Abstract

Hyperinflation contributes to dyspnea intensity in COPD. Little is known about the molecular mechanisms underlying hyperinflation and how inhaled corticosteroids (ICS) affect this important aspect of COPD pathophysiology. To investigate the effect of ICS/long-acting β2-agonist (LABA) treatment on both lung function measures of hyperinflation, and the nasal epithelial gene-expression profile in severe COPD. 117 patients were screened and 60 COPD patients entered a 1-month run-in period on low-dose ICS/LABA budesonide/formoterol (BUD/F) 200/6 one inhalation b.i.d. Patients were then randomly assigned to 3-month treatment with either a high dose BDP/F 100/6 two inhalations b.i.d. (n = 31) or BUD/F 200/6 two inhalations b.i.d. (n = 29). Lung function measurements and nasal epithelial gene-expression were assessed before and after 3-month treatment and validated in independent datasets. After 3-month ICS/LABA treatment, residual volume (RV)/total lung capacity (TLC)% predicted was reduced compared to baseline (p < 0.05). We identified a nasal gene-expression signature at screening that associated with higher RV/TLC% predicted values. This signature, decreased by ICS/LABA treatment was enriched for genes associated with increased p53 mediated apoptosis was replicated in bronchial biopsies of COPD patients. Finally, this signature was increased in COPD patients compared to controls in nasal, bronchial and small airways brushings. Short-term ICS/LABA treatment improves RV/TLC% predicted in severe COPD. Furthermore, it decreases the expression of genes involved in the signal transduction by the p53 class mediator, which is a replicable COPD gene expression signature in the upper and lower airways.Trial registration: ClinicalTrials.gov registration number NCT01351792 (registration date May 11, 2011), ClinicalTrials.gov registration number NCT00848406 (registration date February 20, 2009), ClinicalTrials.gov registration number NCT00158847 (registration date September 12, 2005).

Highlights

  • Hyperinflation contributes to dyspnea intensity in Chronic Obstructive Pulmonary Disease (COPD)

  • We found no significant effect of increasing the dose of inhaled corticosteroids (ICS)/LABA treatment on pre- and post-dose residual volume (RV)% predicted, total lung capacity (TLC)% predicted, and ­FEV1% predicted over the 3-month treatment period (Fig. 2A–C)

  • O’Donnell et al showed an improvement in hyperinflation, as reflected by RV and Forced Respiratory Capacity (FRC), following treatment with fluticasone/salmeterol for 2 months, while John et al showed a significant decrease in RV/TLC% predicted after 3-month treatment with extra-fine particle ­beclomethasone[9,10]

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Summary

Introduction

Hyperinflation contributes to dyspnea intensity in COPD. Little is known about the molecular mechanisms underlying hyperinflation and how inhaled corticosteroids (ICS) affect this important aspect of COPD pathophysiology. To investigate the effect of ICS/long-acting β2-agonist (LABA) treatment on both lung function measures of hyperinflation, and the nasal epithelial gene-expression profile in severe COPD. We identified a nasal gene-expression signature at screening that associated with higher RV/TLC% predicted values This signature, decreased by ICS/LABA treatment was enriched for genes associated with increased p53 mediated apoptosis was replicated in bronchial biopsies of COPD patients. Air trapping is present in a considerable proportion of patients, as reflected by an increased residual volume (RV) in relation to total lung capacity (TLC) This trapped air, i.e. hyperinflation that is associated with heterogeneity in patency of the small airways, contributes importantly to the dyspnea intensity experienced by COPD p­ atients[3].

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