纯化大麻二酚的治疗潜力。

Saoirse Elizabeth O'Sullivan, Sanne Skov Jensen, Gitte Nykjaer Nikolajsen, Heidi Ziegler Bruun, Rhenu Bhuller, Julia Hoeng
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引用次数: 2

摘要

大麻二酚(CBD)用于治疗目的正在受到相当大的关注,人们猜测CBD在各种情况下都是有用的。只有一种产品,纯化形式的植物源性CBD溶液(Epidiolex),被批准用于治疗lenox - gastaut综合征,Dravet综合征或结节性硬化症患者的癫痫发作。CBD产品有时含有额外的植物化学物质(如四氢大麻酚(THC)),这使得阳性研究中活性药物成分(API)的鉴定变得困难,因此对CBD治疗证据基础的评估变得复杂。本综述的目的是严格审查仅使用纯化CBD产品的临床研究,以便确定纯化CBD可能有益的适应症。支持使用CBD的临床证据最多的领域是治疗焦虑症(7项非对照研究和17项随机对照试验的阳性数据)、精神病和精神分裂症(1项非对照研究和8项随机对照试验的阳性数据)、创伤后应激障碍(2项非对照研究和4项随机对照试验的阳性数据)和药物滥用(2项非对照研究和3项随机对照试验的阳性数据)。七项不受控制的研究支持使用CBD改善睡眠质量,但这只在一项小型随机对照试验中得到了验证。有限的证据支持使用CBD治疗帕金森病(3项阳性对照研究和2项阳性随机对照试验)、自闭症(3项阳性随机对照试验)、戒烟(2项阳性随机对照试验)、移植物抗宿主病和肠通透性(各1项阳性随机对照试验)。目前的随机对照试验证据不支持将纯化的口服CBD用于疼痛(至少作为急性镇痛药)或治疗COVID症状、癌症、亨廷顿舞蹈症或2型糖尿病。总之,已发表的临床证据确实支持在癫痫以外的多种适应症中使用纯化CBD。然而,证据基础受到试验数量的限制,这些试验只调查CBD的急性效应,在健康志愿者中测试CBD,或者在非常小的患者数量中测试CBD。所有适应症都需要大规模的验证性3期试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The therapeutic potential of purified cannabidiol.

The therapeutic potential of purified cannabidiol.

The therapeutic potential of purified cannabidiol.

The therapeutic potential of purified cannabidiol.

The use of cannabidiol (CBD) for therapeutic purposes is receiving considerable attention, with speculation that CBD can be useful in a wide range of conditions. Only one product, a purified form of plant-derived CBD in solution (Epidiolex), is approved for the treatment of seizures in patients with Lennox-Gastaut syndrome, Dravet syndrome, or tuberous sclerosis complex. Appraisal of the therapeutic evidence base for CBD is complicated by the fact that CBD products sometimes have additional phytochemicals (like tetrahydrocannabinol (THC)) present, which can make the identification of the active pharmaceutical ingredient (API) in positive studies difficult. The aim of the present review is to critically review clinical studies using purified CBD products only, in order to establish the upcoming indications for which purified CBD might be beneficial. The areas in which there is the most clinical evidence to support the use of CBD are in the treatment of anxiety (positive data in 7 uncontrolled studies and 17 randomised controlled trials (RCTs)), psychosis and schizophrenia (positive data in 1 uncontrolled study and 8 RCTs), PTSD (positive data in 2 uncontrolled studies and 4 RCTs) and substance abuse (positive data in 2 uncontrolled studies and 3 RCTs). Seven uncontrolled studies support the use of CBD to improve sleep quality, but this has only been verified in one small RCT. Limited evidence supports the use of CBD for the treatment of Parkinson's (3 positive uncontrolled studies and 2 positive RCTs), autism (3 positive RCTs), smoking cessation (2 positive RCTs), graft-versus-host disease and intestinal permeability (1 positive RCT each). Current RCT evidence does not support the use of purified oral CBD in pain (at least as an acute analgesic) or for the treatment of COVID symptoms, cancer, Huntington's or type 2 diabetes. In conclusion, published clinical evidence does support the use of purified CBD in multiple indications beyond epilepsy. However, the evidence base is limited by the number of trials only investigating the acute effects of CBD, testing CBD in healthy volunteers, or in very small patient numbers. Large confirmatory phase 3 trials are required in all indications.

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