Abstract |
From the Childhood Asthma Management Program cohort, which was randomly assigned to receive budesonide, nedocromil, or placebo for 4-6 years, we determined the prevalence of and factors associated with at least 1% per year loss in postbronchodilator FEV(1)% predicted. Participants who had a significant reduction in postbronchodilator FEV(1)% predicted (SRP), comprised 25.7% of the cohort (n = 990). Using logistic regression, predictors of SRP at baseline were younger age (p = 0.0005), male sex (p < 0.0001), clinic (p = 0.02), and higher postbronchodilator FEV(1)% predicted (p = 0.02). Examination of the SRPs indicated that the effect of baseline lung function was such that the higher the lung function, the less steep the reduction in postbronchodilator FEV(1)% predicted (p < 0.0001). A similar proportion of SRPs was found in each treatment group. Among the SRPs, the rate of reduction in postbronchodilator FEV(1)% predicted was similar in all treatment groups. At a single site where biomarker assessment was performed, SRPs also had more prominent eosinophilic inflammation during the washout period. The course and mechanisms of lung function reduction or slow lung growth velocity in children with asthma must be defined.
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Authors | Ronina A Covar, Joseph D Spahn, James R Murphy, Stanley J Szefler, Childhood Asthma Management Program Research Group |
Journal | American journal of respiratory and critical care medicine
(Am J Respir Crit Care Med)
Vol. 170
Issue 3
Pg. 234-41
(Aug 01 2004)
ISSN: 1073-449X [Print] United States |
PMID | 15028558
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Biomarkers
- Bronchodilator Agents
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Topics |
- Administration, Inhalation
- Age Distribution
- Asthma
(diagnosis, drug therapy, metabolism, physiopathology)
- Biomarkers
(analysis)
- Bronchodilator Agents
(therapeutic use)
- Child
- Child, Preschool
- Cohort Studies
- Disease Progression
- Female
- Forced Expiratory Volume
(drug effects)
- Humans
- Inflammation
(drug therapy, metabolism)
- Logistic Models
- Male
- Respiratory Function Tests
(statistics & numerical data)
- Sex Distribution
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