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Postmortem MRI and histology demonstrate differential iron accumulation and cortical myelin organization in early- and late-onset Alzheimer's disease.
- Source :
-
Neurobiology of aging [Neurobiol Aging] 2018 Feb; Vol. 62, pp. 231-242. Date of Electronic Publication: 2017 Oct 28. - Publication Year :
- 2018
-
Abstract
- Previous MRI studies reported cortical iron accumulation in early-onset (EOAD) compared to late-onset (LOAD) Alzheimer disease patients. However, the pattern and origin of iron accumulation is poorly understood. This study investigated the histopathological correlates of MRI contrast in both EOAD and LOAD. T2*-weighted MRI was performed on postmortem frontal cortex of controls, EOAD, and LOAD. Images were ordinally scored using predefined criteria followed by histology. Nonlinear histology-MRI registration was used to calculate pixel-wise spatial correlations based on the signal intensity. EOAD and LOAD were distinguishable based on 7T MRI from controls and from each other. Histology-MRI correlation analysis of the pixel intensities showed that the MRI contrast is best explained by increased iron accumulation and changes in cortical myelin, whereas amyloid and tau showed less spatial correspondence with T2*-weighted MRI. Neuropathologically, subtypes of Alzheimer's disease showed different patterns of iron accumulation and cortical myelin changes independent of amyloid and tau that may be detected by high-field susceptibility-based MRI.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Adult
Aged
Aged, 80 and over
Amyloid beta-Peptides metabolism
Autopsy
Disease Susceptibility
Female
Humans
Male
Middle Aged
tau Proteins metabolism
Alzheimer Disease diagnostic imaging
Alzheimer Disease pathology
Cerebral Cortex metabolism
Cerebral Cortex pathology
Diffusion Magnetic Resonance Imaging
Iron metabolism
Myelin Sheath metabolism
Myelin Sheath pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1558-1497
- Volume :
- 62
- Database :
- MEDLINE
- Journal :
- Neurobiology of aging
- Publication Type :
- Academic Journal
- Accession number :
- 29195086
- Full Text :
- https://doi.org/10.1016/j.neurobiolaging.2017.10.017