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MDMA-Assisted Therapy for Treatment-Resistant Posttraumatic Stress Disorder (PTSD) – One step further toward a patient-centered treatment pathway
INTRODUCTION: PTSD is a chronic, debilitating condition with limited treatment efficacy. Accessing traumatic memories often leads to overwhelming distress, impacting treatment process. Current approved pharmacological treatments have exhibited small to moderate effects when compared with placebo. Ev...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567733/ http://dx.doi.org/10.1192/j.eurpsy.2022.1731 |
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author | Pratas Penedos, S. Freire, M.J. Fonseca, I. Franco, A. Ribeiro, N. Moreno, L. Magalhães, M.M. Afonso, P.A. Alves, I.M. Paulino, L. Ramos, C. Figueiredo, M.M. Madruga, L. Gamito, A. |
author_facet | Pratas Penedos, S. Freire, M.J. Fonseca, I. Franco, A. Ribeiro, N. Moreno, L. Magalhães, M.M. Afonso, P.A. Alves, I.M. Paulino, L. Ramos, C. Figueiredo, M.M. Madruga, L. Gamito, A. |
author_sort | Pratas Penedos, S. |
collection | PubMed |
description | INTRODUCTION: PTSD is a chronic, debilitating condition with limited treatment efficacy. Accessing traumatic memories often leads to overwhelming distress, impacting treatment process. Current approved pharmacological treatments have exhibited small to moderate effects when compared with placebo. Evidence suggests 3,4,-methylene-dioxymethamphetamine(MDMA)-assisted psychotherapy as a viable option for refractory PTSD. OBJECTIVES: Comprehensive review of early clinical research, proposed mechanisms, safety and emerging therapeutic models. METHODS: Eligible studies will be identified through strategic search of MEDLINE. RESULTS: Pre-clinical and imaging studies suggest memory reconsolidation and fear extinction as candidate psychological and neurological mechanisms, involving MDMA’s combined effects of increasing serotonergic activity, as well the release of oxytocin and brain-derived neurotrophic factor in key memory and emotional circuits. Resulting reduction in amygdala and insula activation and increasing connectivity between the amygdala and hippocampus may create a “tolerance window” of neuroplasticity for emotional engagement and reprocessing of traumatic memories during psychotherapy. Early clinical trials report impressive and durable reduction in PTSD symptoms, with a safety profile comparable to that of SSRIs. A recently completed randomized, double-blind, placebo-controlled phase 3 trial reported full remission of PTSD symptoms in 67% of patients at 2 months, with no increase in suicidality, cardiovascular events or abuse behavior. Emerging treatment models underline the importance of unmedicated therapeutic sessions for preparation for the experience and subsequent integration as essential for full benefit and safety of the clinical context. CONCLUSIONS: The psychological impact associated with the COVID-19 pandemic is an reminder of the emotional and economic burden associated with PTSD. MDMA-assisted therapy may be a breakthrough approach meriting further multidisciplinary investment and clinical research. DISCLOSURE: No significant relationships. |
format | Online Article Text |
id | pubmed-9567733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-95677332022-10-17 MDMA-Assisted Therapy for Treatment-Resistant Posttraumatic Stress Disorder (PTSD) – One step further toward a patient-centered treatment pathway Pratas Penedos, S. Freire, M.J. Fonseca, I. Franco, A. Ribeiro, N. Moreno, L. Magalhães, M.M. Afonso, P.A. Alves, I.M. Paulino, L. Ramos, C. Figueiredo, M.M. Madruga, L. Gamito, A. Eur Psychiatry Abstract INTRODUCTION: PTSD is a chronic, debilitating condition with limited treatment efficacy. Accessing traumatic memories often leads to overwhelming distress, impacting treatment process. Current approved pharmacological treatments have exhibited small to moderate effects when compared with placebo. Evidence suggests 3,4,-methylene-dioxymethamphetamine(MDMA)-assisted psychotherapy as a viable option for refractory PTSD. OBJECTIVES: Comprehensive review of early clinical research, proposed mechanisms, safety and emerging therapeutic models. METHODS: Eligible studies will be identified through strategic search of MEDLINE. RESULTS: Pre-clinical and imaging studies suggest memory reconsolidation and fear extinction as candidate psychological and neurological mechanisms, involving MDMA’s combined effects of increasing serotonergic activity, as well the release of oxytocin and brain-derived neurotrophic factor in key memory and emotional circuits. Resulting reduction in amygdala and insula activation and increasing connectivity between the amygdala and hippocampus may create a “tolerance window” of neuroplasticity for emotional engagement and reprocessing of traumatic memories during psychotherapy. Early clinical trials report impressive and durable reduction in PTSD symptoms, with a safety profile comparable to that of SSRIs. A recently completed randomized, double-blind, placebo-controlled phase 3 trial reported full remission of PTSD symptoms in 67% of patients at 2 months, with no increase in suicidality, cardiovascular events or abuse behavior. Emerging treatment models underline the importance of unmedicated therapeutic sessions for preparation for the experience and subsequent integration as essential for full benefit and safety of the clinical context. CONCLUSIONS: The psychological impact associated with the COVID-19 pandemic is an reminder of the emotional and economic burden associated with PTSD. MDMA-assisted therapy may be a breakthrough approach meriting further multidisciplinary investment and clinical research. DISCLOSURE: No significant relationships. Cambridge University Press 2022-09-01 /pmc/articles/PMC9567733/ http://dx.doi.org/10.1192/j.eurpsy.2022.1731 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstract Pratas Penedos, S. Freire, M.J. Fonseca, I. Franco, A. Ribeiro, N. Moreno, L. Magalhães, M.M. Afonso, P.A. Alves, I.M. Paulino, L. Ramos, C. Figueiredo, M.M. Madruga, L. Gamito, A. MDMA-Assisted Therapy for Treatment-Resistant Posttraumatic Stress Disorder (PTSD) – One step further toward a patient-centered treatment pathway |
title | MDMA-Assisted Therapy for Treatment-Resistant Posttraumatic Stress Disorder (PTSD) – One step further toward a patient-centered treatment pathway |
title_full | MDMA-Assisted Therapy for Treatment-Resistant Posttraumatic Stress Disorder (PTSD) – One step further toward a patient-centered treatment pathway |
title_fullStr | MDMA-Assisted Therapy for Treatment-Resistant Posttraumatic Stress Disorder (PTSD) – One step further toward a patient-centered treatment pathway |
title_full_unstemmed | MDMA-Assisted Therapy for Treatment-Resistant Posttraumatic Stress Disorder (PTSD) – One step further toward a patient-centered treatment pathway |
title_short | MDMA-Assisted Therapy for Treatment-Resistant Posttraumatic Stress Disorder (PTSD) – One step further toward a patient-centered treatment pathway |
title_sort | mdma-assisted therapy for treatment-resistant posttraumatic stress disorder (ptsd) – one step further toward a patient-centered treatment pathway |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9567733/ http://dx.doi.org/10.1192/j.eurpsy.2022.1731 |
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