Body mass index (BMI) does not predict responses to psilocybin
Meg J Spriggs, Bruna Giribaldi, Taylor Lyons, Fernando E Rosas, Laura S Kärtner, Tobias Buchborn, Hannah M Douglass, Leor Roseman, Christopher Timmermann, David Erritzøe, David J Nutt, Robin L Carhart-Harris
Journal of Psychopharmacology November 14, 2022 DOI: 10.1177/02698811221131994 via OpenAlex
Summary
AI-generated from the abstractA fixed 25 mg dose of psilocybin produces similar acute psychedelic effects and improvements in well-being regardless of body mass index (BMI). Pooling data from three therapeutic studies, results support the null hypothesis that BMI does not predict overall intensity of the altered state, mystical experiences, perceptual changes, or emotional breakthroughs. There was weak evidence that lower BMI participants reported greater 'dread of ego dissolution,' but BMI did not meaningfully add to predictions beyond age, sex, and study. Mystical-type experiences and emotional breakthroughs strongly predicted well-being improvements, but BMI did not. These findings suggest body weight-adjusted dosing may be unnecessary, supporting fixed dosing to reduce practical and financial burdens on psychedelic therapy scalability.
Study at a glance
| Characteristics | Observational cohort Peer reviewed |
|---|---|
| Intervention | Psilocybin |
| Dose | 25 mg |
| Duration | 2-week follow-up |
| Topics | Psychedelic-assisted therapy |
| Keywords | 5-ht2a Bayes factor Body mass index Classic psychedelic |
| Citations | 15 |
| Key finding | BMI does not predict the intensity of acute psychedelic effects or improvements in well-being after a fixed 25 mg dose of psilocybin in a therapeutic context. |
Abstract
Background: Psilocybin is a serotonin type 2A (5-HT 2A ) receptor agonist and naturally occurring psychedelic. 5-HT 2A receptor density is known to be associated with body mass index (BMI), however, the impact of this on psilocybin therapy has not been explored. While body weight-adjusted dosing is widely used, this imposes a practical and financial strain on the scalability of psychedelic therapy. This gap between evidence and practice is caused by the absence of studies clarifying the relationship between BMI, the acute psychedelic experience and long-term psychological outcomes. Method: Data were pooled across three studies using a fixed 25 mg dose of psilocybin delivered in a therapeutic context to assess whether BMI predicts characteristics of the acute experience and changes in well-being 2 weeks later. Supplementing frequentist analysis with Bayes Factors has enabled for conclusions to be drawn regarding the null hypothesis. Results: Results support the null hypothesis that BMI does not predict overall intensity of the altered state, mystical experiences, perceptual changes or emotional breakthroughs during the acute experience. There was weak evidence for greater ‘dread of ego dissolution’ in participants with lower BMI, however, further analysis suggested BMI did not meaningfully add to the combination of the other covariates (age, sex and study). While mystical-type experiences and emotional breakthroughs were strong predictors of improvements in well-being, BMI was not. Conclusions: These findings have important implications for our understanding of pharmacological and extra-pharmacological contributors to psychedelic-assisted therapy and for the standardization of a fixed therapeutic dose in psychedelic-assisted therapy.