Loebl Tsafrir, Angarita Gustavo A, Pachas Gladys N, Huang Kai-Lin, Lee Sang H, Nino Johanna, Logvinenko Tanya, Culhane Melissa A, Evins A Eden
Center for Addiction Medicine of the Department of Psychiatry and the Biostatistics Center of Massachusetts General Hospital, Harvard Medical School, Boston, Mass. 02114, USA.
J Clin Psychiatry. 2008 Mar;69(3):480-6. doi: 10.4088/jcp.v69n0321.
There is no approved pharmaco-therapy for cocaine dependence. Risperidone is an atypical antipsychotic drug with combined dopamine-2/serotonin-2 (D(2)/5-HT(2)) antagonist activity that has been effective in reducing cocaine use in some animal studies. We tested the efficacy of a long-acting, injectable preparation of risperidone on cocaine use in active cocaine users.
Thirty-one cocaine-dependent men who met DSM-IV diagnostic criteria for current cocaine dependence entered a 12-week, randomized, double-blind, placebo-controlled trial of intramuscular risperidone, 25 mg every other week. The primary outcome measure was cocaine use as measured by urinary concentration of cocaine metabolites. Secondary outcomes were self-report of cocaine use and craving, depressive symptoms as measured by the Hamilton Rating Scale for Depression (HAM-D), and adverse events. Participants were recruited during a 12-month period from October 2005 to September 2006.
Both groups reduced their cocaine use during the study. There were no between-group differences in the primary measure of cocaine use (urinary metabolites [F = 0.7, p = .41]) or on craving measures. Those assigned to risperi-done reported significantly worsened depressive symptoms (mean +/- SD HAM-D change scores: +7.4 +/- 8.8 vs. -2.3 +/- 5.8, respectively, F = 7.5, p = .018) and gained significantly more weight (mean weight change: +6.3 +/- 9.4 lb vs. -4.0 +/- 8.9 lb, respectively, F = 4.65, p = .044) than those assigned to placebo.
Treatment with long-acting injectable risperidone in active cocaine users was not associated with reduction in cocaine use or craving and was associated with worsening of depressive symptoms and weight gain.
clinicaltrials.gov Identifier: NCT00385801.
目前尚无获批用于治疗可卡因依赖的药物疗法。利培酮是一种非典型抗精神病药物,具有多巴胺-2/5-羟色胺-2(D₂/5-HT₂)联合拮抗剂活性,在一些动物研究中已证明其可有效减少可卡因使用量。我们测试了长效注射用利培酮对活跃可卡因使用者可卡因使用情况的疗效。
31名符合《精神疾病诊断与统计手册》第四版(DSM-IV)当前可卡因依赖诊断标准的男性可卡因依赖者,进入一项为期12周的随机、双盲、安慰剂对照试验,接受每两周注射25毫克利培酮的治疗。主要疗效指标是通过尿液中可卡因代谢物浓度来衡量可卡因使用情况。次要疗效指标包括可卡因使用和渴求的自我报告、用汉密尔顿抑郁量表(HAM-D)测量的抑郁症状以及不良事件。研究对象于2005年10月至2006年9月的12个月期间招募。
两组在研究期间可卡因使用量均有所减少。在可卡因使用的主要指标(尿液代谢物[F = 0.7,p = 0.41])或渴求指标方面,两组之间没有差异。与服用安慰剂的人相比,服用利培酮的人报告抑郁症状明显加重(平均±标准差HAM-D变化得分分别为+7.4±8.8和-2.3±5.8,F = 7.5,p = 0.018),体重增加也明显更多(平均体重变化分别为+6.3±9.4磅和-4.0±8.9磅,F = 4.65,p = 0.044)。
在活跃可卡因使用者中,使用长效注射用利培酮治疗与可卡因使用量或渴求的减少无关,且与抑郁症状加重和体重增加有关。
美国国立医学图书馆临床试验注册库标识符:NCT00385801。