Paterson Louise M, Flechais Remy S A, Murphy Anna, Reed Laurence J, Abbott Sanja, Boyapati Venkataramana, Elliott Rebecca, Erritzoe David, Ersche Karen D, Faluyi Yetunde, Faravelli Luca, Fernandez-Egea Emilio, Kalk Nicola J, Kuchibatla Shankar S, McGonigle John, Metastasio Antonio, Mick Inge, Nestor Liam, Orban Csaba, Passetti Filippo, Rabiner Eugenii A, Smith Dana G, Suckling John, Tait Roger, Taylor Eleanor M, Waldman Adam D, Robbins Trevor W, Deakin J F William, Nutt David J, Lingford-Hughes Anne R
Centre for Neuropsychopharmacology, Imperial College London, London, UK.
Neuroscience and Psychiatry Unit, University of Manchester, Manchester, UK.
J Psychopharmacol. 2015 Sep;29(9):943-60. doi: 10.1177/0269881115596155. Epub 2015 Aug 5.
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.
药物和酒精依赖是全球性问题,会带来巨大的社会成本。预防复发的治疗方法很少,因此迫切需要进一步研究支撑复发回路的脑机制。帝国理工学院-剑桥-曼彻斯特(ICCAM)平台研究是针对这一问题的一种实验医学方法:利用功能磁共振成像(fMRI)技术和选择性药理学工具,旨在探索可卡因、酒精、阿片类药物依赖者以及健康个体中假定复发途径的神经药理学,为未来的药物开发提供信息。由于招募困难和人员流失,成瘾研究通常涉及小样本。我们在三个中心建立了该平台,以评估多中心方法解决这些问题的可行性。在一项金钱激励延迟任务、一项抑制控制任务和一项唤起图像任务中,使用μ-阿片受体、多巴胺D3受体(DRD3)和神经激肽1(NK1)受体的选择性拮抗剂(纳曲酮、GSK598809、沃氟匹坦/阿瑞匹坦),采用安慰剂对照、随机、交叉设计,研究奖励、冲动性和情绪反应性的药理学调节。在两年内,共进行了609次扫描,155名个体在基线时接受了扫描。人员流失率较低,大多数个体有足够的积极性完成所有五个阶段(n = 87)。我们在此描述研究设计、主要目标、招募人数、样本特征,并解释测试假设和预期的研究结果。