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      The relationship between childhood trauma, dopamine release and dexamphetamine-induced positive psychotic symptoms: a [ 11C]-(+)-PHNO PET study

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          Abstract

          Childhood trauma is a risk factor for psychosis. Amphetamine increases synaptic striatal dopamine levels and can induce positive psychotic symptoms in healthy individuals and patients with schizophrenia. Socio-developmental hypotheses of psychosis propose that childhood trauma and other environmental risk factors sensitize the dopamine system to increase the risk of psychotic symptoms, but this remains to be tested in humans. We used [ 11C]-(+)-PHNO positron emission tomography to measure striatal dopamine-2/3 receptor (D 2/3R) availability and ventral striatal dexamphetamine-induced dopamine release in healthy participants ( n = 24). The relationships between dexamphetamine-induced dopamine release, dexamphetamine-induced positive psychotic symptoms using the Positive and Negative Syndrome Scale (PANSS), and childhood trauma using the Childhood Trauma Questionnaire (CTQ) were assessed using linear regression and mediation analyses, with childhood trauma as the independent variable, dexamphetamine-induced dopamine release as the mediator variable, and dexamphetamine-induced symptoms as the dependent variable. There was a significant interaction between childhood trauma and ventral striatal dopamine release in predicting dexamphetamine-induced positive psychotic symptoms (standardized β = 1.83, p = 0.003), but a mediation analysis was not significant (standardized β = −0.18, p = 0.158). There were no significant effects of dopamine release and childhood trauma on change in negative ( p = 0.280) or general PANSS symptoms ( p = 0.061), and there was no relationship between ventral striatal baseline D 2/3R availability and positive symptoms ( p = 0.368). This indicates childhood trauma and dopamine release interact to influence the induction of positive psychotic symptoms. This is not consistent with a simple sensitization hypothesis, but suggests that childhood trauma moderates the cognitive response to dopamine release to make psychotic experiences more likely.

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          The environment and schizophrenia.

          Psychotic syndromes can be understood as disorders of adaptation to social context. Although heritability is often emphasized, onset is associated with environmental factors such as early life adversity, growing up in an urban environment, minority group position and cannabis use, suggesting that exposure may have an impact on the developing 'social' brain during sensitive periods. Therefore heritability, as an index of genetic influence, may be of limited explanatory power unless viewed in the context of interaction with social effects. Longitudinal research is needed to uncover gene-environment interplay that determines how expression of vulnerability in the general population may give rise to more severe psychopathology.
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            Childhood trauma, psychosis and schizophrenia: a literature review with theoretical and clinical implications.

            To review the research addressing the relationship of childhood trauma to psychosis and schizophrenia, and to discuss the theoretical and clinical implications. Relevant studies and previous review papers were identified via computer literature searches. Symptoms considered indicative of psychosis and schizophrenia, particularly hallucinations, are at least as strongly related to childhood abuse and neglect as many other mental health problems. Recent large-scale general population studies indicate the relationship is a causal one, with a dose-effect. Several psychological and biological mechanisms by which childhood trauma increases risk for psychosis merit attention. Integration of these different levels of analysis may stimulate a more genuinely integrated bio-psycho-social model of psychosis than currently prevails. Clinical implications include the need for staff training in asking about abuse and the need to offer appropriate psychosocial treatments to patients who have been abused or neglected as children. Prevention issues are also identified.
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              Excess early mortality in schizophrenia.

              Schizophrenia is often referred to as one of the most severe mental disorders, primarily because of the very high mortality rates of those with the disorder. This article reviews the literature on excess early mortality in persons with schizophrenia and suggests reasons for the high mortality as well as possible ways to reduce it. Persons with schizophrenia have an exceptionally short life expectancy. High mortality is found in all age groups, resulting in a life expectancy of approximately 20 years below that of the general population. Evidence suggests that persons with schizophrenia may not have seen the same improvement in life expectancy as the general population during the past decades. Thus, the mortality gap not only persists but may actually have increased. The most urgent research agenda concerns primary candidates for modifiable risk factors contributing to this excess mortality, i.e., side effects of treatment and lifestyle factors, as well as sufficient prevention and treatment of physical comorbidity.
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                Author and article information

                Contributors
                +44(0) 20 8383 3446 , tarik.dahoun@conted.ox.ac.uk
                oliver.howes@kcl.ac.uk
                Journal
                Transl Psychiatry
                Transl Psychiatry
                Translational Psychiatry
                Nature Publishing Group UK (London )
                2158-3188
                11 November 2019
                11 November 2019
                2019
                : 9
                : 287
                Affiliations
                [1 ]ISNI 0000 0001 0705 4923, GRID grid.413629.b, Psychiatric Imaging Group, Robert Steiner MRI Unit, , MRC London Institute of Medical Sciences, Hammersmith Hospital, ; London, W12 0NN UK
                [2 ]ISNI 0000 0001 2113 8111, GRID grid.7445.2, Institute of Clinical Sciences, Faculty of Medicine, , Imperial College London, Hammersmith Hospital, ; London, W12 0NN UK
                [3 ]ISNI 0000 0004 1936 8948, GRID grid.4991.5, Department of Psychiatry, , University of Oxford, Warneford Hospital, ; Oxford, OX37 JX UK
                [4 ]ISNI 0000 0001 2322 6764, GRID grid.13097.3c, Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience (IoPPN), , King’s College London, ; London, SE5 8AF UK
                [5 ]ISNI 0000000121901201, GRID grid.83440.3b, Max Planck UCL Centre for Computational Psychiatry and Ageing Research, , University College London, Russell Square House, ; 10-12 Russell Square, London, WC1B 5EH UK
                [6 ]ISNI 0000000121901201, GRID grid.83440.3b, Wellcome Centre for Human Neuroimaging (WCHN), , University College London, ; London, WC1N 3AR UK
                [7 ]ISNI 0000000121901201, GRID grid.83440.3b, Division of Psychiatry, , University College London, 6th Floor, Maple House, ; 149 Tottenham Court Road, London, WC1T 7NF UK
                [8 ]ISNI 0000000121901201, GRID grid.83440.3b, Institute of Cognitive Neuroscience, , University College London, 17 Queen Square, ; London, WC1N 3AZ UK
                [9 ]ISNI 0000000121901201, GRID grid.83440.3b, Clinical Psychopharmacology Unit, Research Department of Clinical, Educational and Health Psychology, , University College London, ; 1-19 Torrington Place, London, WC1E 6BT UK
                [10 ]ISNI 0000 0004 0612 2754, GRID grid.439749.4, NIHR University College London Hospitals Biomedical Research Centre, , University College Hospital, ; London, W1T 7DN UK
                [11 ]ISNI 0000000121901201, GRID grid.83440.3b, Translational Psychiatry Research Group, Research Department of Mental Health Neuroscience, Division of Psychiatry, , University College London, 6th Floor, Maple House, ; 149 Tottenham Court Road, London, WC1T 7NF UK
                Author information
                http://orcid.org/0000-0003-1102-2566
                http://orcid.org/0000-0002-7661-8881
                Article
                627
                10.1038/s41398-019-0627-y
                6848217
                31712556
                61471d8f-50bf-4de4-95d9-2b863d20339f
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 19 January 2019
                : 17 September 2019
                : 20 October 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100001923, DH | NIHR | Health Services Research Programme (NIHR Health Services Research Programme);
                Funded by: FundRef https://doi.org/10.13039/100004440, Wellcome Trust (Wellcome);
                Funded by: FundRef https://doi.org/10.13039/501100000691, Academy of Medical Sciences;
                Funded by: FundRef https://doi.org/10.13039/100000874, Brain and Behavior Research Foundation (Brain & Behavior Research Foundation);
                Funded by: FundRef https://doi.org/10.13039/501100000272, DH | National Institute for Health Research (NIHR);
                Funded by: FundRef https://doi.org/10.13039/501100009187, RCUK | MRC | Medical Research Foundation;
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Clinical Psychology & Psychiatry
                neuroscience,psychiatric disorders
                Clinical Psychology & Psychiatry
                neuroscience, psychiatric disorders

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