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Publication bias in randomized trials of psilocybin for depression: a Robust Bayesian Meta-Analysis

Çağrı Özkurt

preprint DOI: 10.31234/osf.io/6gy8v_v1 (opens in new tab)

Summary

AI-generated from the abstract

A re-analysis of 12 randomized controlled trials on psilocybin for depression found moderate evidence of publication bias, with a bias-corrected effect size about 41% smaller than originally reported. The original analysis reported a large effect (g = 0.90), but after accounting for selective reporting using Robust Bayesian Meta-Analysis, the effect dropped to about 0.53, with a credible interval that includes zero. This evidence of bias disappeared when open-label studies were excluded, suggesting expectancy-driven effects rather than suppressed negative results. The findings do not overturn the original conclusions but indicate greater uncertainty than previously thought.

Study at a glance

Characteristics Re-analysis of a living systematic review Randomized Open-label
Intervention Psilocybin
Key finding After accounting for publication bias, the effect of psilocybin on depression symptoms is about 41% smaller than originally reported, with a credible interval spanning zero.

Abstract

A recent living systematic review in Nature Mental Health found psilocybin reduced depression symptoms across 12 randomized controlled trials, with pooled effect g = 0.90. The original analysis assessed publication bias using Egger’s test, non-significant — but this test has limited power with few studies and cannot produce a bias-corrected estimate. We re-analysed the same open dataset using Robust Bayesian Meta-Analysis (RoBMA), which simultaneously estimates evidence for a treatment effect, heterogeneity, and publication bias. We find moderate evidence for publication bias (Bayes Factor = 3.89). After accounting for selective reporting, the bias-corrected effect (g ≈ 0.53) is ~41% smaller than published, with a credible interval spanning to zero. This evidence dissipates when open-label studies are excluded, suggesting expectancy-driven artefacts rather than file-drawer suppression. These findings do not overturn the original conclusions but indicate greater uncertainty than the frequentist analysis implies.

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