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Effects of Psilocybin-Assisted Therapy on Major Depressive Disorder: A Randomized Clinical Trial

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TLDR
This randomized clinical trial examines the efficacy of psilocybin as an adjunct to psychotherapy and other treatments for major depressive disorder.
Abstract
Importance Major depressive disorder (MDD) is a substantial public health burden, but current treatments have limited effectiveness and adherence. Recent evidence suggests that 1 or 2 administrations of psilocybin with psychological support produces antidepressant effects in patients with cancer and in those with treatment-resistant depression. Objective To investigate the effect of psilocybin therapy in patients with MDD. Design, Setting, and Participants This randomized, waiting list–controlled clinical trial was conducted at the Center for Psychedelic and Consciousness Research at Johns Hopkins Bayview Medical Center in Baltimore, Maryland. Adults aged 21 to 75 years with an MDD diagnosis, not currently using antidepressant medications, and without histories of psychotic disorder, serious suicide attempt, or hospitalization were eligible to participate. Enrollment occurred between August 2017 and April 2019, and the 4-week primary outcome assessments were completed in July 2019. A total of 27 participants were randomized to an immediate treatment condition group (n = 15) or delayed treatment condition group (waiting list control condition; n = 12). Data analysis was conducted from July 1, 2019, to July 31, 2020, and included participants who completed the intervention (evaluable population). Interventions Two psilocybin sessions (session 1: 20 mg/70 kg; session 2: 30 mg/70 kg) were given (administered in opaque gelatin capsules with approximately 100 mL of water) in the context of supportive psychotherapy (approximately 11 hours). Participants were randomized to begin treatment immediately or after an 8-week delay. Main Outcomes and Measures The primary outcome, depression severity was assessed with the GRID-Hamilton Depression Rating Scale (GRID-HAMD) scores at baseline (score of ≥17 required for enrollment) and weeks 5 and 8 after enrollment for the delayed treatment group, which corresponded to weeks 1 and 4 after the intervention for the immediate treatment group. Secondary outcomes included the Quick Inventory of Depressive Symptomatology-Self Rated (QIDS-SR). Results Of the randomized participants, 24 of 27 (89%) completed the intervention and the week 1 and week 4 postsession assessments. This population had a mean (SD) age of 39.8 (12.2) years, was composed of 16 women (67%), and had a mean (SD) baseline GRID-HAMD score of 22.8 (3.9). The mean (SD) GRID-HAMD scores at weeks 1 and 4 (8.0 [7.1] and 8.5 [5.7]) in the immediate treatment group were statistically significantly lower than the scores at the comparable time points of weeks 5 and 8 (23.8 [5.4] and 23.5 [6.0]) in the delayed treatment group. The effect sizes were large at week 5 (Cohend = 2.5; 95% CI, 1.4-3.5;P  Conclusions and Relevance Findings suggest that psilocybin with therapy is efficacious in treating MDD, thus extending the results of previous studies of this intervention in patients with cancer and depression and of a nonrandomized study in patients with treatment-resistant depression. Trial Registration ClinicalTrials.gov Identifier:NCT03181529

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Trial of Psilocybin versus Escitalopram for Depression.

TL;DR: In a phase 2, double-blin... as mentioned in this paper, double-blind comparison between psilocybin and established treatments for depression is conducted using a double-labeling system.
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The Subjective Effects of Psychedelics Are Necessary for Their Enduring Therapeutic Effects.

TL;DR: It is proposed that the subjective effects of psychedelics are necessary for their enduring beneficial effects and that these subjective effects account for the majority of their benefit.
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Psilocybin induces rapid and persistent growth of dendritic spines in frontal cortex in vivo.

TL;DR: In this article, the authors used chronic two-photon microscopy to image longitudinally the apical dendritic spines of layer 5 pyramidal neurons in the mouse medial frontal cortex and found that a single dose of psilocybin led to ∼10% increases in spine size and density.
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Psilocybin induces rapid and persistent growth of dendritic spines in frontal cortex in vivo

TL;DR: In this paper, the authors used chronic two-photon microscopy to image longitudinally the apical dendritic spines of layer 5 pyramidal neurons in the mouse medial frontal cortex and found that a single dose of psilocybin led to ∼10% increases in spine size and density.
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Harnessing psilocybin: antidepressant-like behavioral and synaptic actions of psilocybin are independent of 5-HT2R activation in mice.

TL;DR: For example, the authors showed that a single injection of psilocybin reversed anhedonic responses assessed with the sucrose preference and female urine preference tests in chronically stressed male mice, and suggested that altered perception may not be required for its antidepressant effects.
References
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TL;DR: The amended (revised) Beck Depression Inventory (BDI-IA) and theBeck Depression Inventory-II (BDi-II) were self-administered to 140 psychiatric outpatients with various psychiatric disorders.
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The PHQ-9: A new depression diagnostic and severity measure

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