酒精线索暴露范式作为酒精使用障碍药物开发的筛选工具:一个重要的回顾。

IF 2.7 Q2 SUBSTANCE ABUSE
Dylan E Kirsch, Erica N Grodin, Lorenzo Leggio, Sherry A McKee, Lindsay R Meredith, Ethan H Mereish, Robert Miranda, Steven J Nieto, Stephanie S O'Malley, Joseph P Schacht, Lara A Ray
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引用次数: 0

摘要

酒精线索暴露范式在酒精使用障碍(AUD)研究中有着悠久而丰富的历史,有助于识别危险因素,将渴望视为核心症状,理解AUD神经生物学,以及开发药物和行为治疗方法。本综述的目的是评估酒精提示暴露范式作为AUD药物开发筛选工具的效用,并为改进范式提供建议。首先,我们回顾了支持酒精线索暴露范式的预测有效性和临床适用性的证据。其次,我们检查了目前在AUD药物治疗研究中实施范式的实践。第三,我们强调了需要改进的几个领域,并为该范式的实现提供了建议。最后,我们概述了关键结论和可操作的未来方向。综上所述,尽管酒精提示暴露范式在AUD药物治疗研究中已经建立了基础,但其未来的成功取决于在大规模研究中对方案进行完善和标准化以及验证结果测量的共同努力。解决这些优先事项可以加速AUD新疗法的开发和监管批准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The alcohol cue-exposure paradigm as a screening tool for alcohol use disorder medication development: A critical review.

The alcohol cue-exposure paradigm has a long and rich history in alcohol use disorder (AUD) research, contributing to the identification of risk factors, the recognition of craving as a core symptom, the understanding of AUD neurobiology, and the development of both pharmacological and behavioral treatments. The goal of this review was to evaluate the utility of the alcohol cue-exposure paradigm as a screening tool for AUD medication development and to provide recommendations for refinement of the paradigm. First, we review evidence supporting the predictive validity and clinical applicability of the alcohol cue-exposure paradigm. Second, we examine current practices in implementing the paradigm in AUD pharmacotherapy studies. Third, we highlight several areas for refinement and offer recommendations for the implementation of this paradigm. Finally, we outline key conclusions and actionable future directions. In summary, while the alcohol cue-exposure paradigm has an established foundation in the study of AUD pharmacotherapies, its future success hinges on a concerted effort to refine and standardize protocols and validate outcome measures in large-scale studies. Addressing these priorities could accelerate the development and regulatory approval of novel treatments for AUD.

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CiteScore
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