Department of Neurology, University of Colorado Anschutz Medical Campus School of Medicine, Aurora, Colorado, USA.
Department of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Anschutz Medical Campus, Aurora, Colorado, USA.
Mov Disord. 2024 May;39(5):863-875. doi: 10.1002/mds.29768. Epub 2024 Mar 15.
Cannabis use is frequent in Parkinson's disease (PD), despite inadequate evidence of benefits and risks.
The aim is to study short-term efficacy and tolerability of relatively high cannabidiol (CBD)/low Δ-9-tetrahydrocannabinol (THC) to provide preliminary data for a longer trial.
Persons with PD with ≥20 on motor Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) who had negative cannabis testing took cannabis extract (National Institute of Drug Abuse) oral sesame oil solution for 2 weeks, increasing to final dose of 2.5 mg/kg/day. Primary outcome was change in motor MDS-UPDRS from baseline to final dose.
Participants were randomized to CBD/THC (n = 31) or placebo (n = 30). Mean final dose (CBD/THC group) was 191.8 ± 48.9 mg CBD and 6.4 ± 1.6 mg THC daily. Motor MDS-UPDRS was reduced by 4.57 (95% CI, -8.11 to -1.03; P = 0.013) in CBD/THC group, and 2.77 (-4.92 to -0.61; P = 0.014) in placebo; the difference between groups was non-significant: -1.80 (-5.88 to 2.27; P = 0.379). Several assessments had a strong placebo response. Sleep, cognition, and activities of daily living showed a treatment effect, favoring placebo. Overall adverse events were mild and reported more in CBD/THC than placebo group. On 2.5 mg/kg/day CBD plasma level was 54.0 ± 33.8 ng/mL; THC 1.06 ± 0.91 ng/mL.
The brief duration and strong placebo response limits interpretation of effects, but there was no benefit, perhaps worsened cognition and sleep, and there was many mild adverse events. Longer duration high quality trials that monitor cannabinoid concentrations are essential and would require improved availability of research cannabinoid products in the United States. © 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
尽管大麻使用在帕金森病(PD)中的益处和风险证据不足,但仍较为常见。
本研究旨在研究相对高剂量的大麻二酚(CBD)/低 Δ-9-四氢大麻酚(THC)的短期疗效和耐受性,为更长时间的试验提供初步数据。
MDS-UPDRS 运动评分≥20 的 PD 患者,且大麻检测结果为阴性,服用大麻提取物(国家药物滥用研究所)口服芝麻油溶液,为期 2 周,逐渐增加至最终剂量 2.5mg/kg/天。主要结局为从基线到最终剂量时运动 MDS-UPDRS 的变化。
参与者被随机分配至 CBD/THC 组(n=31)或安慰剂组(n=30)。CBD/THC 组的平均最终剂量为 191.8±48.9mg CBD 和 6.4±1.6mg THC/天。CBD/THC 组运动 MDS-UPDRS 评分降低 4.57(95%CI,-8.11 至 -1.03;P=0.013),安慰剂组降低 2.77(-4.92 至 -0.61;P=0.014);两组间差异无统计学意义:-1.80(-5.88 至 2.27;P=0.379)。多项评估显示出强烈的安慰剂反应。睡眠、认知和日常生活活动方面,治疗效果有利于安慰剂。总体不良事件轻微,且 CBD/THC 组报告的不良事件多于安慰剂组。2.5mg/kg/天的 CBD 血浆水平为 54.0±33.8ng/mL;THC 为 1.06±0.91ng/mL。
短暂的试验持续时间和强烈的安慰剂反应限制了对效果的解释,但没有益处,可能会恶化认知和睡眠,且有许多轻微的不良事件。需要进行持续时间更长、质量更高的试验,同时监测大麻素浓度,这在美国需要提高研究用大麻素产品的可获得性。