Johns Hopkins University School of Medicine, Department of Psychiatry and Behavioral Sciences, Baltimore, MD, 21224, USA.
Johns Hopkins University School of Medicine, Department of Psychiatry and Behavioral Sciences, Baltimore, MD, 21224, USA.
Drug Alcohol Depend. 2019 Dec 1;205:107650. doi: 10.1016/j.drugalcdep.2019.107650. Epub 2019 Oct 20.
Methadone maintenance is an effective treatment for opioid use disorder (OUD), yet many methadone-maintained patients (MMPs) struggle with cocaine use during OUD recovery. The current study aimed to identify whether prefrontal cortex (PFC) activity during a risky decision-making task was associated with cocaine use during a 90-day follow-up in MMPs.
MMPs (N = 28) attended a single neuroimaging session wherein PFC activity was measured using functional near-infrared spectroscopy (fNIRS) during the Balloon Analogue Risk Task (BART). Trait impulsivity was assessed via the Barratt Impulsiveness Scale version 11 (BIS-11). Following the neuroimaging session, MMPs were tracked via electronic health records for 90 days to determine treatment outcomes including cocaine use verified by urine drug screens.
During the BART, MMPs who used cocaine displayed increased neural activity in the right PFC during active decision-making (F = 14.75, p = 0.001) and the right dorsolateral PFC during active minus passive decision-making (F = 5.56, p = 0.028) compared to participants who did not use cocaine. Receiver operating characteristic curves confirmed that neural activity in the right PFC during active decision-making (AUC = 0.841, 95% CI, 0.697-0.985, p = 002), and in the right dorsolateral PFC during active minus passive decision-making (AUC = 0.805, 95% CI, 0.643-0.968, p = 0.006) was associated with continued cocaine use. MMPs who used cocaine versus those who did not reported increased trait impulsivity on the BIS-11 Total Score (t=-2.28, p = 0.031).
The fNIRS device is portable, relatively easy to use, and potentially feasible for use in methadone outpatient programs to assess propensity for negative treatment outcomes such as continued cocaine use.
美沙酮维持治疗是治疗阿片类药物使用障碍(OUD)的有效方法,但许多美沙酮维持治疗患者(MMP)在 OUD 康复期间仍存在可卡因使用问题。本研究旨在确定在风险决策任务期间的前额叶皮层(PFC)活动是否与 MMP 在 90 天随访期间的可卡因使用有关。
MMP(n=28)参加了一次单一的神经影像学会议,在该会议期间,使用功能近红外光谱(fNIRS)在气球模拟风险任务(BART)期间测量 PFC 活动。特质冲动性通过巴瑞特冲动量表第 11 版(BIS-11)进行评估。在神经影像学会议之后,通过电子健康记录对 MMP 进行了 90 天的跟踪,以确定治疗结果,包括通过尿液药物检测证实的可卡因使用情况。
在 BART 期间,与未使用可卡因的参与者相比,使用可卡因的 MMP 在主动决策时右前额叶皮层的神经活动增加(F=14.75,p=0.001),在主动决策减去被动决策时右背外侧前额叶皮层的神经活动增加(F=5.56,p=0.028)。接受者操作特征曲线证实,在主动决策时右前额叶皮层的神经活动(AUC=0.841,95%CI,0.697-0.985,p=0.002),以及在主动决策减去被动决策时右背外侧前额叶皮层的神经活动(AUC=0.805,95%CI,0.643-0.968,p=0.006)与持续可卡因使用相关。与未使用可卡因的参与者相比,使用可卡因的 MMP 报告 BIS-11 总分的特质冲动性增加(t=-2.28,p=0.031)。
fNIRS 设备便携、使用相对简单,并且有可能在美沙酮门诊计划中用于评估负面治疗结果(如持续可卡因使用)的倾向。