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托吡酯对饮酒冲动及酒精主观效应的影响:一项初步实验室研究。

Effects of topiramate on urge to drink and the subjective effects of alcohol: a preliminary laboratory study.

作者信息

Miranda Robert, MacKillop James, Monti Peter M, Rohsenow Damaris J, Tidey Jennifer, Gwaltney Chad, Swift Robert, Ray Lara, McGeary John

机构信息

Center for Alcohol and Addiction Studies, Brown University, Providence, Rhode Island 02912, USA.

出版信息

Alcohol Clin Exp Res. 2008 Mar;32(3):489-97. doi: 10.1111/j.1530-0277.2007.00592.x. Epub 2008 Jan 22.

Abstract

BACKGROUND

Topiramate was recently reported to be efficacious in reducing drinking rates and craving among individuals with alcohol dependence in a randomized controlled trial, but dose effects could not be determined. This laboratory study systematically examined the dose-dependent effects of topiramate on cue-elicited craving and other putative mechanisms of its pharmacotherapeutic effects on drinking.

METHODS

Male and female heavy drinkers (n = 61) were randomized to 1 of 3 medication conditions (200 mg/d; 300 mg/d; placebo) in a double-blind study. Participants reached the target dose after a 32-day titration period, then were stabilized for approximately 1 week. All then participated in a laboratory assessment of alcohol cue reactivity and of the subjective effects of a moderate dose of alcohol.

RESULTS

Both doses of topiramate reduced the frequency of heavy drinking during the titration period as compared to placebo. However, topiramate did not affect self-reported craving for alcohol during the titration period, during the cue reactivity protocol, or in response to the alcohol challenge procedure. Topiramate reduced the stimulating effects of alcohol ingestion compared to placebo, but only in the 200 mg group.

CONCLUSIONS

The results of this study support previous findings that topiramate reduces drinking, but the behavioral mechanism underlying this effect does not appear to be attenuation of craving for alcohol as measured using the approaches employed in this study. Rather, the results tentatively suggest that topiramate may exert its beneficial effects by altering the subjective experiences of alcohol consumption. Limitations of the current study are discussed and complementary methods are recommended for future studies, such as the use of behavioral economic paradigms and ecological momentary assessment.

摘要

背景

在一项随机对照试验中,最近有报告称托吡酯在降低酒精依赖个体的饮酒率和渴望方面有效,但无法确定剂量效应。这项实验室研究系统地考察了托吡酯对线索诱发的渴望以及其对饮酒的药物治疗作用的其他假定机制的剂量依赖性效应。

方法

在一项双盲研究中,将61名男性和女性重度饮酒者随机分为3种药物治疗组之一(200毫克/天;300毫克/天;安慰剂)。参与者在32天的滴定期后达到目标剂量,然后稳定约1周。随后所有人都参与了一项关于酒精线索反应性和中等剂量酒精主观效应的实验室评估。

结果

与安慰剂相比,两种剂量的托吡酯在滴定期均降低了重度饮酒的频率。然而,托吡酯在滴定期、线索反应性试验期间或对酒精激发程序的反应中均未影响自我报告的对酒精的渴望。与安慰剂相比,托吡酯降低了酒精摄入的刺激作用,但仅在200毫克组中。

结论

本研究结果支持先前的发现,即托吡酯可减少饮酒,但这种效应的行为机制似乎并非如本研究采用的方法所测量的那样是减轻对酒精的渴望。相反,结果初步表明托吡酯可能通过改变饮酒的主观体验发挥其有益作用。讨论了当前研究的局限性,并为未来研究推荐了补充方法,如使用行为经济学范式和生态瞬时评估。

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