The Imperial College Cambridge Manchester (ICCAM) platform study: An experimental medicine platform for evaluating new drugs for relapse prevention in addiction. Part A: Study description

上瘾 冲动性 心理学 κ-阿片受体 神经药理学 功能磁共振成像 酒精依赖 奖励制度 精神科 医学 临床心理学 类阿片 神经科学 内科学 受体 化学 生物化学
作者
Louise M. Paterson,Remy Flechais,Anna Murphy,Laurence Reed,Sanja Abbott,Venkataramana Boyapati,Richard M. Elliott,David Erritzøe,Karen D. Ersche,Yetunde Faluyi,Luca Faravelli,Emilio Fernández-Egea,Nicola J. Kalk,Shankar Kuchibatla,John McGonigle,Antonio Metastasio,Inge Mick,Liam Nestor,Csaba Orban,Filippo Passetti,Eugenii A. Rabiner,Dana Smith,John Suckling,Roger Tait,Eleanor Taylor,Adam D. Waldman,Trevor W. Robbins,Bill Deakin,David Nutt,Anne Lingford-Hughes,Iccam Platform
出处
期刊:Journal of Psychopharmacology [SAGE]
卷期号:29 (9): 943-960 被引量:27
标识
DOI:10.1177/0269881115596155
摘要

Drug and alcohol dependence are global problems with substantial societal costs. There are few treatments for relapse prevention and therefore a pressing need for further study of brain mechanisms underpinning relapse circuitry. The Imperial College Cambridge Manchester (ICCAM) platform study is an experimental medicine approach to this problem: using functional magnetic resonance imaging (fMRI) techniques and selective pharmacological tools, it aims to explore the neuropharmacology of putative relapse pathways in cocaine, alcohol, opiate dependent, and healthy individuals to inform future drug development. Addiction studies typically involve small samples because of recruitment difficulties and attrition. We established the platform in three centres to assess the feasibility of a multisite approach to address these issues. Pharmacological modulation of reward, impulsivity and emotional reactivity were investigated in a monetary incentive delay task, an inhibitory control task, and an evocative images task, using selective antagonists for µ-opioid, dopamine D3 receptor (DRD3) and neurokinin 1 (NK1) receptors (naltrexone, GSK598809, vofopitant/aprepitant), in a placebo-controlled, randomised, crossover design. In two years, 609 scans were performed, with 155 individuals scanned at baseline. Attrition was low and the majority of individuals were sufficiently motivated to complete all five sessions (n=87). We describe herein the study design, main aims, recruitment numbers, sample characteristics, and explain the test hypotheses and anticipated study outputs.

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