Asthma is one of the most common chronic illnesses and it disproportionately affects inner-city African Americans. The prevalence rate of asthma has been estimated to be as high as 20 percent among inner-city African Americans which is 2-3 times higher than the national prevalence rate. Moreover, inner-city African Americans experience greater morbidity and have higher asthma-related mortality than others. There are striking differences in environmental exposures between inner-city and suburban homes that may explain the disproportionate asthma burden in the inner-city population. For example, Mus m 1, the major mouse allergen, is found in 95 percent of inner-city homes, and is found in 100-fold higher concentrations in inner-city homes than in suburban homes. In addition, mouse is a well-recognized cause of occupational asthma, and as many as 20 percent of inner-city homes have levels of airborne mouse allergen that are as high as levels seen in some occupational settings. The striking prevalence and high levels of Mus m 1, a known causative agent of occupational asthma, suggest that Mus m 1 may be a significant contributor to inner-city asthma morbidity. For these reasons, we hypothesize that (i) mouse allergen exposure causes asthma morbidity among inner- city asthmatics and (2) mouse allergen elicits an allergen-specific inflammatory response in the airways of inner-city asthmatics with IgE-sensitization to mouse. In order to establish the link between household mouse allergen exposure and asthma morbidity in inner-city, we propose repeatedly assessing household Mus m 1 levels, and asthma-related health care utilization and symptoms in a cohort of inner-city children and young adults with asthma. In addition, we will conduct nasal and bronchial challenges to mouse allergen in order to determine if skin test sensitivity to mouse allergen predicts airways symptoms and allergic inflammatory responses to mouse allergen. The findings from these studies will directly inform public health strategies to reduce the inner-city asthma burden, and lend critical insight into the clinical implications of a positive skin test to mouse in the inner-city population.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI070630-01
Application #
7132426
Study Section
Special Emphasis Panel (ZRG1-IRAP-Q (01))
Program Officer
Dong, Gang
Project Start
2006-07-01
Project End
2011-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
1
Fiscal Year
2006
Total Cost
$367,875
Indirect Cost
Name
Johns Hopkins University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
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Little, Frédéric F; Delgado, Diana M; Wexler, Philip J et al. (2014) Salivary inflammatory mediator profiling and correlation to clinical disease markers in asthma. PLoS One 9:e84449
Matsui, E C (2014) Environmental exposures and asthma morbidity in children living in urban neighborhoods. Allergy 69:553-8
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Rivera-Mariani, Félix E; Matsui, Elizabeth C; Breysse, Patrick N (2014) Performance of the halogen immunoassay to assess airborne mouse allergen-containing particles in a laboratory animal facility. J Expo Sci Environ Epidemiol 24:3-8
McCormack, Meredith C; Aloe, Charles; Curtin-Brosnan, Jean et al. (2013) Guideline-recommended fractional exhaled nitric oxide is a poor predictor of health-care use among inner-city children and adolescents receiving usual asthma care. Chest 144:923-929

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