Gonzalez Gerardo, Sevarino Kevin, Sofuoglu Mehmet, Poling Jim, Oliveto Alison, Gonsai Kishor, George Tony P, Kosten Thomas R
Department of Psychiatry, Yale University School of Medicine, West Haven, CT, USA.
Addiction. 2003 Nov;98(11):1625-32. doi: 10.1046/j.1360-0443.2003.00544.x.
We sought to evaluate the safety and efficacy of the GABAergic agent tiagabine in reducing cocaine use among methadone-treated patients.
Ten-week randomized double-blind placebo-controlled trial.
Opiate Treatment Research Program, Veteran's Affairs Connecticut Healthcare System in West Haven, Connecticut, USA.
The participants were 45 cocaine-dependent methadone-treated patients who were predominately Caucasian (75.6%), male (77.8%) and never married (53%) with an average age of 38 years (SD = 6.5).
Comparison groups received tiagabine 12 mg/day (n = 15), tiagabine 24 mg/day (n = 15) or placebo (n = 15).
Baseline assessments included the Structured Clinical Interview for DSM-IV, the Addiction Severity Index, a urine drug test, self-reported use and opiate withdrawal scales. Urine drug tests were performed thrice weekly.
Treatment retention was over 80% for all treatment groups. The sample mean (+/- SE) of cocaine-free urines for the first week after study entry and before tiagabine was started was 1.16 (0.19) urines/week. During weeks 9 and 10 cocaine-free urines increased significantly from baseline by 33% with high-dose tiagabine (24 mg/day), by 14% with low-dose tiagabine (12 mg/day) and decreased by 10% with placebo (hierarchical linear model, Z= 2.03; P < 0.05). Self-reported cocaine use also decreased significantly more with active medications than with placebo.
Tiagabine at 24 mg/day was well tolerated among these methadone-treated patients with only one reporting headache. Tiagabine appears to be a promising GABAergic medication that moderately improves cocaine-free urines.
我们试图评估γ-氨基丁酸能药物噻加宾在减少美沙酮治疗患者可卡因使用方面的安全性和有效性。
为期十周的随机双盲安慰剂对照试验。
美国康涅狄格州韦斯特黑文退伍军人事务康涅狄格医疗系统的阿片类药物治疗研究项目。
45名依赖可卡因且接受美沙酮治疗的患者,主要为白种人(75.6%),男性(77.8%),从未结婚(53%),平均年龄38岁(标准差=6.5)。
比较组分别接受12毫克/天的噻加宾(n = 15)、24毫克/天的噻加宾(n = 15)或安慰剂(n = 15)。
基线评估包括《精神疾病诊断与统计手册》第四版的结构化临床访谈、成瘾严重程度指数、尿液药物检测、自我报告的使用情况和阿片类药物戒断量表。每周进行三次尿液药物检测。
所有治疗组的治疗保留率均超过80%。研究开始后且在开始使用噻加宾之前的第一周,无可卡因尿液的样本均值(±标准误)为每周1.16(0.19)次尿液检测结果。在第9周和第10周,高剂量噻加宾(24毫克/天)组无可卡因尿液从基线水平显著增加33%,低剂量噻加宾(12毫克/天)组增加14%,安慰剂组减少10%(分层线性模型,Z = 2.03;P < 0.05)。与安慰剂相比,使用活性药物后自我报告的可卡因使用量也显著减少。
在这些接受美沙酮治疗的患者中,24毫克/天的噻加宾耐受性良好,只有一人报告有头痛症状。噻加宾似乎是一种有前景的γ-氨基丁酸能药物,可适度增加无可卡因尿液的次数。