Whole-brain white matter disruption in semantic and nonfluent variants of primary progressive aphasia

被引:55
作者
Schwindt, Graeme C. [1 ,2 ,3 ]
Graham, Naida L. [4 ,5 ]
Rochon, Elizabeth [4 ,5 ]
Tang-Wai, David F. [6 ,7 ]
Lobaugh, Nancy J. [2 ,3 ]
Chow, Tiffany W. [6 ,8 ,9 ]
Black, Sandra E. [1 ,2 ,3 ,5 ,6 ,8 ]
机构
[1] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
[2] Sunnybrook Hlth Sci Ctr, LC Campbell Cognit Neurol Res Unit, Toronto, ON M4N 3M5, Canada
[3] Sunnybrook Res Inst, Brain Sci Res Program, Toronto, ON, Canada
[4] Univ Toronto, Dept Speech Language Pathol, Toronto, ON, Canada
[5] Toronto Rehabil Inst, Toronto, ON, Canada
[6] Univ Toronto, Dept Med Neurol, Toronto, ON, Canada
[7] Toronto Western Hosp, Univ Hlth Network, Div Neurol, Toronto, ON M5T 2S8, Canada
[8] Rotman Res Inst, Toronto, ON, Canada
[9] Univ Toronto, Dept Psychiat Geriatr Psychiat, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
primary progressive aphasia; semantic dementia; nonfluent progressive aphasia; white matter; diffusion tensor imaging; FRONTOTEMPORAL LOBAR DEGENERATION; DIFFUSION; DEMENTIA; SEGMENTATION; ATROPHY; MRI; HYPOMETABOLISM; ABNORMALITIES; PATHOLOGY; CONSENSUS;
D O I
10.1002/hbm.21484
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Semantic (svPPA) and nonfluent (nfPPA) variants of primary progressive aphasia are associated with distinct patterns of cortical atrophy and underlying pathology. Little is known, however, about their contrasting spread of white matter disruption and how this relates to grey matter (GM) loss. We undertook a structural MRI study to investigate this relationship. We used diffusion tensor imaging, tract-based spatial statistics, and voxel-based morphometry to examine fractional anisotropy (FA) and directional diffusivities in nine patients with svPPA and nine patients with nfPPA, and compared them to 16 matched controls after accounting for global GM atrophy. Significant differences in topography of white matter changes were found, with more ventral involvement in svPPA patients and more widespread frontal involvement in nfPPA individuals. However, each group had both ventral and dorsal tract changes, and both showed spread of diffusion abnormalities beyond sites of local atrophy. There was a clear dissociation in sensitivity of diffusion tensor imaging measures between groups. SvPPA patients showed widespread changes in FA and radial diffusivity, whereas changes in axial diffusivity were more restricted and proximal to sites of GM atrophy. NfPPA patients showed isolated changes in FA, but widespread axial and radial diffusivity changes. These findings reveal the extent of white matter disruption in these variants of PPA after accounting for GM loss. Further, they suggest that differences in the relative sensitivity of diffusion metrics may reflect differences in the nature of underlying white matter pathology in these two subtypes. Hum Brain Mapp, 2013. (c) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:973 / 984
页数:12
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