| Literature DB >> 18979777 |
Jurgen Fripp1, Pierrick Bourgeat, Parnesh Raniga, Oscar Acosta, Victor Villemagne, Gareth Jones, Graeme O'keefe, Christopher Rowe, Sébastien Ourselin, Olivier Salvado.
Abstract
Beta-amyloid (Abeta) plaques are one of the neuropathological hallmarks of Alzheimer's disease (AD) and can be quantified using the marker 11C PiB. As l1C PiB PET images have limited anatomical information, an Magnetic Resonance Image (MRI) is usually acquired to perform the spatial normalization needed for population analysis. We designed and evaluated a high dimensional spatial normalization approach that only uses the 11C PiB PET image. The non-rigid registration (NRR) is based on free form deformation (FFD) modelled using B-splines. To compensate for the limited anatomical information, the FFD is constrained to an allowable transform space using a model trained from MR registrations. Abeta deposition is dependent on disease staging, so a spatially normalized 11C PiB PET appearance model selects and refines the atlas. The approach was compared with MR NRR using data from healthy elderly, mild cognitive impaired and Alzheimer disease participants. Using segmentation propagation, an average Dice similarity coefficient of 0.64 and 0.73 was obtained for white and gray matter. The R-squared correlation between the uptake obtained in the frontal, parietal, occipital and temporal was 0.789, 0.843, 0.871 and 0.964. These are very promising results, considering the low resolution of 11C PiB PET images.Entities:
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Year: 2008 PMID: 18979777 DOI: 10.1007/978-3-540-85988-8_53
Source DB: PubMed Journal: Med Image Comput Comput Assist Interv