Depression is among the most prevalent of all psychiatric disorders. Consistent with the NIH objectives of promoting discovery in the brain and behavioral sciences to fuel research on the causes of mental disorders and charting mental illness trajectories to determine when, where, and how to intervene, a critical public health priority is the development of methods for identifying and altering factors and mechanisms that increase individuals'vulnerability to depression. Offspring of depressed parents are known to be at elevated risk for developing depression;consequently, assessing these children has been an important strategy for elucidating factors associated with the increased risk for psychiatric disorder. To date, however, few studies have gone beyond documenting the magnitude of this risk to examine specific mechanisms that might underlie the intergenerational transmission of risk for depression. Over the last four years we have worked hard to recruit and test a large, carefully diagnosed, sample of 10- to 14-year-old never-disordered girls at either high or low familial risk for depression. Each girl has a biological mother who either has experienced recurrent episodes of Major Depressive Disorder (MDD) during her daughter's lifetime (high risk) or has never experienced an episode of any Axis-I disorder (low risk). Although the high-risk girls are asymptomatic, we have found that they nevertheless already exhibit characteristics of MDD, including selective attention to sad faces, higher and more prolonged cortisol secretion in response to a laboratory stressor, higher levels of awakening cortisol, smaller hippocampi, and anomalous neural functioning both in response to reward and punishment and while experiencing and regulating a sad mood. Because we began recruiting the girls in this study at this young age only four years ago, we have not yet been able to examine fully whether these difficulties predict the subsequent onset of a first episode of MDD. Therefore, we propose to conduct a 54-month follow-up diagnostic session with this sample and to add a second fMRI scan to assess differences in the stability of neural structure and function between high-risk girls who do, and who do not, develop MDD. We also propose to recruit a new sample of high-risk daughters, to teach them either through attentional bias training or through real-time neurofeedback training to alter mechanisms that we posit underlie the development of MDD, and to assess both short- and long-term effects of modulating these mechanisms. We propose to examine immediate changes in stress reactivity, cognitive biases, and reward processing as a function of training. We also propose to conduct an 18-month follow-up assessment to examine longer-term effects of training on specific clinical constructs, such as levels of depressive symptoms, coping strategies, and the onset of MDD. This project will yield new insights concerning psychological and biological risk factors for MDD, and will provide important information that can be used to develop innovative and effective approaches to the prevention of depression.

Public Health Relevance

This project promises to improve our understanding of psychological and biological mechanisms that increase risk for depression, a devastating psychiatric condition that affects one-quarter of the world's population, that starts early in life and frequently becomes chronic and unrelenting. Understanding these mechanisms will help us to develop more effective approaches to the prevention of clinical depression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
3R01MH074849-09S1
Application #
8795890
Study Section
Biobehavioral Mechanisms of Emotion, Stress and Health Study Section (MESH)
Program Officer
Garriock, Holly A
Project Start
2005-07-01
Project End
2016-01-31
Budget Start
2014-02-01
Budget End
2015-01-31
Support Year
9
Fiscal Year
2014
Total Cost
$88,628
Indirect Cost
$33,408
Name
Stanford University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Foland-Ross, Lara C; Cooney, Rebecca E; Joormann, Jutta et al. (2014) Recalling happy memories in remitted depression: a neuroimaging investigation of the repair of sad mood. Cogn Affect Behav Neurosci 14:818-26
Singh, Manpreet K; Chang, Kiki D; Kelley, Ryan G et al. (2014) Early signs of anomalous neural functional connectivity in healthy offspring of parents with bipolar disorder. Bipolar Disord 16:678-89
Foland-Ross, Lara C; Hamilton, Paul; Sacchet, Matthew D et al. (2014) Activation of the medial prefrontal and posterior cingulate cortex during encoding of negative material predicts symptom worsening in major depression. Neuroreport 25:324-9
Sacchet, Matthew D; Prasad, Gautam; Foland-Ross, Lara C et al. (2014) CHARACTERIZING WHITE MATTER CONNECTIVITY IN MAJOR DEPRESSIVE DISORDER: AUTOMATED FIBER QUANTIFICATION AND MAXIMUM DENSITY PATHS. Proc IEEE Int Symp Biomed Imaging 11:592-595
Asarnow, Lauren D; Thompson, Renee J; Joormann, Jutta et al. (2014) Children at risk for depression: memory biases, self-schemas, and genotypic variation. J Affect Disord 159:66-72
Monroe, Scott M; Slavich, George M; Gotlib, Ian H (2014) Life stress and family history for depression: the moderating role of past depressive episodes. J Psychiatr Res 49:90-5
Foland-Ross, Lara C; Hardin, Michael G; Gotlib, Ian H (2013) Neurobiological markers of familial risk for depression. Curr Top Behav Neurosci 14:181-206
Kircanski, K; Mazur, H; Gotlib, I H (2013) Behavioral activation system moderates self-referent processing following recovery from depression. Psychol Med 43:1909-19
Furman, Daniella J; Waugh, Christian E; Bhattacharjee, Kalpa et al. (2013) Interoceptive awareness, positive affect, and decision making in major depressive disorder. J Affect Disord 151:780-5
Foland-Ross, Lara C; Hamilton, J Paul; Joormann, Jutta et al. (2013) The neural basis of difficulties disengaging from negative irrelevant material in major depression. Psychol Sci 24:334-44

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