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Assessing the risk of symptom worsening in psilocybin-assisted therapy for depression: A systematic review and individual participant data meta-analysis

Otto Simonsson, Per Carlbring, Robin Carhart-Harris, Alan K Davis, David J Nutt, Roland R Griffiths, David Erritzøe, Simon B Goldberg

Psychiatry Research July 23, 2023 DOI: 10.1016/j.psychres.2023.115349 via OpenAlex

Summary

AI-generated from the abstract

In a meta-analysis of three psilocybin trials for depression involving 102 participants, clinically significant symptom worsening occurred for a minority of those receiving psilocybin or escitalopram (about 10%) and for a majority of those in the waitlist condition (63.6%). The psilocybin arm showed a lower likelihood of symptom worsening compared to waitlist and no difference compared to escitalopram. The authors note the limitation of a relatively small sample size.

Study at a glance

Characteristics Meta-analysis Peer reviewed
Sample size 102
Population Participants in psilocybin trials for depression
Interventions psilocybin escitalopram waitlist
Dose two-dose
Topics Depression Psilocybin
Keywords Meta-analysis Psilocybin therapy Clinical depression treatment Psychedelic medicine Mental health research
Citations 24
Key finding Clinically significant symptom worsening occurred for about 10% of participants in the psilocybin and escitalopram conditions and for 63.6% in the waitlist condition, with psilocybin showing a lower likelihood of worsening versus waitlist and no difference versus escitalopram.

Abstract

We conducted a meta-analysis using individual participant data from three, two-dose psilocybin trials for depression (N = 102) with the aim of assessing the risk of symptom worsening. Clinically significant symptom worsening occurred for a minority of participants in the psilocybin and escitalopram conditions (∼10%) and for a majority of participants in the waitlist condition (63.6%). Using data from the two trials with control arms, the psilocybin arm showed a lower likelihood of symptom worsening versus waitlist, and no difference in the likelihood of symptom worsening versus escitalopram. The limitation of a relatively small sample size should be addressed in future studies.

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