In this revised application, the Imaging Core will provide imaging and data management support for the Center projects that integrate human and rodent-model studies to explore the role of fragmented patterns of maternal signals in increasing the vulnerability of developing individuals to mental illness. In the context of the Core, we will assess structural changes in the brains of children and rodents, using volumetry and DTI. We will also perform fMRI, testing the common hypothesis of Projects 1 and 4, pertaining to brain network shifts provoked by fragmented sensory patterns early in life. The Imaging Core has four basic goals: (i) To acquire, transfer, and store imaging data; (ii) To perform single subject image analysis, group analysis using advanced statistical inference, and multivariate modeling; (iii) To develop and execute automatic and high-speed processing pipelines for the imaging data; and (iv) To maintain quality control, data security, and data integrity. Specifically, we will acquire three types of magnetic resonance imaging (MRI) data, including structural, diffusion tensor (DTI), and functional images (fMRI), and will undertake analysis using advanced methods to test the stated hypotheses of Projects 1, 2, 3. and 4. Further, we will manage data transfers and pipelines, creating processing streams that maximize semiautomatic methods for image preprocessing, anatomical parcellation, and statistical inference, and implement parallel computer algorithms to decrease analysis times using cluster and grid computers. Guided by the helpful suggestions raised by Reviewers of the original application, the Revised Core section provides detailed information about Core facilities. Personnel expertise, and individual methodologies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
5P50MH096889-05
Application #
9265949
Study Section
Special Emphasis Panel (ZMH1-ERB-L)
Project Start
Project End
2019-04-30
Budget Start
2017-05-01
Budget End
2018-04-30
Support Year
5
Fiscal Year
2017
Total Cost
$432,019
Indirect Cost
$72,003
Name
University of California Irvine
Department
Type
Domestic Higher Education
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92617
Glynn, Laura M; Stern, Hal S; Howland, Mariann A et al. (2018) Measuring novel antecedents of mental illness: the Questionnaire of Unpredictability in Childhood. Neuropsychopharmacology :
Bolton, Jessica L; Molet, Jenny; Regev, Limor et al. (2018) Anhedonia Following Early-Life Adversity Involves Aberrant Interaction of Reward and Anxiety Circuits and Is Reversed by Partial Silencing of Amygdala Corticotropin-Releasing Hormone Gene. Biol Psychiatry 83:137-147
Bolton, Jessica L; Ruiz, Christina M; Rismanchi, Neggy et al. (2018) Early-life adversity facilitates acquisition of cocaine self-administration and induces persistent anhedonia. Neurobiol Stress 8:57-67
Gunn, Benjamin G; Sanchez, Gissell A; Lynch, Gary et al. (2018) Hyper-diversity of CRH interneurons in mouse hippocampus. Brain Struct Funct :
Leal, Stephanie L; Yassa, Michael A (2018) Integrating new findings and examining clinical applications of pattern separation. Nat Neurosci 21:163-173
Fox, Molly; Sandman, Curt A; Davis, Elysia Poggi et al. (2018) A longitudinal study of women's depression symptom profiles during and after the postpartum phase. Depress Anxiety 35:292-304
Singh-Taylor, A; Molet, J; Jiang, S et al. (2018) NRSF-dependent epigenetic mechanisms contribute to programming of stress-sensitive neurons by neonatal experience, promoting resilience. Mol Psychiatry 23:648-657
Riley, Jeffrey D; Chen, E Elinor; Winsell, Jessica et al. (2018) Network specialization during adolescence: Hippocampal effective connectivity in boys and girls. Neuroimage 175:402-412
Glynn, Laura M; Howland, Mariann A; Fox, Molly (2018) Maternal programming: Application of a developmental psychopathology perspective. Dev Psychopathol 30:905-919
Sandman, Curt A; Curran, Megan M; Davis, Elysia Poggi et al. (2018) Cortical Thinning and Neuropsychiatric Outcomes in Children Exposed to Prenatal Adversity: A Role for Placental CRH? Am J Psychiatry 175:471-479

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