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大麻衍生的大麻二酚在酒精使用障碍中的安全性、耐受性和临床效果的初步随机试验。

A preliminary randomized trial of the safety, tolerability, and clinical effects of hemp-derived cannabidiol in alcohol use disorder.

作者信息

Mueller Raeghan L, Hooper Jake F, Ellingson Jarrod M, Olsavsky Aviva K, Rzasa-Lynn Rachael, Bryan Angela D, Bidwell L Cinnamon, Hutchison Kent E

机构信息

Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, CO, United States.

Children's Hospital Colorado, Aurora, CO, United States.

出版信息

Front Psychiatry. 2025 Apr 28;16:1516351. doi: 10.3389/fpsyt.2025.1516351. eCollection 2025.

DOI:10.3389/fpsyt.2025.1516351
PMID:40357520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12066606/
Abstract

INTRODUCTION

Cannabidiol (CBD) has recently gained attention for its potential therapeutic effects in substance use disorders, including Alcohol Use Disorder (AUD). This study examined the potential therapeutic effects of commercially available products containing CBD with and without a small amount of tetrahydrocannabinol (THC) on alcohol use and craving among individuals with moderate to severe AUD.

METHODS

In this feasibility study, a total of 44 participants were randomized to one of three conditions: full-spectrum CBD ( = 13, fsCBD - <0.3% THC), broad-spectrum CBD ( = 15, bsCBD - without THC), or placebo control ( = 16) for 8 weeks. The study was designed to assess the safety and tolerability of these treatments and to evaluate whether CBD demonstrated any clinical effects (Clinicaltrials.gov Identifier: NCT04873453; https://clinicaltrials.gov/study/NCT04873453). It was hypothesized that both CBD conditions would be well tolerated and would reduce drinking, alcohol dependence, and craving compared to placebo.

RESULTS

Analyses of attrition and side effect data indicated no significant differences across conditions, suggesting that both bsCBD and fsCBD were well tolerated. Individuals receiving fsCBD demonstrated reductions in craving but no reduction in drinks per drinking day.

DISCUSSION

In this pilot study, safety profiles fsCBD and bsCBD were similar, and fsCBD was associated with a greater reduction in craving and AUD symptoms relative to both bsCBD and placebo. Future studies with larger sample sizes will be necessary to replicate and extend these findings by addressing the question of whether a small amount of THC may work synergistically with CBD.

摘要

引言

大麻二酚(CBD)最近因其在物质使用障碍,包括酒精使用障碍(AUD)中的潜在治疗作用而受到关注。本研究调查了含有CBD且含有或不含有少量四氢大麻酚(THC)的市售产品对中度至重度酒精使用障碍患者的酒精使用和渴望的潜在治疗作用。

方法

在这项可行性研究中,共有44名参与者被随机分为三个组之一:全谱CBD组(n = 13,fsCBD - THC含量<0.3%)、广谱CBD组(n = 15,bsCBD - 不含THC)或安慰剂对照组(n = 16),为期8周。该研究旨在评估这些治疗方法的安全性和耐受性,并评估CBD是否具有任何临床效果(Clinicaltrials.gov标识符:NCT04873453;https://clinicaltrials.gov/study/NCT04873453)。假设与安慰剂相比,两种CBD组的耐受性良好,并且会减少饮酒、酒精依赖和渴望。

结果

对损耗和副作用数据的分析表明,各组之间没有显著差异,这表明bsCBD和fsCBD的耐受性都很好。接受fsCBD的个体渴望程度降低,但每日饮酒量没有减少。

讨论

在这项初步研究中,fsCBD和bsCBD的安全性概况相似,并且相对于bsCBD和安慰剂,fsCBD与更大程度地减少渴望和酒精使用障碍症状相关。未来需要进行更大样本量的研究,通过解决少量THC是否可能与CBD协同作用的问题来复制和扩展这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/64bec353f475/fpsyt-16-1516351-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/bdda3d621b04/fpsyt-16-1516351-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/64f40079c018/fpsyt-16-1516351-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/b599cfd8cd09/fpsyt-16-1516351-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/a800d10b03ff/fpsyt-16-1516351-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/64bec353f475/fpsyt-16-1516351-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/bdda3d621b04/fpsyt-16-1516351-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/64f40079c018/fpsyt-16-1516351-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/b599cfd8cd09/fpsyt-16-1516351-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/a800d10b03ff/fpsyt-16-1516351-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c9/12066606/64bec353f475/fpsyt-16-1516351-g005.jpg

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本文引用的文献

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Efficacy of cannabidiol alone or in combination with Δ-9-tetrahydrocannabinol for the management of substance use disorders: An umbrella review of the evidence.大麻二酚单独或与Δ-9-四氢大麻酚联合用于物质使用障碍管理的疗效:证据的综合评价。
Addiction. 2025 May;120(5):813-834. doi: 10.1111/add.16745. Epub 2025 Feb 13.
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Psychosocial treatment options for adolescents and young adults with alcohol use disorder: systematic review and meta-analysis.针对患有酒精使用障碍的青少年和青年的心理社会治疗方案:系统评价与荟萃分析。
Front Public Health. 2024 Jul 23;12:1371497. doi: 10.3389/fpubh.2024.1371497. eCollection 2024.
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Service-level barriers to and facilitators of accessibility to treatment for problematic alcohol use: a scoping review.
服务层面上,阻碍和促进有问题的酒精使用治疗可及性的因素:范围综述。
Front Public Health. 2023 Dec 1;11:1296239. doi: 10.3389/fpubh.2023.1296239. eCollection 2023.
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Pharmacotherapy for Alcohol Use Disorder: A Systematic Review and Meta-Analysis.酒精使用障碍的药物治疗:系统评价和荟萃分析。
JAMA. 2023 Nov 7;330(17):1653-1665. doi: 10.1001/jama.2023.19761.
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Cannabidiol tempers alcohol intake and neuroendocrine and behavioural correlates in alcohol binge drinking  adolescent rats. Focus on calcitonin gene-related peptide's brain levels.大麻二酚调节酒精 binge 饮 用青少年大鼠的酒精摄入量和神经内分泌及行为相关物,重点关注降钙素基因相关肽的脑水平。
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Comparative Pharmacokinetics of Commercially Available Cannabidiol Isolate, Broad-Spectrum, and Full-Spectrum Products.市售大麻二酚(CBD)分离物、广谱和全谱产品的比较药代动力学。
Eur J Drug Metab Pharmacokinet. 2023 Jul;48(4):427-435. doi: 10.1007/s13318-023-00839-3. Epub 2023 Jun 19.
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Cannabidiol regulates behavioral and brain alterations induced by spontaneous alcohol withdrawal.大麻二酚可调节自发性酒精戒断引起的行为和大脑改变。
Neuropharmacology. 2023 Aug 1;233:109549. doi: 10.1016/j.neuropharm.2023.109549. Epub 2023 Apr 19.
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Psychopharmacology (Berl). 2023 May;240(5):1119-1129. doi: 10.1007/s00213-023-06349-z. Epub 2023 Mar 20.
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Cannabidiol Effect on Cue-Induced Craving for Individuals with Opioid Use Disorder Treated with Buprenorphine: A Small Proof-of-Concept Open-Label Study.大麻二酚对接受丁丙诺啡治疗的阿片类物质使用障碍患者线索诱导性渴求的影响:一项小型概念验证性开放标签研究。
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