ASSESSING THE CONCORDANCE BETWEEN FRACTIONAL EXHALED NITRIC OXIDE LEVELS AND BLOOD EOSINOPHIL COUNTS FOR GUIDING INHALED CORTICOSTEROID THERAPY IN THE PREVENTION OF EXACERBATIONS IN CHRONIC OBSTRUCTIVE PULMONARY DISEASE
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Abstract
Background: In addition to the well-established role of blood eosinophils, fractional exhaled nitric oxide, a noninvasive inflammatory biomarker, has been proposed as a potential alternative or complementary tool to guide inhaled corticosteroid use for the prevention of exacerbations in chronic obstructive pulmonary disease. Objectives: 1. To evaluate the concordance between fractional exhaled nitric oxide levels and blood eosinophil counts; 2. To determine the optimal FeNO cut-off values for guiding inhaled corticosteroid therapy based on blood eosinophil thresholds in the prevention of COPD exacerbations. Materials and methods: A cross-sectional descriptive study was conducted in 64 patients with chronic obstructive pulmonary disease. Results: Among the 64 COPD patients, 60.9% had FeNO levels ≥25 ppb, with a mean age of 67.38 ± 9.81 years. Patients with FeNO ≥25 ppb had higher rates of smoking, asthma, and chronic rhinosinusitis, along with higher mMRC scores and lower FEV₁ values. Blood eosinophil counts differed significantly between FeNO groups, with the FeNO ≥25 ppb group predominantly exhibiting blood eosinophil counts ≥300 cells/µL. FeNO showed a strong positive correlation with blood eosinophil counts (r = 0.819). The optimal FeNO cutoff values for predicting inhaled corticosteroid indication were 26.5 ppb for blood eosinophils ≥300 cells/µL and 12.7 ppb for blood eosinophils ≥100 cells/µL, both demonstrating high sensitivity and specificity. Conclusion: FeNO levels are strongly correlated with blood eosinophil counts in patients with chronic obstructive pulmonary disease and represent a valuable noninvasive biomarker to support guidance on inhaled corticosteroid use for the prevention of COPD exacerbations.
Keywords
Fractional exhaled nitric oxide, inhaled corticosteroids, chronic obstructive pulmonary disease
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