Article Text

Download PDFPDF

Reduction in sputum neutrophil and eosinophil numbers by the PDE4 inhibitor roflumilast in patients with COPD
Free
  1. Diana C Grootendorst1,
  2. Stefanie A Gauw1,
  3. Renate M Verhoosel1,
  4. Peter J Sterk1,
  5. Jeannette J Hospers2,
  6. Dirk Bredenbröker2,
  7. Thomas D Bethke2,
  8. Pieter S Hiemstra1,
  9. Klaus F Rabe1
  1. 1
    Department of Pulmonology, Leiden University Medical Center, Leiden, The Netherlands
  2. 2
    ALTANA Pharma AG, Konstanz, Germany
  1. Dr Diana C Grootendorst, Department of Pulmonology C3-P, Leiden University Medical Center, P O Box 9600, 2300 RC Leiden, The Netherlands; d.c.Grootendorst{at}lumc.nl

Abstract

Background: Roflumilast is a targeted oral once-daily administered phosphodiesterase 4 (PDE4) inhibitor with clinical efficacy in chronic obstructive pulmonary disease (COPD). Results from in vitro studies with roflumilast indicate that it has anti-inflammatory properties that may be applicable for the treatment of COPD.

Methods: In a crossover study, 38 patients with COPD (mean (SD) age 63.1 (7.0) years, post-bronchodilator forced expiratory volume in 1 s (FEV1) 61.0 (12.6)% predicted) received 500 μg roflumilast or placebo once daily for 4 weeks. Induced sputum samples were collected before and after 2 and 4 weeks of treatment. Differential and absolute cell counts were determined in whole sputum samples. Markers of inflammation were determined in sputum supernatants and blood. Spirometry was performed weekly.

Results: Roflumilast significantly reduced the absolute number of neutrophils and eosinophils/g sputum compared with placebo by 35.5% (95% CI 15.6% to 50.7%; p = 0.002) and 50.0% (95% CI 26.8% to 65.8%; p<0.001), respectively. The relative proportion of sputum neutrophils and eosinophils was not affected by treatment (p>0.05). Levels of soluble interleukin-8, neutrophil elastase, eosinophil cationic protein and α2-macroglobulin in sputum and the release of tumour necrosis factor α from blood cells were significantly reduced by roflumilast compared with placebo treatment (p<0.05 for all). Post-bronchodilator FEV1 improved significantly during roflumilast compared with placebo treatment with a mean difference between treatments of 68.7 ml (95% CI 12.9 to 124.5; p = 0.018).

Conclusion: PDE4 inhibition by roflumilast treatment for 4 weeks reduced the number of neutrophils and eosinophils, as well as soluble markers of neutrophilic and eosinophilic inflammatory activity in induced sputum samples of patients with COPD. This anti-inflammatory effect may in part explain the concomitant improvement in post-bronchodilator FEV1.

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Footnotes

  • This study was financially supported by ALTANA Pharma AG, Konstanz, Germany. The study was designed by DCG, PJS, DB, TDB, PSH and KFR. Data collection was performed by DCG, SAG and RMV. Altana monitored all collected data. Statistical analysis was performed by DCG, PJS, PSH and KFR and confirmed by an independent statistician (Dr G Rippin, Omnicare Clinical Research, Biometrics International). DCG, PJS, PSH and KFR interpreted the data and wrote the manuscript, which was subsequently discussed with and approved by ALTANA. All investigators and ALTANA agreed upon submission of the manuscript to Thorax.

  • Competing interests: DCG, SAG and RMV have no declared conflict of interest. The Department of Pulmonology, and thereby PJS (staff member), PSH (staff member) and KFR (head of the department), has received grants from ALTANA Pharma, Novartis, Bayer, AstraZeneca, Pfizer, MSD, Exhale Therapeutics, Boehringer Ingelheim, Roche and GSK in the years 2001–6. PSH has participated as a speaker in various meetings co-financed by various pharmaceutical companies. KFR has been a consultant, participated in Advisory Board Meetings and received lecture fees from AstraZeneca, ALTANA Pharma, MSD and GSK. KFR holds no stock or other equities in pharmaceutical companies. JJH, DB and TDB are employees of ALTANA Pharma.

  • Abbreviations:
    COPD
    chronic obstructive pulmonary disease
    ECP
    eosinophil cationic protein
    FEV1
    forced expiratory volume in 1 s
    FVC
    forced vital capacity
    IL
    interleukin
    LPS
    lipopolysaccharide
    PDE
    phosphodiesterase
    TNFα
    tumour necrosis factor α