Gastao Cruz1, Andrew Phair1, Carlos Velasco1, René M. Botnar1, and Claudia Prieto1
1King's College London, London, United Kingdom
Synopsis
Cardiac Magnetic Resonance Fingerprinting (MRF) produces co-registered,
multi-parametric maps from highly accelerated acquisitions. Low rank methods
leveraging temporal information have enabled highly undersampled MRF
reconstructions. However, residual aliasing from these reconstructions can potentially
propagate through the MRF framework into the parametric maps. Region-Optimized Virtual
coils have recently been proposed for undersampled reconstructions in
conventional imaging, by suppressing unwanted sources of aliasing signal. Here
we combine both methods and investigate its performance in Cardiac Magnetic
Resonance Fingerprinting.
INTRODUCTION:
Cardiac Magnetic Resonance Fingerprinting (MRF)1,2 has been
investigated for myocardial tissue characterization. In 2D, breath-hold
acquisitions are commonly employed to minimize respiratory motion, limiting the
available scan time to the duration of a feasible breath-hold. Additionally,
ECG-triggering used to minimize cardiac motion reduces scan efficiency, and consequently
cardiac MRF requires highly accelerated acquisitions. Low rank models3,4,5
have been deployed in MRF to cope with the acceleration requirements. MRF
requires the residual artefacts to be incoherent, otherwise they may propagate
into the parametric maps. Recently, Region-Optimized Virtual coils (ROVir)6
have been proposed to suppress unwanted signal in the FOV, which may otherwise
contribute to residual aliasing, demonstrating improved performance in
conventional Cartesian undersampled imaging. In cardiac MRF, subcutaneous fat
(or other strong signal sources) can introduce coherent artefacts and
potentially introduce errors in the maps. Here, we combine ROVir with a Low
Rank Inversion (LRI) and investigate its feasibility for cardiac MRF.METHODS:
The proposed ROVir+LRI framework integrates the optimal coil combination
from ROVir into the subspace constrained LRI reconstruction for cardiac MRF
(Fig. 1). First, a ROI is select around the myocardium, marking the “signal”
region $$$ A $$$; the complementary region in the FOV is considered as “interference”
region $$$ B $$$. According to the ROVir theory6, there is a set of linear
weight vectors
that maximizes the
signal-to-interference ratio: $$$ SIR(w_i) = \frac{w_i^HAw_i}{w_i^HBw_i} $$$. The vectors $$$ w_i $$$ can
be found by solving $$$Aw_i = \lambda Bw_i$$$ via a
generalized eigenvalue decomposition. Once found, $$$ w_i $$$ can be
applied to the coil sensitivities and k-space data to suppress signal from
region $$$ B $$$, while maintaining signal from region $$$ A $$$. These “virtual” coils and k-space data can
then be used in a subspace constrained reconstruction3,4,5. Here, we
follow the LRI notation, where the set of singular images $$$ y $$$ (compressing the temporal contrast dynamics) is
obtained by solving: $$ \hat{y} = \mathit{argmin}_y \left \| AFC' U_r y - s' \right \| _2 ^2 $$, where $$$ A $$$ is
the sampling trajectory, $$$F$$$ is the Fourier transform, $$$C'$$$ are “virtual” ROVir coil sensitivities, $$$ Ur $$$ are
the left singular vectors following a singular value decomposition of the MRF
dictionary and $$$s'$$$ are
“virtual” ROVir k-space data. Following the reconstruction, the MRF parametric
maps may be obtained by standard template matching of $$$y$$$ to the MRF dictionary. EXPERIMENTS:
Eight healthy subjects were scanned at a 1.5T scanner (Philips Ingenia)
using a cardiac MRF sequence for simultaneous T1/T2 mapping. The MRF sequence
was ECG-triggered, employing Inversion Recovery (for T1) and T2 preparation
pulses (for T2) as described in previous work.7 Imaging parameters
included field of view (FOV) = 315x315 mm2; 8
mm slice thickness; resolution = 1.75x1.75 mm2; TE/TR = 0.9/7.1 ms;
gradient echo readout; 6-10º sinusoidally varying flip angle; 1080 time-points;
nominal scan time 18s. Acquired data was reconstructed with LRI and with ROVir+LRIRESULTS:
A comparison of LRI and ROVir+LRI revealed that in the majority of cases
(6/8), both methods produced virtually the same results (Fig. 2). There were
two cases were residual artefacts were present in the T1/T2 LRI maps, but were
reduced in T1/T2 ROVir+LRI maps (Fig. 3 and Fig. 4). In both cases, the
residual coherent aliasing was due to strong signal sources (e.g. off-resonant
excitations and/or fat) in the edges of the FOV.CONCLUSION:
The feasibility of Region-Optimized
Virtual coils plus Low Rank Inversion was investigated for cardiac MR
Fingerprinting. Preliminary results indicate similar performance in most cases,
however in some situations ROVir+LRI can reduce coherent aliasing and improve
map quality. Future work will compare this approach with other methods of coil
selection.Acknowledgements
This work was supported by EPSRC (EP/P001009,
EP/P032311/1, EP/P007619/1) and Wellcome EPSRC Centre for Medical Engineering
(NS/ A000049/1).References
1. Hamilton JI, Jiang Y, Chen Y, et al. MR
fingerprinting for rapid quantification of myocardial T 1 , T 2
, and proton spin density. MRM 2017;77:1446–1458.
2. Jaubert
O, Cruz G, Bustin A, Schneider T, Botnar RM, Prieto C. Dixon-cMRF : cardiac
tissue characterization using three-point Dixon MR fingerprinting. 2019:5–7 doi: 10.1002/mrm.26216.2.
3.
McGivney DF, Pierre E, Ma
D, et al. SVD compression for magnetic resonance fingerprinting in the time
domain. IEEE Trans. Med. Imaging 2014;33:2311–2322 doi: 10.1109/TMI.2014.2337321.
4.
Zhao B, Setsompop K,
Adalsteinsson E, et al. Improved magnetic resonance fingerprinting
reconstruction with low-rank and subspace modeling. Magn. Reson. Med.
2018;79:933–942 doi: 10.1002/mrm.26701.
5.
Assländer J, Cloos MA,
Knoll F, Sodickson DK, Hennig J, Lattanzi R. Low rank alternating direction
method of multipliers reconstruction for MR fingerprinting. Magn. Reson. Med.
2018;79:83–96 doi: 10.1002/mrm.26639.
6.
Kim D,
Cauley SF, Nayak KS, Leahy RM, Haldar JP. Region‐optimized virtual (ROVir)
coils: Localization and/or suppression of spatial regions using sensor‐domain
beamforming. Magnetic Resonance in Medicine. 2021 Jul;86(1):197-212.
7.
Cruz G, Qi H, Jaubert O, Kuestner T, Schneider
T, Botnar RM, Prieto C. Generalized low‐rank nonrigid motion‐corrected
reconstruction for MR fingerprinting. Magnetic Resonance in Medicine. 2021 Oct
2.