This application seeks support to investigate the neurodevelopmental origins and etiology of major depressive disorder. Specifically, we propose to test a """"""""fetal programming"""""""" model of depression in which adverse conditions during the fetal period-as indicated by exposure to maternal hypothalamic-pituitary- adrenal (HPA) hormones, elevated maternal pro-inflammatory cytokines;early social adversity;and genetic susceptibility, combine to contribute to a trajectory of elevated lifetime risk for major depression. This project also addresses the challenge of health disparities, which for depression are marked and persistent, and which remain an NIH priority area. We propose that the social origins of depression are, in part, neurodevelopmental in nature, and that understanding the developmental pathways to depression will not only yield significant insights into etiology, but will also advance the objective of reducing disparities.
The aims of this application are: 1) to investigate the combined influences of atypical fetal stress- response pathways and social adversity in relation to the lifetime risk of major depressive disorder;and 2) to investigate gene-environment interactions during the prenatal period in the development of depression. The following hypotheses will be tested. 1) The long-term impact of prenatal risks-as indicated by maternal pro- inflammatory cytokines and maternal HPA activity-for major depression will be heightened under adverse social conditions. Hypothesis 1a is that the combination of maternal-fetal stress, as indicated by elevated levels of inflammatory cytokines (IL-1, IL-6, and TNF-) during mid-gestation, and social adversity will be associated with an increased lifetime risk and recurrence of major depression. Hypothesis 1b is that levels of HPA hormones (increased CRH and decreased DHEAS and hCG) during mid-gestation will be associated with the lifetime risk and recurrence of major depression most strongly among individuals born in the context of social adversity 2) Social adversity during pregnancy and early infancy, in combination with genetic susceptibility to depression, with be associated with an elevated lifetime risk of depression. Hypothesis 2 is that polymorphisms in genes associated with HPA circuitry and in genes with prior replicated evidence of environmentally dependent effects on depression, will be associated with an increased risk of depression most strongly among children born in the context of social adversity. This application involves data from a 50-year investigation of a well-established birth cohort, the New England Family Study, which is uniquely capable of addressing the prenatal determinants of mental illness. The applicant is a social epidemiologist whose long-term career objectives are to discover the developmental pathways leading to major depression, and to identify modifiable pathways in order to reduce the public health burden of depression.

Public Health Relevance

The aim of this project is to investigate the combined influences of the fetal exposures, genetic susceptibility, and social adversity to the neurodevelopmental origins of major depression. By integrating the social determinants of depression with fetal biologic risk factors, we aim to significantly increase our understanding of the early life origins of depression. We also aim to identify potentially modifiable pathways in order to reduce disparities in depression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH087544-03
Application #
8089557
Study Section
Special Emphasis Panel (ZMH1-ERB-L (06))
Program Officer
Garriock, Holly A
Project Start
2009-09-25
Project End
2013-06-30
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
3
Fiscal Year
2011
Total Cost
$323,730
Indirect Cost
Name
Harvard University
Department
Social Sciences
Type
Schools of Public Health
DUNS #
149617367
City
Boston
State
MA
Country
United States
Zip Code
02115
Gilman, Stephen E; Hornig, Mady; Ghassabian, Akhgar et al. (2017) Socioeconomic disadvantage, gestational immune activity, and neurodevelopment in early childhood. Proc Natl Acad Sci U S A 114:6728-6733
Pabayo, Roman; Fuller, Daniel; Goldstein, Risë B et al. (2017) Income inequality among American states and the conditional risk of post-traumatic stress disorder. Soc Psychiatry Psychiatr Epidemiol 52:1195-1204
Hung, Galen Chin-Lun; Pietras, Stefanie A; Carliner, Hannah et al. (2016) Cognitive ability in childhood and the chronicity and suicidality of depression. Br J Psychiatry 208:120-7
Gilman, S E; Cherkerzian, S; Buka, S L et al. (2016) Prenatal immune programming of the sex-dependent risk for major depression. Transl Psychiatry 6:e822
Pabayo, Roman; Kawachi, Ichiro; Gilman, Stephen E (2015) US State-level income inequality and risks of heart attack and coronary risk behaviors: longitudinal findings. Int J Public Health 60:573-88
Chin-Lun Hung, Galen; Hahn, Jill; Alamiri, Bibi et al. (2015) Socioeconomic disadvantage and neural development from infancy through early childhood. Int J Epidemiol 44:1889-99
Gilman, S E; Ni, M Y; Dunn, E C et al. (2015) Contributions of the social environment to first-onset and recurrent mania. Mol Psychiatry 20:329-36
Slopen, Natalie; Loucks, Eric B; Appleton, Allison A et al. (2015) Early origins of inflammation: An examination of prenatal and childhood social adversity in a prospective cohort study. Psychoneuroendocrinology 51:403-13
Santavirta, Torsten; Santavirta, Nina; Betancourt, Theresa S et al. (2015) Long term mental health outcomes of Finnish children evacuated to Swedish families during the second world war and their non-evacuated siblings: cohort study. BMJ 350:g7753
Pabayo, Roman; Kawachi, Ichiro; Gilman, Stephen E (2014) Income inequality among American states and the incidence of major depression. J Epidemiol Community Health 68:110-5

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