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伐尼克兰、纳曲酮及其联合用药治疗重度饮酒吸烟者:初步神经影像学研究结果

Varenicline, naltrexone, and their combination for heavy-drinking smokers: preliminary neuroimaging findings.

作者信息

Ray Lara A, Courtney Kelly E, Ghahremani Dara G, Miotto Karen, Brody Arthur, London Edythe D

机构信息

Departments of Psychology .

出版信息

Am J Drug Alcohol Abuse. 2015 Jan;41(1):35-44. doi: 10.3109/00952990.2014.927881. Epub 2014 Jun 20.

Abstract

RATIONALE

Heavy drinking smokers constitute a sizeable and hard-to-treat subgroup of smokers, for whom tailored smoking cessation therapies are not yet available.

OBJECTIVE

The present study used a double-blind, randomized, 2 × 2 medication design, testing varenicline alone (VAR; 1 mg twice daily), naltrexone alone (NTX; 25 mg once daily), varenicline plus naltrexone, and placebo for effects on neural activation to cigarette cues in a sample (n = 40) of heavy drinking daily smokers (≥10 cigarettes/day).

METHODS

All participants were tested after a 10-12-day titration period designed to reach steady state on the target medication. Participants underwent functional neuroimaging (fMRI) for examination of brain responses to visual smoking-related (vs. neutral) cues.

RESULTS

Region of interest (ROI) analyses of brain responses to Cigarette vs. Neutral Cues indicated that the combination of VAR + NTX was associated with reduced activation of the bilateral anterior cingulate cortex as compared to placebo and to NTX alone. Exploratory whole-brain analyses also indicated significant differences in brain activation during cigarette cues in the active medications versus placebo condition. All medications suppressed left nucleus accumbens activation relative to placebo, suggesting the possibility that both medications, either alone or in combination, reduce neural signals associated with appetitive behavior.

CONCLUSIONS

Although preliminary, these neuroimaging findings indicate that clinical studies of the combination of VAR + NTX for heavy drinkers trying to quit smoking may be warranted.

摘要

理论依据

重度饮酒吸烟者是吸烟者中规模较大且难以治疗的亚组,目前尚无针对他们的量身定制的戒烟疗法。

目的

本研究采用双盲、随机、2×2药物设计,在每日重度饮酒吸烟者(≥10支/天)样本(n = 40)中,测试伐尼克兰单独使用(VAR;每日2次,每次1mg)、纳曲酮单独使用(NTX;每日1次,每次25mg)、伐尼克兰加纳曲酮以及安慰剂对香烟线索的神经激活作用。

方法

所有参与者在经过10 - 12天的滴定期后进行测试,该滴定期旨在使目标药物达到稳态。参与者接受功能神经成像(fMRI)检查,以检测大脑对视觉吸烟相关(与中性相对)线索的反应。

结果

对香烟与中性线索的大脑反应进行感兴趣区域(ROI)分析表明,与安慰剂和单独使用NTX相比,VAR + NTX组合与双侧前扣带回皮质激活减少有关。探索性全脑分析还表明,在活跃药物与安慰剂条件下,香烟线索期间大脑激活存在显著差异。相对于安慰剂,所有药物均抑制了左侧伏隔核的激活,这表明两种药物单独或联合使用都有可能减少与食欲行为相关的神经信号。

结论

尽管这些神经成像结果是初步的,但表明针对试图戒烟的重度饮酒者进行VAR + NTX联合用药的临床研究可能是有必要的。

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