Department of Psychology, Center on Alcoholism, Substance Abuse and Addictions, University of New Mexico, Albuquerque, NM, USA.
Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Germany.
Addict Biol. 2017 Nov;22(6):1528-1539. doi: 10.1111/adb.12427. Epub 2016 Aug 2.
Researchers have sought to distinguish between individuals whose alcohol use disorder (AUD) is maintained by drinking to relieve negative affect ('relief drinkers') and those whose AUD is maintained by the rewarding effects of alcohol ('reward drinkers'). As an opioid receptor antagonist, naltrexone may be particularly effective for reward drinkers. Acamprosate, which has been shown to down-regulate the glutamatergic system, may be particularly effective for relief drinkers. This study sought to replicate and extend prior work (PREDICT study; Glöckner-Rist et al. ) by examining dimensions of reward and relief temptation to drink and subtypes of individuals with distinct patterns of reward/relief temptation. We utilized data from two randomized clinical trials for AUD (Project MATCH, n = 1726 and COMBINE study, n = 1383). We also tested whether classes of reward/relief temptation would predict differential response to naltrexone and acamprosate in COMBINE. Results replicated prior work by identifying reward and relief temptation factors, which had excellent reliability and construct validity. Using factor mixture modeling, we identified five distinct classes of reward/relief temptation that replicated across studies. In COMBINE, we found a significant class-by-acamprosate interaction effect. Among those most likely classified in the high relief/moderate reward temptation class, individuals had better drinking outcomes if assigned to acamprosate versus placebo. We did not find a significant class-by-naltrexone interaction effect. Our study questions the orthogonal classification of drinkers into only two types (reward or relief drinkers) and adds to the body of research on moderators of acamprosate, which may inform clinical decision making in the treatment of AUD.
研究人员试图区分那些因缓解负面情绪而饮酒导致酒精使用障碍(AUD)的个体(“缓解饮酒者”)和那些因酒精的奖赏效应而导致 AUD 的个体(“奖赏饮酒者”)。作为一种阿片受体拮抗剂,纳曲酮可能对奖赏饮酒者特别有效。已证明具有下调谷氨酸能系统作用的安非他酮可能对缓解饮酒者特别有效。本研究旨在通过检查与奖赏和缓解饮酒相关的维度以及具有不同奖赏/缓解饮酒相关模式的个体亚型,复制和扩展之前的工作(PREDICT 研究;Glöckner-Rist 等人)。我们利用了两项针对 AUD 的随机临床试验的数据(项目 MATCH,n = 1726;COMBINE 研究,n = 1383)。我们还测试了奖赏/缓解饮酒相关维度是否可以预测 COMBINE 中纳曲酮和安非他酮的不同反应。结果复制了之前的工作,确定了奖赏和缓解饮酒相关维度,这些维度具有良好的可靠性和结构有效性。使用因子混合模型,我们在两个研究中识别了五个不同的奖赏/缓解饮酒相关维度类别。在 COMBINE 研究中,我们发现了奖赏/缓解饮酒相关维度与安非他酮之间的显著交互作用。在那些最有可能被归类为高缓解/中奖赏饮酒相关维度的个体中,如果分配到安非他酮而非安慰剂,他们的饮酒结果会更好。我们没有发现奖赏/缓解饮酒相关维度与纳曲酮之间的显著交互作用。我们的研究质疑将饮酒者仅分为两种类型(奖赏或缓解饮酒者)的正交分类,并增加了对安非他酮的调节因素的研究,这可能为 AUD 的治疗提供临床决策依据。