Patients with recurrent major depression have abnormalities in a broad array of emotional and cognitive functions. Recently functional imaging studies have developed emotional tasks to elicit brain activation responses under standardized conditions. These studies implicate a circuit including the amygdala, the affective division of the anterior cingulate (ACad) and dorsolateral prefrontal cortex (DLPFC) in emotional regulation. The amygdala detects critical emotional information, especially threats. The ACad assesses salience of motivational cues, particularly based on amygdala input, detects conflict and regulates emotional responses. The DLPFC has a critical role in supporting a wide range of cognitive control functions. The goal of the current project is to determine which elements of the emotional circuit are dysfunctional in major depression. We propose to use functional magnetic resonance imaging (fMRI) in depressed (n = 50) and matched control (n = 50) subjects studied before and after a course of antidepressant treatment. We will use two standard cognitive paradigms in which emotion is manipulated to help elucidate the cognitive-emotional interace: a 2-back emotional working memory task and a matching task producing emotional conflict. We will determine whether depression involves a primary dysfunction in amygdala, ACad, or DLPFC. In addition, we hypothesize that depressed subjects will have normalization of abnormal brain activation with treatment. The proposed study has the potential to substantially advance our understanding of the precise nature and mechanisms underlying cognitive-emotional dysregulation in major depression. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
3R01MH064821-02S1
Application #
7010224
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Meinecke, Douglas L
Project Start
2003-07-01
Project End
2007-05-31
Budget Start
2005-01-01
Budget End
2005-05-31
Support Year
2
Fiscal Year
2005
Total Cost
$75,151
Indirect Cost
Name
Washington University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Yang, Zhen; Oathes, Desmond J; Linn, Kristin A et al. (2018) Cognitive Behavioral Therapy Is Associated With Enhanced Cognitive Control Network Activity in Major Depression and Posttraumatic Stress Disorder. Biol Psychiatry Cogn Neurosci Neuroimaging 3:311-319
Shou, Haochang; Yang, Zhen; Satterthwaite, Theodore D et al. (2017) Cognitive behavioral therapy increases amygdala connectivity with the cognitive control network in both MDD and PTSD. Neuroimage Clin 14:464-470
Satterthwaite, T D; Cook, P A; Bruce, S E et al. (2016) Dimensional depression severity in women with major depression and post-traumatic stress disorder correlates with fronto-amygdalar hypoconnectivty. Mol Psychiatry 21:894-902
D'Angelo, Gina M; Weissfeld, Lisa A (2013) Application of copulas to improve covariance estimation for partial least squares. Stat Med 32:685-96
Sheline, Yvette I (2011) Depression and the hippocampus: cause or effect? Biol Psychiatry 70:308-9
Sheline, Yvette I; Price, Joseph L; Yan, Zhizi et al. (2010) Resting-state functional MRI in depression unmasks increased connectivity between networks via the dorsal nexus. Proc Natl Acad Sci U S A 107:11020-5
Sheline, Yvette I; Barch, Deanna M; Price, Joseph L et al. (2009) The default mode network and self-referential processes in depression. Proc Natl Acad Sci U S A 106:1942-7
Fales, Christina L; Barch, Deanna M; Rundle, Melissa M et al. (2009) Antidepressant treatment normalizes hypoactivity in dorsolateral prefrontal cortex during emotional interference processing in major depression. J Affect Disord 112:206-11
Fales, Christina L; Barch, Deanna M; Rundle, Melissa M et al. (2008) Altered emotional interference processing in affective and cognitive-control brain circuitry in major depression. Biol Psychiatry 63:377-84