A spiral projection acquisition scheme was used for 3D MR fingerprinting to achieve isotropic resolution of 1.2x1.2x1.2 mm3 with FOV of 240x240x240 mm3 for whole brain T1 and T2 mapping within 4.3 minutes.
Purpose
To develop a fast three-dimensional (3D) magnetic resonance fingerprinting (MRF) method based on spiral projection acquisition to achieve high resolution isotropic quantitative mapping.Acquisition trajectories based on spiral projection imaging (SPI) 4,5 was implemented for 3D slab-selective MR fingerprinting with fast imaging with steady state precession (FISP) readout 6. As Figure 1(a) shows, rotating spiral readouts were acquired for 600 time points (TRs) per each group repetition (GR) and 30 group repetitions for whole scan. The spiral trajectory was firstly rotated about z-axis to fully sample a plane like a “disk”. This disk was then rotated about x-axis to fill a sphere in k-space. Since the necessary number of spirals to fill a disk is much less than the necessary number of disks to fill a sphere (30 compared to 200 in this work), spiral rotates 12° about z-axis by group repetitions and about x-axis at golden angle (111.25°) by time points within each group repetition to minimize total acquisition time.
Pulse sequence design was shown in Figure 2a. Varying flip angles were illustrated in Figure 2b while TRs were set as constant value of 11 ms with the number of time points = 600. The number of group repetition was 30 and the identical pulse sequence was used for each group except for rotated acquisition trajectories. The interval between sequential group repetition was 2 seconds. Therefore, the total scan time was 4 minutes and 16 seconds. The isotropic spatial resolution of 1.2x1.2x1.2 mm3 was achieved for the identified parametric maps in a field of view (FOV) of 240x240x240 mm3 and matrix size of 200x200x200. The measurements of a phantom and in vivo brains were performed on a Siemens 3T Prisma scanner with a 64 channel head coil.
Reconstruction is achieved by following these steps, shown in figure 1. First, acquired spiral interleaves was combined from all group repetitions into a disk-like trajectory at each time point. Second, the inverse NUFFT operator was applied to k-space data with a sliding-window strategy 7. Third, the reconstructed image frames were matched to a sliding-windowed MRF dictionary (calculated by EPG algorithm 8) to generate parametric maps.
Figure 3 shows the result of a phantom (comprised of three solutions with different concentration of agar and MnCl2) study. The T1 and T2 values obtained by the proposed method (shown in Figure 2e) were close to the ones from the gold standard method (IR-SE for T1 and SE for T2), without bias which often occurs in 2D MRF due to defective slice profile of RF excitation 9.
Figure 4 shows the T1 (a) and T2 (b) maps of different slices and different orientations for an in vivo study. Some regions of interest were marked by blue characters, respectively corresponding to the caudate nucleus, putamen, hippocampus, parietal white matter and frontal white matter from a to e. Their specific T1 and T2 values were listed in Table 1.
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