Functional networks related to cocaine dependence and its treatment and relapse

与可卡因依赖及其治疗和复发相关的功能网络

• 批准号: 9026859
• 负责人: Jiansong Xu
• 金额: $ 25.1万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-05-01 至 2019-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9026859
• 关键词: Abstinence; Aftercare; Attention; Biological Markers; Brain; Brain region; Cocaine; Cocaine Dependence; Conflict (Psychology); Confusion; Data; Data Set; Dimensions; Dorsal; Drug abuse; Drug usage; Equilibrium; Functional Magnetic Resonance Imaging; Heterogeneity; Incentives; Inpatients; Insula of Reil; Linear Models; Midbrain structure; Motivation; Nature; Neurons; Outcome; Outpatients; Participant; Pathological Gambling; Patients; Recovery; Relapse; Reporting; Research; Research Personnel; Rewards; Sampling; Signal Transduction; Source; Staging; Substance Use Disorder; Task Performances; Testing; Thalamic structure; Treatment outcome; Urine; Ventral Striatum; addiction; base; blood oxygen level dependent; cocaine use; cognitive control; diagnostic biomarker; effective therapy; follow-up; independent component analysis; insight; neural correlate; neuropathology; neuropsychiatric disorder; non-drug; novel strategies; predictive marker; public health relevance; theories; therapy development

 DESCRIPTION (provided by applicant): This application responds to PAR-13-080 - Accelerating the Pace of Drug Abuse Research Using Existing Data. Functional magnetic resonance imaging (fMRI) and the traditional general-linear-model-based analysis (GLM-BA) have been used to assess neural correlates of cocaine dependence (CD) and other neuropsychiatric disorders. However, these studies have reported inconsistent findings including reduced and increased brain activity in patients relative to healthy controls (HCs), and have not been able to provide a clear picture on CD neuropathology and define reliable biomarkers for CD treatment. Investigators have suggested multiple factors such as addiction stages of patients contributing to conflicting findings. We recently applied spatial independent component analysis (sICA) to several fMRI datasets and found extensive overlaps of functional networks (FNs) with opposite timecourses of task-related activities. Based on these findings, we predict: 1) that blood-oxygenation-level-dependent (BOLD) signal mixtures reflecting concurrent co-localized activation and deactivation (CCAD) of different neurons in the same voxels contribute to the opposite findings, while CCAD is determined by balanced excitation and inhibition and functional heterogeneity in the brain; 2) that due to the nature of signal mixtures,a reduced brain deactivation might be expressed as an increased BOLD signal and misinterpreted as a greater brain activation by studies using GLM-BA, which cannot differentiate mixed signals from same voxels; and 3) that sICA will overcome the limitation of GLM-BA and reveal consistent fMRI findings in patients, because sICA can separate signal mixtures from the same voxels into different FNs, and thus mitigate the confusion of reduced deactivation vs. increased activation. For testing our predictions and better understanding CD neuropathology, this project will use sICA to perform secondary analyses on fMRI data acquired from 419 participants, including 179 HCs and 196 CD patients. They performed fMRI tasks for assessing cognitive control and/or monetary reward/loss- motivation. Most patients were treated for CD and followed for 3 ~ 12 months after treatment. We hypothesize that sICA will consistently reveal reduced task-related modulations of FNs related to cognitive control and/or reward/loss-motivation in CD patients relative to HCs, increased (i.e., "recovery") modulations of these FNs in patients after effective treatment for CD, and positive correlations between greater modulations of these FNs and better long-term outcomes after treatment. Findings supporting our hypotheses will not only provide a consistent insight into CD neuropathology and reconcile extant conflicting data, but also demonstrate that task- related modulations in FNs related to cognitive control and/or reward/loss-motivation in CD patients as revealed by sICA are excellent candidates for reliable diagnostic and predictive biomarkers for optimizing and developing CD treatments. Furthermore, these findings will have a sustained, powerful impact on fMRI theories and practices in a general and broad sense and will help move the entire field forward.

 描述(由申请人提供)：本申请响应PAR-13-080-使用现有数据加快药物滥用研究的步伐。功能磁共振成像(FMRI)和传统的基于一般线性模型的分析(GLM-BA)已被用于评估可卡因依赖(CD)和其他神经精神障碍的神经相关性。然而，这些研究报告了不一致的发现，包括与健康对照组(HCS)相比，患者的脑活动减少和增加，并且无法提供CD神经病理的清晰图像，并为CD治疗定义可靠的生物标志物。调查人员提出了多种因素，如患者的成瘾阶段，导致了相互矛盾的发现。我们最近将空间独立分量分析(SICA)应用于几个fMRI数据集，发现功能网络(FN)与任务相关活动的相反时间来源存在广泛重叠。基于这些发现，我们预测：1)反映同一体素中不同神经元的同时共定位激活和失活(CCAD)的血氧水平依赖(BOLD)信号混合物有助于相反的发现，而CCAD是由大脑中平衡的兴奋和抑制以及功能异质性决定的；2)由于信号混合物的性质，大脑失活的减少可能表现为BOLD信号的增加，并被GLM-BA研究误解为更大的大脑激活，GLM-BA研究无法区分混合信号和相同的体素；3)SICA将克服GLM-BA的局限性，并在患者中显示一致的fMRI结果，因为SICA可以将来自相同体素的信号混合分离到不同的FN中，从而缓解了减少失活和增加激活的困惑。为了验证我们的预测并更好地了解CD神经病理学，本项目将使用SICA对419名参与者的fMRI数据进行二次分析，其中包括179名HCS患者和196名CD患者。他们执行fMRI任务，以评估认知控制和/或金钱奖励/损失动机。多数患者接受CD治疗，治疗后随访3~12个月。我们假设，SICA将持续揭示与认知控制和/或奖赏/丧失动机相关的任务相关的FN调节减少，CD患者在CD有效治疗后这些FN的调节增加(即“恢复”)，以及这些FN的更大调节与治疗后更好的长期结果之间的正相关关系。支持我们假设的结果不仅将为CD的神经病理学提供一致的见解并调和现有的相互矛盾的数据，而且还表明SICA揭示的与CD患者的认知控制和/或奖赏/丧失动机相关的FN中的任务相关调节是优化和开发CD治疗的可靠诊断和预测生物标志物的极佳候选。此外，这些发现将对一般和广泛意义上的功能磁共振成像理论和实践产生持续、强大的影响，并将有助于推动整个领域向前发展。