School of Psychological Sciences, Macquarie University, Sydney, NSW, Australia.
Department of Psychiatry, School of Clinical Sciences, Monash University, Clayton, VIC, Australia.
J Psychopharmacol. 2024 Aug;38(8):701-711. doi: 10.1177/02698811241254831. Epub 2024 Jun 14.
Some recent research and commentary have suggested that most or all the effects reported by people who microdose psychedelics may be explained by expectations or placebo effects. In this rapid review, we aimed to evaluate the strength of evidence for a placebo explanation of the reported effects of microdosing. We conducted a PubMed search for all studies investigating psychedelic microdosing with controlled doses and a placebo comparator. We identified 19 placebo-controlled microdosing studies and summarised all positive and null findings across this literature. Risk of bias was assessed using the Cochrane risk-of-bias tool for randomised trials. The reviewed papers indicated that microdosing with LSD and psilocybin leads to changes in neurobiology, physiology, subjective experience, affect, and cognition relative to placebo. We evaluate methodological gaps and challenges in microdosing research and suggest eight reasons why current claims that microdosing is predominately a placebo are premature and possibly wrong: (1) there have been only a small number of controlled studies; (2) studies have had small sample sizes; (3) there is evidence of dose-dependent effects; (4) studies have only investigated the effects of a small number of doses; (5) the doses investigated may have been too small; (6) studies have looked only at non-clinical populations; (7) studies so far have been susceptible to selection bias; and (8) the measured impact of expectancy is small. Considering the available evidence, we conclude that it is not yet possible to determine whether microdosing is a placebo.
一些最近的研究和评论表明,大多数或所有报告的迷幻剂微剂量使用者的效果可能可以用预期或安慰剂效应来解释。在这个快速综述中,我们旨在评估报告的迷幻剂微剂量效应的安慰剂解释的证据强度。我们在 PubMed 上搜索了所有使用受控剂量和安慰剂对照剂研究迷幻剂微剂量的研究。我们确定了 19 项安慰剂对照微剂量研究,并总结了该文献中的所有阳性和阴性结果。使用 Cochrane 随机试验偏倚风险工具评估了偏倚风险。已审查的论文表明,与安慰剂相比,LSD 和裸盖菇素的微剂量会导致神经生物学、生理学、主观体验、情绪和认知发生变化。我们评估了微剂量研究中的方法学差距和挑战,并提出了当前声称微剂量主要是安慰剂的说法过早且可能错误的八个原因:(1)仅有少数对照研究;(2)研究样本量小;(3)有剂量依赖性效应的证据;(4)研究仅调查了少数剂量的效果;(5)研究的剂量可能太小;(6)研究仅观察了非临床人群;(7)迄今为止,研究易受选择偏倚影响;(8)预期的测量影响较小。考虑到现有证据,我们得出的结论是,目前还无法确定微剂量是否是安慰剂。