Physiological motion remains a major challenge for cardiac PET-MR. Here we propose a framework for non-rigid respiratory motion-corrected simultaneous Coronary MR Angiography (CMRA) and cardiac PET. Motion estimated from low-resolution MR image navigators and from CMRA data itself is used for correcting CMRA and PET datasets to the same respiratory position. The proposed CMRA approach was validated in ten healthy subjects. Results from the PET-CMRA framework on three patients show that motion-corrected PET images have improved sharpness compared to uncorrected reconstructions, whereas motion-corrected CMRA images have improved coronary vessel length and sharpness compared to uncorrected and translational-corrected images.
PET-MR acquisition consists of an ECG-triggered free-breathing CMRA sequence simultaneously acquired with cardiac list mode PET data (Fig1a). CMRA data is acquired using a 3D T1-weighted spoiled gradient echo sequence with a fully sampled golden-step Cartesian spiral profile order sampling trajectory(3). A low-resolution 2D image navigator (iNAV)(4) is acquired at each cardiac cycle by spatially encoding low flip angle start-up echoes preceding the CMRA acquisition. Fat saturation and adiabatic T2 preparation pulses are performed to improve contrast between blood and myocardium. The iNAVs are used to estimate foot-head and right-left motion in a beat-to-beat fashion, providing translational motion estimates to correct the MR data. Foot-head motion is used to bin both the PET and MR data (Fig1b). 3D non-rigid motion between respiratory bins is estimated from MR images reconstructed at each respiratory position and is then used for correcting the CMRA (directly in the reconstruction(5)) and the emission and attenuation PET datasets to the same respiratory position.
Ten healthy subjects were scanned on a Biograph mMR scanner (Siemens Healthcare, Germany) using a prototype implementation of the proposed sequence (304x304x40-48 matrix size, 1x1x2mm3 resolution TR/TE=3.7/1.7ms, FA=15°, T2prep=50ms). A subject-specific trigger delay and acquisition window (89 to 119ms) were set coinciding mid-diastolic rest period. For the iNAV, 14 start-up echoes (same FOV as CMRA, FA=3º) were used. Additionally, a gated and tracked image (6mm gating window, tracking scaling factor=0.6) was acquired for comparison. The whole PET-MR framework was tested in three oncology patients (scanned 2.2 hours after injection of 319.7 MBq of 18F-FDG, on average), using the same acquisition parameters described for the healthy subjects. List-mode PET data was acquired during the whole CMRA acquisition (~10min).
CMRA data was reconstructed with the proposed translation plus non-rigid motion correction (TC+GMD), 2D translational motion correction only (TC) and without motion correction (NMC). PET image reconstruction was performed in Siemens e7 Tools (OSEM, 3 iterations, 21 subsets, PSF modelling, 2.03x2.08x2.08mm3 resolution, 127x344x344 matrix size). Three reconstructions were performed for PET data: reconstruct-transform-average(6) motion-corrected (MC), uncorrected (NMC) and Gated reconstruction at end-expiration.
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