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      Cognitive Behavioral Therapy Is Associated With Enhanced Cognitive Control Network Activity in Major Depression and Posttraumatic Stress Disorder

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          Abstract

          BACKGROUND

          Both major depressive disorder (MDD) and posttraumatic stress disorder (PTSD) are characterized by depressive symptoms, abnormalities in brain regions important for cognitive control, and response to cognitive behavioral therapy (CBT). However, whether a common neural mechanism underlies CBT response across diagnoses is unknown.

          METHODS

          Brain activity during a cognitive control task was measured using functional magnetic resonance imaging in 104 participants: 28 patients with MDD, 53 patients with PTSD, and 23 healthy control subjects; depression and anxiety symptoms were determined on the same day. A patient subset ( n = 31) entered manualized CBT and, along with controls ( n = 19), was rescanned at 12 weeks. Linear mixed effects models assessed the relationship between depression and anxiety symptoms and brain activity before and after CBT.

          RESULTS

          At baseline, activation of the left dorsolateral prefrontal cortex was negatively correlated with Montgomery–Åsberg Depression Rating Scale scores across all participants; this brain–symptom association did not differ between MDD and PTSD. Following CBT treatment of patients, regions within the cognitive control network, including ventrolateral prefrontal cortex and dorsolateral prefrontal cortex, showed a significant increase in activity.

          CONCLUSIONS

          Our results suggest that dimensional abnormalities in the activation of cognitive control regions were associated primarily with symptoms of depression (with or without controlling for anxious arousal). Furthermore, following treatment with CBT, activation of cognitive control regions was similarly increased in both MDD and PTSD. These results accord with the Research Domain Criteria conceptualization of mental disorders and implicate improved cognitive control activation as a transdiagnostic mechanism for CBT treatment outcome.

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          Most cited references36

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          Effects of attention and emotion on face processing in the human brain: an event-related fMRI study.

          We used event-related fMRI to assess whether brain responses to fearful versus neutral faces are modulated by spatial attention. Subjects performed a demanding matching task for pairs of stimuli at prespecified locations, in the presence of task-irrelevant stimuli at other locations. Faces or houses unpredictably appeared at the relevant or irrelevant locations, while the faces had either fearful or neutral expressions. Activation of fusiform gyri by faces was strongly affected by attentional condition, but the left amygdala response to fearful faces was not. Right fusiform activity was greater for fearful than neutral faces, independently of the attention effect on this region. These results reveal differential influences on face processing from attention and emotion, with the amygdala response to threat-related expressions unaffected by a manipulation of attention that strongly modulates the fusiform response to faces.
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            Current and lifetime comorbidity of the DSM-IV anxiety and mood disorders in a large clinical sample.

            The comorbidity of current and lifetime DSM-IV anxiety and mood disorders was examined in 1,127 outpatients who were assessed with the Anxiety Disorders Interview Schedule for DSM-IV: Lifetime version (ADIS-IV-L). The current and lifetime prevalence of additional Axis I disorders in principal anxiety and mood disorders was found to be 57% and 81%, respectively. The principal diagnostic categories associated with the highest comorbidity rates were mood disorders, posttraumatic stress disorder (PTSD), and generalized anxiety disorder (GAD). A high rate of lifetime comorbidity was found between the anxiety and mood disorders; the lifetime association with mood disorders was particularly strong for PTSD, GAD, obsessive-compulsive disorder, and social phobia. The findings are discussed in regard to their implications for the classification of emotional disorders.
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              Functional neuroimaging of major depressive disorder: a meta-analysis and new integration of base line activation and neural response data.

              Functional neuroimaging investigations of major depressive disorder can advance both the neural theory and treatment of this debilitating illness. Inconsistency of neuroimaging findings and the use of region-of-interest approaches have hindered the development of a comprehensive, empirically informed neural model of major depression. In this context, the authors sought to identify reliable anomalies in baseline neural activity and neural response to affective stimuli in major depressive disorder. The authors applied voxel-wise, whole-brain meta-analysis to neuroimaging investigations comparing depressed to healthy comparison groups with respect to baseline neural activity or neural response to positively and/or negatively valenced stimuli. Relative to healthy subjects, those with major depression had reliably higher baseline activity, bilaterally, in the pulvinar nucleus. The analysis of neural response studies using negative stimuli showed greater response in the amygdala, insula, and dorsal anterior cingulate cortex and lower response in the dorsal striatum and dorsolateral prefrontal cortex in individuals with major depressive disorder than in healthy subjects. The meta-analytic results support an elegant and neuroanatomically viable model of the salience of negative information in major depressive disorder. In this proposed model, high baseline pulvinar activity in depression first potentiates responding of the brain's salience network to negative information; next, and owing potentially to low striatal dopamine levels in depression, this viscerally charged information fails to propagate up the cortical-striatal-pallidalthalamic circuit to the dorsolateral prefrontal cortex for contextual processing and reappraisal.
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                Author and article information

                Journal
                101671285
                44575
                Biol Psychiatry Cogn Neurosci Neuroimaging
                Biol Psychiatry Cogn Neurosci Neuroimaging
                Biological psychiatry. Cognitive neuroscience and neuroimaging
                2451-9030
                6 April 2018
                28 December 2017
                April 2018
                19 April 2018
                : 3
                : 4
                : 311-319
                Affiliations
                Center for Neuromodulation in Depression and Stress (ZY, DJO, TDS, PAC, EKS, YIS) and Brain and Behavior Laboratory (TDS), Department of Psychiatry, Department of Biostatistics, Epidemiology, and Informatics (KAL, HS), Department of Radiology (PAC, YIS), and Department of Neurology (YIS), University of Pennsylvania, Philadelphia, Pennsylvania; and Department of Psychological Sciences (SEB), Center for Trauma Recovery, University of Missouri, St. Louis, Missouri
                Author notes
                Address correspondence to Yvette I. Sheline, M.D., M.S., Department of Psychiatry, 3700 Hamilton Walk, Richards D307, University of Pennsylvania, Philadelphia, PA 19104; sheline@ 123456mail.med.upenn.edu
                Article
                NIHMS957832
                10.1016/j.bpsc.2017.12.006
                5908226
                29628063
                b4a605d9-9827-4a2c-9f8f-9a4448778c9c

                This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/).

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                Categories
                Article

                affective disorders,cognitive behavioral therapy,cognitive control,dimensionality,mdd,ptsd,rdoc

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