重复低剂量LSD治疗成人ADHD的安全性和有效性

IF 22.5 1区 医学 Q1 PSYCHIATRY
Lorenz Mueller, Joyce Santos de Jesus, Yasmin Schmid, Felix Müller, Anna Becker, Aaron Klaiber, Isabelle Straumann, Dino Luethi, Eline C. H. M. Haijen, Petra P. M. Hurks, Kim P. C. Kuypers, Matthias E. Liechti
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Data were analyzed from March 22, 2024, to August 19, 2024. Outpatient treatment was provided at 2 centers: University Hospital in Basel, Switzerland, and Maastricht University in the Netherlands. Adults aged 18 to 65 years with a prior ADHD diagnosis who presented with moderate to severe symptoms (Adult Investigator Symptom Rating Scale [AISRS] score ≥26 and Clinical Global Impression Severity score ≥4) were eligible for inclusion. Key exclusion criteria included selected current major psychiatric or somatic disorders and the use of potentially interacting medications.InterventionParticipants received either LSD (20 μg) or placebo twice weekly for 6 weeks (total of 12 doses).Main Outcome and MeasuresThe primary outcome was the change in ADHD symptoms from baseline to week 6, assessed by the AISRS and analyzed with a mixed-effects model for repeated measures.ResultsA total of 53 participants were randomized to LSD (n = 27) or placebo (n = 26). 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引用次数: 0

摘要

微剂量致幻剂,包括麦角酸二乙胺(LSD),因其对包括注意力缺陷/多动障碍(ADHD)在内的几种精神疾病的潜在益处而受到关注。然而,LSD在减少ADHD症状方面的功效尚不清楚。目的与安慰剂比较,确定重复低剂量LSD减轻ADHD症状的安全性和有效性。设计、环境和参与者:这是一项为期6周、多中心、双盲、安慰剂对照、平行组的2A期随机临床试验,于2021年12月17日至2023年12月4日进行。数据分析时间为2024年3月22日至2024年8月19日。门诊治疗由两个中心提供:瑞士巴塞尔大学医院和荷兰马斯特里赫特大学。年龄在18岁至65岁之间,既往诊断为ADHD且出现中度至重度症状(成人调查员症状评定量表[AISRS]评分≥26分,临床总体印象严重性评分≥4分)的成年人符合纳入条件。主要排除标准包括选定的当前主要精神或躯体疾病以及使用可能相互作用的药物。参与者接受LSD (20 μg)或安慰剂治疗,每周两次,持续6周(共12剂)。主要结局和测量主要结局是ADHD症状从基线到第6周的变化,由AISRS评估并使用重复测量的混合效应模型进行分析。结果53名受试者随机分为LSD组(n = 27)和安慰剂组(n = 26)。参与者平均(SD)年龄为37(12)岁,22名参与者(42%)为女性。LSD组AISRS平均改善为- 7.1点(95% CI, - 10.1至- 4.0)。安慰剂组AISRS平均改善- 8.9点(95% CI, - 12.0至- 5.8),组间无差异。总体而言,LSD在生理上是安全的,在心理上是可耐受的。结论和相关性:在这项随机临床试验中,在门诊环境中反复给药低剂量LSD是安全的,但在减轻ADHD症状方面并不比安慰剂更有效。临床试验注册号:NCT05200936
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and Efficacy of Repeated Low-Dose LSD for ADHD Treatment in Adults
ImportanceMicrodosing psychedelics, including lysergic acid diethylamide (LSD), has gained attention for its potential benefits in several psychiatric disorders, including attention-deficit/hyperactivity disorder (ADHD). However, LSD’s efficacy in reducing ADHD symptoms remains unknown.ObjectiveTo determine the safety and efficacy of repeated low doses of LSD in reducing ADHD symptoms compared with placebo.Design, Setting, and ParticipantsThis was a 6-week, multicenter, double-blind, placebo-controlled, parallel-group phase 2A randomized clinical trial conducted between December 17, 2021, and December 4, 2023. Data were analyzed from March 22, 2024, to August 19, 2024. Outpatient treatment was provided at 2 centers: University Hospital in Basel, Switzerland, and Maastricht University in the Netherlands. Adults aged 18 to 65 years with a prior ADHD diagnosis who presented with moderate to severe symptoms (Adult Investigator Symptom Rating Scale [AISRS] score ≥26 and Clinical Global Impression Severity score ≥4) were eligible for inclusion. Key exclusion criteria included selected current major psychiatric or somatic disorders and the use of potentially interacting medications.InterventionParticipants received either LSD (20 μg) or placebo twice weekly for 6 weeks (total of 12 doses).Main Outcome and MeasuresThe primary outcome was the change in ADHD symptoms from baseline to week 6, assessed by the AISRS and analyzed with a mixed-effects model for repeated measures.ResultsA total of 53 participants were randomized to LSD (n = 27) or placebo (n = 26). Mean (SD) participant age was 37 (12) years, and 22 participants (42%) were female. The LSD group presented a mean AISRS improvement of −7.1 points (95% CI, −10.1 to −4.0). The placebo group presented a mean AISRS improvement of −8.9 points (95% CI, −12.0 to −5.8), with no difference between groups. LSD was physically safe and psychologically well tolerated overall.Conclusions and RelevanceIn this randomized clinical trial, repeated low-dose LSD administration was safe in an outpatient setting, but it was not more efficacious than placebo in reducing ADHD symptoms.Trial RegistrationClinicalTrials.gov Identifier: NCT05200936
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来源期刊
JAMA Psychiatry
JAMA Psychiatry PSYCHIATRY-
CiteScore
30.60
自引率
1.90%
发文量
233
期刊介绍: JAMA Psychiatry is a global, peer-reviewed journal catering to clinicians, scholars, and research scientists in psychiatry, mental health, behavioral science, and related fields. The Archives of Neurology & Psychiatry originated in 1919, splitting into two journals in 1959: Archives of Neurology and Archives of General Psychiatry. In 2013, these evolved into JAMA Neurology and JAMA Psychiatry, respectively. JAMA Psychiatry is affiliated with the JAMA Network, a group of peer-reviewed medical and specialty publications.
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