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重新审视致幻剂诱发精神病的证据:综述概述、系统评价及人类研究的荟萃分析

Reconsidering evidence for psychedelic-induced psychosis: an overview of reviews, a systematic review, and meta-analysis of human studies.

作者信息

Sabé Michel, Sulstarova Adi, Glangetas Alban, De Pieri Marco, Mallet Luc, Curtis Logos, Richard-Lepouriel Héléne, Penzenstadler Louise, Seragnoli Federico, Thorens Gabriel, Zullino Daniele, Preller Katrin, Böge Kerem, Leucht Stefan, Correll Christoph U, Solmi Marco, Kaiser Stefan, Kirschner Matthias

机构信息

Division of Adult Psychiatry, Department of Psychiatry, University Hospitals of Geneva, 2, Chemin du Petit-Bel-Air, CH-1226, Thonex, Switzerland.

Faculty of Medicine, University of Geneva, Geneva, Switzerland.

出版信息

Mol Psychiatry. 2025 Mar;30(3):1223-1255. doi: 10.1038/s41380-024-02800-5. Epub 2024 Nov 27.

Abstract

BACKGROUND

Persons with schizophrenia are excluded from psychedelic-assisted therapy due to concerns about the risk of triggering or worsening psychosis. However, there is limited meta-analytic data on the risk of psychedelic-induced psychosis in individuals with pre-existing psychotic disorders.

METHODS

We conducted a systematic review, meta-analysis, and overview of reviews to assess the incidence of psychedelic-induced psychosis and symptom exacerbation in schizophrenia. Our pre-registered protocol (CRD42023399591) covered: LSD, psilocybin, mescaline, DMT, and MDMA, using data from Embase, PubMed, PsyARTICLES, PsyINFO, and trial registries up to November 2023. A random-effects model was used to calculate psychosis incidence, with standardized assessments of study quality.

RESULTS

From 131 publications, we analyzed 14 systematic reviews, 20 reviews, 35 randomized-controlled trials (RCTs), 10 case-control studies, 30 uncontrolled trials (UCTs), and 22 cohort studies, most of which were low quality. Meta-analysis of nine studies showed an incidence of psychedelic-induced psychosis at 0.002% in population studies, 0.2% in UCTs, and 0.6% in RCTs. In UCTs including individuals with schizophrenia, 3.8% developed long-lasting psychotic symptoms. Of those with psychedelic-induced psychosis, 13.1% later developed schizophrenia. Sensitivity analyses confirmed the results.

CONCLUSION

In summary, the reviewed evidence suggests that schizophrenia might not be a definite exclusion criterion for clinical trials exploring safety and efficacy of psychedelics for treatment-resistant depression and negative symptoms. However, given the low quality and limited number of studies, more high-quality research is needed, and a conservative approach is recommended until further data is available.

摘要

背景

由于担心引发或加重精神病风险,精神分裂症患者被排除在迷幻剂辅助治疗之外。然而,关于已有精神障碍个体发生迷幻剂所致精神病风险的荟萃分析数据有限。

方法

我们进行了一项系统评价、荟萃分析及综述概述,以评估精神分裂症患者中迷幻剂所致精神病及症状加重的发生率。我们预先注册的方案(CRD42023399591)涵盖:麦角酸二乙胺(LSD)、裸盖菇素、三甲氧苯乙胺、二甲基色胺(DMT)和3,4-亚甲基二氧甲基苯丙胺(MDMA),使用截至2023年11月来自Embase、PubMed、PsyARTICLES、PsyINFO及试验注册库的数据。采用随机效应模型计算精神病发生率,并对研究质量进行标准化评估。

结果

从131篇出版物中,我们分析了14项系统评价、20项综述、35项随机对照试验(RCT)、10项病例对照研究、30项非对照试验(UCT)和22项队列研究,其中大多数质量较低。对9项研究的荟萃分析表明,在人群研究中迷幻剂所致精神病的发生率为0.002%,在非对照试验中为0.2%,在随机对照试验中为0.6%。在纳入精神分裂症患者的非对照试验中,3.8%出现了持久的精神病症状。在那些发生迷幻剂所致精神病的患者中,13.1%后来发展为精神分裂症。敏感性分析证实了结果。

结论

总之,所审查的证据表明,对于探索迷幻剂治疗难治性抑郁症和阴性症状的安全性和有效性的临床试验,精神分裂症可能不是明确的排除标准。然而,鉴于研究质量低且数量有限,需要更多高质量的研究,在有更多数据之前,建议采取保守方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/709f/11835720/9f6b949d8889/41380_2024_2800_Fig1_HTML.jpg

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