Zhang Sheng, Hu Sien, Sinha Rajita, Potenza Marc N, Malison Robert T, Li Chiang-Shan R
Department of Psychiatry, Yale University, New Haven, CT 06519, USA; Connecticut Mental Health Center, New Haven, CT 06519, USA.
Department of Psychiatry, Yale University, New Haven, CT 06519, USA; Child Study Center, Yale University, New Haven, CT 06520, USA; Department of Neuroscience, Yale University, New Haven, CT 06520, USA; Interdepartmental Neuroscience Program, Yale University, New Haven, CT 06520, USA.
Neuroimage Clin. 2016 Aug 4;12:348-58. doi: 10.1016/j.nicl.2016.08.006. eCollection 2016.
Cocaine dependence is associated with deficits in cognitive control. Previous studies demonstrated that chronic cocaine use affects the activity and functional connectivity of the thalamus, a subcortical structure critical for cognitive functioning. However, the thalamus contains nuclei heterogeneous in functions, and it is not known how thalamic subregions contribute to cognitive dysfunctions in cocaine dependence. To address this issue, we used multivariate pattern analysis (MVPA) to examine how functional connectivity of the thalamus distinguishes 100 cocaine-dependent participants (CD) from 100 demographically matched healthy control individuals (HC). We characterized six task-related networks with independent component analysis of fMRI data of a stop signal task and employed MVPA to distinguish CD from HC on the basis of voxel-wise thalamic connectivity to the six independent components. In an unbiased model of distinct training and testing data, the analysis correctly classified 72% of subjects with leave-one-out cross-validation (p < 0.001), superior to comparison brain regions with similar voxel counts (p < 0.004, two-sample t test). Thalamic voxels that form the basis of classification aggregate in distinct subclusters, suggesting that connectivities of thalamic subnuclei distinguish CD from HC. Further, linear regressions provided suggestive evidence for a correlation of the thalamic connectivities with clinical variables and performance measures on the stop signal task. Together, these findings support thalamic circuit dysfunction in cognitive control as an important neural marker of cocaine dependence.
可卡因成瘾与认知控制缺陷有关。先前的研究表明,长期使用可卡因会影响丘脑的活动和功能连接,丘脑是对认知功能至关重要的皮层下结构。然而,丘脑包含功能各异的核团,目前尚不清楚丘脑亚区域如何导致可卡因成瘾中的认知功能障碍。为了解决这个问题,我们使用多变量模式分析(MVPA)来研究丘脑的功能连接如何区分100名可卡因成瘾参与者(CD)和100名人口统计学匹配的健康对照个体(HC)。我们通过对停止信号任务的功能磁共振成像数据进行独立成分分析,对六个与任务相关的网络进行了特征描述,并使用MVPA根据丘脑与六个独立成分的体素连接性来区分CD和HC。在一个无偏的不同训练和测试数据模型中,该分析在留一法交叉验证中正确分类了72%的受试者(p < 0.001),优于具有相似体素数量的比较脑区(p < 0.004,双样本t检验)。构成分类基础的丘脑体素聚集在不同的子簇中,这表明丘脑亚核的连接性可区分CD和HC。此外,线性回归为丘脑连接性与停止信号任务的临床变量和表现指标之间的相关性提供了提示性证据。总之,这些发现支持丘脑回路在认知控制中的功能障碍是可卡因成瘾的一个重要神经标志物。