Speaker
Dr
Claude Comtat
(Frédéric Joliot Hospital Facility, CEA/DSV/DRM, Orsay, France)
Description
High resolution PET imaging is now a well established technique not only for small
animal, but also for human brain studies. The ECAT HRRT brain PET scanner (Siemens
Molecular Imaging) is characterized by an effective isotropic spatial resolution of
2.5 mm, about a factor of 2 better than for state-of-the-art whole-body clinical PET
scanners. Although the absolute sensitivity of the HRRT (6.5 %) for a point source in
the center of the field-of-view is increased relative to whole-body scanners
(typically 4.5 %) thanks to a larger co-polar aperture, the sensitivity in terms of
volumetric resolution (75 µm3 at best for whole-body scanners and 16 µm3 for the
HRRT) is much lower. This constraint has an impact on the performance of image
reconstruction techniques, in particular for dynamic studies. Standard reconstruction
methods used with clinical whole-body PET scanners are not optimal for this
application. Specific methods had to be developed, based on fully 3D iterative
techniques.
In this study, we present the performance of several implementations of the fully 3D
sinogram-based OSEM (Ordered Subset Expectation Maximization) image reconstruction
algorithm, with different noise (weighting scheme) and spatial resolution models.
Their performance was evaluated for the neuronal dopamine transporter (DAT) imaging
in humans with the HRRT, using a selective DAT radioligand ([11C]-PE2I). Eleven
healthy volunteers were scanned, and the striatum binding potential (BP) of
[11C]-PE2I was calculated using a simplified reference model with the cerebellum as
the non-specific binding region. Another set of eleven healthy volunteers was scanned
on the whole-body ECAT EXACT HR+ scanner (Siemens Molecular Imaging) using the same
protocol. The BP values obtained on the HR+ with a well validated analytic
reconstruction technique (3DRP) were considered as the reference.
The BP values obtained with the HRRT were validated against the HR+ reference values
by post-processing the HRRT images to match the partial volume effect of the HR+
images. The use of a simplified noise model in the HRRT reconstruction algorithm
introduces a systematic quantitative bias in the activity measured in the image when
the relative amount of random coincidences is high, for example at the beginning of a
dynamic acquisition. The modeling of a realistic intrinsic spatial resolution allows
noise amplification in the image to be reduced, in particular at very low count
levels (for frame duration of the order of one minute or later frames for 11C labeled
radioligands). These results validate the use of the HRRT for cerebral DAT imaging in
humans, and show the importance of using a realistic modeling of the acquisition
process in the reconstruction algorithm for high resolution dynamic brain PET imaging.
Author
Dr
Claude Comtat
(Frédéric Joliot Hospital Facility, CEA/DSV/DRM, Orsay, France)
Co-authors
Dr
Andrew Reader
(School of Chimical Engineering & Analytical Science, The University of Manchester, Manchester, United Kingdom)
Mr
Bataille Frédéric
(Frédéric Joliot Hospital Facility, CEA/DSV/DRM, Orsay, France)
Dr
Claire Leroy
(ty, URM 0205, INSERM-CEA, Orsay, France)
Mr
Florent Sureau
(Frédéric Joliot Hospital Facility, CEA/DSV/DRM, Orsay, France)
Dr
Maria-João Santagio-Ribeiro
(Frédéric Joliot Hospital Facility, CEA/DSV/DRM, Orsay, France)
Dr
Régine Trébossen
(Frédéric Joliot Hospital Facility, CEA/DSV/DRM, Orsay, France)