Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA (KGL, JP, MM, MT, PF, KMK); Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA (KS).
J Addict Med. 2022;16(2):157-163. doi: 10.1097/ADM.0000000000000842.
Varenicline is a partial agonist at the α2β4 and α6β2 nAChR receptors and a full agonist at α7 receptors. Both α7 and α6β2 receptors are implicated in the neural reward circuitry activated by cocaine use. A preliminary clinical trial suggested that varenicline treatment reduced cocaine use. This trial was intended to replicate and extend the findings of the previous trial.
This was a 12-week, double-blind, placebo-controlled clinical trial involving 156 subjects with DSM IV cocaine dependence. Subjects received up to 2 mg of varenicline or identical placebo daily along with weekly relapse prevention psychotherapy. The primary outcome measure was cocaine use measured by thrice-weekly urine drug screens. Additional outcome measures included end of study cocaine abstinence, cocaine craving, cocaine withdrawal symptom severity, cigarette use, and global improvement measure by the Clinical Global Improvement Scale.
End of study cocaine abstinence, measured by urine drug screens during the last 3 weeks of the trial, was not different between groups (8% in the varenicline treated subjects and versus 9% in placebo-treated subjects). Generalized estimating equations analysis of urine drug screen results showed no significant difference between groups in cocaine abstinence over the 12 weeks of the trial. There were no significant differences between the 2 groups in cocaine craving or cocaine withdrawal symptom severity. Varenicline was well-tolerated. There were no medication-associated serious adverse events.
Varenicline plus cognitive-behavioral therapy does not seem to be an efficacious treatment for cocaine dependence.
伐伦克林是一种 α2β4 和 α6β2 烟碱型乙酰胆碱受体的部分激动剂,也是 α7 受体的完全激动剂。α7 和 α6β2 受体都与可卡因使用激活的神经奖励回路有关。一项初步的临床试验表明,伐伦克林治疗可减少可卡因的使用。本试验旨在复制和扩展先前试验的结果。
这是一项为期 12 周、双盲、安慰剂对照的临床试验,涉及 156 名符合 DSM-IV 可卡因依赖的受试者。受试者每天接受高达 2mg 的伐伦克林或相同的安慰剂,同时每周接受复发预防心理治疗。主要结局指标是通过每周三次的尿液药物筛查测量可卡因的使用情况。其他结局指标包括研究结束时的可卡因戒断、可卡因渴求、可卡因戒断症状严重程度、吸烟情况以及临床总体改善量表(Clinical Global Improvement Scale)的总体改善测量。
研究结束时的可卡因戒断情况(通过试验最后 3 周的尿液药物筛查测量),两组之间没有差异(伐伦克林治疗组为 8%,安慰剂治疗组为 9%)。尿液药物筛查结果的广义估计方程分析显示,两组在试验的 12 周内可卡因戒断率没有显著差异。两组在可卡因渴求或可卡因戒断症状严重程度方面没有显著差异。伐伦克林耐受良好。没有与药物相关的严重不良事件。
伐伦克林联合认知行为疗法似乎对可卡因依赖不是一种有效的治疗方法。