscle myosin heavy-chain isoforms, myosin light-chain kinase, and the phosphorylated form of the regulatory light chain of myosin. Neither mucosal eosinophilia nor neutrophilia, epithelial damage, or SBM thickness reflected asthma severity. In contrast, higher numbers of fibroblasts (p < 0.001), an increase in collagen type III deposition (p < 0.020), larger mucous gland (p < 0.040) and ASM (p < 0.001) areas, augmented ASM cell size (p < 0.001), and myosin light-chain kinase expression (p < 0.005) distinguished patients with severe persistent asthma from patients with milder disease or with chronic obstructive pulmonary disease. Stepwise multivariate regression analysis established that fibroblast numbers and ASM cell size were negatively associated with prebronchodilator and postbronchodilator FEV1 values in patients with asthma. We conclude that fibroblast accumulation and ASM hypertrophy in proximal airways are selective determinants of severe persistent asthma.
Languageeng
Pub Type(s)Journal Article
PubMed ID12531777
  
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