Open AccessMRI and flortaucipir relationships in Alzheimer's phenotypes are heterogeneous
Author(s) -
Josephs Keith A.,
Tosakulwong Nirubol,
GraffRadford Jonathan,
Weigand Stephen D.,
Buciuc Marina,
Machulda Mary M.,
Jones David T.,
Schwarz Christopher G.,
Senjem Matthew L.,
ErtekinTaner Nilufer,
Kantarci Kejal,
Boeve Bradley F.,
Knopman David S.,
Jack Clifford R.,
Petersen Ronald C.,
Lowe Val J.,
Whitwell Jennifer L.
Publication year - 2020
Publication title -
annals of clinical and translational neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.824
H-Index - 42
ISSN - 2328-9503
DOI - 10.1002/acn3.51038
Subject(s) - neocortex , entorhinal cortex , phenotype , hippocampal formation , medicine , pathology , grey matter , voxel , hippocampus , alzheimer's disease , atrophy , concordance , voxel based morphometry , brain size , neuroscience , magnetic resonance imaging , white matter , disease , psychology , biology , radiology , genetics , psychiatry , gene
Abstract Objective To assess the relationships between MRI volumetry and [ 18 F]flortaucipir PET of typical and atypical clinical phenotypes of Alzheimer’s disease, by genarian (age by decade). Methods Five‐hundred and sixty‐four participants including those with typical ( n = 86) or atypical ( n = 80) Alzheimer’s dementia and normal controls ( n = 398) underwent apolipoprotein E genotyping, MRI, flortaucipir, and 11 C‐PiB; all 166 Alzheimer’s participants were beta‐amyloid positive and all controls were beta‐amyloid negative. Grey matter volume and flortaucipir standard uptake value ratios were calculated for hippocampus, entorhinal cortex, and neocortex. Ratios of hippocampal‐to‐neocortical and entorhinal‐to‐neocortical volume and flortaucipir uptake were also calculated. Linear regression models assessed relationships among regional volume, flortaucipir uptake, and ratios and phenotypes, within three genarians (50–59, 60–69, and 70+). Voxel‐level analyses were also performed. Results For 50–59 greater medial temporal atrophy and flortaucipir uptake was observed in the typical compared with atypical phenotype. The typical phenotype also showed greater frontal neocortex uptake with the voxel‐level analysis. For 60–69 and 70+ there was greater hippocampal volume loss in the typical compared with atypical phenotype while only the 60–69, but not the 70+ group, showed a difference in hippocampal flortaucipir uptake. We also observed a pattern for higher neocortical flortaucipir uptake to correlate with younger age decade for both phenotypes. Interpretation MRI volumetry versus flortaucipir PET relationships differ across Alzheimer’s clinical phenotypes, and also within phenotype across age decades. This suggests that there is potential risk of masked effects by not accounting for genarian in participants with beta‐amyloid and tau‐positive biomarker defined Alzheimer’s disease.