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Characterizing White Matter Tract Degeneration in Syndromic Variants of Alzheimer's Disease: A Diffusion Tensor Imaging Study.

Authors :
Madhavan A
Schwarz CG
Duffy JR
Strand EA
Machulda MM
Drubach DA
Kantarci K
Przybelski SA
Reid RI
Senjem ML
Gunter JL
Apostolova LG
Lowe VJ
Petersen RC
Jack CR
Josephs KA
Whitwell JL
Source :
Journal of Alzheimer's disease : JAD [J Alzheimers Dis] 2016; Vol. 49 (3), pp. 633-43.
Publication Year :
2016

Abstract

Background: Different clinical syndromes can arise from Alzheimer's disease (AD) neuropathology, including dementia of the Alzheimer's type (DAT), logopenic primary progressive aphasia (lvPPA), and posterior cortical atrophy (PCA).<br />Objective: To assess similarities and differences in patterns of white matter tract degeneration across these syndromic variants of AD.<br />Methods: Sixty-four subjects (22 DAT, 24 lvPPA, and 18 PCA) that had diffusion tensor imaging and showed amyloid-β deposition on PET were assessed in this case-control study. A whole-brain voxel-based analysis was performed to assess differences in fractional anisotropy, mean diffusivity, axial diffusivity, and radial diffusivity across groups.<br />Results: All three groups showed overlapping diffusion abnormalities in a network of tracts, including fornix, corpus callosum, posterior thalamic radiations, superior longitudinal fasciculus, inferior longitudinal fasciculus, inferior fronto-occipital fasciculus, and uncinate fasciculus. Subtle regional differences were also observed across groups, with DAT particularly associated with degeneration of fornix and cingulum, lvPPA with left inferior fronto-occipital fasciculus and uncinate fasciculus, and PCA with posterior thalamic radiations, superior longitudinal fasciculus, posterior cingulate, and splenium of the corpus callosum.<br />Conclusion: These findings show that while each AD phenotype is associated with degeneration of a specific structural network of white matter tracts, striking spatial overlap exists among the three network patterns that may be related to AD pathology.

Details

Language :
English
ISSN :
1875-8908
Volume :
49
Issue :
3
Database :
MEDLINE
Journal :
Journal of Alzheimer's disease : JAD
Publication Type :
Academic Journal
Accession number :
26484918
Full Text :
https://doi.org/10.3233/JAD-150502