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Short-term longitudinal variation in exhaled nitric oxide fraction predicts future moderate-to-severe exacerbations
Zhaoqian Gong1,2, Hailun Huang1,2, Xueying Zhao3,2
1Chronic Airways Diseases Laboratory, Department of Respiratory and Critical Care Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Background:
Fractional exhaled nitric oxide (F ENO) reflects type 2 airway inflammation, yet the prognostic utility of longitudinal F ENO changes in COPD remains unclear. We aim to explore whether 6-month F ENO variation patterns predict subsequent moderate-to-severe exacerbations in COPD patients receiving triple therapy.
Methods:
We prospectively evaluated COPD patients receiving triple inhaled therapy from 2023 to 2024. Four F ENO-related variables were used to derive F ENO variation phenotypes via K-means unsupervised clustering.
Results:
Three distinct F ENO-variation phenotypes were identified: a High F ENO-Persistently Elevated subtype (Cluster 1, 11.2%), a High F ENO-Declining subtype (Cluster 2, 20.3%) and a Low F ENO-Stable subtype (Cluster 3, 68.5%). During 6-12 months of follow-up, 75 patients (33.8%) experienced a moderate-to-severe exacerbation. Compared with Cluster 3, both Cluster 1 (OR 6.97, 95% CI 2.38-20.47) and Cluster 2 (OR 20.08, 95% CI 7.01-57.58) were independently associated with future exacerbations (p<0.001). The final prediction model incorporating F ENO variation phenotypes demonstrated excellent discrimination (AUC 0.889) and provided greater net clinical benefit than models using traditional clinical predictors alone (p=0.004). Subgroup analyses revealed consistent effect sizes across categories of age, prior-year exacerbations, baseline FEV1 % predicted, symptom burden, smoking status and proportion of days covered, supporting the robustness and internal consistency of the F ENO-variation phenotyping approach.
Conclusion:
Short-term longitudinal F ENO variation over 6 months was independently associated with future moderate-to-severe exacerbations in COPD patients receiving triple therapy, supporting risk stratification and hypothesis generation for future interventional studies rather than direct treatment guidance.
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