Distinct white matter alterations following severe stroke Longitudinal DTI study in neglect

被引:44
|
作者
Umarova, Roza M. [1 ,2 ,3 ,4 ]
Beume, Lena [1 ,2 ,3 ]
Reisert, Marco [5 ]
Kaller, Christoph P. [1 ,2 ,3 ]
Kloeppel, Stefan [2 ,3 ,4 ,7 ]
Mader, Irina [2 ,6 ]
Glauche, Volkmar [1 ,2 ]
Kiselev, Valerij G. [5 ]
Catani, Marco [8 ]
Weiller, Cornelius [1 ,2 ,3 ]
机构
[1] Univ Freiburg, Fac Med, Med Ctr, Dept Neurol, Freiburg, Germany
[2] Univ Freiburg, Fac Med, Med Ctr, Freiburg Brain Imaging, Freiburg, Germany
[3] Univ Freiburg, Fac Med, Med Ctr, BrainLinks BrainTools Cluster Excellence, Freiburg, Germany
[4] Univ Freiburg, Fac Med, Med Ctr, Dept Psychiat & Psychotherapy, Freiburg, Germany
[5] Univ Freiburg, Fac Med, Med Ctr, Dept Radiol,Med Phys, Freiburg, Germany
[6] Univ Freiburg, Fac Med, Med Ctr, Dept Neuroradiol, Freiburg, Germany
[7] Univ Bern, Univ Hosp Old Age Psychiat, Bern, Switzerland
[8] Kings Coll London, Inst Psychiat, NatBrainLab, London, England
关键词
WALLERIAN DEGENERATION; STRUCTURAL CONNECTIVITY; HEMISPATIAL NEGLECT; RADIAL DIFFUSIVITY; WATER DIFFUSION; SPATIAL NEGLECT; VISUAL NEGLECT; RECOVERY; DEMYELINATION; NEUROANATOMY;
D O I
10.1212/WNL.0000000000003843
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To distinguish white matter remodeling directly induced by stroke lesion from that evoked by remote network dysfunction, using spatial neglect as a model. Methods: 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. Results: 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. Conclusions: 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.
引用
收藏
页码:1546 / 1555
页数:10
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