Department of Psychiatry and Behavioral Neuroscience, Wayne State University School of Medicine, Detroit, Michigan, USA.
Center for Complex Systems and Brain Sciences, Florida Atlantic University, Boca Raton, Florida, USA.
Hum Brain Mapp. 2020 Sep;41(13):3594-3607. doi: 10.1002/hbm.25032. Epub 2020 May 21.
Directional network interactions underpin normative brain function in key domains including associative learning. Schizophrenia (SCZ) is characterized by altered learning dynamics, yet dysfunctional directional functional connectivity (dFC) evoked during learning is rarely assessed. Here, nonlinear learning dynamics were induced using a paradigm alternating between conditions (Encoding and Retrieval). Evoked fMRI time series data were modeled using multivariate autoregressive (MVAR) models, to discover dysfunctional direction interactions between brain network constituents during learning stages (Early vs. Late), and conditions. A functionally derived subnetwork of coactivated (healthy controls [HC] ∩ SCZ] nodes was identified. MVAR models quantified directional interactions between pairs of nodes, and coefficients were evaluated for intergroup differences (HC ≠ SCZ). In exploratory analyses, we quantified statistical effects of neuroleptic dosage on performance and MVAR measures. During Early Encoding, SCZ showed reduced dFC within a frontal-hippocampal-fusiform network, though during Late Encoding reduced dFC was associated with pathways toward the dorsolateral prefrontal cortex (dlPFC). During Early Retrieval, SCZ showed increased dFC in pathways to and from the dorsal anterior cingulate cortex, though during Late Retrieval, patients showed increased dFC in pathways toward the dlPFC, but decreased dFC in pathways from the dlPFC. These discoveries constitute novel extensions of our understanding of task-evoked dysconnection in schizophrenia and motivate understanding of the directional aspect of the dysconnection in schizophrenia. Disordered directionality should be investigated using computational psychiatric approaches that complement the MVAR method used in our work.
方向网络相互作用是包括联想学习在内的关键领域中规范大脑功能的基础。精神分裂症(SCZ)的特征是学习动力学改变,但很少评估学习过程中功能失调的定向功能连接(dFC)。在这里,使用交替条件(编码和检索)的范式诱导非线性学习动力学。使用多变量自回归(MVAR)模型对诱发 fMRI 时序列数据进行建模,以发现学习阶段(早期与晚期)和条件下大脑网络成分之间功能失调的方向相互作用。确定了一个共同激活的功能衍生子网(健康对照组 [HC]∩SCZ]节点)。MVAR 模型量化了节点对之间的定向相互作用,并评估了组间差异(HC≠SCZ)的系数。在探索性分析中,我们量化了神经递质剂量对性能和 MVAR 测量的影响。在早期编码过程中,SCZ 显示出额-海马-梭状回网络内的 dFC 减少,但在晚期编码过程中,dFC 减少与通向背外侧前额叶皮层(dlPFC)的途径有关。在早期检索过程中,SCZ 显示出通向和来自背侧前扣带皮层的 dFC 增加,但在晚期检索过程中,患者显示出通向 dlPFC 的 dFC 增加,而来自 dlPFC 的 dFC 减少。这些发现构成了我们对精神分裂症中任务诱发的去连接理解的新扩展,并促使我们理解精神分裂症中去连接的方向性方面。使用补充我们工作中使用的 MVAR 方法的计算精神病学方法,应该研究紊乱的方向性。