Voxel-Based Analysis of Amyloid-Burden Measured with [11C]PiB PET in a Double Transgenic Mouse Model of Alzheimer’s Disease
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The purpose of this study is to validate the feasibility of a voxel-based analysis of in vivo amyloid-β positron emission tomography (PET) imaging studies in transgenic mouse models of Alzheimer’s disease.
We performed [11C]PiB PET imaging in 20 APP/PS1 mice and 16 age-matched controls, and histologically determined the individual amyloid-β plaque load. Using SPM software, we performed a voxel-based group comparison plus a regression analysis between PiB retention and actual plaque load, both thresholded at pFWE < 0.05. In addition, we carried out an individual ROI analysis in every animal.
The automated voxel-based group comparison allowed us to identify voxels with significantly increased PiB retention in the cortical and hippocampal regions in transgenic animals compared to controls. The voxel-based regression analysis revealed a significant association between this signal increase and the actual cerebral plaque load. The validity of these results was corroborated by the individual ROI-based analysis.
Voxel-based analysis of in vivo amyloid-β PET imaging studies in mouse models of Alzheimer’s disease is feasible and allows studying the PiB retention patterns in whole brain maps. Furthermore, the selected approach in our study also allowed us to establish a quantitative relation between tracer retention and actual plaque pathology in the brain in a voxel-wise manner.
Key wordsAlzheimer’s disease Double transgenic Mouse model Positron emission tomography Pittsburgh compound B Magnetic resonance imaging Voxel-based Statistical parametric mapping Amyloid precursor protein Presenilin 1
Positron emission tomography
Pittsburgh compound B, [11C]-6-OH-BTA-1
Region of interest
Statistical parametric mapping
Magnetic resonance imaging
Amyloid precursor protein
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