The study of multiple indices of diffusion, including axial (DA), radial (DR) and mean diffusion (MD), as well as fractional
anisotropy (FA), enables WM damage in Alzheimer’s disease (AD) to be assessed in detail. Here, tract-based spatial statistics
(TBSS) were performed on scans of 40 healthy elders, 19 non-amnestic MCI (MCIna) subjects, 14 amnestic MCI (MCIa)
subjects and 9 AD patients. Significantly higher DA was found in MCIna subjects compared to healthy elders in the right
posterior cingulum/precuneus. Significantly higher DA was also found in MCIa subjects compared to healthy elders in the
left prefrontal cortex, particularly in the forceps minor and uncinate fasciculus. In the MCIa versus MCIna comparison,
significantly higher DA was found in large areas of the left prefrontal cortex. For AD patients, the overlap of FA and DR
changes and the overlap of FA and MD changes were seen in temporal, parietal and frontal lobes, as well as the corpus
callosum and fornix. Analysis of differences between the AD versus MCIna, and AD versus MCIa contrasts, highlighted
regions that are increasingly compromised in more severe disease stages. Microstructural damage independent of gross
tissue loss was widespread in later disease stages. Our findings suggest a scheme where WM damage begins in the core
memory network of the temporal lobe, cingulum and prefrontal regions, and spreads beyond these regions in later stages.
DA and MD indices were most sensitive at detecting early changes in MCIa.
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