Water/fat separation is a classical problem for in vivo proton MRI. Although many methods have been proposed to address this problem, robust water/fat separation remains a challenge, especially in the presence of large amplitude of static field inhomogeneities. This problem is challenging because of the nonuniqueness of the solution for an isolated voxel. This paper tackles the problem using a statistically motivated formulation that jointly estimates the complete field map and the entire water/fat images. This formulation results in a difficult optimization problem that is solved effectively using a novel graph cut algorithm, based on an iterative process where all voxels are updated simultaneously. The proposed method has good theoretical properties, as well as an efficient implementation. Simulations and in vivo results are shown to highlight the properties of the proposed method and compare it to previous approaches. Twenty-five cardiac datasets acquired on a short, wide-bore scanner with different slice orientations were used to test the proposed method, which produced robust water/fat separation for these challenging datasets. This paper also shows example applications of the proposed method, such as the characterization of intramyocardial fat.

Multiple sclerosis is characterized by inflammatory demyelination and irreversible axonal injury leading to permanent neurological disabilities. Diffusion tensor imaging demonstrates an improved capability over standard magnetic resonance imaging to differentiate axon from myelin pathologies. However, the increased cellularity and vasogenic oedema associated with inflammation cannot be detected or separated from axon/myelin injury by diffusion tensor imaging, limiting its clinical applications. A novel diffusion basis spectrum imaging, capable of characterizing water diffusion properties associated with axon/myelin injury and inflammation, was developed to quantitatively reveal white matter pathologies in central nervous system disorders. Tissue phantoms made of normal fixed mouse trigeminal nerves juxtaposed with and without gel were employed to demonstrate the feasibility of diffusion basis spectrum imaging to quantify baseline cellularity in the absence and presence of vasogenic oedema. Following the phantom studies, in vivo diffusion basis spectrum imaging and diffusion tensor imaging with immunohistochemistry validation were performed on the corpus callosum of cuprizone treated mice. Results demonstrate that in vivo diffusion basis spectrum imaging can effectively separate the confounding effects of increased cellularity and/or grey matter contamination, allowing successful detection of immunohistochemistry confirmed axonal injury and/or demyelination in middle and rostral corpus callosum that were missed by diffusion tensor imaging. In addition, diffusion basis spectrum imaging-derived cellularity strongly correlated with numbers of cell nuclei determined using immunohistochemistry. Our findings suggest that diffusion basis spectrum imaging has great potential to provide non-invasive biomarkers for neuroinflammation, axonal injury and demyelination coexisting in multiple sclerosis.

Partial separability (PS) and sparsity have been previously used to enable reconstruction of dynamic images from undersampled (k, t)-space data. This paper presents a new method to use PS and sparsity constraints jointly for enhanced performance in this context. The proposed method combines the complementary advantages of PS and sparsity constraints using a unified formulation, achieving significantly better reconstruction performance than using either of these constraints individually. A globally convergent computational algorithm is described to efficiently solve the underlying optimization problem. Reconstruction results from simulated and in vivo cardiac MRI data are also shown to illustrate the performance of the proposed method.

Water/fat separation in the presence of B 0 field inhomogeneity is a problem of considerable practical importance in MRI. This article describes two complementary methods for estimating the water/fat images and the field inhomogeneity map from Dixontype acquisitions. One is based on variable projection (VARPRO) and the other on linear prediction (LP). The VARPRO method is very robust and can be used in low signal-to-noise ratio conditions because of its ability to achieve the maximum-likelihood solution. The LP method is computationally more efficient, and is shown to perform well under moderate levels of noise and field inhomogeneity.

Purpose To propose and evaluate P-LORAKS, a new calibrationless parallel imaging reconstruction framework. Theory and Methods LORAKS is a flexible and powerful framework that was recently proposed for constrained MRI reconstruction. LORAKS was based on the observation that certain matrices constructed from fully-sampled k-space data should have low rank whenever the image has limited support or smooth phase, and made it possible to accurately reconstruct images from undersampled or noisy data using low-rank regularization. This paper introduces P-LORAKS, which extends LORAKS to the context of parallel imaging. This is achieved by combining the LORAKS matrices from different channels to yield a larger but more parsimonious low-rank matrix model of parallel imaging data. This new model can be used to regularize the reconstruction of undersampled parallel imaging data, and implicitly imposes phase, support, and parallel imaging constraints without needing to calibrate phase, support, or sensitivity profiles. Results The capabilities of P-LORAKS are evaluated with retrospectively undersampled data and compared against existing parallel MRI reconstruction methods. Results show that P-LORAKS can improve parallel imaging reconstruction quality, and can enable the use of new k-space trajectories that are not compatible with existing reconstruction methods. Conclusion The P-LORAKS framewok provides a new and effective way to regularize parallel imaging reconstruction.

Magnetic resonance (MR) fingerprinting is a new quantitative imaging paradigm, which simultaneously acquires multiple MR tissue parameter maps in a single experiment. In this paper, we present an estimation-theoretic framework to perform experiment design for MR fingerprinting. Specifically, we describe a discrete-time dynamic system to model spin dynamics, and derive an estimation-theoretic bound, i.e., the Cramér-Rao bound (CRB), to characterize the signal-to-noise ratio (SNR) efficiency of an MR fingerprinting experiment. We then formulate an optimal experiment design problem, which determines a sequence of acquisition parameters to encode MR tissue parameters with the maximal SNR efficiency, while respecting the physical constraints and other constraints from the image decoding/reconstruction process. We evaluate the performance of the proposed approach with numerical simulations, phantom experiments, and in vivo experiments. We demonstrate that the optimized experiments substantially reduce data acquisition time and/or improve parameter estimation. For example, the optimized experiments achieve about a factor of two improvement in the accuracy of T2 maps, while keeping similar or slightly better accuracy of T1 maps. Finally, as a remarkable observation, we find that the sequence of optimized acquisition parameters appears to be highly structured rather than randomly/pseudorandomly varying as is prescribed in the conventional MR fingerprinting experiments.

There has been significant recent interest in fast imaging with sparse sampling. Conventional imaging methods are based on ShannonNyquist sampling theory. As such, the number of required samples often increases exponentially with the dimensionality of the image, which limits achievable resolution in high-dimensional scenarios. The partially-separable function (PSF) model has previously been proposed to enable sparse data sampling in this context. Existing methods to leverage PSF structure utilize tailored data sampling strategies, which enable a specialized two-step reconstruction procedure. This work formulates the PSF reconstruction problem using the matrix-recovery framework. The explicit matrix formulation provides new opportunities for data acquisition and image reconstruction with rank constraints. Theoretical results from the emerging field of low-rank matrix recovery (which generalizes theory from sparse-vector recovery) and our empirical results illustrate the potential of this new approach.

Purpose To propose and evaluate a novel multidimensional approach for imaging sub-voxel tissue compartments called Diffusion-Relaxation Correlation Spectroscopic Imaging (DR-CSI). Theory and Methods Multi-exponential modeling of MR diffusion or relaxation data is commonly used to infer the many different microscopic tissue compartments that contribute signal to macroscopic MR imaging voxels. However, multi-exponential estimation is known to be difficult and ill-posed. Observing that this ill-posedness is theoretically reduced in higher dimensions, DR-CSI uses a novel multidimensional imaging experiment that jointly encodes diffusion and relaxation information, and then uses a novel constrained reconstruction technique to generate a multidimensional diffusion-relaxation correlation spectrum for every voxel. The peaks of the multidimensional spectrum are expected to correspond to the distinct tissue microenvironments that are present within each macroscopic imaging voxel. Results Using numerical simulations, experiment data from a custom-built phantom, and experiment data from a mouse model of traumatic spinal cord injury, DR-CSI is demonstrated to provide substantially better multi-compartment resolving power compared to conventional diffusion- and relaxation-based methods. Conclusion The DR-CSI approach provides powerful new capabilities for resolving the different components of multi-compartment tissue models, and can be leveraged to significantly expand the insights provided by MRI in studies of tissue microstructure.