Neuroimaging of Epilepsy Laboratory, McConnell Brain Imaging Centre and Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Department of Psychology, Neuropsychology Unit, McGill University, Montreal, Quebec, Canada.
Brain. 2019 Mar 1;142(3):688-699. doi: 10.1093/brain/awz009.
Neuroimaging studies have consistently shown distributed brain anomalies in epilepsy syndromes associated with a focal structural lesion, particularly mesiotemporal sclerosis. Conversely, a system-level approach to focal cortical dysplasia has been rarely considered, likely due to methodological difficulties in addressing variable location and topography. Given the known heterogeneity in focal cortical dysplasia histopathology, we hypothesized that lesional connectivity consists of subtypes with distinct structural signatures. Furthermore, in light of mounting evidence for focal anomalies impacting whole-brain systems, we postulated that patterns of focal cortical dysplasia connectivity may exert differential downstream effects on global network topology. We studied a cohort of patients with histologically verified focal cortical dysplasia type II (n = 27), and age- and sex-matched healthy controls (n = 34). We subdivided each lesion into similarly sized parcels and computed their connectivity to large-scale canonical functional networks (or communities). We then dichotomized connectivity profiles of lesional parcels into those belonging to the same functional community as the focal cortical dysplasia (intra-community) and those adhering to other communities (inter-community). Applying hierarchical clustering to community-reconfigured connectome profiles identified three lesional classes with distinct patterns of functional connectivity: decreased intra- and inter-community connectivity, a selective decrease in intra-community connectivity, and increased intra- as well as inter-community connectivity. Hypo-connectivity classes were mainly composed of focal cortical dysplasia type IIB, while the hyperconnected lesions were type IIA. With respect to whole-brain networks, patients with hypoconnected focal cortical dysplasia and marked structural damage showed only mild imbalances, while those with hyperconnected subtle lesions had more pronounced topological alterations. Correcting for interictal epileptic discharges did not impact connectivity patterns. Multivariate structural equation analysis provided a mechanistic model of such complex, diverging interactions, whereby the focal cortical dysplasia structural makeup shapes its functional connectivity, which in turn modulates whole-brain network topology.
神经影像学研究一致表明,在与局灶性结构性病变相关的癫痫综合征中,存在分布式脑异常,特别是内侧颞叶硬化。相反,局灶性皮质发育不良的系统级方法很少被考虑,可能是由于在解决位置和拓扑结构多变性方面存在方法学困难。鉴于局灶性皮质发育不良的组织病理学存在明显的异质性,我们假设病变的连通性由具有不同结构特征的亚型组成。此外,鉴于越来越多的证据表明局灶性异常会影响全脑系统,我们假设局灶性皮质发育不良的连通模式可能会对全局网络拓扑结构产生不同的下游影响。我们研究了一组经组织学证实的 II 型局灶性皮质发育不良患者(n = 27)和年龄、性别匹配的健康对照组(n = 34)。我们将每个病变分为大小相似的区,并计算它们与大型规范功能网络(或社区)的连通性。然后,我们将病变区的连通性分布分为与局灶性皮质发育不良相同的功能社区(内社区)和其他社区(外社区)。应用层次聚类对社区重新配置的连接组图谱进行分析,确定了具有不同功能连通模式的三种病变类型:内社区和外社区的连通性均降低,内社区的连通性选择性降低,以及内社区和外社区的连通性均增加。低连通性类主要由 IIB 型局灶性皮质发育不良组成,而高连通性病变则由 IIA 型组成。就全脑网络而言,低连通性局灶性皮质发育不良和明显结构性损伤的患者仅表现出轻微的失衡,而高连通性细微病变的患者则表现出更明显的拓扑改变。纠正癫痫发作间期放电并不影响连通性模式。多变量结构方程分析提供了一种复杂、发散相互作用的机制模型,即局灶性皮质发育不良的结构性构成塑造了其功能连通性,进而调节全脑网络拓扑结构。