Physics-based Reconstruction Methods for Magnetic Resonance Imaging
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Physics-based Reconstruction Methods for Magnetic Resonance Imaging arXiv:2010.01403v1 [eess.IV] 3 Oct 2020 Xiaoqing Wang1,2 , Zhengguo Tan1,2 , Nick Scholand1,2 , Volkert Roeloffs1 , Martin Uecker1,2,3,4 1 Institute for Diagnostic and Interventional Radiology, University Medical Center Göttingen, Göttingen, Germany 2 German Centre for Cardiovascular Research (DZHK), Partner Site Göttingen, Göttingen, Germany 3 Cluster of Excellence “Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells” (MBExC), University of Göttingen, Göttingen, Germany 4 Campus Institute Data Science (CIDAS), University of Göttingen, Göttingen, Germany 30. September 2020 Abstract Conventional Magnetic Resonance Imaging (MRI) is hampered by long scan times and only qualitative image contrasts that prohibit a direct com- parison between different systems. Instead of assuming a fixed Fourier relationship, model-based reconstructions explicitly model the physical laws that govern the MRI signal generation. By formulating image re- construction as an inverse problem, quantitative maps of the underlying physical parameters can then be extracted directly from efficiently ac- quired k-space signals without intermediate image reconstruction – ad- dressing both shortcomings of conventional MRI at the same time. This review will discuss basic concepts of model-based reconstructions and re- port about our experience in developing several model-based methods over the last decade using selected examples. Keywords: Magnetic Resonance Imaging, model-based reconstruction, inverse problems Submitted to Philosophical Transactions of the Royal Society A. Correspondence to: Martin Uecker, email: martin.uecker@med.uni-goettingen.de 1
1 Introduction First physics-based reconstruction methods for parametric mapping appeared in the literature more than a decade ago [1, 2, 3] and constitute now a major research area in the field of Magnetic Resonance Imaging (MRI). [4, 5, 6, 7, 8, 9, 10, 11, 12] Model-based reconstruction is based on modelling the physics of the MRI signal and has been used, for example, to estimate T1 [13, 5, 8, 7, 12, 14], T2 relaxation [3, 15, 9, 16], for T2? estimation and water-fat separation [17, 18, 19, 20], as well as for quantification of flow [10] and diffusion [21, 22]. Quantita- tive maps of the underlying physical parameters can then be extracted directly from the measurement data without intermediate image reconstruction. This di- rect reconstruction has two major advantages: First, the full signal is described by a model based on few parameter maps only and intermediate image recon- struction is waived. This renders model-based techniques much more efficient in exploiting the available information than conventional two-step methods. Sec- ond, as a specific signal behaviour is no longer required for image reconstruction, MRI sequences can now be designed that have an optimal sensitivity to the pa- rameters of interest. Once the underlying physical parameters are estimated, arbitrary contrast-weighted images can be generated synthetically by evaluating the signal model for a specific sequence and acquisition parameters. 2 MRI Signal In typical MRI experiments, the proton spins are polarized by bringing them into a strong external field. The spins then start to precess with a character- istic Larmor frequency and can be manipulated using additional on-resonant radio-frequency pulses and further gradient fields. The dynamical behaviour of the magnetization is described by the Bloch-Torrey equations that describe the physics of magnetic resonance including effects from relaxation, flow and diffu- sion. As a fully computer-controlled imaging method, MRI is extremely flexible and the underlying physics enables access to a variety of tissue and imaging sys- tem specific parameters such as relaxation constants, flow velocities, diffusion, temperature, magnetic fields, etc. The measured MRI signal corresponds to the complex-valued transversal magnetization M = Mx + iMy which is obtained by quadrature demodulation from the voltage induced in the receive coils. In a multi-coil experiment this sig- nal is proportional to the transversal magnetization weighted by the sensitivity of each receive coil: Z yj (t) = cj (~r) M (x, B, t, ~r) d~r (1) Here, cj is the complex-valued sensitivity of the jth coil and M the complex- valued transversal magnetization at time t and position ~r. The magnetization depends on some physical parameters x and the externally controlled magnetic fields B(t, ~r), i.e. gradient fields and radio-frequency pulses, and can be obtained 2
coil sensitivities physics parameter maps model signal evolution Figure 1: The forward operator F can be formally factorized into operator M that describes the spin physics, the multiplication with the coil sensitivities C, the (non-uniform) Fourier transform F, and a sampling operator P. by solving the Bloch-Torrey equations (or, if motion of spins can be neglected, by solving the Bloch equations at each point). While equation 1 can be exploited directly for model-based reconstruction [23], many other model-based methods use some simplifying approximations to reduce the computational complexity. Often, segmentation in time is used by assuming that the magnetization is constant around certain time points, e.g. around echo times T En with n ∈ 1, . . . , N . The effect of magnetic field gradients can then be separated out into a phase term which is defined by the k-space trajectory ~k(t). This separation often allows the use of simplified models for the magnetization and, more importantly, the use of fast (non-uniform) Fourier transform algorithms for the gradient-encoding term. We derive the following - still very generic - model: Z ~ yn,j (t) = ei2π~r·k(t) cj (~r)M (x, tn , ~r)d~r (2) Based on this model, we define a nonlinear forward operator F : x 7→ y that maps the unknown parameters x to the acquired data y (see Fig. 1). The defining feature of physics-modelling reconstruction is the addition of a signal model M into the forward operator F . The specific signal model depends on the applied sequence protocol and specifies which tissue and/or hardware characteristics can be estimated. Often, an analytical model can be derived from the Bloch equations using hard-pulse approximations. For many typical MRI sequences important parameter dependencies are exponentials. Table 1 lists some of these analytical signals models. If the applied sequence protocol does not lend itself to an analytical signal ex- pression, the Bloch equations need to be integrated as signal model directly. 3
parameter sequence type signal relaxation rate R1 inversion recovery a − (1 + a) · e−tn R1/a relaxation rate R2 spin-echo e−R2 tn ∗ relaxation rate R2? gradient-echo e−R2 tn field B0 gradient-echo ei2π·fB0 tn chemical shift gradient-echo P i2πfp tn pe ~ flow velocity ~v bipolar gradient ei~v·Vn ~T diffusion tensor D bipolar gradient e−bn Dbn Table 1: Basic analytical signal models for physical parameter dependencies in common MRI sequences. This integration becomes challenging for iterative reconstructions, because of the estimation of the signals derivatives. Current techniques exploit finite dif- ference methods [9, 23] or sensitivity analysis of the Bloch equations [24]. 3 Nonlinear Reconstruction Using a nonlinear forward operator F : x 7→ y that maps the unknown param- eters x to the acquired data y, we can formulate the image reconstruction as a nonlinear optimization problem: X x̂ = argmin kF (x) − yk22 + λQ(xc ) + λi Ri (x) (3) x i Data fidelity is ensured by kF (x) − yk22 and regularization terms Ri can be added to introduce prior knowledge. This framework is very general, combin- ing parallel imaging, compressed sensing, and model-based reconstruction in a unified reconstruction. Often the coil sensitivities are estimate before, but they could also be included as unknowns in x. Paired with suitable sampling schemes, this yields fully calibrationless methods that do not require additional calibration scans [12, 25, 26, 10, 27, 28]. Moreover, model-based reconstructions allow a direct application of sparsity-promoting regularizations to the physical parameters for performance improvement [3, 6, 22, 12]. However, the high non-convexity of model-based reconstruction makes this method sensible to the initial guess and relative scaling of the derivatives of each parameter map. These issues can often be addressed with a reasonable initial guess and a proper preconditioning. Algorithms to solve the nonlinear inverse problems include gradient descent, the variable projection methods [29], the method of nonlinear conjugate gradient [30], Newton-type methods [31] where the nonlinear problem is linearized in each Newton step and the linearized 4
subproblem is solved using the method of conjugate gradients, FISTA [32] or ADMM[33], or alternate minimization [6]. Sequence Flip Angle TR/TE/∆TE Bandwidth Matrix Spokes TA FOV Slice ° ms Hz/px s mm mm IR-FLASH 6 4.10 / 2.58 630 256 × 256 1020 4 192 5 ME-SE 90/180 2000 / 9.9 / 9.9 390 256 × 256 25 × 16 80 192 3 ME-FLASH 5 9.81 / 1.31 / 1.23 1090 200 × 200 33 × 7 0.3 1 320 5 PC-FLASH 10 4.46 / 2.96 1250 210 × 210 2×7 15 320 5 fmSSFP2 15 4.5 / 2.25 840 192 × 192 4 × 101 × 40 137 192 1 1 acquisition time per frame 2 3D Stack-Of-Stars sequence with 40 partitions (1000 prep scans) Table 2: Detailed parameters of MR sequences capable of mapping physical parameters listed in Table 1. Data for the following examples was obtained on a Siemens Skyra 3T scan- ner (Siemens Healthcare GmbH, Erlangen, Germany) from volunteers without known illness after obtaining written informed consent and with approval of the local ethics committee. Acquisition parameters can be found in Table 2. The images were reconstructed using the BART toolbox [34]. 3.1 T1 and T2 Mapping For T1 mapping, a inversion-recovery (IR) FLASH sequence was used. Following a non-selective inversion pulse, data was continuously acquired using a radial FLASH readout with a tiny golden angle (≈ 23.63◦ ) between successive spokes. The magnetization signal M (t) for single-shot radial IR-FLASH reads ∗ Mtk (~r) = Mss (~r) − Mss (~r) + M0 (~r) · e−tk ·R1 (~r) (4) with Mss the steady-state magnetization, M0 the equilibrium magnetization, and R1∗ the effective relaxation rate. tk is the inversion time which is defined as the center of each acquisition window. A radial multi-echo spin echo (ME-SE) sequence was employed for T2 map- ping. Data was acquired with 25 excitations and 16 echoes. The golden angle (≈ 111.25◦ ) was used between successive radial spokes. The magnetization sig- nal M (t) for radial multi-echo spin echo at echo time tk follows an exponential decay Mtk (~r) = M0 · e−tk ·R2 (~r) with M0 the spin density map, R2 = 1/T2 the transverse relaxation rate. This simple exponential model does not take stim- ulated echoes into account, but a more complicated analytical model exits for this case [35]. Quantitative parameter maps for both acquisitions are estimated using the nonlinear model-based reconstruction. I.e., the estimation of parameter maps (Mss , M0 , R1∗ )T or parameter maps (M 0, R2 )T , respectively, and coil sensitivity maps (c1 , . . . , cN )T is formulated as a nonlinear inverse problem with a joint `1 -Wavelet regularization applied to the parameter maps and the Sobolev norm to the coil sensitivity maps. This nonlinear inverse problem is then solved by 5
(A) EstimatedTT11 Estimated EstimatedT Estimated T12 5 6 1.8 Ground Truth 0.18 Ground Truth 4 10 7 1.4 0.14 3 1.0 0.10 9 1 2 8 0.6 0.06 0.2 0.02 1 2 3 4 5 6 7 8 9 10 1 2 3 4 5 6 7 8 9 10 0.4 0.8 1.2 1.6 2.0 0 0.05 0.10 0.15 0 Tubes Tubes T1 / s T2 / s (B) T1 / s 2.0 1.6 1.2 0.8 0.4 Mss M0 R 1* T1 0 T2 / s 0.15 0.10 0.05 M0 R2 T2 0 Figure 2: (A). (Leftmost) Model-based reconstructed T1 map and (left mid- dle) the ROI-analysed quantitative T1 values for the numerical phantom using the single-shot IR radial FLASH sequence. (Right middle and rightmost) Simi- lar results for T2 mapping using the multi-echo spin-echo sequence. (B). (Top) The reconstructed parameter maps (Mss , M0 , R1∗ )T for the T1 model and (bot- tom) (M0 , R2 )T for the T2 model with the corresponding T1 / T2 maps in the rightmost column. the IRGNM-FISTA algorithm [12]. After estimation of the parameters T1 and T2 maps can be calculated. To evaluate the quantitative accuracy of the model-based methods, numeri- cal phantoms with different T1 relaxation times (ranging from 200 ms to 2000 ms with a step size of 200 ms for each tube, and 3000 ms for the background), T2 relaxation times (ranging from 20 ms to 200 ms with a step size of 20 ms for each tube, and 1000 ms for the background) were simulated, respectively. The k-space data were derived from the analytical Fourier representation of an el- lipse assuming an array of eight circular receiver coils surrounding the phantom without overlap. Fig. 2 (A) presents the estimated T1, T2 maps and the corresponding ROI- analyzed quantitative values for the numerical phantom using model-based re- constructions. Good quantitative accuracy is confirmed for both model-based 6
Water Fat R2* B0 Figure 3: Real-time liver images acquired during free-breathing using a radial multi-echo (ME) FLASH sequence. Model-based reconstruction directly and jointly estimates separated water and fat images, as well as R2? and B0 field maps. T1 and T2 mapping methods. Fig. 2 (B) demonstrates model-based recon- structed three and two physical parameter maps, the corresponding T1 and T2 maps for the retrospective T1 and T2 models on human brain studies. More- over, synthetic images were computed for all inversion/echo times and the image series were then converted into movies showing the contrast changes in the sup- plementary Videos 1 and 2. 3.2 Water/Fat Separation and R2∗ Mapping Quantitative T2∗ mapping can be achieved via multi-echo gradient-echo sam- pling. With prolonged echo-train readout, the acquired multi-echo signal fol- lows, ∗ Mn = ρ · e−R2 ·TEn · ei2π·fB0 ·TEn (5) where R2∗ and fB0 is the inverse of T2∗ and B0 field inhomogeneity, respectively. TEn denotes the nth echo time. On the other hand, when the imaging voxel contains distinct protons resonating at different frequencies, the magnetization ρ can be split into multiple compartments. For instance, chemical shift between water and fat induces phase modulation, therefore, X ∗ Mn = (W + F · ei2πfp ·TEn ) · e−R2 ·TEn · ei2π·fB0 ·TEn (6) p where W and F are the water and fat magnetization, respectively. fp is the pth fat-spectrum peak frequency. In practice, usually the 6-peak fat spectrum [36] is used. Here, a multi-echo (ME) radial FLASH sequence [28] was used to acquire liver data during free breathing. The Sobolev-norm weight was applied to the B0 field inhomogeneity and coil sensitivity maps. Joint `1-Wavelet regularization was applied to other parameter maps. As shown in Figure 3 and supplementary 7
Video 3, high-quality respiratory-resolved water/fat separation as well as R2∗ and fB0 maps can be achieved even with undersampled multi-echo radial acquisition (33 spokes per echo and 7 echoes in total). 3.3 Phase-Contrast Velocity Mapping In phase-contrast flow MRI, velocity-encoding gradients (i.e. bipolar gradients with equal area but opposite polarity) are used to encode flow-induced phases. Flowing spins with constant velocities during the bipolar gradient result in net phase (proportional to the product between the gradient area and velocity), whereas static spins result in zero phase. However, MR signal is in general complex-valued due to the use of receiver coils. To compute the quantitative velocity maps, a reference measurement without flow-encoding gradients is re- quired such that the phase difference between the reference and flow-encoded measurement excludes the background phase. Therefore, the mathematical modelling of the phase-contrast flow MRI signal can be written as ~ Mk = ρ · ei~v·Vk . (7) ~v is the velocity and Vk is the velocity-encoding for the kth measurement. For through-plane velocity mapping, V ~0 = 0 for the reference and V1 = π/VENC the velocity-encoded measurement perpendicular to the imaging plane, respec- tively. Here, VENC is the maximum measurable velocity in the unit of cm s−1 and inversely proportional to the first moment of the bipolar velocity-encoding gradient. ρ is the shared anatomical image between the two measurements. Multi-dimensional velocity mapping can be used as in 4D flow MRI [37]. Multi- dimensional mapping was also used for real-time imaging of flow with model- based reconstruction [38]. A phase-contrast flow MRI sequence with radial sampling and through-plane velocity-encoding gradient was used to measure the in-vivo aortic blood flow ve- locities. Two types of reconstructions were performed: model-based reconstruc- tion [10, 27] based on the model in 7, and a parallel imaging reconstruction on both reference and flow-encoded measurements followed by a phase-difference computation. Fig. 4 shows the reconstructed velocity map from the model- based reconstruction and phase-difference computation. Supplementary Video 4 displays the dynamic velocity maps of the whole 15-second scan. The later approach employs parallel imaging reconstruction on the reference and the flow- encoding measurement separately and then computes the phase difference be- tween the reconstructed reference and flow-encoded images. With the direct regularization on the phase-difference map, the proposed model-based recon- struction is able to largely remove background random phase noise. 4 Linear Subspace Reconstruction In contrast to nonlinear models, in linear subspace methods the signal curves t 7→ M (x, t, ~r) are approximated using a linear combination of basis functions 8
Model-based Phase Difference Figure 4: Comparison between (top) the model-based reconstruction and (bot- tom) the conventional phase-difference reconstruction. A section crossing the ascending and descending aorta was selected as the imaging slice. Displayed im- ages are (left) anatomical magnitude image and (right) phase-contrast velocity map at systole. With direct phase-difference regularization, the model-based reconstruction largely reduces random background phase noise in the velocity map. 9
[39, 40, 41, 42, 43, 44] , i.e. X M (x, t, ~r) ≈ as (~r)Bs (t) . (8) s The linear basis functions Bs (t) can be generated by simulating a set of repre- sentative signal curves for a range of parameter and performing a singular value decomposition to obtain a good representation. With known coil sensitivities, this leads to a linear inverse problem for the subspace coefficients: X â = argmin ky − PF CBak22 + λi Ri (x) (9) a i After reconstruction of the subspace coefficients as , the parameters x need to be obtained in a separate step. This can be achieved by predicting complete magnetization maps for all time points and fitting a nonlinear signal model. This can be done point-wise, so is much easier than doing a full nonlinear reconstruction. Still, for multi-parametric mapping efficient techniques to map between coefficients and parameters are required [44]. Linear subspace methods have several advantages. Linear subspace models linear problems without local minima. Due to their linearity, they also inher- ently avoid model violations stemming from partial volume effects. Because the matrix multiplication with the basis and other operations commute, they admit a computationally advantageous formulation that allows computation in the subspace [45, 41]. 4.1 T1 Mapping Alternatively, T1 maps were also reconstructed using the subspace method. Similar to [43], the T1 dictionary was constructed using 1000 different 1/R1∗ values linearly range from 5–5000 ms, combining with 100 Mss values from 0.01 · M0 to M0 . This results in 100,000 exponential curves in the dictionary. A subset of such a dictionary is shown in Fig. 5 (left). The other parame- ters are TR = 4.10 ms, 20 spokes per frame, 51 frame in total. The simulated curves are highly correlated and can be represented by only a few principle com- ponents Fig. 5. For easier comparison, the subspace-constraint reconstruction used the coil sensitivity maps estimated using model-based T1 reconstruction. The resulting linear problem was then solved using conjugate gradient or FISTA algorithm in BART. The coefficient maps were then projected back to image series where the 3-parameter fit is applied for each voxel according to equation (4). Fig. 6 (A) shows estimated phantom T1 maps using a variant number of complex coefficients of the linear subspace-based reconstruction with L2 regu- larization. Lower number of coefficients causes bias for quantitative T1 mapping (especially for tubes with short T1s) while higher number of coefficients brings noise in the final T1 maps. Therefore 4 coefficient maps were chosen to com- promise between quantitative accuracy and precision. Fig. 6 (B) compares the 10
(A) Inversion Recovery Signal Simulation (B) Multi-Gradient-Echo Signal Simulation Figure 5: Demonstration of subspace-based methods for (A) single-shot inversion-recovery and (B) multi-gradient-echo signal, respectively. (Left) Sim- ulated (top) T1 relaxation and (bottom) T2∗ relaxation and off-resonance phase modulation curves. (Center) Plot of the first 30 principle components. (Right) The temporal subspace curves that can be linearly combined to form (top) T1 relaxations and (bottom) multi-gradient-echo relaxations. 11
Linear Subspace Model (A) Reference 2 Coeffs. 3 Coeffs 4 Coeffs 5 Coeffs T1 / s 2.0 1.6 1.2 0.8 0.4 0 40 32 Rel. diff (%) x 2.5 24 16 8 0.047 0.032 0.026 0.027 0 (B) Reference 0.05 0.1 0.2 0.5 T1 / s 2.0 1.6 1.2 0.8 0.4 0 40 32 Rel. diff (%) x 2.5 24 16 8 0.027 0.026 0.027 0.041 0 Nonlinear Model (C) Reference 0.05 0.1 0.2 0.5 T1 / s 2.0 1.6 1.2 0.8 0.4 0 40 32 Rel. diff (%) x 2.5 24 16 8 0.022 0.021 0.022 0.025 0 Figure 6: Comparison of linear and nonlinear model-based reconstructions on the simulated phantom. (A). Linear subspace reconstructed T1 maps using 2, 3, 4, 5 complex coefficients and their relative difference to the reference. (B). Linear subspace reconstructed T1 maps using 4 complex coefficients with changing regularization parameters. (C). Model-based reconstructed T1 maps using different regularization strengths. Please note all reconstructions are done with L2-regularizations. The normalized relative errors to the reference are presented on the left-bottom of each figure. 12
(A) x1 Coefficients x5 (B) T1 / s Linear Subspace 2.0 1.6 1.2 0.8 0.4 0 T1 / s 2.0 Nonlinear 1.6 1.2 0.8 0.4 0 Figure 7: (A) Reconstructed 4 complex coefficient maps using the linear sub- space method for a human brain study. (B) Synthesized images (at inversion time 40 ms, 400 ms, 800 ms, 4000 ms) using (top) the above 4 complex coeffi- cient maps of the linear subspace method and (bottom) the 3 physical maps of the nonlinear model-based reconstruction, respectively. The corresponding T1 maps are presented in the rightmost column. effects of regularization strength. Similarly, low value of the regularization pa- rameter brings noise while high regularization strength causes bias. A value of 0.1 was then chosen to compromise T1 accuracy and precision. Fig. 6 (C) then shows the effects of regularization for the model-based reconstruction. A value of 0.1 was selected as it has the least normalized error. The low normalized relative errors on the optimized T1 maps reflect both linear subspace and nonlinear model-based methods can generate T1 maps with good accuracy while nonlinear model-based reconstruction has a slightly better performance (i.e., less normalized relative errors). With the above settings, Fig. 7 (A) depicts the four main coefficient maps estimated using the linear subspace method for a brain study. In this case, a joint `1 -Wavelet sparsity regularization was applied to the maps with a strength of 0.0015 to improve the precision. Fig. 7 (B) presents the synthesized images along with the corresponding T1 maps using (top) the above four coefficient maps for the linear subspace and (bottom) the 3 physical parameter maps for nonlinear model-based reconstructions, where a similar joint `1 -Wavelet sparsity is applied with the regularization parameter 0.09. Again, both linear subspace and nonlinear methods could generate high-quality synthesized images and T1 maps while the nonlinear methods have slightly less noise and better sharpness. Although linear subspace reconstruction has been demonstrated to be a fast 13
RSS magn. subspace fmSSFP phase +180° 0° -180° synth. magn. bSSFP Figure 8: Reconstructed subspace coefficients maps (top) along with its root- sum-squares composite image for a individual slice within the acquired 3D vol- ume. Synthesized bSSFP images are computed from these coefficient maps for different virtual frequency offsets (bottom). and robust quantitative parameter mapping technique, it might not be directly applicable to MR signals with phase modulation along echo trains. For instance, multi-gradient-echo signals are known to be modulated by off-resonance-induced phases. A dictionary of multi-gradient-echo magnitude and phase signals was simulated with 256 × 256 R2∗ and fB0 combinations linearly ranging from 10 to 1000 s−1 and from -200 to 200 Hz, respectively. Fig. 5 displays the magnitude and phase evolution of 7 randomly-selected dictionary entries. The magnitude signal follows the exponential decay, while phase wrappings occur with large field inhomogeneity and long echo train read- out. More importantly, the SVD analysis of the signal dictionary shows that at least 26 principal components are required to represent the complex signal behaviour. 4.2 Frequency-Modulated SSFP Conventional balanced steady-state free precession (bSSFP) sequences exhibit a high signal-to-noise ratio (SNR) but suffer from possible signal voids in regions with certain off-resonance distributions. These voids or banding artifacts can be removed when multiple images are acquired with different transmitter phase cy- cles. Foxall and coworkers demonstrated that bSSFP sequences are tolerant to small but continuous changes in transmitter frequency [46]. In [42] we exploited this method to develop a time-efficient alternative to phase-cycled bSSFP that waives intermediate preparation phases in phase-cycled bSSFP to establish dif- 14
ferent steady-states. Image reconstruction is performed in the low-frequency Fourier subspace and yields banding-free images with close-to-optimal SNR. To this end, a frequency-modulated SSFP (fmSSFP) pulse sequence [46] was combined with 3D stack-of-stars data acquisition such that a single full sweep through the spectral response profile was obtained. Aligned partitions allowed to decouple the reconstruction problem into individual slices by a 1D inverse Fourier transform. After coil sensitivity estimation [47], image reconstruction was performed by solving a linear subspace-constrained reconstruction problem using a local low rank regularization. As a subspace basis, the four lowest order Fourier modes were chosen. From the obtained complex-valued coefficient maps a composite image is derived in a root-sum-squares manner and synthesized bSSFP images are computed for different virtual frequency offsets. 5 Discussion In the past decades various techniques were developed to accelerate quantita- tive MRI. One very general way is to exploit complementary information from spatially distinct receiver coils, called parallel imaging (PI) [48, 49, 50]. Others make use of the fact that MR images are usually sparse in a certain transform domain and combined with incoherent sampling and nonlinear image recon- struction algorithms it is called compressed sensing (CS) [51]. Exploiting this prior knowledge about a compressible image, CS can recover MR images from highly undersampled data [52, 53]. Other approaches combine PI and CS with efficient non-Cartesian sampling schemes [53]. When it comes to parameter mapping, beside of the already mentioned sparsity constraints, also low-rank constraints or joint sparsity can be exploited along the parameter dimension to accelerate the acquisition time [13, 54, 55, 56]. Generally speaking, the method above usually consist of two steps: first re- construction of contrast-weighted images from undersampled datasets and sec- ond, the subsequent voxel-by-voxel fitting/matching. In contrast, model-based reconstructions integrate the underlying MR physics into the forward model, enabling estimation of MR physical images (parameter maps) directly from the undersampled k-space, bypassing the intermediate steps of image reconstruc- tion and pixel-wise fitting/matching completely. This kind of method has the advantages of only reconstructing the desired parameter maps instead of a set of contrast-weighted images, i.e., reducing the number of unknowns tremendously. Model-based reconstructions are, in general, memory demanding and time consuming as all the data has to be hold in memory simultaneously during iterations. However, modern computational devices such as GPUs have enabled faster reconstructions. For example, the computation time for model-based T1 reconstruction presented here has been reduced from around 4 hours in CPU (40-core 2.3 GHz Intel Xeon E5-2650 server with a RAM size of 512 GB) to 6 minutes using GPUs (Tesla V100 SXM2, NVIDIA, Santa Clara, CA). Other smart computational strategies [45] may also be employed to reduce the memory and computational time. 15
Tremendous progress in the fields of machine learning / deep learning has sparked a huge interest in applying these methods to different MRI applications including image reconstruction [57, 58]. However, so far only few applications exist that target accelerated parameter mapping directly [59, 60, 61, 62]. Magnetic Resonance Fingerprintig (MRF) [63] is an alternative technique to perform time-efficient multi-parametric mapping leveraging high undersampling factors. In its original formulation, parameter maps are reconstructed in a two- step procedere. First, time series are generated by an inverse NUFFT operation agnostic to any physical signal model. Second, parameter maps are generated by pixel-wise matching of the obtained time series with a precomputed dictio- nary consisting of simulated signal prototypes. The proposed decoupling into a linear reconstruction of time series and a nonlinear fitting problem solved by exhaustive search results in comparatively short reconstruction times and does not require analytical signal models. These two advantages rendered MRF a very popular approach in the recent years. This two-step procedere, however, comes at a cost. The initial model-agnostic gridding operation results in heavily aliased signal time courses. Aliasing can be removed only partially by pixel-wise matching, as no information on the sampling pattern is available in that step, and might deteriorate or bias the obtained parameter maps. Recent works have tried to overcome this inherent drawback of the two-step method by iterating between time and parameter domain [64] or by formulating the reconstruction as a nonlinear problem that integrates the physical signal model and additional im- age priors [6] similar to the discussed model-based approaches. Also techniques combining iterative reconstructions and grid searches on dictionaries were de- veloped [65]. For a recent review that discusses the basic concept of MRF also in the context of other quantitative methods see [66]. 6 Conclusion By formulating image reconstruction as an inverse problem, model-based recon- struction techniques can estimate quantitative maps of the underlying physical parameters directly from the acquired k-space signals without intermediate im- age reconstruction. While this is computationally demanding, it enables very efficient quantitative MRI. Acknowledgments The authors would like to thank Mr. Ansgar Simon Adler for help with the phase-contrast flow MRI experiment, Dr. Sebastian Rosenzweig for helpful di- cussions and improvements to the figures, and Dr. Tobias Block for the radial spin-echo sequence. 16
Funding Statement This work was supported by the DZHK (German Centre for Cardiovascular Research), by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under grant TA 1473/2-1 / UE 189/4-1 and under Germany’s Ex- cellence Strategy—EXC 2067/1-390729940, and funded in part by NIH under grant U24EB029240. Data Accessibility All model-based reconstructions were performed with the BART toolbox. Scripts to reproduce the examples shown in this work are available at https://github. com/mrirecon/physics-recon. Data are available at DOI: 10.5281/zenodo.4060287. References [1] C. Graff, Z. Li, A. Bilgin, M. I. Altbach, A. F. Gmitro, and E. W. Clarkson. Iterative t2 estimation from highly undersampled radial fast spin-echo data. In Proc. Int. Soc. Mag. Reson. Med., volume 14, 2006. [2] V. T. Olafsson, D. C. Noll, and J. A. Fessler. Fast Joint Reconstruction of Dynamic R2∗ and Field Maps in Functional MRI. IEEE Trans. Med. Imag., 27(9):1177–1188, 2008. [3] K. T. Block, M. Uecker, and J. Frahm. Model-Based Iterative Recon- struction for Radial Fast Spin-Echo MRI. IEEE Trans. Med. Imaging, 28(11):1759–1769, 2009. [4] Jeffrey A. Fessler. Model-based image reconstruction for mri. IEEE Signal Process. Mag., 27(4):81–89, 2010. [5] Johannes Tran-Gia, Daniel Stäb, Tobias Wech, Dietbert Hahn, and Herbert Köstler. Model-based acceleration of parameter mapping (MAP) for satura- tion prepared radially acquired data. Magn. Reson. Med., 70(6):1524–1534, 2013. [6] B. Zhao, F. Lam, and Z. Liang. Model-based mr parameter mapping with sparsity constraints: Parameter estimation and performance bounds. IEEE Trans. Med. Imaging, 33(9):1832–1844, 2014. [7] Johannes Tran-Gia, Sotirios Bisdas, Herbert Köstler, and Uwe Klose. A model-based reconstruction technique for fast dynamic T1 mapping. Magn. Reson. Imaging, 34(3):298–307, 2016. [8] Volkert Roeloffs, Xiaoqing Wang, Tilman J. Sumpf, Markus Untenberger, Dirk Voit, and Jens Frahm. Model-based reconstruction for t1 mapping 17
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