Cardiac Magnetic Resonance Fingerprinting (cMRF) has been recently proposed to reduce scan time by estimating simultaneously T1, T2 and M0 in a single breath-hold acquisition. Additionally, cardiac fat images may carry additional diagnostic information and promising results have been shown for epicardial fat volume quantification, characterisation of cardiac masses and detection of fibro-fatty infiltrations. Here we extend cMRF with a three-point Dixon encoding (Dixon-cMRF) for enhanced myocardium tissue characterisation by providing T1, T2, M0 for both water and fat, from which an additional fat fraction map can be computed. The feasibility of Dixon-cMRF was evaluated in 5 healthy subjects.
The proposed Dixon-cMRF is a 2D ECG-triggered cMRF acquisition with an optimised4 three-echo Dixon GRE readout. Acquisition is performed with a golden radial trajectory with one radial spoke per time-point; varying magnetization preparation modules and varying flip angles (Fig.1). A subject-specific dictionary is computed using slice profile corrected extended phase graph simulations taking into account the corresponding ECG signal.
In MRF, the dictionary D can be compressed in the temporal direction to allow faster reconstruction of compressed time-point images and faster matching5,6. The compression is defined as $$$\widetilde{X} =U_R^H X$$$ , where X is a set of time-point images, $$$\widetilde{X}$$$ are the corresponding compressed singular images obtained by applying the Hermitian conjugate of the temporal singular vectors U of D truncated at an appropriate rank R. Here we show that the water fat separation problem can be also solved in the compressed domain.
The compressed images $$$\widetilde{S_k}$$$ for each echo k were reconstructed separately using HD-PROST7 which proposes a novel multi-contrast patch-based low rank regularized reconstruction for MRF. Considering the water (W) and fat (F) images, $$$\widetilde{S_k}$$$ can be written as8
\[\widetilde{S_k} =U_R^H S_k=U_R^H (W+Fe^{i2\pi\Delta f t_k } ) e^{i2\pi\Delta f_{B_0}(t_k-t_1) }\]
\[=(\widetilde{W} + \widetilde{F} e^{i2\pi\Delta f t_k } ) e^{i2\pi\Delta f_{B_0}(t_k-t_1) }\]
Where $$$\Delta f$$$ is the precession frequency difference between fat and water, $$$\Delta f_{B_0}$$$ the one induced by B0 field inhomogeneities and $$$t_k$$$ is TE of echo k.
This signal formulation leads to the classical Dixon problem in the compressed domain which was solved for by using a 3-point Dixon separation method9. A B0 estimate is obtained from the high signal to noise ratio (SNR) first singular images and used to obtain $$$\widetilde{W}$$$ and $$$\widetilde{F}$$$ the water and fat compressed time series. T1, T2 and M0 maps are obtained through dot product matching for both water and fat. Additionally, a fat fraction map10 can be obtained from the fat and water M0 maps.
Dixon-cMRF was acquired in 5 healthy subjects on a 1.5T scanner (Ingenia, Philips Healthcare) and compared to 1st echo cMRF, and conventional MOLLI11, SASHA12 and T2GRASE13 mapping techniques with the same spatial resolution. Dixon-cMRF imaging parameters include: TR/TE1/TE2/TE3= 7.5/2/3.6/5.2 ms, 2x2mm2 resolution, FOV=256x256mm2, 8mm slice thickness, 187.5ms diastolic acquisition window, ~15s scan time.
Whole FOV Dixon-cMRF results showing no water-fat swaps is presented in Fig.2 for a representative subject. A zoom in on the heart compares Dixon-cMRF maps to the maps obtained from the 1st echo data. Dixon-cMRF shows a better delineation of the myocardial wall in the presence of water and fat partial volume, which can affect T1 and T2 maps. The additional fat fraction map obtained from the water and fat M0 maps is also shown in Fig.2.
T1,T2 and M0 maps obtained from Dixon-cMRF are compared to the conventional techniques MOLLI, SASHA, T2GRASE and Dixon in Fig. 3. T1 and T2 values were measured in the septum for all subjects and reported in Fig. 4. Average T1 measurement and standard deviation for SASHA, MOLLI and Dixon-cMRF are 1121±111 ms, 1001±47 ms and 1013±41 ms respectively. T2 values for T2GRASE and Dixon-cMRF are 50.4±3.7 ms and 48.2±3.7 ms. Consistent high-quality maps were obtained for all subjects as shown in Fig.5.
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