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      Reduction in social anxiety after MDMA-assisted psychotherapy with autistic adults: a randomized, double-blind, placebo-controlled pilot study

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          Abstract

          Rationale

          Standard therapeutic approaches to reduce social anxiety in autistic adults have limited effectiveness. Since 3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy shows promise as a treatment for other anxiety disorders, a blinded, placebo-controlled pilot study was conducted.

          Objectives

          To explore feasibility and safety of MDMA-assisted psychotherapy for reduction of social fear and avoidance that are common in the autistic population.

          Methods

          Autistic adults with marked to very severe social anxiety were randomized to receive MDMA (75 to 125 mg, n = 8) or inactive placebo (0 mg, n = 4) during two 8-h psychotherapy sessions (experimental sessions) in a controlled clinical setting. Double-blinded experimental sessions were spaced approximately 1 month apart with 3 non-drug psychotherapy sessions following each. The primary outcome was change in Leibowitz Social Anxiety Scale (LSAS) Total scores from Baseline to one month after the second experimental session. Outcomes were measured again six months after the last experimental session.

          Results

          Improvement in LSAS scores from baseline to the primary endpoint was significantly greater for MDMA group compared to the placebo group ( P = 0.037), and placebo-subtracted Cohen’s d effect size was very large ( d = 1.4, CI − 0.074, 2.874). Change in LSAS scores from baseline to 6-month follow-up showed similar positive results ( P = 0.036), with a Cohen’s d effect size of 1.1 (CI − 0.307, 2.527). Social anxiety remained the same or continued to improve slightly for most participants in the MDMA group after completing the active treatment phase.

          Conclusions

          This pilot trial demonstrated rapid and durable improvement in social anxiety symptoms in autistic adults following MDMA-assisted psychotherapy. Initial safety and efficacy outcomes support expansion of research into larger samples to further investigate this novel treatment for social anxiety.

          Trial registration

          clinicaltrials.gov identifier, NCT02008396

          Electronic supplementary material

          The online version of this article (10.1007/s00213-018-5010-9) contains supplementary material, which is available to authorized users.

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          Most cited references31

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          Assessment of Individual Differences in Empathy

          Mark Davis (2018)
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            GABA system dysfunction in autism and related disorders: from synapse to symptoms.

            Autism spectrum disorders (ASDs) are neurodevelopmental syndromes characterised by repetitive behaviours and restricted interests, impairments in social behaviour and relations, and in language and communication. These symptoms are also observed in a number of developmental disorders of known origin, including Fragile X Syndrome, Rett Syndrome, and Foetal Anticonvulsant Syndrome. While these conditions have diverse etiologies, and poorly understood pathologies, emerging evidence suggests that they may all be linked to dysfunction in particular aspects of GABAergic inhibitory signalling in the brain. We review evidence from genetics, molecular neurobiology and systems neuroscience relating to the role of GABA in these conditions. We conclude by discussing how these deficits may relate to the specific symptoms observed. Copyright © 2012 Elsevier Ltd. All rights reserved.
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              Brain serotonin and dopamine transporter bindings in adults with high-functioning autism.

              Autism is a neurodevelopmental disorder that is characterized by repetitive and/or obsessive interests and behavior and by deficits in sociability and communication. Although its neurobiological underpinnings are postulated to lie in abnormalities of the serotoninergic and dopaminergic systems, the details remain unknown. To determine the occurrence of changes in the binding of serotonin and dopamine transporters, which are highly selective markers for their respective neuronal systems. Using positron emission tomography, we measured the binding of brain serotonin and dopamine transporters in each individual with the radioligands carbon 11 ((11)C)-labeled trans-1,2,3,5,6,10-beta-hexahydro-6-[4-(methylthio)phenyl]pyrrolo-[2,1-a]isoquinoline ([(11)C](+)McN-5652) and 2beta-carbomethoxy-3-beta-(4-fluorophenyl)tropane ([(11)C]WIN-35,428), respectively. Statistical parametric mapping was used for between-subject analysis and within-subject correlation analysis with respect to clinical variables. Participants recruited from the community. Twenty men (age range, 18-26 years; mean [SD] IQ, 99.3 [18.1]) with autism and 20 age- and IQ-matched control subjects. Serotonin transporter binding was significantly lower throughout the brain in autistic individuals compared with controls (P < .05, corrected). Specifically, the reduction in the anterior and posterior cingulate cortices was associated with the impairment of social cognition in the autistic subjects (P < .05, corrected). A significant correlation was also found between repetitive and/or obsessive behavior and interests and the reduction of serotonin transporter binding in the thalamus (P < .05, corrected). In contrast, the dopamine transporter binding was significantly higher in the orbitofrontal cortex of the autistic group (P < .05, corrected in voxelwise analysis). In the orbitofrontal cortex, the dopamine transporter binding was significantly inversely correlated with serotonin transporter binding (r = -0.61; P = .004). The brains of autistic individuals have abnormalities in both serotonin transporter and dopamine transporter binding. The present findings indicate that the gross abnormalities in these neurotransmitter systems may underpin the neurophysiologic mechanism of autism. Our sample was not characteristic or representative of a typical sample of adults with autism in the community.
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                Author and article information

                Contributors
                adanforth@labiomed.org
                cgrob@labiomed.org
                cstruble.md@gmail.com
                alli@mapsbcorp.com
                nwalker@ciis.edu
                ilsa@mapsbcorp.com
                berra@maps.org
                amy@mapsbcorp.com
                Journal
                Psychopharmacology (Berl)
                Psychopharmacology (Berl.)
                Psychopharmacology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0033-3158
                1432-2072
                8 September 2018
                8 September 2018
                2018
                : 235
                : 11
                : 3137-3148
                Affiliations
                [1 ]ISNI 0000 0001 0157 6501, GRID grid.239844.0, Los Angeles Biomedical Research Institute, , Harbor-UCLA Medical Center, ; Box 498, 1000 West Carson Blvd., Torrance, CA 90509 USA
                [2 ]ISNI 0000 0001 0157 6501, GRID grid.239844.0, Department of Psychiatry, , Harbor-UCLA Medical Center, ; Box 498, 1000 West Carson Blvd., Torrance, CA 90509 USA
                [3 ]MAPS Public Benefit Corporation, 1115 Mission Street, Santa Cruz, CA 95060 USA
                [4 ]GRID grid.462142.7, School of Undergraduate Studies, , California Institute of Integral Studies, ; 1453 Mission Street, San Francisco, CA 94103 USA
                [5 ]GRID grid.429422.b, Multidisciplinary Association for Psychedelic Studies, ; 1115 Mission Street, Santa Cruz, CA 95060 USA
                Article
                5010
                10.1007/s00213-018-5010-9
                6208958
                30196397
                70b08bc3-7d1a-4589-971a-6a2ccd0c9bcd
                © The Author(s) 2018

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.

                History
                : 12 June 2018
                : 20 August 2018
                Funding
                Funded by: Multidisciplinary Association for Psychedelic Studies
                Award ID: NA
                Award Recipient :
                Categories
                Original Investigation
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2018

                Pharmacology & Pharmaceutical medicine
                social anxiety,mdma,3,4-methylenedioxymethamphetamine,mdma-assisted psychotherapy,autism,asperger’s,liebowitz social anxiety scale,psychedelics,anxiety

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