Literature DB >> 22515393

Associated demographics of persistent exhaled nitric oxide elevation in treated asthmatics.

K Matsunaga1, S Yanagisawa, T Hirano, T Ichikawa, A Koarai, K Akamatsu, H Sugiura, Y Minakata, K Matsunaga1, T Kawayama, M Ichinose.   

Abstract

BACKGROUND: The fraction of exhaled nitric oxide (FENO) is reduced by anti-inflammatory treatment in asthma. However, the FENO level is also regulated by individual demographics and there is considerable variation among clinically stable patients.
OBJECTIVE: We hypothesized that some demographics may be responsible for persistent FENO elevation despite inhaled corticosteroids (ICS) therapy in asthma.
METHODS: This was a prospective observational study. We initially screened 250 stable asthmatics and determined the FENO cut-off point for identifying poorly controlled asthma defined by one of the following criteria: Asthma control test <20, or forced expiratory volume in one-second % of predicted <80%, or peak expiratory flow variability <80% (Study 1). After 12-weeks, 229 patients who maintained high or low FENO were selected and the independent factors which might contribute to a high FENO were examined (Study 2).
RESULTS: A FENO level >39.5 p.p.b. yielded 67% sensitivity and 76% specificity for identifying the patients with poorly controlled asthma. The persistent high FENO group (≥ 40 p.p.b.) was more likely to be ex-smokers, to show evidence of atopy (positive specific IgE, higher serum IgE and blood eosinophils), and to have allergic comorbidities. Especially, past smoking history, blood eosinophils, and chronic rhinosinusitis were identified to be independent predictors of high FENO. Neither the dose of ICS nor other medication use showed any difference between the groups. CONCLUSIONS AND CLINICAL RELEVANCE: These results suggested that past smoking history, blood eosinophilia, and chronic rhinosinusitis are involved in the persistent airway inflammation detected by FENO. Although their relative contributions on FENO values should be further quantified, clarification of the features of the subjects with high FENO might provide clues for adjustment of the treatment approach in asthma.
© 2011 Blackwell Publishing Ltd.

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Year:  2012        PMID: 22515393     DOI: 10.1111/j.1365-2222.2011.03945.x

Source DB:  PubMed          Journal:  Clin Exp Allergy        ISSN: 0954-7894            Impact factor:   5.018


  4 in total

1.  A trial of oral corticosteroids for persistent systemic and airway inflammation in severe asthma.

Authors:  Keiji Oishi; Tsunahiko Hirano; Ryo Suetake; Syuichiro Ohata; Yoshikazu Yamaji; Kosuke Ito; Nobutaka Edakuni; Kazuto Matsunaga
Journal:  Immun Inflamm Dis       Date:  2017-05-04

Review 2.  Fractional exhaled nitric oxide as a determinant for the clinical course of asthma: a systematic review.

Authors:  Charlotte Suppli Ulrik; Peter Lange; Ole Hilberg
Journal:  Eur Clin Respir J       Date:  2021-02-24

3.  Storage conditions for stability of offline measurement of fractional exhaled nitric oxide after collection for epidemiologic research.

Authors:  Yoshiko Yoda; Naruhito Otani; Hideki Hasunuma; Hiroshi Kanegae; Masayuki Shima
Journal:  BMC Pulm Med       Date:  2012-11-02       Impact factor: 3.317

Review 4.  Blood eosinophil counts in the general population and airways disease: a comprehensive review and meta-analysis.

Authors:  Victoria S Benson; Sylvia Hartl; Neil Barnes; Nicholas Galwey; Melissa K Van Dyke; Namhee Kwon
Journal:  Eur Respir J       Date:  2022-01-13       Impact factor: 16.671

  4 in total

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