Neuroimaging of Epilepsy Laboratory, Department of Neurology and McConnell Brain Imaging Centre, Montreal Neurological Institute and Hospital, McGill University, Montreal, Quebec, Canada.
Brain. 2017 Aug 1;140(8):2133-2143. doi: 10.1093/brain/awx145.
Neuroimaging studies of malformations of cortical development have mainly focused on the characterization of the primary lesional substrate, while whole-brain investigations remain scarce. Our purpose was to assess large-scale brain organization in prevalent cortical malformations. Based on experimental evidence suggesting that distributed effects of focal insults are modulated by stages of brain development, we postulated differential patterns of network anomalies across subtypes of malformations. We studied a cohort of patients with focal cortical dysplasia type II (n = 63), subcortical nodular heterotopia (n = 44), and polymicrogyria (n = 34), and compared them to 82 age- and sex-matched controls. Graph theoretical analysis of structural covariance networks indicated a consistent rearrangement towards a regularized architecture characterized by increased path length and clustering, as well as disrupted rich-club topology, overall suggestive of inefficient global and excessive local connectivity. Notably, we observed a gradual shift in network reconfigurations across subgroups, with only subtle changes in focal cortical dysplasia type II, moderate effects in heterotopia and maximal effects in polymicrogyria. Analysis of resting state functional connectivity also revealed gradual network changes, with most marked rearrangement in polymicrogyria; contrary to findings in the structural domain, however, functional architecture was characterized by decreases in both local and global parameters. Diverging results in the structural and functional domain were supported by formal structure-function coupling analysis. Our findings support the concept that time of insult during corticogenesis impacts the severity of topological network reconfiguration. Specifically, late-stage malformations, typified by polymicrogyria, may selectively disrupt the formation of large-scale cortico-cortical networks and thus lead to a more profound impact on whole-brain organization than early stage disturbances of predominantly radial migration patterns observed in cortical dysplasia type II, which likely affect a relatively confined cortical territory.
神经影像学研究皮质发育畸形主要集中在原发性病变基质的特征描述上,而全脑研究仍然很少。我们的目的是评估常见皮质畸形的大脑整体组织。基于实验证据表明,局灶性损伤的弥散效应受大脑发育阶段的调节,我们假设在畸形的亚型之间存在网络异常的差异模式。我们研究了一组局灶性皮质发育不良 II 型(n = 63)、皮质下结节性异位(n = 44)和多微小脑回畸形(n = 34)患者,并将其与 82 名年龄和性别匹配的对照组进行比较。结构协方差网络的图论分析表明,存在向正则化结构的一致重排,其特征为路径长度和聚类增加,以及富区拓扑破坏,总体上提示全局连接效率低下和局部连接过度。值得注意的是,我们观察到网络重排在亚组之间逐渐变化,局灶性皮质发育不良 II 型变化轻微,异位症影响中等,多微小脑回畸形影响最大。静息状态功能连接分析也揭示了网络的逐渐变化,多微小脑回畸形的变化最为明显;然而,与结构域的发现相反,功能结构的特征是局部和全局参数都减少。结构和功能域的发散结果得到了正式的结构-功能耦合分析的支持。我们的研究结果支持这样一种概念,即在皮质发生过程中损伤的时间会影响拓扑网络重排的严重程度。具体而言,晚期畸形,以多微小脑回畸形为代表,可能会选择性地破坏大尺度皮质-皮质网络的形成,从而对全脑组织产生比皮质发育不良 II 型中观察到的主要为放射状迁移模式的早期干扰更深远的影响,后者可能影响相对受限的皮质区域。