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Published on: April 13, 2010
Urinary bromotyrosine measures asthma control and predicts asthma exacerbations in children
Samuel H Wedes1, Weijia Wu, Suzy A A Comhair
1Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, OH 44195, USA.
Insights
Urinary bromotyrosine, a marker of eosinophil activity, effectively tracks asthma control in children. High levels predict a significantly increased risk of future asthma exacerbations.
Area of Science:
- Biochemistry
- Pulmonology
- Pediatrics
Background:
- Asthma control is crucial for managing pediatric respiratory health.
- Eosinophil-mediated inflammation contributes to asthma severity.
- Noninvasive biomarkers are needed to monitor asthma control and predict exacerbations.
Purpose of the Study:
- To evaluate urinary bromotyrosine as a noninvasive marker for tracking asthma control in children.
- To assess the predictive value of urinary bromotyrosine for future asthma exacerbations.
Main Methods:
- Recruited children with asthma for clinic visits.
- Collected urine samples for bromotyrosine analysis.
- Gathered spirometry, exhaled nitric oxide, and Asthma Control Questionnaire data.
- Followed up participants for 6 weeks to monitor asthma exacerbations.
Main Results:
- Urinary bromotyrosine levels significantly correlated with asthma control scores (Asthma Control Questionnaire).
- High baseline bromotyrosine levels were associated with inadequately controlled asthma (18.1-fold increased likelihood).
- High bromotyrosine levels predicted a greater risk of asthma exacerbations within 6 weeks (4.0-fold increased likelihood).
Conclusions:
- Urinary bromotyrosine serves as a valuable noninvasive biomarker for assessing asthma control in pediatric patients.
- This marker effectively predicts the risk of subsequent asthma exacerbations, aiding in proactive management strategies.
Objectives:
To determine the usefulness of urinary bromotyrosine, a noninvasive marker of eosinophil-catalyzed protein oxidation, in tracking with indexes of asthma control and in predicting future asthma exacerbations in children.
Study Design:
Children with asthma were recruited consecutively at the time of clinic visit. Urine was obtained, along with spirometry, exhaled nitric oxide, and Asthma Control Questionnaire data. Follow-up phone calls were made 6 weeks after enrollment.
Results:
Fifty-seven participants were enrolled. Urinary bromotyrosine levels tracked significantly with indexes of asthma control as assessed by Asthma Control Questionnaire scores at baseline (R = 0.38, P = .004) and follow-up (R = 0.39, P = .008). Participants with high baseline levels of bromotyrosine were 18.1-fold (95% CI 2.1-153.1, P = .0004) more likely to have inadequately controlled asthma and 4.0-fold more likely (95% CI 1.1-14.7, P = .03) to have an asthma exacerbation (unexpected emergency department visit; doctor's appointment or phone call; oral or parenteral corticosteroid burst; acute asthma-related respiratory symptoms) over the ensuing 6 weeks. Exhaled nitric oxide levels did not track with Asthma Control Questionnaire data; and immunoglobulin E, eosinophil count, spirometry, and exhaled nitric oxide levels failed to predict asthma exacerbations.
Conclusions:
Urinary bromotyrosine tracks with asthma control and predicts the risk of future asthma exacerbations in children.
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