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Please use this identifier to cite or link to this item: http://apo.ansto.gov.au/dspace/handle/10238/9030

Title: Simulation-based optimisation of the PET data processing for partial saturation approach protocols
Authors: Wimberley, C
Angelis, G
Boisson, F
Callaghan, PD
Fischer, K
Pichler, BJ
Meikle, SR
Grégoire, MC
Reilhac, A
Keywords: Positron computed tomography
Kinetics
Simulation
Monte Carlo method
Data processing
Saturation
Dopamine
Receptors
Issue Date: 15-Aug-2014
Publisher: Elsevier B.V.
Citation: Wimberley, C., Angelis, G., Boisson, F., Callaghan, P., Fischer, K., Pichler, B. J.,Meikle, S. R, Grégoire, M. C. & Reilhac, A. (2014). Simulation-based optimisation of the PET data processing for partial saturation approach protocols. NeuroImage, 97, 29-40. doi:https://doi.org/10.1016/j.neuroimage.2014.04.010
Abstract: Positron emission tomography (PET) with [11C]Raclopride is an important tool for studying dopamine D2 receptor expression in vivo. [11C]Raclopride PET binding experiments conducted using the Partial Saturation Approach (PSA) allow the estimation of receptor density (Bavail) and the in vivo affinity appKD. The PSA is a simple, single injection, single scan experimental protocol that does not require blood sampling, making it ideal for use in longitudinal studies. In this work, we generated a complete Monte Carlo simulated PET study involving two groups of scans, in between which a biological phenomenon was inferred (a 30% decrease of Bavail), and used it in order to design an optimal data processing chain for the parameter estimation from PSA data. The impact of spatial smoothing, noise removal and image resolution recovery technique on the statistical detection was investigated in depth. We found that image resolution recovery using iterative deconvolution of the image with the system point spread function associated with temporal data denoising greatly improves the accuracy and the statistical reliability of detecting the imposed phenomenon. Before optimisation, the inferred Bavail variation between the two groups was underestimated by 42% and detected in 66% of cases, while a false decrease of appKD by 13% was detected in more than 11% of cases. After optimisation, the calculated Bavail variation was underestimated by only 3.7% and detected in 89% of cases, while a false slight increase of appKD by 3.7% was detected in only 2% of cases. We found during this investigation that it was essential to adjust a factor that accounts for difference in magnitude between the non-displaceable ligand concentrations measured in the target and in the reference regions, for different data processing pathways as this ratio was affected by different image resolutions. © 2014 Elsevier B.V..
URI: https://doi.org/10.1016/j.neuroimage.2014.04.010
http://apo.ansto.gov.au/dspace/handle/10238/9030
ISSN: 1053-8119
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