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Publication : Brain microstructure abnormalities in the 3xTg-AD mouse - A diffusion MRI and morphology correlation study.

First Author  Falangola MF Year  2022
Journal  Magn Reson Imaging Volume  94
Pages  48-55 PubMed ID  36116712
Mgi Jnum  J:348654 Mgi Id  MGI:7642282
Doi  10.1016/j.mri.2022.09.002 Citation  Falangola MF, et al. (2022) Brain microstructure abnormalities in the 3xTg-AD mouse - A diffusion MRI and morphology correlation study. Magn Reson Imaging 94:48-55
abstractText  The widely studied triple transgenic (3xTg-AD) mouse provides a robust model of Alzheimer's disease (AD) with region dependent patterns of progressive amyloid-beta (Ass) and tau pathology. Using diffusion MRI (dMRI), we investigated the sensitivity of dMRI measures in capturing AD pathology associated microstructure alterations in older 3xTg-AD mice, and the degree to which dMRI changes correlate with measurements of Abeta and tau pathology. 3xTg-AD and normal control (NC) mice, 15 to 21 months of age, were used in this study. In vivo dMRI data were acquired for the generation of diffusion tensor (DT) and diffusional kurtosis (DK) measures within the hippocampus and fimbria (Fi). For these same brain regions, Abeta and tau pathology were quantified by morphological analysis of Ass1-42 and AT8 immunoreactivity. Two-tailed, two-sample t-tests were performed to assess group differences in each brain region of interest (ROI), with the Benjamini-Hochberg false discovery rate (FDR) method being applied to adjust for multiple comparisons. Spearman correlation coefficients were calculated to investigate associations between diffusion and morphological measures. Our results revealed, depending on the brain region, DT and DK measures were able to detect group differences. In the dorsal hippocampus (HD), fractional anisotropy (FA) was significantly higher in the 3xTg-AD mice compared with NC mice. In the subiculum (SUB), FA, axial diffusivity (D(||)) and radial kurtosis (K( upper left and right quadrants)) were significantly higher in 3xTg-AD mice compared with NC mice. Morphological quantification of Ass1-42 and AT8 immunoreactivity showed elevated Ass and tau in the Fi, ventral hippocampus (HV) and SUB of 3xTg-AD mice. The presence of Abeta and tau was significantly correlated with several DT and DK measures, particularly in the SUB, where an increase in tau correlated with an increase in mean kurtosis (MK) and K( upper left and right quadrants). This work demonstrates significant dMRI differences between older 3xTg-AD and NC mice in the hippocampus and Fi. Significant correlations were found between dMRI and morphological measures of Abeta and tau pathology. These results support the potential of dMRI-derived parameters as biomarkers of AD pathology. Since the imaging methods employed here are easily translatable to clinical MRI, our results are also relevant for human AD patients.
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