重复低剂量LSD在成人多动症治疗中的安全性和有效性:一项随机临床试验
Lorenz Mueller1,2, Joyce Santos de Jesus1,2, Yasmin Schmid1,2
1Division of Clinical Pharmacology and Toxicology, University Hospital Basel, Basel, Switzerland.
JAMA psychiatry
|March 19, 2025
概括
对注意力缺陷/多动性障碍 (ADHD) 的微剂量lysergic acid diethylamide (LSD) 发现是安全的,但不比安慰剂更有效. 这项为期6周的试验显示,在LSD和安慰剂组之间,症状减轻没有显著差异.
科学领域:
- 精神病学是一个精神病学.
- 神经科学是一个神经科学.
- 药理学 药理学是指药理学的学科.
背景情况:
- 微剂量的迷幻药物,如 lysergic acid diethylamide (LSD) 正在用于精神疾病的研究中.
- 注意缺陷/多动障碍 (ADHD) 是一种目前尚不清楚LSD功效的疾病.
- 需要研究LSD在管理ADHD症状中的潜在治疗效果.
研究的目的:
- 评估重复低剂量lysergic acid diethylamide (LSD) 给患有注意力缺陷/多动症障碍 (ADHD) 的成年人的安全性和疗效.
- 为了比较LSD微量剂与安慰剂在6周内减少ADHD症状的影响.
主要方法:
- 进行了为期6周的多中心,双盲,安慰剂控制,并行组2A期随机临床试验.
- 患有中度至重度ADHD症状的参与者 (N=53) 每周两次接受20微克LSD或安慰剂.
- 用成年调查者症状评分表 (AISRS) 评估ADHD症状的变化,并用混合效应模型分析重复测量.
主要成果:
- 在LSD组 (改善7.1分) 和安慰剂组 (改善8.9分) 之间,没有观察到ADHD症状平均改善 (AISRS得分) 的统计学上显著差异.
- 莱瑟基酸二甲基胺 (LSD) 的使用在门诊环境中被发现是身体安全的,并且在心理上被容忍得很好.
- 这项研究包括53名参与者,其中27名被随机分配给LSD,26名被分配给安慰剂,平均年龄为37岁,42%是女性.
结论:
- 在门诊环境中,重复服用低剂量的lysergic acid diethylamide (LSD) 对患有注意力缺陷/多动症障碍 (ADHD) 的成年人是安全的.
- 这项研究没有发现证据表明微剂量LSD在减少ADHD症状方面比安慰剂更有效.
- 可能需要进一步的研究来探索其他剂量或涉及LSD治疗ADHD的治疗方法.
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