Healthy Clinical Trial
Official title:
The Functional Neuroanatomy of Emotion Regulation in Major Depressive Disorder (MDD)
This study will evaluate emotional processing biases in the brain while viewing facial expressions in adults with current or remitted major depressive disorder and healthy volunteers.
The goal of this research is to elucidate the neurophysiological abnormalities associated
with processing emotionally valenced stimuli in MDD. Neuroimaging technology has led to the
identification of specific abnormalities in the amygdala, ventral striatum and medial
prefrontal cortex in response to affective pictures. Much of the knowledge involving these
structures in emotion processing has been elucidated through animal models including
classical fear conditioning and reversal-learning paradigms. Functional magnetic resonance
imaging (fMRI) studies have applied similar techniques in humans to study emotional
processing. The amygdala has been shown to play a role in the learning of fear (aversive)
conditioning to emotional stimuli, the ventral striatum has been shown to play a role in
appetitive conditioning, and areas of the prefrontal cortex are recruited for extinction of
conditioned responses. These areas have also been implicated as key structures in the
abnormal expression of emotion in MDD. Dysregulation of connections between the amygdala and
prefrontal cortex has been hypothesized to influence depressed subjects' tendency to ruminate
on emotional events and memories, which may be associated with an inability to properly
regulate emotional processing through habituation and extinction mechanisms. Research
suggests that depressed individuals have an impaired ability to disengage from or habituate
to emotional stimuli perceived as sad.
In addition to studying emotional processing at a conscious, cortical level, significant
evidence suggests that many aspects of emotional processing occur below conscious awareness,
at a preconscious level. The technique of backward masking assesses the automaticity of
emotional processing and responses to affective stimuli. In MDD, backward masking serves to
avoid confounding interpretation by the presence of other cognitive processing, which may
result from depressed subjects perseverating on emotional stimuli. The proposed study builds
on previous fMRI research to investigate neurophysiological differences in the processing of
aversively conditioned emotional stimuli in depressed compared to healthy individuals. Using
fMRI technology and a variation of the paradigm developed by Morris et al., subjects with MDD
will be classically conditioned to the presence of an unmasked specific target face (angry or
sad) and the subsequent neural responses to the stimuli will be assessed utilizing the
backward masking technique. The BOLD hemodynamic response and rates of habituation and
extinction to the faces will be compared between depressed subjects with MDD and healthy
controls, currently depressed versus currently remitted subjects with MDD, and MDD subjects
pre- and post-antidepressant therapy.
The present amendment proposes to include an additional paradigm in the testing battery. This
new paradigm has been extensively examined under different pharmacological manipulations, and
in healthy individuals undergoing fMRI but has yet to be examined in patient populations. The
task complements the paradigms presently included by extending the research to encompass
appetitive as well as aversive emotional processing.
This research will be used to evaluate neural processes involved in emotional dysregulation
in MDD and may direct future research to potential therapeutic approaches for the treatment
of mood and anxiety disorders with abnormalities in emotional processing.
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