Umarova Roza M, Beume Lena, Reisert Marco, Kaller Christoph P, Klöppel Stefan, Mader Irina, Glauche Volkmar, Kiselev Valerij G, Catani Marco, Weiller Cornelius
From the Department of Neurology (R.M.U., L.B., C.P.K., V.G., C.W.), Freiburg Brain Imaging (R.M.U., L.B., C.P.K., S.K., I.M., V.G., C.W.), BrainLinks-BrainTools Cluster of Excellence (R.M.U., L.B., C.P.K., S.K., C.W.), Department of Psychiatry and Psychotherapy (R.M.U., S.K.), Medical Physics, Department of Radiology (M.R., V.G.K.), and Department of Neuroradiology (I.M.), Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Germany; University Hospital of Old Age Psychiatry (S.K.), University of Bern, Switzerland; and NatBrainLab (M.C.), Institute of Psychiatry, King's College London, UK.
Neurology. 2017 Apr 18;88(16):1546-1555. doi: 10.1212/WNL.0000000000003843. Epub 2017 Mar 22.
To distinguish white matter remodeling directly induced by stroke lesion from that evoked by remote network dysfunction, using spatial neglect as a model.
We examined 24 visual neglect/extinction patients and 17 control patients combining comprehensive analyses of diffusion tensor metrics and global fiber tracking with neuropsychological testing in the acute (6.3 ± 0.5 days poststroke) and chronic (134 ± 7 days poststroke) stroke phases.
Compared to stroke controls, patients with spatial neglect/extinction displayed longitudinal white matter alterations with 2 defining signatures: (1) perilesional degenerative changes characterized by congruently reduced fractional anisotropy and increased radial diffusivity (RD), axial diffusivity, and mean diffusivity, all suggestive of direct axonal damage by lesion and therefore nonspecific for impaired attention network and (2) transneuronal changes characterized by an increased RD in contralesional frontoparietal and bilateral occipital connections, suggestive of primary periaxonal involvement; these changes were distinctly related to the degree of unrecovered neglect symptoms in chronic stroke, hence emerging as network-specific alterations.
The present data show how stroke entails global alterations of lesion-spared network architecture over time. Sufficiently large lesions of widely interconnected association cortex induce distinct, large-scale structural reorganization in domain-specific network connections. Besides their relevance to unrecovered domain-specific symptoms, these effects might also explain mechanisms of domain-general deficits in stroke patients, pointing to potential targets for therapeutic intervention.
以空间忽视作为模型,区分由中风病灶直接引起的白质重塑与由远程网络功能障碍引起的白质重塑。
我们对24名视觉忽视/消退患者和17名对照患者进行了检查,在中风急性期(中风后6.3±0.5天)和慢性期(中风后134±7天),将扩散张量指标和全局纤维追踪的综合分析与神经心理学测试相结合。
与中风对照组相比,空间忽视/消退患者表现出纵向白质改变,有两个特征性表现:(1)病灶周围退行性改变,其特征为各向异性分数一致性降低,径向扩散率(RD)、轴向扩散率和平均扩散率增加,所有这些都提示病变直接导致轴突损伤,因此对注意力网络受损不具有特异性;(2)跨神经元改变,其特征为对侧额顶叶和双侧枕叶连接的RD增加,表示原发性轴突周围受累;这些改变与慢性中风中未恢复的忽视症状程度明显相关,因此表现为网络特异性改变。
目前的数据表明中风如何随着时间推移导致未受损伤的网络结构发生整体改变。广泛相互连接的联合皮质的足够大的病灶会在特定领域的网络连接中引起明显的大规模结构重组。除了与未恢复的特定领域症状相关外,这些影响还可能解释中风患者的一般领域缺陷机制,指出治疗干预的潜在靶点。