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Urinary eosinophil protein X in childhood asthma: relation with changes in disease control and eosinophilic airway
Marianne Nuijsink1, Wim C J Hop, Peter J Sterk
1Department of Pediatric Respiratory Medicine, Juliana Children's Hospital, HAGA Teaching Hospital, P.O. Box 60605, 2506 LP, The Hague, The Netherlands.
Insights
Urothelial epithelial cells in urine (uEPX) showed weak correlations with lung function (FEV(1)) and eosinophil levels (% eos) in children with atopic asthma. These findings suggest uEPX is unlikely to be a reliable biomarker for monitoring individual asthma control.
Area of Science:
- Pediatric Pulmonology
- Allergy and Immunology
- Biomarker Discovery
Background:
- Asthma control and airway inflammation are critical in managing pediatric atopic asthma.
- Identifying reliable biomarkers for monitoring asthma is essential for personalized treatment.
Purpose of the Study:
- To evaluate the cross-sectional and longitudinal associations between urinary epithelial cells (uEPX) and established asthma control markers.
- To determine if uEPX can serve as a biomarker for eosinophilic airway inflammation and lung function in children.
Main Methods:
- Longitudinal study of 205 atopic asthmatic children treated with inhaled fluticasone over 2 years.
- Measurements included uEPX, symptom scores, forced expiratory volume in one second (FEV(1)), and sputum eosinophils (% eos) at baseline and yearly intervals.
Main Results:
- Negative correlations were observed between uEPX and FEV(1) at all time points.
- Within-patient changes in uEPX correlated negatively with changes in FEV(1) and % eos.
- No significant associations were found between uEPX and asthma symptom scores.
Conclusions:
- While uEPX showed correlations with FEV(1) and % eos in children with atopic asthma, the weak associations and wide scatter suggest limited utility.
- uEPX is unlikely to be a practical biomarker for monitoring asthma control in individual children.
Abstract:
The aim of this study was to assess cross-sectional and longitudinal correlations between uEPX and other markers of asthma control and eosinophilic airway inflammation. Methods. We measured uEPX at baseline, after 1 year and after 2 years in 205 atopic asthmatic children using inhaled fluticasone. At the same time points, we assessed symptom scores (2 weeks diary card), lung function (forced expiratory volume in one second (FEV(1))), airway hyperresponsiveness (AHR), and percentage eosinophils in induced sputum (% eos). Results. We found negative correlations between uEPX and FEV(1) at baseline (r = -0.18, P = 0.01), after 1 year (r = -0.25, P < 0.01) and after 2 years (r = -0.21, P = 0.02). Within-patient changes of uEPX showed a negative association with FEV(1) changes (at 1 year: r = -0.24, P = 0.01; at 2 years: r = -0.21, P = 0.03). Within-patient changes from baseline of uEPX correlated with changes in % eos. No relations were found between uEPX and symptoms. Conclusion. In this population of children with atopic asthma, uEPX correlated with FEV(1) and % eos, and within-subjects changes in uEPX correlated with changes in FEV(1) and % eos. As the associations were weak and the scatter of uEPX wide, it seems unlikely that uEPX will be useful as a biomarker for monitoring asthma control in the individual child.
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