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Published on: November 4, 2010
Clinical significance of the bronchodilator response in children with severe asthma
Andrea M Coverstone1, Leonard B Bacharier1, Bradley S Wilson2
1Department of Pediatrics, Washington University School of Medicine in Saint Louis, St. Louis, Missouri.
Insights
Severe asthma in children is linked to airway reversibility. Factors like smoke exposure, FeNO, IgE, and low neutrophils predict bronchodilator response, indicating poorer asthma control.
Area of Science:
- Pediatric Pulmonology
- Asthma Research
- Respiratory Medicine
Background:
- Investigating characteristics associated with airflow obstruction reversibility and bronchodilator response in children with severe asthma.
- Utilizing data from the Severe Asthma Research Program (SARP).
Purpose of the Study:
- To identify factors predicting bronchodilator (BD) response in children with severe asthma.
- To understand the relationship between BD response and asthma control and healthcare utilization.
Main Methods:
- Cross-sectional analysis of children aged 6-17 with nonsevere asthma (NSA) and severe asthma (SA).
- Spirometry performed before and after albuterol administration to assess reversibility (≥12% increase in FEV1).
- Maximal reversibility determined with escalating albuterol doses.
Main Results:
- Severe asthma, secondhand smoke exposure, and higher fractional exhaled nitric oxide (FeNO) were associated with increased odds of airway reversibility.
- Higher prebronchodilator FEV1% predicted was linked to decreased odds of reversibility.
- In SARP III, blood neutrophils, immunoglobulin E (IgE), and FEV1% predicted correlated with BD reversibility.
- Children with BD response showed greater healthcare utilization and reduced lung function at enrollment and follow-up.
Conclusions:
- Lung function (FEV1% predicted) predicts BD response in pediatric asthma.
- Smoke exposure, elevated FeNO or IgE, and low peripheral blood neutrophils increase the likelihood of BD reversibility.
- BD response identifies a pediatric asthma phenotype characterized by low lung function and poor control.
Background:
Our objective was to determine those characteristics associated with reversibility of airflow obstruction and response to maximal bronchodilation in children with severe asthma through the Severe Asthma Research Program (SARP).
Methods:
We performed a cross-sectional analysis evaluating children ages 6 to 17 years with nonsevere asthma (NSA) and severe asthma (SA). Participants underwent spirometry before and after 180 µg of albuterol to determine reversibility (≥12% increase in FEV1 ). Participants were then given escalating doses up to 720 µg of albuterol to determine their maximum reversibility.
Results:
We evaluated 230 children (n = 129 SA, n = 101 NSA) from five centers across the United States in the SARP I and II cohorts. SA (odds ratio [OR], 2.08, 95% confidence interval [CI], 1.05-4.13), second-hand smoke exposure (OR, 2.81, 95%CI, 1.23-6.43), and fractional exhaled nitric oxide (FeNO; OR, 1.97, 95%CI, 1.35-2.87) were associated with increased odds of airway reversibility after maximal bronchodilation, while higher prebronchodilator (BD) FEV1 % predicted (OR, 0.91, 95%CI, 0.88-0.94) was associated with decreased odds. In an analysis using the SARP III cohort (n = 186), blood neutrophils, immunoglobulin E (IgE), and FEV1 % predicted were significantly associated with BD reversibility. In addition, children with BD response have greater healthcare utilization. BD reversibility was associated with reduced lung function at enrollment and 1-year follow-up though less decline in lung function over 1 year compared to those without reversibility.
Conclusions:
Lung function, that is FEV1 % predicted, is a predictor of BD response in children with asthma. Additionally, smoke exposure, higher FeNO or IgE level, and low peripheral blood neutrophils are associated with a greater likelihood of BD reversibility. BD response can identify a phenotype of pediatric asthma associated with low lung function and poor asthma control.
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