Clinical Brain Networks Group, QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.
Wesley Medical Research Institute, Wesley Hospital, Auchenflower, QLD, Australia.
NEJM Evid. 2023 Sep;2(9):EVIDoa2300012. doi: 10.1056/EVIDoa2300012. Epub 2023 Jun 7.
Tourette syndrome is characterized by chronic motor and vocal tics. There is preliminary evidence of benefit from cannabis products containing Δ9-tetrahydrocannabinol (THC) and that coadministration of cannabidiol (CBD) improves the side-effect profile and safety. METHODS: In this double-blind, crossover trial, participants with severe Tourette syndrome were randomly assigned to a 6-week treatment period with escalating doses of an oral oil containing 5 mg/ml of THC and 5 mg/ml of CBD, followed by a 6-week course of placebo, or vice versa, separated by a 4-week washout period. The primary outcome was the total tic score on the Yale Global Tic Severity Scale (YGTSS; range, 0 to 50 [higher scores indicate greater severity of symptoms]). Secondary outcomes included video-based assessment of tics, global impairment, anxiety, depression, and obsessive-compulsive symptoms. Outcomes were correlated with plasma levels of cannabinoid metabolites. A computerized cognitive battery was administered at the beginning and the end of each treatment period. RESULTS: Overall, 22 participants (eight female participants) were enrolled. Reduction in total tic score (at week 6 relative to baseline) as measured by the YGTSS was 8.9 (±7.6) in the active group and 2.5 (±8.5) in the placebo group. In a linear mixed-effects model, there was a significant interaction of treatment (active/placebo) and visit number on tic score (coefficient = −2.28; 95% confidence interval, −3.96 to −0.60; P=0.008), indicating a greater decrease (improvement) in tics under active treatment. There was a correlation between plasma 11-carboxy-tetrahydrocannabinol levels and the primary outcome, which was attenuated after exclusion of an outlier. The most common adverse effect in the placebo period was headache (n=7); in the active treatment period, it was cognitive difficulties, including slowed mentation, memory lapses, and poor concentration (n=8). CONCLUSIONS: In severe Tourette syndrome, treatment with THC and CBD reduced tics and may reduce impairment due to tics, anxiety, and obsessive-compulsive disorder; although in some participants this was associated with slowed mentation, memory lapses, and poor concentration. (Funded by the Wesley Medical Research Institute, Brisbane, and the Lambert Initiative for Cannabinoid Therapeutics, a philanthropically-funded research organization at the University of Sydney, Australia; Australian and New Zealand Clinical Trials Registry number, ACTRN12618000545268.)
妥瑞氏综合征的特征为慢性运动性和发声性抽搐。有初步证据表明,含有 Δ9-四氢大麻酚(THC)的大麻产品有疗效,而同时使用大麻二酚(CBD)可以改善副作用特征和安全性。方法:在这项双盲、交叉试验中,严重妥瑞氏综合征患者被随机分配到为期 6 周的治疗期,接受含有 5mg/ml THC 和 5mg/ml CBD 的口服油治疗,随后是 6 周的安慰剂治疗,或反之,其间有 4 周的洗脱期。主要结局是耶鲁总体抽动严重程度量表(YGTSS;范围,0 至 50[得分越高表示症状越严重])的总抽动评分。次要结局包括视频评估抽动、总体损伤、焦虑、抑郁和强迫症状。结果与大麻素代谢物的血浆水平相关。在每个治疗期的开始和结束时,进行了计算机化认知测试。结果:共有 22 名参与者(8 名女性参与者)入组。YGTSS 测量的抽动总评分(与基线相比,第 6 周)在治疗组中降低了 8.9(±7.6),在安慰剂组中降低了 2.5(±8.5)。在线性混合效应模型中,治疗(活性/安慰剂)和就诊次数对抽动评分的交互作用有显著差异(系数为-2.28;95%置信区间,-3.96 至-0.60;P=0.008),表明在活性治疗下抽动减少(改善)幅度更大。血浆 11-羧基-四氢大麻酚水平与主要结局之间存在相关性,但在排除一个异常值后,这种相关性减弱。安慰剂期最常见的不良反应是头痛(n=7);在活性治疗期,认知困难,包括思维迟钝、记忆力减退和注意力不集中(n=8)是最常见的不良反应。结论:在严重妥瑞氏综合征中,THC 和 CBD 的治疗可减少抽动,并可能减少因抽动、焦虑和强迫症引起的损伤;尽管在某些参与者中,这与思维迟钝、记忆力减退和注意力不集中有关。(由澳大利亚布里斯班韦斯利医学研究所和澳大利亚悉尼大学的慈善资助研究组织 Lambert 大麻素治疗倡议资助;澳大利亚和新西兰临床试验注册编号,ACTRN12618000545268。)