Abstract
Asthma in inner-city children is often severe and difficult to control. Residence in poor and urban areas confers increased asthma morbidity even after adjusting for ethnicity, age, and gender. Higher exposure to household pests, such as cockroaches and mice, pollutants and tobacco smoke exposure, poverty, material hardship, poor-quality housing, differences in health care quality, medication compliance, and heath care access also contribute to increased asthma morbidity in this population. Since 1991, the National Institutes of Allergy and Infectious Diseases established research networks: the National Cooperative Inner-City Asthma Study (NCICAS), the Inner-City Asthma Study (ICAS), and the Inner-City Asthma Consortium (ICAC), to improve care for this at risk population. The most striking finding of the NCICAS is the link between asthma morbidity and the high incidence of allergen sensitization and exposure, particularly cockroach. The follow-up ICAS confirmed that reductions in household cockroach and dust mite were associated with reduction in the inner-city asthma morbidity. The ICAC studies have identified that omalizumab lowered fall inner-city asthma exacerbation rate; however, the relationship between inner-city asthma vs immune system dysfunction, respiratory tract infections, prenatal environment, and inner-city environment is still being investigated. Although challenging, certain interventions for inner-city asthma children have shown promising results. These interventions include family-based interventions such as partnering families with asthma-trained social workers, providing guidelines driven asthma care as well as assured access to controller medication, home-based interventions aim at elimination of indoor allergens and tobacco smoke exposure, school-based asthma programs, and computer/web-based asthma programs.
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Abbreviations
- ACE:
-
Asthma Control Evaluation
- ACT:
-
Asthma Control Test
- APIC:
-
Asthma Phenotypes in the Inner City
- ASMA:
-
Asthma Self-Management for Adolescents
- CASI:
-
Composite Asthma Severity Index
- CDC:
-
Center for Disease Control
- COAST:
-
Childhood Origins of Asthma study
- CXCL 1:
-
C-X-C motif chemokine ligand 1
- DMRs:
-
Differentially methylated regions
- ED:
-
Emergency department
- ETS:
-
Environmental tobacco smoke
- FAB:
-
Facilitated allergen binding
- FeNO:
-
Fractional exhaled nitric oxide
- ICAC:
-
Inner-City Asthma Consortium
- ICAS:
-
Inner-City Asthma Study
- ICATA:
-
Inner-City Anti-IgE Therapy for Asthma
- IFN:
-
Interferon
- Ig:
-
Immunoglobulin
- IL:
-
Interleukin
- ISAAC:
-
International Study of Asthma and Allergies in Childhood
- IT:
-
Immunotherapy
- MAIT:
-
Mucosal-associated invariant T cells
- NAEPP:
-
National Asthma Education and Prevention Program
- NCICAS:
-
National Cooperative Inner-City Asthma Study
- NHIS:
-
National Health Interview Survey
- NHLBI:
-
National Heart, Lung, and Blood Institute
- NIAID:
-
National Institutes of Allergy and Infectious Diseases
- NIH:
-
National Institute of Health
- NKT cells:
-
Natural killer T cells
- PBMCs:
-
Peripheral blood mononuclear cells
- PM:
-
Particulate matter
- PROSE:
-
Preventative Omalizumab or Step-Up Therapy for Fall Exacerbations
- RSV:
-
Respiratory syncytial virus
- SARP:
-
Severe Asthma Research Program
- SAMPRO:
-
School-based Asthma Management Program
- SICAS:
-
School Inner-City Asthma Study
- SCIT:
-
Subcutaneous immunotherapy
- SLIT:
-
Sublingual immunotherapy
- Th 2:
-
T helper 2
- Th 17:
-
T helper 17
- URECA:
-
Urban Environment and Childhood Asthma Study
- UC:
-
Urgent care
- US:
-
United States
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Poowuttikul, P., Saini, S. & Seth, D. Inner-City Asthma in Children. Clinic Rev Allerg Immunol 56, 248–268 (2019). https://doi.org/10.1007/s12016-019-08728-x
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DOI: https://doi.org/10.1007/s12016-019-08728-x