The role of the psychedelic experience in psilocybin treatment for treatment-resistant depression
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
39706482
DOI
10.1016/j.jad.2024.12.061
PII: S0165-0327(24)02049-4
Knihovny.cz E-resources
- Keywords
- Dose-response, Psilocybin, Psychedelic, Psychedelic experience, Randomized-control trial, Treatment-resistant depression,
- MeSH
- Depressive Disorder, Treatment-Resistant * drug therapy psychology MeSH
- Depressive Disorder, Major * drug therapy psychology MeSH
- Adult MeSH
- Hallucinogens * therapeutic use administration & dosage adverse effects MeSH
- Middle Aged MeSH
- Humans MeSH
- Surveys and Questionnaires MeSH
- Psilocybin * therapeutic use administration & dosage adverse effects MeSH
- Psychiatric Status Rating Scales MeSH
- Treatment Outcome MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Hallucinogens * MeSH
- Psilocybin * MeSH
OBJECTIVE: To determine the relationships between psilocybin dose, psychedelic experiences, and therapeutic outcome in treatment-resistant depression. METHODS: For treatment-resistant depression, 233 participants received a single dose of 25, 10, or 1 mg of COMP360 psilocybin (a proprietary, pharmaceutical-grade synthesized psilocybin formulation, developed by the sponsor, Compass Pathfinder Ltd.) with psychological support. The resulting psychedelic experience (Five-Dimensional Altered States of Consciousness questionnaire [5D-ASC] and Emotional Breakthrough Inventory [EBI]) were measured. These proximal variables and outcome 3 weeks post-administration (change in Montgomery-Åsberg Depression Rating Scale [MADRS]) were explored using correlation analysis. RESULTS: The mean intensity of psychedelic effects was dose-related, but distributions of scores for different doses overlapped considerably. Depression response correlated with select aspects of the psychedelic experience overall and for individual doses. At the 25 mg dose, 5D-ASC dimensions Oceanic Boundlessness (Pearson correlation coefficient r = -0.508) and Visual Restructuralization (r = -0.516), and EBI (r = -0·637) were the variables with the strongest correlation to the Week 3 change from Baseline in MADRS score. LIMITATIONS: The existence of correlation does not establish causation and exploratory findings require further replication, preferably in larger independent samples. CONCLUSIONS: The intensity of psychedelic experience overlaps widely across doses and mitigates the risk of unblinding to dose. Correlations between psychedelic experience and outcome suggest specificity in psilocybin's mechanism of action. Quality and intensity of psychedelic experience may be a measure of pharmacodynamic effect and reveal an effective dose response phenomenon for single oral doses.
Compass Pathfinder Ltd London UK
Compass Pathways Inc New York United States
Department of Psychiatry University of California San Diego San Diego CA United States
Kadima Neuropsychiatry Institute San Diego CA United States
Parc Sanitari Sant Joan de Déu Barcelona Spain; Sant Joan de Déu Research Foundation Barcelona Spain
Stanford University Department of Psychiatry and Behavioral Sciences Stanford CA United States
The National Institute of Mental Health Klecany Czech Republic
University Medical Centre Groningen Department of Psychiatry Groningen the Netherlands
References provided by Crossref.org