Incremental efficacy systematic review and meta-analysis of psilocybin-for-depression RCTs.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Nicholas C Borgogna, Tyler Owen, Dan Petrovitch, Jacob Vaughn, David A L Johnson, Louis A Pagano, Stephen L Aita, Benjamin D Hill
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引用次数: 0

Abstract

Rationale: Psilocybin is a potentially paradigm-shifting depression intervention. We conducted a systematic review and meta-analysis of psilocybin-for-depression randomized controlled trials (RCTs).

Objectives: Systematically assess harm reporting, risk of bias, action mechanism specification, and incremental therapeutic effect sizes in the psilocybin-for-depression RCT literature.

Methods: Assessed databases included PsycINFO, CINAHL, Embase, Medline, Web of Science, and Scopus. Search terms "Psilocybin" or "Psychedelic" were paired with "Depression", and "Randomized Controlled Trial" or "RCT".

Results: We identified k = 9 RCTs (k = 10 subgroups) involving n = 602 participants (56% psilocybin). Five studies had low/very low harm quality reporting, opposed to two with high. Most studies demonstrated a high risk of bias. Therapeutic mechanisms of action (MoAs) were discussed in varying detail but rarely assessed in original publications. Psilocybin was moderately superior to controls at reducing depression (g = 0.62; 95% CI = 0.27, 0.98). Effects were heterogenous (τ = .47). Smaller studies evidenced stronger effects that favored psilocybin (Egger's b0 = 3.63, p = .014). Almost all studies documented financial conflicts of interests.

Conclusion: Psilocybin demonstrates significant depression reduction relative to controls. However, researchers, clinicians, and stakeholders should consider several contextual factors. Effects were moderate and attenuated in larger and better-controlled studies. Harms reporting and risk of bias was high, though partly driven by unique challenges of psilocybin research. MoAs were variably specified but rarely assessed; suggesting it is unclear how depression is reduced. We advise researchers conduct RCTs with active control conditions, larger samples, and include MoA assessments. Independent RCTs from researchers without financial conflicts of interest are needed.

裸盖菇素治疗抑郁症随机对照试验的增量疗效系统评价和荟萃分析。
理由:裸盖菇素是一种潜在的范式转换抑郁症干预措施。我们对裸盖菇素治疗抑郁症的随机对照试验(rct)进行了系统回顾和荟萃分析。目的:系统评估裸盖菇素治疗抑郁症的RCT文献中的危害报告、偏倚风险、作用机制规范和增量治疗效果大小。方法:评估的数据库包括PsycINFO、CINAHL、Embase、Medline、Web of Science和Scopus。搜索词“裸盖菇素”或“迷幻药”与“抑郁症”、“随机对照试验”或“随机对照试验”配对。结果:我们确定了k = 9个随机对照试验(k = 10个亚组),涉及n = 602名参与者(56%裸盖菇素)。5项研究的危害质量报告为低/极低,2项为高。大多数研究表明存在较高的偏倚风险。治疗机制的作用(MoAs)讨论了不同的细节,但很少评估在原始出版物。裸盖菇素在减轻抑郁方面略优于对照组(g = 0.62;95% ci = 0.27, 0.98)。效果是异质性的(τ = 0.47)。较小规模的研究表明,裸盖菇素的效果更强(Egger’s b0 = 3.63, p = 0.014)。几乎所有的研究都记录了经济利益冲突。结论:裸盖菇素相对于对照组有明显的抑郁减轻作用。然而,研究人员、临床医生和利益相关者应该考虑几个背景因素。在规模更大、对照更好的研究中,效果是中等和减弱的。危害报告和偏倚风险很高,尽管部分原因是裸盖菇素研究的独特挑战。moa的具体规定各不相同,但很少进行评估;这表明目前还不清楚抑郁症是如何减少的。我们建议研究人员进行具有主动对照条件、较大样本量的随机对照试验,并包括MoA评估。需要来自没有经济利益冲突的研究人员的独立随机对照试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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