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Published on: November 4, 2010
Racial differences in physiologic parameters related to asthma among middle-class children
C L Joseph1, D R Ownby, E L Peterson
1Henry Ford Health System, Detroit, MI 48202, USA.
Insights
African-American children exhibit greater airway hyperresponsiveness and higher total IgE levels than European-American children, suggesting a predisposition to asthma. These findings highlight critical racial disparities in pediatric asthma severity.
Area of Science:
- Pediatric Allergy and Immunology
- Respiratory Medicine
- Public Health
Background:
- Asthma disproportionately affects African-American (AA) children compared to European-American (EA) children in the US.
- Existing research often overlooks non-urban, middle-class AA populations.
Purpose of the Study:
- To investigate racial disparities in physiological factors contributing to pediatric asthma severity.
- To compare airway responsiveness and immunoglobulin E (IgE) levels between AA and EA children.
Main Methods:
- Cross-sectional study of 569 children aged 6-8 years in suburban Detroit.
- Evaluations included spirometry, methacholine challenge, and total serum IgE measurement.
- Data analysis controlled for gender, age, socioeconomic status, and parental smoking.
Main Results:
- AA children showed significantly higher methacholine reactivity (42% vs. 22%) and total IgE levels (60.6 vs. 27.5 IU/mL) than EA children.
- A significant association between total IgE and airway responsiveness was observed in EA children, but not in AA children.
- These racial differences persisted after adjusting for multiple confounding factors.
Conclusions:
- Findings confirm racial disparities in lung function, airway responsiveness, and IgE.
- A novel racial difference in the IgE-airway responsiveness relationship was identified.
- Results suggest a potential predisposition to asthma in African-American children.
Background:
Asthma morbidity and mortality are higher in the United States for African-American (AA) children when compared to European-American (EA) children.
Study Objectives:
To explore racial differences in physiologic factors associated with pediatric asthma severity.
Design:
Cross-sectional.
Methods:
We analyzed data from two groups of children in suburban Detroit, one of which contains non-urban, middle-class AA children, a group not usually included in childhood asthma studies. All children were 6 to 8 years of age. Clinical evaluations included medical history, physical examination, skin testing, spirometry, and methacholine challenge.
Results:
The study population (n = 569) was 14% African American, 51% of the participants were male, and the mean age was 6.8 +/- 0.4 years. Socioeconomic status (parental education) was similar overall by race, although some strata-specific differences were observed. The prevalence of physician-diagnosed asthma was 10% for both AA and EA groups. AA children were more reactive to methacholine than EA children (42% vs 22%, respectively; p = 0.001), and had significantly higher total IgE than EA children (geometric mean, 60. 6 vs 27.5 IU/mL; p = 0.001). Serum IgE was related to methacholine reactivity in EA children (p = 0.001), but not AA children (p = 0. 73). These differences remained after adjustment for gender, age, parental education, parental smoking, and maternal smoking during pregnancy.
Conclusions:
Our data support previous reports of racial differences in lung volume, airway responsiveness, and serum IgE concentrations. We found a racial difference in the relationship between total serum IgE and airway responsiveness that is unreported elsewhere. Overall, our results suggest that AA children may be predisposed to asthma.
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Additionally, environmental and genetic factors play crucial roles in determining an individual's susceptibility to asthma and the severity of their condition.
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