Quantitative magnetic resonance imaging (MRI) enables the quantification of biomarkers and the detection of tissue changes. Recently, various magnetic resonance fingerprinting (MRF) sequences were proposed to enable simultaneous quantification of T1 and T2/T2*relaxation times. In this study, we demonstrate motion sensitivity of the original MRF and MRF-EPI. Intensity-based image registration is used in six healthy subjects to eliminate motion artifacts in MRF-EPI. The effectiveness is demonstrated by a significant improvement in the Dice coefficient. As the algorithm is independent of patient and slice, it facilitates motion robust acquisition of parameters maps with MRF ready for clinical use.
NUMERICAL SIMULATION: Original MRF and MRF-EPI were simulated in a Shepp-Logan phantom using Bloch-equations, with π1 and π2/π2*(π2 for original MRF and π2* for MRF-EPI) in the in-vivo range. Sequence parameters of original MRF and MRF-EPI were chosen as previously described1,2. Motion was induced in two sets of experiments by corrupting 1 second worth of images: 1) Variable amplitude (0°-20° rotation, 0-20 pixel translation) at the beginning of the measurement. 2) Fixed motion amplitude (14º rotation and 10 pixel translation), with varying time of onset of the motion. The resulting π1 and π2/π2*-maps from the motion corrupted fingerprints were determined and the mean deviation from the ground truth was calculated.
IN-VIVO EXPERIMENTS: In-vivo measurements of 6 healthy volunteers (4 male, 27±3 years) were acquired with MRF-EPI on a 3 T whole-body scanner (Siemens Trio) using a 32-channel head-array-coil, with following sequence parameters: TE/TR=17-78ms/80-755ms, flip angle=4-58°, FOV=220x220x140mm3, voxel size=1.7x1.7x5.0mm3, band-width=1136Hz/pixel, partial-Fourier=5/8, GRAPPA rate=3, acquisition time slice=10s, total number of baseline images=160. To demonstrate motion sensitivity and to validate correction, subjects were instructed to turn their heads by 20 degrees 2 seconds after the scan start. Subsequently, a reference measurement without motion was acquired for each test person.
MOTION CORRECTION: Motion correction was performed using rigid geometric transformation based on mutual information with a 1+1 evolution strategy with following parameters: maximum iteration=1000, initial radius=0.0156, epsilon=1.5·10-6, growth factor=1.05. The first image was selected as reference due to the highest SNR. The motion correction is evaluated by means of visual assessment of parameter maps and quantitative assessment of Dice indices. The scan series are statistically compared using Student’s t-test on the log-transformed indices of baseline image 10 (before motion) and 99 (after motion).
Simulation results show high motion sensitivity of both MRF methods, even to small displacements (Fig. 1). π1 quantification is particularly susceptible to motion in the early parts of the scan, while π2 and π2* are more resilient to motion with a uniform sensitivity profile throughout the measurement (Fig. 2). Artifacts such as blurred edges are clearly visible in the simulated parameter maps generated from motion corrupted data (Fig. 1,2). This can be confirmed by in-vivo measurements. Both, π1 and π2* parameter maps show artifacts such as ghosting and fuzziness (Fig. 4). However, image artifacts are successfully mitigated with the proposed intensity based co-registration method (Fig. 4). The correction significantly increases the Dice index from 90% in the presence of motion to 97% after correction (p < 0.002 Fig. 5), which is comparable to data without motion (p = 0.264 Fig 5).
Although residual motion sensitivity is present in MRF, our data indicates, that MRF-EPI can be reliably performed in the presence of motion, by employing retrospective image registration on the baseline images. This fosters motion robustness, which can benefit the clinical use of quantitative MRI.
1. Ma D, Gulani V, Seiberlich N, Liu K, Sunshine JL, Duerk JL, et al. Magnetic resonance fingerprinting. Nature. 2013 Mar 14;495(7440):187–92.
2. Rieger B, Zimmer F, Zapp J, Weingärtner S, Schad LR. Magnetic resonance fingerprinting using echo-planar imaging: Joint quantification of T1 and T2∗ relaxation times. Magn Reson Med. 2016 Dec 1;n/a-n/a.