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Thorax 2007;62:938-943 doi:10.1136/thx.2006.071068
  • Chronic obstructive pulmonary disease

Effect of salmeterol/fluticasone propionate on airway inflammation in COPD: a randomised controlled trial

  1. Jean Bourbeau1,
  2. Pota Christodoulopoulos1,
  3. Francois Maltais2,
  4. Yasuhiro Yamauchi3,
  5. Ronald Olivenstein1,
  6. Qutayba Hamid3
  1. 1
    Respiratory Epidemiology and Clinical Research Unit, Montreal Chest Institute, McGill University Health Centre, Montréal, Quebec, Canada
  2. 2
    Centre de recherche, Hôpital Laval, Institut Universitaire de cardiologie et de pneumologie, Université Laval, Québec, Canada
  3. 3
    Meakins Christie Laboratories, McGill University, Montréal, Quebec, Canada
  1. Professor Qutayba Hamid, Meakins Christie Laboratories, McGill University, 3626 St Urbain Street, Montreal, Quebec, Canada H2X 2P2; qutayba.hamid{at}mcgill.ca
  • Received 31 August 2006
  • Accepted 5 April 2007
  • Published Online First 8 June 2007

Abstract

Background: Airway inflammation in chronic obstructive pulmonary disease (COPD) is characterised by infiltration of CD8+ T cells and CD68+ macrophages and an increased number of neutrophils, whereas few studies have described the presence of eosinophils. Although the anti-inflammatory effects of corticosteroids in stable COPD are unclear, recent studies suggest that combination therapy could be beneficial. A study was therefore undertaken to evaluate combined salmeterol/fluticasone propionate (SFC) and fluticasone propionate (FP) alone on inflammatory cells in the airways of patients with COPD.

Methods: Patients were treated in a randomised, double blind, parallel group, placebo-controlled trial with either a combination of 50 µg salmeterol and 500 µg FP twice daily (SFC, n = 19, 19 men, mean age 62 years), 500 µg FP twice daily (n = 20, 15 men, mean age 64 years) or placebo (n = 21, 17 men, mean age 66 years) for 3 months. At the start and end of treatment bronchoscopy with bronchial biopsies was performed and the numbers of CD8+ T lymphocytes, CD68+ macrophages, neutrophils and eosinophils were measured.

Results: CD8+ cells were significantly reduced by SFC compared with placebo (difference −98.05 cells/mm2; 95% CI −143.14 to −52.9; p<0.001). Such a marked effect was not seen with FP alone (−44.67 cells/mm2; 95% CI −90.92 to 1.57; p = 0.06). CD68+ macrophages were also reduced by SFC compared with placebo (difference −31.68 cells/mm2; 95% CI −61.07 to −2.29; p = 0.03) but not by FP. SFC did not significantly change neutrophils and eosinophils compared with placebo.

Conclusions: SFC has airway anti-inflammatory effects not seen with inhaled corticosteroids alone.

Footnotes

  • This study was funded by an unrestricted research grant from GlaxoSmithKline.

  • Competing interests: None.

  • Abbreviations:
    BAL
    bronchoalveolar lavage
    COPD
    chronic obstructive pulmonary disease
    CRQ
    Chronic Respiratory Questionnaire
    FEV1
    forced expiratory volume in 1 s
    FP
    fluticasone propionate
    FVC
    forced vital capacity
    SFC
    salmeterol xinafoate/fluticasone propionate
    Tlco
    carbon monoxide transfer factor

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