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Magnetic Resonance Fingerprinting Reconstruction and Dictionary Matching with Compensation of Frequency Drifts
Rasim Boyacioglu1 and Mark Griswold1
1Radiology, Case Western Reserve University, Cleveland, OH, United States

Synopsis

Magnetic Resonance Fingerprinting (MRF) maps multiple tissue properties and system parameters simultaneously. The accuracy of MRF maps depends on the simulation of all possible system properties into the signal evolutions via the Bloch equations. We have observed frequency drifts during MRF scans, similar to those seen in fMRI scans, which might cause various artifacts if not accounted for. Here, it is shown that 2D MRF frequency drifts can be compensated with a simple dictionary update. For correction of 3D MRF frequency drifts, a novel reconstruction framework is introduced. Results show significant improvements on quantitative maps for 2D and 3D MRF.

Introduction

Magnetic Resonance Fingerprinting (MRF) is a novel imaging technique capable of simultaneous mapping of multiple tissue and system properties1. MRF data is typically acquired with fast sampling of highly undersampled k-space with a temporally variable FA/TR. The reconstructed MRF signal evolutions are assumed to be encoded by the underlying tissue properties which are then obtained with dictionary matching. The dictionary is simulated considering the possible tissue and system property ranges (field inhomogeneities, slice profile, etc.). Because of this, the accuracy of MRF maps depends on the exact knowledge of system properties throughout the acquisition. Recent experiments revealed ~4-5 Hz/min scanner frequency drifts during continuous 2D MRF acquisitions due to the eddy currents from fast switching gradients. If not accounted for, any discrepancy between the expected and the real on-resonance frequency might cause problems in the dictionary matching stage. Here we incorporate experimental measurements of frequency drifts into dictionary generation and suggest a novel MRF reconstruction framework for 3D. Improved image quality is shown when these drifts are taken into account.

Methods

Recently, MRF with quadratic RF phase2 (MRFqRF) was introduced to map off-resonance and T2*, in addition to T1 and T2. Since MRFqRF is particularly sensitive to frequency drifts with artifacts as blurring in T1 maps and overestimation of Γ, it is a good candidate to test our hypothesis.
2D MRFqRF brain data3: 256x256 matrix size, 1.2x1.2 mm2 resolution, 5 mm slice thickness, 3516 time points (tp). 3D MRFqRF brain data4: 24 partitions (Np), same acquisition parameters as in 2D (Figure 1) but with 3D excitation and phase encoding in z-direction with no acceleration. Also for reference, 3D FISP MRF data (matching MRFqRF FOV) were also acquired. Informed consent with IRB approval was obtained prior to the data acquisition.
For frequency drift estimation, we acquired 10 consecutive 2D MRFqRF scans and calculated the mean off-resonance change per TR over an ROI. Then, for frequency drift compensated MRFqRF dictionary, every entry was updated every TR with an increment of the resulting mean frequency drift of 0.0013 Hz/TR within the Bloch simulations. Dictionary and the data were compressed with randomized SVD5 (rSVD) prior to the reconstruction. The dictionary was also undersampled in the tissue property dimension. Quadratic interpolation6 recovers the high resolution in the tissue property dimension. The same 2D MRFqRF data were reconstructed with the generic and frequency drift compensated MRF dictionary.
During generic 3D MRF reconstruction each k-space partition is compressed to Nk rank with the compression matrix calculated from rSVD of the standard dictionary (Figure 2a). Then, Nk fully sampled k-space data go through non-uniform FFT and the resulting Nk images get matched to the compressed dictionary. However, in the case of frequency drift, each partition will have a frequency offset of an integer multiple of tp*0.0013 Hz compared to the very first time point in the acquisition. In this case, the compression matrix, even though it’s calculated from the frequency drift compensated 2D dictionary, would only apply to the first partition and not the others. To overcome this problem, we suggest a new framework for 3D MRF reconstruction (Figure2b) where we calculate one SVD that can compress all partitions than might have slightly different signal evolutions due to the drift. The same 3D MRFqRF data were reconstructed with the generic and frequency drift corrected dictionary for comparison.

Results

2D results are shown in Figure 3. Frequency drift correction mainly improves the underestimation of T1 over the whole brain but most dramatically in ventricles. Γ values are overall decreased and T2* contrast gets sharper.
Improvement in 3D T1 maps is noteworthy (Figure 4). Compared to FISP, there’s significant blurring in T1 maps with standard reconstruction which is practically corrected with frequency drift compensation. 3D Γ maps might be improved the most (Figure 5) since with frequency drift it does not have to explain all the frequencies that existed in the voxel throughout the acquisition. 3D T2* maps have similar contrast to 2D T2* maps.

Discussion and Conclusions

Here, upon the observation of scanner frequency drifts during dynamic MRFqRF scans and its possible effects, two potential retrospective correction schemes are suggested. For 2D MRF, the dictionary can be updated with manual increments of measured frequency drifts to compensate for unexpected differences between the acquired data and the dictionary. For 3D MRF, a new reconstruction framework is introduced. The results show significant improvements especially for T1 and T2* maps.
The frequency drift is specific to our system and sequence and could be different on other scanners. Here this value was manually hardcoded into the dictionary but one can also consider making a frequency drift dimension in the dictionary (assuming its time evolution, i.e. linear) and obtain the frequency drift with dictionary matching.
3D reconstruction framework introduced here opens the door to different and optimized sequence parameters for each partition. Thus, MRF optimization problem may have more degrees of freedom and not be limited to number of time points per partition.
In conclusion, it is necessary to compensate for the frequency drift in MRF, especially for bSSFP based MRF sequences, to obtain accurate quantitative maps and a simple retrospective framework achieving that was described.

Acknowledgements

This work is supported by Siemens Healthcare.

References

1. Ma D, Gulani V, Seiberlich N, et al. Magnetic resonance fingerprinting. Nature 2013;495: 187–192.

2. Wang C, Coppo S, Mehta B, et al. Magnetic resonance fingerprinting with quadratic RF phase for measurement of T2* simultaneously with δf ,T1, and T2. Magn Reson Med 2019 81(3):1849-1862.

3. Wang C, Boyacioglu R, McGivney D, et al. Magnetic Resonance Fingerprinting with Pure Quadratic RF Phase. ISMRM proceedings 2019, p4552.

4. Boyacioglu R, Wang C, Ma D et al. 3D Magnetic Resonance Fingerprinting with Quadratic RF Phase. ISMRM proceedings 2019, p806.

5. Yang M, Ma D, Jiang Y, et al. Low rank approximation methods for MR fingerprinting with large scale dictionaries. Magn Reson Med 2018 79(4):2392-2400.

6. McGivney D, Boyacioglu R, Jiang Y, et al. Towards Continuous Tissue Property Resolution in MR Fingerprinting using a Quadratic Inner Product Model. ISMRM proceedings 2019, p4526.

Figures

Figure 1. a) Flip angle and b) TR for the MRFqRF sequence with 3516 time points. The RF phase is modulated with a quadratic function, causing the on-resonance frequency to change linearly in time (c) and making it possible to encode all the frequencies (d) between -1/(2*TR) and 1/(2*TR). Another parameter, Γ, describing the intra-voxel frequency dispersion around a center frequency is simulated in the dictionary and the corresponding match is used to calculate T2*. The other acquisition parameters: TE = 2.2 ms, 300x300 mm2 FOV for 2D and 300x300*120 mm3 FOV for 3D.

Figure 2. a) For generic 3D MRF reconstruction, all partitions are compressed with the same matrix. However, in the case of frequency drift, signal evolutions differ between partitions as the frequency accumulates during the acquisition. To address this, a new Np X tp dictionary is formed with the repetition of the FA/TR/phase pattern by Np times and with frequency drift increments throughout the whole acquisition. A new compression matrix is calculated with rSVD and each partition is compressed after it is inserted in its corresponding place in a Np by Np*tp matrix as illustrated in b).

Figure 3. T2 values are hardly changed between different reconstructions. Off-resonance maps are shifted overall but the contrast between the tissues is preserved. T1 underestimation is resolved with frequency drift correction (blue arrows). The major improvement on Γ maps with narrower frequency distributions expresses itself in T2* maps as elevated values and sharper contrast (red arrow). Please note the corrected Γ in white matter which is supposed to be on the lower end of Γ range.

Figure 4. 3D T1 and T2 maps of the same slice plotted for FISP MRF, generic MRFqRF and MRFqRF with frequency drift correction. It can be observed that T1 improvement in 3D is significantly more than 2D, this is probably due to accrued frequency over much longer 3D acquisition. The T1 FISP contrast between gray matter and white matter is replicated with drift correction whereas the generic reconstruction has elevated blurring throughout the slice (blue arrows).

Figure 5. Γ and T2* maps for the same slices from 3D data shown in Figure 4. The most dramatic improvement is seen with Γ and by extension with T2* maps. The generic reconstruction suffers from severe inhomogeneity artifacts in the frontal and temporal lobes around air-tissue interfaces. Frequency drift corrected reconstruction is able to incorporate those effects in to the dictionary and thus be significantly less sensitive and recover the typical T2* contrast.

Proc. Intl. Soc. Mag. Reson. Med. 28 (2020)
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