McLean Hospital, Department of Psychiatry, 115 Mill St, Belmont, MA, USA.
J Clin Psychiatry. 2010 May;71(5):634-48. doi: 10.4088/JCP.08r04062gry. Epub 2010 Mar 9.
To critically review the literature on topiramate in the treatment of substance-related disorders.
A PubMed search of human studies published in English through January 2009 was conducted using the following search terms: topiramate and substance abuse, topiramate and substance dependence, topiramate and withdrawal, topiramate and alcohol, topiramate and nicotine, topiramate and cocaine, topiramate and opiates, and topiramate and benzodiazepines.
26 articles were identified and reviewed; these studies examined topiramate in disorders related to alcohol, nicotine, cocaine, methamphetamine, opioids, Ecstasy, and benzodiazepines.
Study design, sample size, topiramate dose and duration, and study outcomes were reviewed.
There is compelling evidence for the efficacy of topiramate in the treatment of alcohol dependence. Two trials show trends for topiramate's superiority over oral naltrexone in alcohol dependence, while 1 trial suggests topiramate is inferior to disulfiram. Despite suggestive animal models, evidence for topiramate in treating alcohol withdrawal in humans is slim. Studies of topiramate in nicotine dependence show mixed results. Human laboratory studies that used acute topiramate dosing show that topiramate actually enhances the pleasurable effects of both nicotine and methamphetamine. Evidence for topiramate in the treatment of cocaine dependence is promising, but limited by small sample size. The data on opioids, benzodiazepines, and Ecstasy are sparse.
Topiramate is efficacious for the treatment of alcohol dependence, but side effects may limit widespread use. While topiramate's unique pharmacodynamic profile offers a promising theoretical rationale for use across multiple substance-related disorders, heterogeneity both across and within these disorders limits topiramate's broad applicability in treating substance-related disorders. Recommendations for future research include exploration of genetic variants for more targeted pharmacotherapies.
批判性地回顾有关托吡酯治疗物质相关障碍的文献。
通过使用以下搜索词,在 2009 年 1 月前以英文发表的人类研究的 PubMed 搜索:topiramate 和 substance abuse、topiramate 和 substance dependence、topiramate 和 withdrawal、topiramate 和 alcohol、topiramate 和 nicotine、topiramate 和 cocaine、topiramate 和 opiates 和 topiramate 和 benzodiazepines。
确定并审查了 26 篇文章;这些研究检查了与酒精、尼古丁、可卡因、冰毒、阿片类药物、摇头丸和苯二氮䓬类药物相关的障碍中的托吡酯。
审查了研究设计、样本量、托吡酯剂量和持续时间以及研究结果。
有强有力的证据表明托吡酯治疗酒精依赖症有效。两项试验显示托吡酯在治疗酒精依赖方面优于口服纳曲酮的趋势,而一项试验表明托吡酯不如戒酒硫。尽管有暗示性的动物模型,但托吡酯治疗人类酒精戒断的证据很少。托吡酯治疗尼古丁依赖的研究结果喜忧参半。使用急性托吡酯给药的人体实验室研究表明,托吡酯实际上增强了尼古丁和冰毒的愉悦效果。托吡酯治疗可卡因依赖的证据很有希望,但受到样本量小的限制。关于阿片类药物、苯二氮䓬类药物和摇头丸的数据很少。
托吡酯治疗酒精依赖症有效,但副作用可能会限制其广泛应用。虽然托吡酯独特的药效学特征为治疗多种物质相关障碍提供了一个有前途的理论依据,但这些障碍在异质性方面的异质性限制了托吡酯在治疗物质相关障碍方面的广泛适用性。对未来研究的建议包括探索用于更有针对性的药物治疗的遗传变异。