Longitudinal rates of atrophy and tau accumulation differ between the visual and language variants of atypical Alzheimer's disease

Author:

Sintini Irene1,Graff‐Radford Jonathan2,Schwarz Christopher G.1,Machulda Mary M.3,Singh Neha Atulkumar2,Carlos Arenn F.2,Senjem Matthew L.14,Jr Clifford R. Jack1,Lowe Val J.1,Josephs Keith A.2,Whitwell Jennifer L.1

Affiliation:

1. Department of Radiology Mayo Clinic Rochester Minnesota USA

2. Department of Neurology Mayo Clinic Rochester Minnesota USA

3. Department of Psychiatry and Psychology Mayo Clinic Rochester Minnesota USA

4. Department of Information Technology Mayo Clinic Rochester Minnesota USA

Abstract

AbstractINTRODUCTIONAtypical variants of Alzheimer's disease (AD) include the visual variant, known as posterior cortical atrophy (PCA), and the language variant, known as logopenic progressive aphasia (LPA). Clinically, rates of disease progression differ between them.METHODSWe evaluated 34 PCA and 29 LPA participants. Structural magnetic resonance imaging and 18F‐flortaucipir positron emission tomography were performed at baseline and at 1‐year follow‐up. Rates of change in tau uptake and grey matter volumes were compared between PCA and LPA with linear mixed‐effects models and voxel‐based analyses.RESULTSPCA had faster rates of occipital atrophy. LPA had faster rates of left temporal atrophy and faster rates of tau accumulation in the parietal, right temporal, and occipital lobes. Age was negatively associated with rates of atrophy and tau accumulation.DISCUSSIONLongitudinal patterns of neuroimaging abnormalities differed between PCA and LPA, although with divergent results for tau accumulation and atrophy.HIGHLIGHTS The language variant of Alzheimer's disease accumulates tau faster than the visual variant. Each variant shows faster rates of atrophy than the other in its signature regions. Age negatively influences rates of atrophy and tau accumulation in both variants.

Funder

National Institutes of Health

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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