Fractional Exhaled Nitric Oxide Falls Progressively During Treated Exacerbations of COPD and Is Discordant with Blood Eosinophil Counts
Dimitrios Potonos, Antonia Assioura, Athena Gogali, Emmanouil D. Oikonomou, Konstantinos Exarchos, Christos Kyriakopoulos, Konstantinos KostikasBackground: The behavior of fractional exhaled nitric oxide (FeNO) during treated COPD exacerbations and its agreement with blood eosinophil counts are poorly characterized. Aims: To describe serial FeNO trajectories across hospitalized COPD exacerbations (AECOPDs), assess concordance between FeNO and blood eosinophils, and test whether these can predict length of stay (LOS). Methods: Prospective cohort of patients hospitalized for AECOPD. FeNO was measured on admission, on day 2 and at discharge; blood eosinophils and post-bronchodilator spirometry on admission and before discharge; and arterial blood gases on admission and on day 2. The admission measurements preceded the first dose of corticosteroid. All patients received guideline-directed treatment, including systemic corticosteroids. Results: Most patients were male (94.7%), with a mean age of 71.7 ± 8.3 years. FeNO fell from 16 (IQR 10–25) ppb on admission to 13.5 (7–20) ppb on day 2 and 9 (6–18) ppb at discharge (p < 0.001). Blood eosinophils fell from 60 (20–150) to 0 (0–40) cells/µL (p < 0.001), and FEV1 increased from 38% to 45% predicted (p < 0.001). Agreement between biomarkers on admission was poor (ρ = 0.21, p = 0.07; κ = 0.08, 95% CI −0.15 to +0.30), and 31 patients (40.8%) were classified differently by the two markers. Admission FeNO (ρ = 0.03, p = 0.79), ΔFeNO (ρ = −0.12, p = 0.31), and admission eosinophils (ρ = −0.08, p = 0.49) were not associated with LOS. Of the patients who were type-2-high on admission (FeNO ≥ 20 ppb), 57% had fallen below that threshold by day 2 and 62% by discharge (71% and 71%, respectively, at ≥25 ppb). Over the admission-to-discharge interval, the changes in the two markers were unrelated once each was adjusted for its own admission value (partial ρ = 0.05, p = 0.73), and there was no agreement on the direction of change (κ = 0.03). Conclusions: FeNO progressively declines during treated AECOPD, alongside a fall in the blood eosinophil count, so that the type-2 label assigned on admission is no longer valid for most patients 48 h later. FeNO and blood eosinophils identified largely non-overlapping patients, and no biomarker predicted length of stay.