Use of exhaled nitric oxide measurement to identify a reactive, at-risk phenotype among patients with asthma

Rationale: Exhaled nitric oxide (FE_NO) is a biomarker of airway inflammation in mild to moderate asthma. However, whether FE_NO levels are informative regarding airway inflammation in patients with severe asthma,whoare refractory to conventional treatment, is unknown. Here, we hypothesized that classification of severe asthma based on airway inflammation as defined by FE_NO levels would identify a more reactive, at-risk asthma phenotype. Methods: FE_NO and major features of asthma, including airway inflammation, airflow limitation, hyperinflation, hyperresponsiveness, and atopy, were determined in 446 individuals with various degrees of asthma severity (175 severe, 271 nonsevere) and 49 healthy subjects enrolled in the Severe Asthma Research Program. Measurements and Main Results: FE_NO levels were similar among patients with severe and nonsevere asthma. The proportion of individuals with high FE_NO levels (>35 ppb) was the same (40%) among groups despite greater corticosteroid therapy in severe asthma. All patients with asthma and high FE_NO had more airway reactivity (maximal reversal in response to bronchodilator administration and by methacholine challenge), more evidence of allergic airway inflammation (sputum eosinophils), more evidence of atopy (positive skin tests, higher serum IgE and blood eosinophils), and more hyperinflation, but decreased awareness of their symptoms. High FE_NO identified those patientswith severeasthmacharacterized by the greatest airflow obstruction and hyperinflation and most frequent use of emergency care. Conclusions: Grouping of asthma by FE_NO provides an independent classification of asthma severity, and among patients with severe asthma identifies the most reactive and worrisome asthma phenotype.