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      MDMA-assisted therapy for severe PTSD: a randomized, double-blind, placebo-controlled phase 3 study

      research-article
      1 , 2 , , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 8 , 10 , 11 , 12 , 5 , 9 , 13 , 5 , 9 , 8 , 9 , 9 , 2 , 14 , 14 , 15 , 16 , 9 , 17 , 18 , 19 , 2 , 20 , 21 , 22 , 23 , 24 , 11 , 25 , 5 , 1 , 5 , 5 , 5 , 4 , 5 , 4
      Nature Medicine
      Nature Publishing Group US
      Drug development, Phase III trials

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          Abstract

          Post-traumatic stress disorder (PTSD) presents a major public health problem for which currently available treatments are modestly effective. We report the findings of a randomized, double-blind, placebo-controlled, multi-site phase 3 clinical trial (NCT03537014) to test the efficacy and safety of 3,4-methylenedioxymethamphetamine (MDMA)-assisted therapy for the treatment of patients with severe PTSD, including those with common comorbidities such as dissociation, depression, a history of alcohol and substance use disorders, and childhood trauma. After psychiatric medication washout, participants ( n = 90) were randomized 1:1 to receive manualized therapy with MDMA or with placebo, combined with three preparatory and nine integrative therapy sessions. PTSD symptoms, measured with the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5, the primary endpoint), and functional impairment, measured with the Sheehan Disability Scale (SDS, the secondary endpoint) were assessed at baseline and at 2 months after the last experimental session. Adverse events and suicidality were tracked throughout the study. MDMA was found to induce significant and robust attenuation in CAPS-5 score compared with placebo ( P < 0.0001, d = 0.91) and to significantly decrease the SDS total score ( P = 0.0116, d = 0.43). The mean change in CAPS-5 scores in participants completing treatment was −24.4 (s.d. 11.6) in the MDMA group and −13.9 (s.d. 11.5) in the placebo group. MDMA did not induce adverse events of abuse potential, suicidality or QT prolongation. These data indicate that, compared with manualized therapy with inactive placebo, MDMA-assisted therapy is highly efficacious in individuals with severe PTSD, and treatment is safe and well-tolerated, even in those with comorbidities. We conclude that MDMA-assisted therapy represents a potential breakthrough treatment that merits expedited clinical evaluation.

          Abstract

          Results from a phase 3, double-blind, randomized, placebo-controlled trial demonstrate that MDMA-assisted therapy is safe and effective in treating severe post-traumatic stress disorder.

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          Most cited references36

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          Posttraumatic stress disorder in the National Comorbidity Survey.

          Data were obtained on the general population epidemiology of DSM-III-R posttraumatic stress disorder (PTSD), including information on estimated life-time prevalence, the kinds of traumas most often associated with PTSD, sociodemographic correlates, the comorbidity of PTSD with other lifetime psychiatric disorders, and the duration of an index episode. Modified versions of the DSM-III-R PTSD module from the Diagnostic Interview Schedule and of the Composite International Diagnostic Interview were administered to a representative national sample of 5877 persons aged 15 to 54 years in the part II subsample of the National Comorbidity Survey. The estimated lifetime prevalence of PTSD is 7.8%. Prevalence is elevated among women and the previously married. The traumas most commonly associated with PTSD are combat exposure and witnessing among men and rape and sexual molestation among women. Posttraumatic stress disorder is strongly comorbid with other lifetime DSM-III-R disorders. Survival analysis shows that more than one third of people with an index episode of PTSD fail to recover even after many years. Posttraumatic stress disorder is more prevalent than previously believed, and is often persistent. Progress in estimating age-at-onset distributions, cohort effects, and the conditional probabilities of PTSD from different types of trauma will require future epidemiologic studies to assess PTSD for all lifetime traumas rather than for only a small number of retrospectively reported "most serious" traumas.
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            Serotonin transporter genetic variation and the response of the human amygdala.

            A functional polymorphism in the promoter region of the human serotonin transporter gene (SLC6A4) has been associated with several dimensions of neuroticism and psychopathology, especially anxiety traits, but the predictive value of this genotype against these complex behaviors has been inconsistent. Serotonin [5- hydroxytryptamine, (5-HT)] function influences normal fear as well as pathological anxiety, behaviors critically dependent on the amygdala in animal models and in clinical studies. We now report that individuals with one or two copies of the short allele of the serotonin transporter (5-HTT) promoter polymorphism, which has been associated with reduced 5-HTT expression and function and increased fear and anxiety-related behaviors, exhibit greater amygdala neuronal activity, as assessed by BOLD functional magnetic resonance imaging, in response to fearful stimuli compared with individuals homozygous for the long allele. These results demonstrate genetically driven variation in the response of brain regions underlying human emotional behavior and suggest that differential excitability of the amygdala to emotional stimuli may contribute to the increased fear and anxiety typically associated with the short SLC6A4 allele.
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              The Clinician-Administered PTSD Scale for DSM-5 (CAPS-5): Development and Initial Psychometric Evaluation in Military Veterans.

              The Clinician-Administered PTSD Scale (CAPS) is an extensively validated and widely used structured diagnostic interview for posttraumatic stress disorder (PTSD). The CAPS was recently revised to correspond with PTSD criteria in the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5; American Psychiatric Association, 2013). This article describes the development of the CAPS for DSM-5 (CAPS-5) and presents the results of an initial psychometric evaluation of CAPS-5 scores in 2 samples of military veterans (Ns = 165 and 207). CAPS-5 diagnosis demonstrated strong interrater reliability (к = .78 to 1.00, depending on the scoring rule) and test-retest reliability (к = .83), as well as strong correspondence with a diagnosis based on the CAPS for DSM-IV (CAPS-IV; к = .84 when optimally calibrated). CAPS-5 total severity score demonstrated high internal consistency (α = .88) and interrater reliability (ICC = .91) and good test-retest reliability (ICC = .78). It also demonstrated good convergent validity with total severity score on the CAPS-IV (r = .83) and PTSD Checklist for DSM-5 (r = .66) and good discriminant validity with measures of anxiety, depression, somatization, functional impairment, psychopathy, and alcohol abuse (rs = .02 to .54). Overall, these results indicate that the CAPS-5 is a psychometrically sound measure of DSM-5 PTSD diagnosis and symptom severity. Importantly, the CAPS-5 strongly corresponds with the CAPS-IV, which suggests that backward compatibility with the CAPS-IV was maintained and that the CAPS-5 provides continuity in evidence-based assessment of PTSD in the transition from DSM-IV to DSM-5 criteria. (PsycINFO Database Record
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                Author and article information

                Contributors
                jennifer.mitchell@ucsf.edu
                Journal
                Nat Med
                Nat Med
                Nature Medicine
                Nature Publishing Group US (New York )
                1078-8956
                1546-170X
                10 May 2021
                10 May 2021
                2021
                : 27
                : 6
                : 1025-1033
                Affiliations
                [1 ]GRID grid.266102.1, ISNI 0000 0001 2297 6811, Department of Neurology, , University of California San Francisco, ; San Francisco, CA USA
                [2 ]GRID grid.266102.1, ISNI 0000 0001 2297 6811, Department of Psychiatry and Behavioral Sciences, , University of California San Francisco, ; San Francisco, CA USA
                [3 ]GRID grid.137628.9, ISNI 0000 0004 1936 8753, Department of Psychiatry, , New York University Grossman School of Medicine, ; New York, NY USA
                [4 ]GRID grid.429422.b, ISNI 0000 0004 5913 2227, Multidisciplinary Association for Psychedelic Studies (MAPS), ; San Jose, CA USA
                [5 ]GRID grid.429422.b, ISNI 0000 0004 5913 2227, MAPS Public Benefit Corporation (MAPS PBC), ; San Jose, CA USA
                [6 ]Kleiman Consulting and Psychological Services, Sayreville, NJ USA
                [7 ]KPG Psychological Services LLC, Brunswick, ME USA
                [8 ]Aguazul-Bluewater Inc., Boulder, CO USA
                [9 ]GRID grid.429422.b, ISNI 0000 0004 5913 2227, MDMA Therapy Training Program, , MAPS Public Benefit Corporation, ; San Jose, CA USA
                [10 ]Nautilus Sanctuary, New York, NY USA
                [11 ]Fluence, Woodstock, NY USA
                [12 ]GRID grid.14003.36, ISNI 0000 0001 2167 3675, Department of Family Medicine and Community Health, , University of Wisconsin School of Medicine and Public Health, ; Madison, WI USA
                [13 ]GRID grid.259828.c, ISNI 0000 0001 2189 3475, Medical University of South Carolina, ; Charleston, SC USA
                [14 ]San Francisco Insight and Integration Center, San Francisco, CA USA
                [15 ]British Columbia Centre on Substance Use, Vancouver, British Columbia Canada
                [16 ]GRID grid.189504.1, ISNI 0000 0004 1936 7558, Boston University School of Medicine, ; Boston, MA USA
                [17 ]GRID grid.413795.d, ISNI 0000 0001 2107 2845, Chaim Sheba Medical Center, ; Tel HaShomer, Israel
                [18 ]Ray Worthy Psychiatry LLC, New Orleans, LA USA
                [19 ]Wholeness Center, Fort Collins, CO USA
                [20 ]New School Research LLC, North Hollywood, CA USA
                [21 ]Zen Therapeutic Solutions, Mt Pleasant, SC USA
                [22 ]GRID grid.17063.33, ISNI 0000 0001 2157 2938, University of Toronto, ; Toronto, Ontario Canada
                [23 ]Dr Simon Amar Inc., Montreal, Quebec Canada
                [24 ]Be’er Ya’akov Ness Ziona Mental Health Center, Be’er Ya’akov, Israel
                [25 ]GRID grid.168010.e, ISNI 0000000419368956, Stanford School of Medicine, ; Stanford, CA USA
                Author information
                http://orcid.org/0000-0002-7567-8129
                http://orcid.org/0000-0001-6174-7317
                http://orcid.org/0000-0003-4674-2969
                http://orcid.org/0000-0002-0489-2806
                http://orcid.org/0000-0003-0902-5282
                http://orcid.org/0000-0001-5353-4653
                Article
                1336
                10.1038/s41591-021-01336-3
                8205851
                33972795
                301d16a8-bf26-4df2-ac85-a3f3b1f6f0a2
                © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021

                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
                : 5 February 2021
                : 2 April 2021
                Funding
                Funded by: Multidisciplinary Association for Psychedelic Studies
                Categories
                Article
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                © The Author(s), under exclusive licence to Springer Nature America, Inc. 2021

                Medicine
                drug development,phase iii trials
                Medicine
                drug development, phase iii trials

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