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      Reduced default mode network suppression during a working memory task in remitted major depression

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          Abstract

          Insufficient default mode network (DMN) suppression was linked to increased rumination in symptomatic Major Depressive Disorder (MDD). Since rumination is known to predict relapse and a more severe course of MDD, we hypothesized that similar DMN alterations might also exist during full remission of MDD (rMDD), a condition known to be associated with increased relapse rates specifically in patients with adolescent onset. Within a cross-sectional functional magnetic resonance imaging study activation and functional connectivity (FC) were investigated in 120 adults comprising 78 drug-free rMDD patients with adolescent- (n = 42) and adult-onset (n = 36) as well as 42 healthy controls (HC), while performing the n-back task. Compared to HC, rMDD patients showed diminished DMN deactivation with strongest differences in the anterior-medial prefrontal cortex (amPFC), which was further linked to increased rumination response style. On a brain systems level, rMDD patients showed an increased FC between the amPFC and the dorsolateral prefrontal cortex, which constitutes a key region of the antagonistic working-memory network. Both whole-brain analyses revealed significant differences between adolescent-onset rMDD patients and HC, while adult-onset rMDD patients showed no significant effects. Results of this study demonstrate that reduced DMN suppression exists even after full recovery of depressive symptoms, which appears to be specifically pronounced in adolescent-onset MDD patients. Our results encourage the investigation of DMN suppression as a putative predictor of relapse in clinical trials, which might eventually lead to important implications for antidepressant maintenance treatment.

          Highlights

          • Reduced default mode network suppression persists even after remission of MDD symptoms.

          • Adolescent-onset rMDD patients show stronger alterations likely reflecting the more severe disease course.

          • The anterior-medial prefrontal cortex appears to be the mediator of these brain network changes in rMDD patients.

          • Reduced default mode network suppression is related to increased rumination.

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          Most cited references62

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          Responses to depression and their effects on the duration of depressive episodes.

          I propose that the ways people respond to their own symptoms of depression influence the duration of these symptoms. People who engage in ruminative responses to depression, focusing on their symptoms and the possible causes and consequences of their symptoms, will show longer depressions than people who take action to distract themselves from their symptoms. Ruminative responses prolong depression because they allow the depressed mood to negatively bias thinking and interfere with instrumental behavior and problem-solving. Laboratory and field studies directly testing this theory have supported its predictions. I discuss how response styles can explain the greater likelihood of depression in women than men. Then I intergrate this response styles theory with studies of coping with discrete events. The response styles theory is compared to other theories of the duration of depression. Finally, I suggest what may help a depressed person to stop engaging in ruminative responses and how response styles for depression may develop.
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            Searching for a baseline: functional imaging and the resting human brain.

            Functional brain imaging in humans has revealed task-specific increases in brain activity that are associated with various mental activities. In the same studies, mysterious, task-independent decreases have also frequently been encountered, especially when the tasks of interest have been compared with a passive state, such as simple fixation or eyes closed. These decreases have raised the possibility that there might be a baseline or resting state of brain function involving a specific set of mental operations. We explore this possibility, including the manner in which we might define a baseline and the implications of such a baseline for our understanding of brain function.
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              Animal models of neuropsychiatric disorders.

              Modeling of human neuropsychiatric disorders in animals is extremely challenging given the subjective nature of many symptoms, the lack of biomarkers and objective diagnostic tests, and the early state of the relevant neurobiology and genetics. Nonetheless, progress in understanding pathophysiology and in treatment development would benefit greatly from improved animal models. Here we review the current state of animal models of mental illness, with a focus on schizophrenia, depression and bipolar disorder. We argue for areas of focus that might increase the likelihood of creating more useful models, at least for some disorders, and for explicit guidelines when animal models are reported.
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                Author and article information

                Contributors
                Journal
                J Psychiatr Res
                J Psychiatr Res
                Journal of Psychiatric Research
                Pergamon Press
                0022-3956
                1879-1379
                1 May 2015
                May 2015
                : 64
                : 9-18
                Affiliations
                [a ]Division of Biological Psychiatry, Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria
                [b ]Department of Psychology, Dresden University of Technology, Dresden, Germany
                [c ]MR Centre of Excellence, Medical University of Vienna, Vienna, Austria
                [d ]Center for Medical Physics and Biomedical Engineering, Medical University of Vienna, Vienna, Austria
                [e ]Department of Child and Adolescent Psychiatry, Medical University of Vienna, Vienna, Austria
                [f ]Center of Physiology and Pharmacology, Institute of Pharmacology, Medical University of Vienna, Vienna, Austria
                Author notes
                []Corresponding author. Division of Biological Psychiatry, Department of Psychiatry and Psychotherapy, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria. Tel.: +43 (1) 40400 35680; fax: +43 (1) 40400 3099. lukas.pezawas@ 123456meduniwien.ac.at
                [1]

                These authors contributed equally to this work.

                Article
                S0022-3956(15)00069-2
                10.1016/j.jpsychires.2015.02.025
                4415908
                25801734
                383d3358-99d0-4cbf-b01c-e8d8f85fad29
                © 2015 The Authors

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

                History
                : 10 September 2014
                : 14 January 2015
                : 26 February 2015
                Categories
                Article

                Clinical Psychology & Psychiatry
                default mode network,functional magnetic resonance imaging,major depressive disorder,remission,rumination,working memory

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