Montoya Ivan D, Gorelick David A, Preston Kenzie L, Schroeder Jennifer R, Umbricht Annie, Cheskin Lawrence J, Lange W Robert, Contoreggi Carlo, Johnson Rolley E, Fudala Paul J
Division of Treatment Research and Development and Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Department of Health and Human Services, Baltimore, MD 21224, USA.
Clin Pharmacol Ther. 2004 Jan;75(1):34-48. doi: 10.1016/j.clpt.2003.09.004.
Buprenorphine is a partial mu-opiate agonist and kappa-opiate antagonist with established efficacy in the treatment of opiate dependence. Its efficacy for cocaine dependence is uncertain. This study evaluated buprenorphine for the treatment of concomitant cocaine and opiate dependence.
Two hundred outpatients currently dependent on both cocaine and opiates were randomly assigned to double-blind groups receiving a sublingual solution of buprenorphine (2, 8, or 16 mg daily, or 16 mg on alternate days, or placebo), plus weekly individual drug abuse counseling, for 13 weeks. The chief outcome measures were urine concentrations of opiate and cocaine metabolites (quantitative) and proportion of urine samples positive for opiates or cocaine (qualitative). Group differences were assessed by use of mixed regression modeling.
The target dose of buprenorphine was achieved in 179 subjects. Subjects receiving 8 or 16 mg buprenorphine daily showed statistically significant decreases in urine morphine levels (P =.0135 for 8 mg and P <.001 for 16 mg) or benzoylecgonine concentrations (P =.0277 for 8 mg and P =.006 for 16 mg) during the maintenance phase of the study. For the 16-mg group, mean benzoylecgonine concentrations fell from 3715 ng/mL during baseline to 186 ng/mL during the withdrawal phase; mean morphine concentrations fell from 3311 ng/mL during baseline to 263 ng/mL during withdrawal. For the 8-mg group, mean benzoylecgonine concentrations fell from 6761 ng/mL during baseline to 676 ng/mL during withdrawal; mean morphine concentrations fell from 3890 ng/mL during baseline to 661 ng/mL during withdrawal. Qualitative urinalysis showed a similar pattern of results. Subjects receiving the highest dose showed concomitant decreases in both urine morphine and benzoylecgonine concentrations. There were no significant group differences in treatment retention or adverse events.
A sublingual buprenorphine solution at 16 mg daily is well tolerated and effective in reducing concomitant opiate and cocaine use. The therapeutic effect on cocaine use appears independent of that on opiate use.
丁丙诺啡是一种μ-阿片受体部分激动剂和κ-阿片受体拮抗剂,在治疗阿片类药物依赖方面已证实具有疗效。其对可卡因依赖的疗效尚不确定。本研究评估了丁丙诺啡治疗同时存在可卡因和阿片类药物依赖的情况。
200名目前同时依赖可卡因和阿片类药物的门诊患者被随机分配至双盲组,接受丁丙诺啡舌下溶液(每日2毫克、8毫克或16毫克,或隔日16毫克,或安慰剂)治疗,外加每周一次的个体药物滥用咨询,为期13周。主要结局指标为阿片类药物和可卡因代谢物的尿液浓度(定量)以及阿片类药物或可卡因检测呈阳性的尿液样本比例(定性)。通过混合回归模型评估组间差异。
179名受试者达到了丁丙诺啡的目标剂量。在研究的维持阶段,每日接受8毫克或16毫克丁丙诺啡治疗的受试者尿液吗啡水平(8毫克组P = 0.0135,16毫克组P < 0.001)或苯甲酰爱康宁浓度(8毫克组P = 0.0277,16毫克组P = 0.006)出现了具有统计学意义的下降。对于16毫克组,苯甲酰爱康宁的平均浓度从基线时的3715纳克/毫升降至戒断阶段的186纳克/毫升;吗啡平均浓度从基线时的3311纳克/毫升降至戒断阶段的263纳克/毫升。对于8毫克组,苯甲酰爱康宁平均浓度从基线时的6761纳克/毫升降至戒断阶段的676纳克/毫升;吗啡平均浓度从基线时的3890纳克/毫升降至戒断阶段的661纳克/毫升。定性尿液分析显示了类似的结果模式。接受最高剂量治疗的受试者尿液吗啡和苯甲酰爱康宁浓度同时下降。在治疗保留率或不良事件方面,各治疗组之间没有显著差异。
每日16毫克的丁丙诺啡舌下溶液耐受性良好,在减少同时使用阿片类药物和可卡因方面有效。对可卡因使用的治疗效果似乎独立于对阿片类药物使用的效果。