Department of Family Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
Department of Family Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
Drug Alcohol Depend. 2018 Aug 1;189:30-36. doi: 10.1016/j.drugalcdep.2018.04.023. Epub 2018 May 25.
Previous studies have suggested that varenicline, an α4β2 nicotinic receptor partial agonist, and α7 nicotinic receptor full agonist, may be effective for the treatment of methamphetamine (MA) dependence due to dopaminergic effects, relief of glutamatergic and cognitive dysfunction, and activation of nicotinic cholinergic systems. This study aimed to determine if varenicline (1 mg BID) resulted in reduced methamphetamine use compared to placebo among treatment-seeking MA-dependent volunteers.
Treatment-seeking MA-dependent volunteers were randomized to varenicline 1 mg twice daily (n = 27) or placebo (n = 25) and cognitive behavioral therapy for 9 weeks. The primary outcomes were the proportion of participants achieving end-of-treatment-abstinence (EOTA, MA-negative urine specimens during weeks 8 and 9) and the treatment effectiveness score (TES, number of MA-negative urine specimens) for varenicline versus placebo.
There was no significant difference in EOTA between varenicline (15%, 4/27) and placebo (20%, 5/25; p = 0.9). There was some suggestion that urinary confirmed medication compliance corresponded with EOTA in the varenicline condition, though it did not reach statistical significance, OR = 1.57 for a 100 ng/ml increase in urine varenicline, p = 0.10, 95% CI (0.99, 3.02). There was no significant difference in mean TES in the varenicline condition (8.6) compared to the placebo condition (8.1), and treatment condition was not a statistically significant predictor of TES, IRR = 1.01, p = 0.9, 95% CI (0.39, 2.70).
The results of this study indicate that 1 mg varenicline BID was not an effective treatment for MA dependence among treatment-seeking MA-dependent volunteers.
先前的研究表明,作为一种 α4β2 烟碱受体部分激动剂和 α7 烟碱受体完全激动剂,伐尼克兰可能通过多巴胺能作用、缓解谷氨酸能和认知功能障碍以及激活烟碱胆碱能系统对治疗甲基苯丙胺(MA)依赖有效。本研究旨在确定与安慰剂相比,在寻求治疗的 MA 依赖志愿者中,每日两次(BID)1mg 伐尼克兰是否会减少 MA 的使用。
寻求治疗的 MA 依赖志愿者被随机分配至伐尼克兰 1mg BID(n=27)或安慰剂(n=25)组,并接受认知行为治疗 9 周。主要结局为治疗结束时的戒断率(EOTA,第 8 和 9 周时 MA 阴性尿样)和伐尼克兰与安慰剂的治疗效果评分(TES,MA 阴性尿样数量)。
EOTA 在伐尼克兰组(15%,4/27)和安慰剂组(20%,5/25)之间无显著差异(p=0.9)。虽然在伐尼克兰条件下,尿液中确认的药物依从性与 EOTA 呈正相关,但并未达到统计学意义,尿液中伐尼克兰增加 100ng/ml,比值比(OR)为 1.57,p=0.10,95%置信区间(CI)(0.99,3.02)。伐尼克兰组的 TES 均值(8.6)与安慰剂组(8.1)相比无显著差异,治疗条件也不是 TES 的统计学显著预测因子,风险比(IRR)为 1.01,p=0.9,95%CI(0.39,2.70)。
本研究结果表明,每日两次 1mg 伐尼克兰对寻求治疗的 MA 依赖志愿者的 MA 依赖无效。