Control of Airway Inflammation Maintained at a Lower Steroid Dose with 100/50 Μg of Fluticasone Propionate/salmeterol

Background: Inhaled corticosteroids (ICSs) have been shown to reverse epithelial damage and decrease lamina reticularis thickness in patients with asthma.Objective: This study investigated whether clinical asthma control and airway inflammation could be maintained after switching therapy from medium-dose fluticasone propionate (FP) to low-dose FP administered with the long-acting beta(2)-agonist (LABA) salmeterol.Methods: Eighty-eight subjects (age, >= 18 years) who, during open-label screening, demonstrated improved asthma control after an increase from 100 mu g of FP twice daily to 250 mu g of FP twice daily were randomized to receive 100150 mu g of FP/salmeterol through.a Diskus inhaler (GlaxoSmithKline, Research Triangle Park, NC) twice daily or continue 250 mu g of FP twice daily through a Diskus inhaler for 24 weeks. Clinical outcomes were monitored, and bronchial biopsy specimens and bronchoalveolar lavage fluid were obtained before and after 24 weeks of treatment.Results: There were no significant differences between treatments with respect to eosinophils in the bronchial mucosa and bronchoalveolar lavage fluid; mucosal mast cells, neutrophils, or CD3(+), CD4(+), CD8(+), or CD25(+) T lymphocytes; or concentration of mediators (GM-CSF, IL-8, and eosinophil cationic protein). The 2 treatments were not different with respect to lamina reticularis thickness. Consistent with the airway inflammatory measures, clinical and physiologic measures of asthma control were also similar.Conclusion: This study demonstrates that control of asthma and airway inflammation is maintained over the 24-week treatment period when patients requiring a medium-dose ICS are switched to a lower-dose ICS with a LABA. Clinical implications: A lower-dose ICS with a LABA is effective in controlling inflammation and providing clinical asthma control, confirming current guideline recommendations.