Improvement of airflow limitation by fluticasone propionate/salmeterol in chronic obstructive pulmonary disease: What is the specific marker?

Keiichiro Akamatsu, Kazuto Matsunaga, Hisatoshi Sugiura, Akira Koarai Hirano, Yoshiaki Minakata, Masakazu Ichinose

Research output: Contribution to journalArticlepeer-review

22 Citations (Scopus)

Abstract

Backgrounds: Inhaled corticosteroids (ICS)/inhaled long-acting beta2-agonists (LABA) combination drugs are widely used for the long-term management of chronic obstructive pulmonary disease (COPD). However, COPD is a heterogeneous condition and treatment with ICS is associated with a higher risk of pneumonia. The identification of a specific marker for predicting the efficacy of ICS/LABA on pulmonary function would be useful in the treatment of COPD. Methods: Fourteen COPD patients receiving tiotropium therapy participated consecutively. The relationship between the baseline exhaled nitric oxide (FENO) levels as well as serum markers and changes in pulmonary function by fluticasone propionate (FP)/salmeterol (SAL) were analyzed. Results: FP/SAL therapy significantly improved forced vital capacity, forced expiratory volume in 1 s (FEV1), and the third phase slope of the single nitrogen washout curve (MTMI.-1.Delta1N2) as well as the FENO level. The baseline FENO levels and positive specific IgE (atopy+) were significantly associated with airway obstructive changes assessed by FEV1 and MTMI.-1.Delta1N2. A baseline FENO level >35 ppb yielded 80.0% sensitivity and 66.7% specificity for identifying the subjects with significant improvement in FEV1 (greater than 200 mL). An atopy+ yielded 60.0% sensitivity and 88.9% specificity for an improvement in FEV1. When combined with FENO > 35 ppb and atopy+, it showed 40% sensitivity and 100.0% specificity for FEV1 improvement. Alternatively, COPD subjects with FENO ≤ 35 ppb and atopydid not show significant improvement in FEV1. Conclusion: Combining FENO and specific IgE may be a useful marker for predicting the response to ICS/LABA on airflow limitation in COPD.

Original languageEnglish
Article numberArticle 36
JournalFrontiers in Pharmacology
VolumeJUL
DOIs
Publication statusPublished - 2011
Externally publishedYes

Keywords

  • Airflow limitation
  • Airway inflammation
  • Atopy
  • Exhaled nitric oxide
  • Inhaled corticosteroid
  • Inhaled long-acting beta-agonist

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)

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