Patterns of Brain Atrophy in Clinical Variants of Frontotemporal Lobar Degeneration

被引:36
作者
Lu, Po H. [1 ]
Mendez, Mario F. [1 ,4 ]
Lee, Grace J. [1 ]
Leow, Alex D. [2 ,5 ,7 ,8 ]
Lee, Hyun-Woo [12 ]
Shapira, Jill [1 ]
Jimenez, Elvira [1 ,4 ]
Boeve, Bradley B. [9 ]
Caselli, Richard J. [10 ]
Graff-Radford, Neill R. [11 ]
Jack, Clifford R. [9 ]
Kramer, Joel H. [6 ]
Miller, Bruce L. [6 ]
Bartzokis, George [2 ,3 ]
Thompson, Paul M. [1 ,2 ]
Knopman, David S. [9 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Lab Neuroimaging, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
[4] Greater Los Angeles VA Healthcare Syst, Neurobehav Unit, Los Angeles, CA USA
[5] Community Psychiat Associates, Sacramento, CA USA
[6] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
[7] Univ Illinois, Dept Psychiat, Chicago, IL 60612 USA
[8] Univ Illinois, Dept Bioengn, Chicago, IL USA
[9] Mayo Clin, Dept Neurol, Rochester, MN USA
[10] Mayo Clin, Dept Neurol, Scottsdale, AZ USA
[11] Mayo Clin, Dept Neurol, Jacksonville, FL 32224 USA
[12] McGill Univ, Dept Phys, Montreal, PQ, Canada
关键词
Frontotemporal dementia; Primary progressive aphasia; Longitudinal study; Magnetic resonance imaging; Tensor-based morphometry; White matter; TENSOR-BASED MORPHOMETRY; PRIMARY-PROGRESSIVE-APHASIA; VOXEL-BASED MORPHOMETRY; WHITE-MATTER CHANGES; ALZHEIMERS-DISEASE; DIAGNOSTIC-CRITERIA; SEMANTIC DEMENTIA; DIFFUSION; MRI; PATHOLOGY;
D O I
10.1159/000345523
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background/Aims: The clinical syndromes of frontotemporal lobar degeneration include behavioral variant frontotemporal dementia (bvFTD) and semantic (SV-PPA) and nonfluent variants (NF-PPA) of primary progressive aphasia. Using magnetic resonance imaging (MRI), tensor-based morphometry (TBM) was used to determine distinct patterns of atrophy between these three clinical groups. Methods: Twenty-seven participants diagnosed with bvFTD, 16 with SV-PPA, and 19 with NF-PPA received baseline and follow-up MRI scans approximately 1 year apart. TBM was used to create three-dimensional Jacobian maps of local brain atrophy rates for individual subjects. Results: Regional analyses were performed on the three-dimensional maps and direct comparisons between groups (corrected for multiple comparisons using permutation tests) revealed significantly greater frontal lobe and frontal white matter atrophy in the bvFTD relative to the SV-PPA group (p < 0.005). The SV-PPA subjects exhibited significantly greater atrophy than the bvFTD in the fusiform gyrus (p = 0.007). The NF-PPA group showed significantly more atrophy in the parietal lobes relative to both bvFTD and SV-PPA groups (p < 0.05). Percent volume change in ventromedial prefrontal cortex was significantly associated with baseline behavioral symptomatology. Conclusion: The bvFTD, SV-PPA, and NF-PPA groups displayed distinct patterns of progressive atrophy over a 1-year period that correspond well to the behavioral disturbances characteristic of the clinical syndromes. More specifically, the bvFTD group showed significant white matter contraction and presence of behavioral symptoms at baseline predicted significant volume loss of the ventromedial prefrontal cortex. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:34 / 50
页数:17
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