Literature DB >> 14629652

Exhaled nitric oxide continues to reflect airway hyperresponsiveness and disease activity in inhaled corticosteroid-treated adult asthmatic patients.

David W Reid1, David P Johns, Bryce Feltis, Chris Ward, E Haydn Walters.   

Abstract

OBJECTIVE: Exhaled nitric oxide (eNO) has been used as a surrogate of airway inflammation in mild asthma. However, whether eNO levels reflect disease activity in symptomatic asthmatics receiving moderate doses of inhaled corticosteroid (ICS) is more uncertain.
METHODOLOGY: To examine the relationship between eNO levels, sputum and blood eosinophils (SpE and PbE), PD(20) methacholine as a marker of airway hyperresponsiveness (AHR) and clinical status in 28 ICS-treated asthmatic subjects with persistent asthma compared to that in 25 symptomatic asthmatics managed with beta2-agonists alone.
RESULTS: As expected, eNO levels were normalized in ICS-treated subjects and significantly elevated in the beta2-agonist only group (P < 0.001). SpE, PbE and PD20M did not differ between asthmatic groups but FEV1 was significantly worse in ICS-treated subjects (P < 0.01). Exhaled NO levels correlated with PbE within both asthmatic groups (P < 0.005), but with SpE only in ICS-untreated subjects (r(s) = 0.6, P < 0.05). In contrast, PD20M was negatively correlated with eNO and PbE in ICS-treated subjects only (r(s) = - 0.4, r(s) = - 0.4, respectively, P < 0.05). SpE and PbE were strongly correlated in both asthmatic groups (r(s) = 0.8, r(s) = 0.7, respectively, P < 0.005). Exhaled NO levels, SpE and PbE were all positively associated with increased nocturnal awakenings ( P < 0.05) in ICS-treated subjects, but not in ICS-untreated subjects.
CONCLUSIONS: In ICS-treated asthma, eNO reflects clinical activity, PbE and AHR but not eosinophilic airway inflammation. Exhaled NO levels are quantitatively and relationally different in asthmatic subjects treated with ICS and continue to have potential for use as a surrogate of asthma pathophysiology in this group.

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Year:  2003        PMID: 14629652     DOI: 10.1046/j.1440-1843.2003.00495.x

Source DB:  PubMed          Journal:  Respirology        ISSN: 1323-7799            Impact factor:   6.424


  7 in total

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Review 4.  Asthma outcomes: pulmonary physiology.

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5.  Ventilation heterogeneity is a major determinant of airway hyperresponsiveness in asthma, independent of airway inflammation.

Authors:  Sue R Downie; Cheryl M Salome; Sylvia Verbanck; Bruce Thompson; Norbert Berend; Gregory G King
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6.  Small airway impairment and bronchial hyperresponsiveness in asthma onset.

Authors:  Bruno Sposato; Marco Scalese; Maria Giovanna Migliorini; Maurizio Di Tomassi; Raffaele Scala
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7.  Diagnostic significance of nitric oxide concentrations in exhaled air from the airways in allergic rhinitis patients.

Authors:  Anna Kłak; Edyta Krzych-Fałta; Bolesław K Samoliński; Marta Zalewska
Journal:  Postepy Dermatol Alergol       Date:  2016-05-16       Impact factor: 1.837

  7 in total

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