The primary aim of the this collaborative R01 application is to conduct a longitudinal neuroimaging study of developmental changes in the function and structure of ventral-prefrontal limbic cortical networks key to emotion processing in a unique cohort of children with preschool onset Major Depressive Disorder (PO-MDD) as they transition from school age to early adolescence. To achieve this goal, we propose to conduct structural and functional neuroimaging at 3 timepoints in healthy and PO-MDD children ascertained as part of an ongoing R01 to Joan Luby, M.D. The proposed study would capture children at the 5th and 6th (final) annual waves of data collection in this continuing R01 and would conduct an additional scan and diagnostic assessment at a subsequent planned wave. Detailed longitudinal diagnostic, psychosocial, biological and family history and parenting data are already available in the study sample. The proposed study provides an invaluable opportunity to examine the effects of depression severity and course, as well as key biological and psychosocial mediators/moderators assessed during early childhood, on the structure and function of prefrontal limbic emotion systems known to be altered in older children and adults with MDD. It will also provide the first available longitudinal data on alterations in brain maturation in childhood MDD. Preliminary neuroimaging data from the study population have been obtained as part of a small NIMH supplement and support several of the specific hypotheses. To characterize differences in regional volume and cortical integrity based on innovative high dimensional computational anatomy approaches, we will focus on the neuromorphometry of the following regions: the ventral medial prefrontal cortex, pregenual cingulate, amygdala and hippocampus. Diffusion tensor imaging (DTI) will also be employed in a complementary fashion to further characterize cortical, subcortical and white matter tract structural integrity. To characterize differences in the functional neuroanatomy of emotion processing in these same regions, we propose to use functional magnetic resonance imaging during an emotion recognition paradigm and to assess functional connectivity. Based on the design of the proposed study and the available well-studied sample with PO-MDD, we will have the unique opportunity to fill a critical gap in the literature and investigate developmental changes in brain maturation related to childhood onset MDD.

Public Health Relevance

The proposed study will address how preschool onset and childhood recurrent depression impact brain development in children. We will address the impact of chronicity and severity of early depressive episodes on the structure and function of brain regions known to be key in emotion processing. The study will conduct 3 scans during school age and early adolescence in children with preschool onset MDD compared to healthy controls. Based on the design of the study, we will also have the opportunity to address the role of risk and protective factors in this process including parent child relationship, stressful life events and social support.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH090786-04
Application #
8437231
Study Section
Special Emphasis Panel (ZRG1-BDCN-N (02))
Program Officer
Garriock, Holly A
Project Start
2010-05-01
Project End
2015-02-28
Budget Start
2013-03-01
Budget End
2014-02-28
Support Year
4
Fiscal Year
2013
Total Cost
$796,766
Indirect Cost
$227,389
Name
Washington University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Pagliaccio, David; Luby, Joan L; Bogdan, Ryan et al. (2014) Stress-system genes and life stress predict cortisol levels and amygdala and hippocampal volumes in children. Neuropsychopharmacology 39:1245-53
Belden, Andy C; Luby, Joan L; Pagliaccio, David et al. (2014) Neural activation associated with the cognitive emotion regulation of sadness in healthy children. Dev Cogn Neurosci 9:136-47
Rogers, Cynthia E; Barch, Deanna M; Sylvester, Chad M et al. (2014) Altered gray matter volume and school age anxiety in children born late preterm. J Pediatr 165:928-35
Bogdan, Ryan; Agrawal, Arpana; Gaffrey, Michael S et al. (2014) Serotonin transporter-linked polymorphic region (5-HTTLPR) genotype and stressful life events interact to predict preschool-onset depression: a replication and developmental extension. J Child Psychol Psychiatry 55:448-57
Luking, Katherine R; Luby, Joan L; Barch, Deanna M (2014) Kids, candy, brain and behavior: age differences in responses to candy gains and losses. Dev Cogn Neurosci 9:82-92
Suzuki, Hideo; Luby, Joan L; Botteron, Kelly N et al. (2014) Early life stress and trauma and enhanced limbic activation to emotionally valenced faces in depressed and healthy children. J Am Acad Child Adolesc Psychiatry 53:800-13.e10
Suzuki, Hideo; Botteron, Kelly N; Luby, Joan L et al. (2013) Structural-functional correlations between hippocampal volume and cortico-limbic emotional responses in depressed children. Cogn Affect Behav Neurosci 13:135-51
Pagliaccio, David; Luby, Joan L; Gaffrey, Michael S et al. (2013) Functional brain activation to emotional and nonemotional faces in healthy children: evidence for developmentally undifferentiated amygdala function during the school-age period. Cogn Affect Behav Neurosci 13:771-89
Gaffrey, Michael S; Luby, Joan L; Barch, Deanna M (2013) Towards the study of functional brain development in depression: an Interactive Specialization approach. Neurobiol Dis 52:38-48
Sylvester, Chad M; Barch, Deanna M; Corbetta, Maurizio et al. (2013) Resting state functional connectivity of the ventral attention network in children with a history of depression or anxiety. J Am Acad Child Adolesc Psychiatry 52:1326-1336.e5

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