Camila Munoz1, Christoph Kolbitsch1,2, and Claudia Prieto1
1Department of Biomedical Engineering, King's College London, London, United Kingdom, 2Division of Medical Physics and Metrological Information Technologies, Physikalisch-Technische Bundesanstalt, Berlin, Germany
Synopsis
MR-based PET motion correction has been shown to improve image quality in
cardiac PET-MR imaging. Here we present a numerical simulation study analysing
the impact of temporal and spatial resolution of motion fields on the final
image quality of myocardial perfusion PET scans in order to find the most
efficient parameters yielding accurate cardiac motion compensation in the
shortest possible scan time. Results show that cardiac motion correction is important
for accurate assessment of myocardial lesions and that temporal resolution of
the motion fields can be strongly optimised without losing diagnostic accuracy,
reducing the total exam time in PET-MR imaging.Introduction
Simultaneous PET-MR
offers the possibility to use high-resolution MR images for motion correction
of PET data. Several studies have shown that this approach leads to a strong
improvement in PET image quality. Here we
present a numerical simulation study analysing the impact of temporal and
spatial resolution of MR motion fields on the final image quality of myocardial
perfusion PET scans in order to find the most efficient motion field parameters
yielding accurate cardiac motion compensation in the shortest possible scan
time.
Methods
A numerical representation of a human torso and parameterised
models of beating heart motion are obtained using a commercially available software
(XCAT(1)). XCAT generates emission maps, where each voxel represents
a tissue dependant standardized uptake value (SUV), and attenuation maps for
each motion state, that are then used as input for PET simulations.
Reconstructed PET images were assessed based on metrics used for clinical
diagnosis including detectability of damaged segments in standard polar plots
computed from the left ventricular myocardium(2), and extent and degree of transmurality (i.e. fraction
of the wall affected) of the lesion.
Four
myocardial lesions with different transmurality (100%, 50% and 25%), extension and
location (anterior and lateral wall) were simulated using realistic 18F-FDG
uptake values(3) in XCAT (Fig.1). Cardiac motion was simulated based
on a normal cardiac cycle with a duration of 1s. Analytical PET simulations
were performed in STIR(4) using the geometry of the Siemens Biograph
mMR scanner (60cm bore size, 8 rings of LSO crystal detectors, 258mm axial
FOV). Motion fields of five temporal (20, 10, 5, 2 and 2* cardiac phases) and
four spatial (2, 4, 5.68 and 9.84mm3 isotropic voxel size)
resolutions were studied. The 2* non-uniform division of the cardiac cycle
groups two thirds of the cardiac cycle around maximum relaxation in one cardiac
phase and the remaining third as the second phase. Image reconstruction was
performed using a motion compensated algorithm(5)
(21 subsets, 3 iterations) with a voxel size of 2.03×2.08×2.08mm3,
a matrix size of 127×285×285 and a 4mm isotropic Gaussian post-filtering.
Additionally, a motion-free image was simulated and reconstructed for reference
purposes, and an uncorrected reconstruction was performed for further
comparison.
Results
For both transmural and
non-transmural perfusion defects, results showed that although image quality
degrades when reducing temporal and spatial resolution of the motion fields,
non-viable myocardium can be detected even without motion correction (Fig.1). For
defects 1 (transmural) and 2 (50% transmural), a resolution of 10mm and 2*
phases allowed to detect more of 90% of the
non-viable segments. For defects 3 (25% transmural) and 4 (50% transmural),
a resolution of 2mm and 2* phases is required to detect more than 90% of the
non-viable segments correctly. For the transmurality analysis both (2mm, 20
phases) and (2mm, 2* phases) lead to accurate results; considering defects 2, 3
and 4, an average error of 7.17
±
3.44% and 5.58
±
1.53% compared to the
motion-free reference was obtained respectively. For defect 4 (50% transmural), located in an
area of large cardiac motion amplitude, when 2 phases are used or no motion
correction is performed, the lesion is erroneously detected as transmural (Fig.
3)
Conclusion
We have presented a
simulation study to assess the impact of spatial and temporal resolution of
motion fields for MR-based beating heart motion
corrected cardiac perfusion PET imaging. Results show that non-viable myocardium
can be detected even without motion correction however motion correction is
essential for accurate estimation of the size and degree of transmurality of
perfusion defects. The non-uniform two-phase division of the cardiac cycle allowed for
achieving less than 10% error in the estimation of extent and transmurality of
all simulated defects using a spatial resolution of 2mm. Thus, temporal
resolution of the motion fields can be significantly reduced without losing
diagnostic accuracy. The subsequent reduction of time allocated for MR-based
motion estimation would potentially allow for acquiring diagnostic MR
information simultaneously with PET, reducing total exam time in PET-MR
clinical routine.
Acknowledgements
This work was supported by the EPSRC
Centre
for Doctoral Training
in Medical
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