Many studies demonstrate that stress exposure in childhood is associated with multiple kinds of illnesses in adulthood. The mechanisms underlying these associations are not yet clear, but there is consideration speculation that inflammation and, more broadly, alteration of the immune system from early stress exposure has an etiological role. What has not been established is the extent to which, and the mechanisms by which, early stress exposure has childhood onset effects on the immune system. Research is now needed to translate adult and a sizable experimental animal literature to pediatric samples; results from these studies would fundamentally shape public and clinical health approaches. The proposed study makes use of the Family Life Project (FLP), an ongoing prospective longitudinal study of 1292 children who were selected using epidemiological methods to oversample stress-exposed children. Indicators of innate and adaptive immune function will be collected from detailed developmental visits when the children are approximately 9 years of age and linked with measures of stress, behavior and psychosocial context data dating back to 2 months of age. Several features of the proposed study provide particular leverage for advancing this field of research, including a) a large epidemiologically-derived sample of pre-adolescent children at elevated psychosocial risk who have been carefully studied since infancy, b) detailed study of the innate and adaptive immune systems, and c) detailed assessment of socio-demographic and proximal family stress across the first decade of life that provide leverage for testing hypotheses about the type and timing of stress exposure, and d) examination of glucocorticoid resistance as a mediating mechanism.
The research aims are to 1) test alternative hypotheses for a link between stress exposures and components of the innate immune system; 2) examine the association between early stress exposure and adaptive immunity, indexed by T cell responses to latent/persistent virus; and 3) determine the associations between behavioral/emotional and somatic symptoms and immune function in stress-exposed children. We also add a fourth exploratory aim: to examine the links between family and socio-demographic risk and illness and functional outcomes. The proposed study will add significant new information to our understanding of if and how stress exposure is associated with childhood onset dysregulated immune outcomes and the mechanisms involved. Findings from the study will provide a much-needed empirical foundation for developmental and clinical models of the interplay between stress and health in children.

Public Health Relevance

Several studies show that stress exposure in childhood is associated with adult disease, but we lack adequate data on the extent to which, and by what mechanisms, stress exposure in childhood has more immediate impact on immune health in childhood. The proposed study capitalizes on an ongoing prospective longitudinal study of an epidemiologically-derived sample that has followed approximately 1,200 at-risk children and families since the target child's birth, the Family Life Project (FLP). The proposed study expands the FLP in an important new dimension: by collecting a blood sample on the children at age 9 years, we will be able to extract multiple indicators of immune health and test novel hypotheses about the timing, type, and tenor of stress on immune markers, as well as examine dynamic processes within the immune system.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
4R01MH097293-04
Application #
9023594
Study Section
Biobehavioral Mechanisms of Emotion, Stress and Health Study Section (MESH)
Program Officer
Zehr, Julia L
Project Start
2013-03-12
Project End
2018-01-31
Budget Start
2016-02-01
Budget End
2017-01-31
Support Year
4
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Rochester
Department
Psychiatry
Type
School of Medicine & Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
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O'Connor, Thomas G; Barrett, Emily S (2014) Mechanisms of prenatal programing: identifying and distinguishing the impact of steroid hormones. Front Endocrinol (Lausanne) 5:52
O'Connor, Thomas G; Moynihan, Jan A; Wyman, Peter A et al. (2014) Depressive symptoms and immune response to meningococcal conjugate vaccine in early adolescence. Dev Psychopathol 26:1567-76
O'Connor, Thomas G; Moynihan, Jan A; Caserta, Mary T (2014) Annual research review: The neuroinflammation hypothesis for stress and psychopathology in children--developmental psychoneuroimmunology. J Child Psychol Psychiatry 55:615-31