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The atrophy pattern in Alzheimer-related PPA is more widespread than that of the frontotemporal lobar degeneration associated variants.
- Source :
-
NeuroImage. Clinical [Neuroimage Clin] 2019; Vol. 24, pp. 101994. Date of Electronic Publication: 2019 Aug 25. - Publication Year :
- 2019
-
Abstract
- Objective: The three recognized variants of primary progressive aphasia (PPA) are associated with different loci of degeneration-left posterior perisylvian in logopenic variant (lvPPA), left frontal operculum in non-fluent variant (nfvPPA), and left rostroventral-temporal in semantic variant (svPPA). Meanwhile, it has become apparent that patients with lvPPA, in which Alzheimer pathology is the norm, frequently have more extensive language deficits-namely semantic and grammatical problems-than is captured in the strict diagnostic recommendations for this variant. We hypothesized that this may be because the degeneration in AD-related PPA typically extends beyond the left posterior perisylvian region.<br />Methods: Magnetic resonance images from 25 PPA patients (9AD-related PPA, 10 svPPA, 6 nfvPPA) and a healthy control cohort were used to calculate cortical thickness in three regions of interest (ROIs). The three ROIs being the left-hemispheric loci of maximal reported degeneration for each of the three variants of PPA.<br />Results: Consistent with past studies, the most severe cortical thinning was in the posterior perisylvian ROI in AD-related PPA; the ventral temporal ROI in svPPA; and the frontal opercular ROI in nfvPPA. Significant cortical thinning in AD-related PPA, however, was evident in all three ROIs. In contrast, thinning in svPPA and nfvPPA was largely restricted to their known peak loci of degeneration.<br />Conclusions: Although cortical degeneration in AD-related PPA is maximal in the left posterior perisylvian region, it extends more diffusely throughout the left hemisphere language network offering a plausible explanation for why the linguistic profile of lvPPA so often includes additional semantic and grammatic deficits.<br /> (Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Aged
Alzheimer Disease complications
Alzheimer Disease diagnostic imaging
Aphasia, Primary Progressive diagnostic imaging
Aphasia, Primary Progressive etiology
Atrophy pathology
Cerebral Cortex diagnostic imaging
Cohort Studies
Female
Frontotemporal Lobar Degeneration complications
Frontotemporal Lobar Degeneration diagnostic imaging
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Alzheimer Disease pathology
Aphasia, Primary Progressive pathology
Cerebral Cortex pathology
Frontotemporal Lobar Degeneration pathology
Subjects
Details
- Language :
- English
- ISSN :
- 2213-1582
- Volume :
- 24
- Database :
- MEDLINE
- Journal :
- NeuroImage. Clinical
- Publication Type :
- Academic Journal
- Accession number :
- 31505368
- Full Text :
- https://doi.org/10.1016/j.nicl.2019.101994