New York State Psychiatric Institute, Division on Substance Use Disorders, 1051 Riverside Drive, New York, NY 10032, USA; Department of Psychiatry, Columbia University Vagelos College of Physicians and Surgeons, 630 West 168(th) Street, New York, NY 10032, USA.
New York State Psychiatric Institute, Division on Substance Use Disorders, 1051 Riverside Drive, New York, NY 10032, USA; Department of Psychiatry, Columbia University Vagelos College of Physicians and Surgeons, 630 West 168(th) Street, New York, NY 10032, USA.
Drug Alcohol Depend. 2021 Aug 1;225:108765. doi: 10.1016/j.drugalcdep.2021.108765. Epub 2021 May 21.
Abstinence remains a standard outcome for potential treatment interventions for Cannabis Use Disorder (CUD). However, there needs to be validation of non-abstinent outcomes. This study explores reductions in self-reported days of use as another viable outcome measure using data from three completed randomized placebo-controlled clinical trials of pharmacological interventions for CUD.
The three trials tested the effect of quetiapine (QTP, n = 113); dronabinol (DRO, n = 156); and lofexidine + dronabinol (LFD, n = 122). Self-reported cannabis use was categorized into three use-groups/week: heavy (5-7 days/week), moderate (2-4 days/week) and light use (0-1 days/week). Multinomial logistic regressions analyzed the treatment by time effect on the likelihood of light and moderate use compared to heavy use in each study.
Across the three trials, there was no significant overall time-by-treatment interaction (QTP: p = .06; DRO: p = .15; LFD: p = .21). However, the odds of moderate compared to heavy use were significantly higher in treatment than in placebo groups starting around the midpoint of each trial. No treatment differences were found between the odds of light compared to heavy use.
While study-end abstinence rates have been a standard treatment outcome for CUD trials, reduction from heavy to moderate use has not been standardly assessed. During the last several weeks of each trial, those on active medication were more likely to move from heavy to moderate use, which suggests that certain medications may be more impactful than previously assessed. Future studies should determine if this pattern is associated with less CUD severity and/or improved quality of life.
禁欲仍然是治疗大麻使用障碍(CUD)的潜在干预措施的标准结果。然而,需要验证非禁欲的结果。本研究使用来自三个已完成的随机安慰剂对照药物干预 CUD 的临床试验的数据,探讨减少自我报告的使用天数作为另一种可行的结果测量方法。
这三项试验测试了喹硫平(QTP,n=113);屈大麻酚(DRO,n=156);和可乐定+屈大麻酚(LFD,n=122)的效果。自我报告的大麻使用分为三组/周:重度(5-7 天/周)、中度(2-4 天/周)和轻度使用(0-1 天/周)。多变量逻辑回归分析了每个研究中治疗与时间对与重度使用相比轻度和中度使用的可能性的影响。
在三项试验中,总体时间与治疗的交互作用没有显著差异(QTP:p=0.06;DRO:p=0.15;LFD:p=0.21)。然而,从试验的中点开始,与安慰剂组相比,中度使用的几率明显高于重度使用。与重度使用相比,轻度使用的几率没有发现治疗差异。
虽然研究结束时的禁欲率一直是 CUD 试验的标准治疗结果,但尚未对从重度到中度使用的减少进行标准评估。在每个试验的最后几周,使用活性药物的人更有可能从重度转为中度使用,这表明某些药物可能比以前评估的更有影响力。未来的研究应该确定这种模式是否与 CUD 严重程度降低和/或生活质量提高有关。