https://www.sciencedirect.com/science/article/pii/S019745801830188X
Highlights
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- Postmortem MRI transverse relaxation (R2) is associated with the linear rate of global cognitive decline in late life and accounts for more than 5% of its variance.
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- The association of R2 with cognitive decline persists after accounting for indices of cerebral vessel disease, namely atherosclerosis, arteriolosclerosis, and cerebral amyloid angiopathy.
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- R2 is also associated with specific components of a nonlinear model of cognitive decline.
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- R2 reflects a dimension of brain tissue integrity not captured by current histopathologic indices and therefore may highlight important targets for future interventions against late life cognitive decline.
ABSTRACT
The
purpose of this study was to determine whether metrics of brain tissue
integrity derived from postmortem MRI are associated with late life
cognitive decline, independent of cerebral vessel disease. Using data
from 554 older adults, we employed voxelwise regression to identify
regions where the postmortem MRI transverse relaxation rate constant R2
was associated with the rate of decline in global cognition. We then
used linear mixed models to investigate the association between a
composite R2 measure and cognitive decline, controlling for
neuropathology including three indices of vessel disease:
atherosclerosis, arteriolosclerosis, and cerebral amyloid angiopathy.
This composite R2 measure was associated with the rate of decline (0.049 unit annually per R2
unit, p<0.0001) and accounted for 6.1% of its variance, beyond
contributions from vessel disease indices and other prominent
age-related neuropathologies. Thus, postmortem brain R2
reflects disease processes underlying cognitive decline that are not
captured by vessel disease indices or other standard neuropathologic
indices and may provide a measure of brain tissue integrity that is
complementary to histopathologic evaluation.
Keywords
- Transverse relaxation;
- R2;
- voxelwise;
- atherosclerosis;
- arteriolosclerosis;
- cerebral amyloid angiopathy
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