Effects of a Short Course of Inhaled Corticosteroids in Noneosinophilic Asthmatic Subjects

Author:

Lemière Catherine1,Tremblay Caroline1,FitzGerald Mark2,Aaron Shawn D3,Leigh Richard4,Boulet Louis-Philippe5,Martin James G6,Nair Parameswaran7,Olivenstein Ronald6,Chaboillez Simone1

Affiliation:

1. Hôpital du Sacré–Cœur de Montréal, Université de Montréal, Montréal, Quebec, Canada

2. Vancouver General Hospital, University of British Columbia Vancouver, British Columbia, Canada

3. Ottawa Hospital, University of Ottawa, Ottawa, Ontario, Canada

4. Institute of Infection, Immunity & Inflammation, University of Calgary, Calgary, Alberta, Canada

5. Laval Hospital, Université Laval, Sainte Foy, Canada

6. Montreal Chest Institute, McGill University Health Centre, Montreal, Quebec, Canada

7. St Joseph’s Healthcare, McMaster University, Hamilton, Ontario, Canada

Abstract

BACKGROUND: Noneosinophilic asthma has been regarded as a distinct phenotype characterized by a poor response to inhaled corticosteroids (ICS).OBJECTIVE: To determine whether noneosinophilic, steroid-naive asthmatic subjects show an improvement in asthma control, asthma symptoms and spirometry after four weeks of treatment with ICS, and whether they further benefit from the addition of a long-acting beta-2 agonists to ICS.METHODS: A randomized, double-blind, placebo-controlled, multicentre study comparing the efficacy of placebo versus inhaled fluticasone propionate 250 μg twice daily for four weeks in mildly uncontrolled, steroid-naive asthmatic subjects with a sputum eosinophil count ≤2%. This was followed by an open-label, four-week treatment period with fluticasone propionate 250 μg/salmeterol 50 μg, twice daily for all subjects.RESULTS: After four weeks of double-blind treatment, there was a statistically significant and clinically relevant improvement in the mean (± SD) Asthma Control Questionnaire score in the ICS-treated group (n=6) (decrease of 1.0±0.5) compared with the placebo group (n=6) (decrease of 0.09±0.4) (P=0.008). Forced expiratory volume in 1 s declined in the placebo group (−0.2±0.2 L) and did not change in the ICS group (0.04±0.1 L) after four weeks of treatment (P=0.02). The open-label treatment with fluticasone propionate 250 μg/salmeterol 50 μg did not produce additional improvements in those who were previously treated for four weeks with inhaled fluticasone alone.CONCLUSION: A clinically important and statistically significant response to ICS was observed in mildly uncontrolled noneosinophilic asthmatic subjects.

Funder

GlaxoSmithKline

Publisher

Hindawi Limited

Subject

Pulmonary and Respiratory Medicine

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