Unbound MEDLINE

Bronchial nitric oxide is related to symptom relief during fluticasone treatment in COPD. The European respiratory journal : official journal of the European Society for Clinical Respiratory Physiology [Eur Respir J] Journal article

 
TitleBronchial nitric oxide is related to symptom relief during fluticasone treatment in COPD.
Author(s)Lehtimäki L, Kankaanranta H, Saarelainen S, Annila I, Aine T, Nieminen R, Moilanen E 
InstitutionMedical School, University of Tampere; and The Science Centre, Tampere University Hospital, Tampere, Finland; and Dept of Respiratory Medicine, Tampere University Hospital, Tampere, Finland.
SourceEur Respir J 2009 Jul 2.
AbstractHigh levels of exhaled nitric oxide (NO) predict favorable response to inhaled corticosteroids in asthma, but the ability of exhaled NO or inflammatory markers in exhaled breath condensate (EBC) to predict steroid-responsiveness in COPD is not known.We measured alveolar and bronchial NO output, levels of leukotriene B4 (LTB4), cysteinyl leukotrienes (cysLTs) and 8-isoprostane in EBC, spirometry, body plethysmography and symptoms in 40 subjects with COPD before and after 4 weeks of treatment with inhaled fluticasone (500 microg b.i.d.).Five subjects (12.5 %) with COPD had significant improvement in lung function during fluticasone treatment, while 20 subjects (50 %) had significant decrease in symptoms. High baseline bronchial NO flux was associated with higher increase in FEV1/FVC (r=0.334, p=0.038) and more symptom relief (r= -0.317, p=0.049) during the treatment. Baseline EBC levels of LTB4, cysLTs or 8-isoprostane were not related to response to fluticasone treatment. Inhaled fluticasone decreased bronchial NO flux but not alveolar NO concentration or markers in EBC.High levels of bronchial NO flux are related to symptom relief and improvement of airway obstruction during treatment with inhaled fluticasone in COPD. Markers of inflammation or oxidative stress in EBC are not related to steroid-responsiveness in COPD.
LanguageENG
Pub Type(s)JOURNAL ARTICLE
PubMed ID19574327
  
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