The Scripps Research Institute, Pearson Center for Alcoholism and Addiction Research, La Jolla, CA 92037, USA.
Neuropsychopharmacology. 2012 Jun;37(7):1689-98. doi: 10.1038/npp.2012.14. Epub 2012 Feb 29.
There are no FDA-approved pharmacotherapies for cannabis dependence. Cannabis is the most widely used illicit drug in the world, and patients seeking treatment for primary cannabis dependence represent 25% of all substance use admissions. We conducted a phase IIa proof-of-concept pilot study to examine the safety and efficacy of a calcium channel/GABA modulating drug, gabapentin, for the treatment of cannabis dependence. A 12-week, randomized, double-blind, placebo-controlled clinical trial was conducted in 50 unpaid treatment-seeking male and female outpatients, aged 18-65 years, diagnosed with current cannabis dependence. Subjects received either gabapentin (1200 mg/day) or matched placebo. Manual-guided, abstinence-oriented individual counseling was provided weekly to all participants. Cannabis use was measured by weekly urine toxicology and by self-report using the Timeline Followback Interview. Cannabis withdrawal symptoms were assessed using the Marijuana Withdrawal Checklist. Executive function was measured using subtests from the Delis-Kaplan Executive Function System. Relative to placebo, gabapentin significantly reduced cannabis use as measured both by urine toxicology (p=0.001) and by the Timeline Followback Interview (p=0.004), and significantly decreased withdrawal symptoms as measured by the Marijuana Withdrawal Checklist (p<0.001). Gabapentin was also associated with significantly greater improvement in overall performance on tests of executive function (p=0.029). This POC pilot study provides preliminary support for the safety and efficacy of gabapentin for treatment of cannabis dependence that merits further study, and provides an alternative conceptual framework for treatment of addiction aimed at restoring homeostasis in brain stress systems that are dysregulated in drug dependence and withdrawal.
目前尚无经美国食品和药物管理局(FDA)批准的用于治疗大麻依赖的药物。大麻是世界上使用最广泛的非法药物,寻求原发性大麻依赖治疗的患者占所有物质使用入院患者的 25%。我们进行了一项 IIa 期概念验证性试点研究,以评估钙通道/GABA 调节药物加巴喷丁治疗大麻依赖的安全性和有效性。这项为期 12 周、随机、双盲、安慰剂对照的临床试验在 50 名无报酬、寻求治疗的 18-65 岁男性和女性门诊患者中进行,这些患者被诊断为当前大麻依赖。受试者接受加巴喷丁(1200mg/天)或匹配的安慰剂治疗。每周为所有参与者提供手动引导、以戒除为导向的个体咨询。通过每周尿液毒理学检测和使用 Timeline Followback 访谈进行自我报告来衡量大麻使用情况。使用大麻戒断症状检查表评估大麻戒断症状。使用 Delis-Kaplan 执行功能系统的子测试来衡量执行功能。与安慰剂相比,加巴喷丁显著减少了尿液毒理学(p=0.001)和 Timeline Followback 访谈(p=0.004)测量的大麻使用,显著降低了大麻戒断症状检查表(p<0.001)测量的大麻戒断症状。加巴喷丁还与执行功能测试的整体表现的显著改善相关(p=0.029)。这项概念验证性试点研究初步支持了加巴喷丁治疗大麻依赖的安全性和有效性,值得进一步研究,并为治疗成瘾提供了另一种概念框架,旨在恢复大脑应激系统的体内平衡,这些系统在药物依赖和戒断中失调。