Puerto Rican (PR) children share a disproportionate burden from asthma in the U.S. We have demonstrated that in PR children, a variety of psychological stressors -including physical or sexual abuse, exposure to violence, and parental psychopathology- are associated with worse asthma outcomes. Puerto Rican children also have reduced response to bronchodilators (short-acting inhaled ?2-agonists, the most commonly used medication for asthma worldwide). We have recently shown that high child stress is associated with reduced response to short-acting inhaled ?2-agonists (bronchodilator response or BDR) in PR children with asthma, and our preliminary results also implicate genetic and epigenetic (DNA methylation) variation in genes involved in stress responses (e.g., ADCYAP1R1) on asthma and BDR. Moreover, external in vitro experiments show that high stress leads to reduced expression of the genes for the ?2-adrenergic receptor (ADRB2) and the glucocorticoid receptor (NR3C1) in white blood cells of children with asthma. While it is known that stress reduces BDR, it is not known whether this can be prevented by treatment with inhaled corticosteroids (ICS), or whether stress reduces response to ICS in vivo. Moreover, we have very limited knowledge of the genetic or epigenetic mechanisms underlying treatment resistance in stressed children. Lack of such knowledge is an important problem, because, without it, gaining the ability to prevent or treat stress-induced asthma morbidity in underserved children is highly unlikely. On the basis of our novel preliminary results, we hypothesize that chronic stress reduces response to inhaled corticosteroids (ICS) and BDR in PR children with asthma, and that these effects are mediated by altered methylation of genes regulating responses to stress, corticosteroids and BDR. To test this hypothesis, we will first determine whether increased stress leads to reduced response to ICS or BDR (even after treatment with ICS) in 300 PR children with asthma (Sp.
Aim 1). We will then test for association between high child stress and genome-wide DNA methylation in respiratory (nasal) epithelium in 550 Puerto Rican children with asthma (Sp.
Aim 2). Next, we will examine whether methylation changes in the top 100 genes identified in Aim 2 are associated with response to ICS or BDR in 300 to 550 PR children with asthma (Sp.
aim 3 a). Finally, we will assess the effects of methylation changes identified in Aim 3a on gene expression (Sp.
Aim 3 b). This proposal should determine whether and how psychosocial stress leads to reduced response to common treatments for asthma control (ICS) and relief of asthma symptoms (short-acting inhaled ?2-agonists) in a high-risk group (Puerto Rican children). To achieve this goal, we have assembled an outstanding multidisciplinary research team.

Public Health Relevance

Psychosocial stress may contribute to asthma morbidity in inner-city and minority children by reducing the efficacy of two commonly used medications for asthma: short-acting inhaled ?2-agonists and inhaled corticosteroids. Elucidating these stress effects and their causal mechanisms will have major implications for asthma management, particularly in children chronically exposed to major stressors: the economically disadvantaged and members of ethnic groups heavily affected by asthma, such as Puerto Ricans.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
2R01HL117191-05
Application #
9316934
Study Section
Infectious Diseases, Reproductive Health, Asthma and Pulmonary Conditions Study Section (IRAP)
Program Officer
Gan, Weiniu
Project Start
2013-08-01
Project End
2021-05-31
Budget Start
2017-06-01
Budget End
2018-05-31
Support Year
5
Fiscal Year
2017
Total Cost
$776,815
Indirect Cost
$154,338
Name
University of Pittsburgh
Department
Pediatrics
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Forno, Erick; Han, Yueh-Ying; Mullen, James et al. (2018) Overweight, Obesity, and Lung Function in Children and Adults-A Meta-analysis. J Allergy Clin Immunol Pract 6:570-581.e10
Forno, Erick; Wang, Ting; Qi, Cancan et al. (2018) DNA methylation in nasal epithelium, atopy, and atopic asthma in children: a genome-wide study. Lancet Respir Med :
Han, Yueh-Ying; Forno, Erick; Canino, Glorisa et al. (2018) Psychosocial risk factors and asthma among adults in Puerto Rico. J Asthma :1-9
Rosser, Franziska; Han, Yueh-Ying; Forno, Erick et al. (2018) Urinary polycyclic aromatic hydrocarbons and allergic sensitization in a nationwide study of children and adults in the United States. J Allergy Clin Immunol 142:1641-1643.e6
Han, Yueh-Ying; Forno, Erick; Shivappa, Nitin et al. (2018) The Dietary Inflammatory Index and Current Wheeze Among Children and Adults in the United States. J Allergy Clin Immunol Pract 6:834-841.e2
Forno, Erick; Han, Yueh-Ying; Libman, Ingrid M et al. (2018) Adiposity and Asthma in a Nationwide Study of Children and Adults in the United States. Ann Am Thorac Soc 15:322-330
Szentpetery, Sylvia E; Han, Yueh-Ying; Brehm, John M et al. (2018) Vitamin D insufficiency, plasma cytokines, and severe asthma exacerbations in school-aged children. J Allergy Clin Immunol Pract 6:289-291.e2
Han, Yueh-Ying; Forno, Erick; Celedón, Juan C (2018) Anxiety and noneosinophilic asthma among adults in the United States. J Allergy Clin Immunol Pract :
Han, Yueh-Ying; Forno, Erick; Boutaoui, Nadia et al. (2018) Vitamin D insufficiency, TH2 cytokines, and allergy markers in Puerto Rican children with asthma. Ann Allergy Asthma Immunol 121:497-498.e1
Han, Yueh-Ying; Rosser, Franziska; Forno, Erick et al. (2018) Exposure to polycyclic aromatic hydrocarbons, vitamin D, and lung function in children with asthma. Pediatr Pulmonol 53:1362-1368

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