Li Li-Juan, Mo Yu, Shi Zhan-Ming, Huang Xing-Bing, Ning Yu-Ping, Wu Hua-Wang, Yang Xin-Hu, Zheng Wei
Department of Neurology, The First Affiliated Hospital of Hainan Medical University, Haikou, China.
Department of Psychology, The Brain Hospital of Guangxi Zhuang Autonomous Region, Liuzhou, China.
Front Psychiatry. 2024 Sep 23;15:1416420. doi: 10.3389/fpsyt.2024.1416420. eCollection 2024.
The purpose of this systematic review of randomized controlled trials (RCTs) was to evaluate the effectiveness, safety, and tolerability of psilocybin in adult patients with major depressive disorder (MDD).
A systematic search (up to September 14, 2023) was conducted for RCTs that examined the efficacy, safety, and tolerability of psilocybin in physically healthy adult patients with MDD. Three independent researchers extracted data from publications where the primary outcome was a change in depressive symptoms, and key secondary outcomes were changes in anxiety symptoms and suicidal ideation, discontinuation rates for any reason, and adverse drug reactions (ADRs).
Five RCTs with 472 adult patients with MDD on psilocybin (n = 274) and controls (n = 198) were included. Two of the five RCTs (40%) reported mixed results, while the other three (60%) found that psilocybin had a beneficial effect on MDD treatment. Four RCTs (80%) assessing the anxiolytic effects of psilocybin for treating MDD found that psilocybin was significantly more effective than the control group in improving anxiety symptoms. Psilocybin was more effective than the control group in improving suicidal ideation in one out of five RCTs. Discontinuation rates were similar for any reason between the psilocybin group (2-13%) and the control group (4-21%) (P > 0.05). Four RCTs (80%) reported ADRs in detail. The most common ADR in both groups was headache.
Psilocybin was effective in improving depressive symptoms in over half of the included studies and reduced anxiety symptoms in patients with MDD. The long-term efficacy and safety of psilocybin for MDD treatment needs to be further investigated in large RCTs.
本随机对照试验(RCT)的系统评价旨在评估裸盖菇素对成年重度抑郁症(MDD)患者的有效性、安全性和耐受性。
对截至2023年9月14日的RCT进行系统检索,这些试验研究了裸盖菇素对身体健康的成年MDD患者的疗效、安全性和耐受性。三名独立研究人员从主要结局为抑郁症状变化、关键次要结局为焦虑症状和自杀意念变化、任何原因导致的停药率以及药物不良反应(ADR)的出版物中提取数据。
纳入了五项RCT,共472名成年MDD患者,其中接受裸盖菇素治疗的有274名,接受对照治疗的有198名。五项RCT中有两项(40%)报告了混合结果,而其他三项(60%)发现裸盖菇素对MDD治疗有有益效果。四项(80%)评估裸盖菇素治疗MDD的抗焦虑作用的RCT发现,裸盖菇素在改善焦虑症状方面明显比对照组更有效。五项RCT中有一项发现,裸盖菇素在改善自杀意念方面比对照组更有效。裸盖菇素组(2 - 13%)和对照组(4 - 21%)因任何原因导致的停药率相似(P > 0.05)。四项(80%)RCT详细报告了ADR。两组中最常见的ADR是头痛。
在超过一半的纳入研究中,裸盖菇素在改善抑郁症状方面有效,并减轻了MDD患者的焦虑症状。裸盖菇素治疗MDD的长期疗效和安全性需要在大型RCT中进一步研究。