Acquisition and Reconstruction Techniques for Fat Quantification Using Magnetic Resonance Imaging

Quantifying the tissue fat concentration is important for several diseases in various organs including liver, heart, skeletal muscle and kidney. Uniquely, MRI can separate the signal from water and fat in-vivo, rendering it the most suitable imaging modality for non-invasive fat quantification. Chemical-shift-encoded MRI is commonly used for quantitative fat measurement due to its unique ability to generate a separate image for water and fat. The tissue fat concentration can be consequently estimated from the two images. However, several confounding factors can hinder the water/fat separation process, leading to incorrect estimation of fat concentration. The inhomogeneities of the main magnetic field represent the main obstacle to water/fat separation. Most existing techniques rely mainly on imposing spatial smoothness constraints to address this problem; however, these often fail to resolve large and abrupt variations in the magnetic field. A novel convex relaxation approach to water/fat separation is proposed. The technique is compared to existing methods, demonstrating its robustness to resolve abrupt magnetic field inhomogeneities. Water/fat separation requires the acquisition of multiple images with different echo-times, which prolongs the acquisition time. Bipolar acquisitions can efficiently acquire the required data in shorter time. However, they induce phase errors that significantly distort the fat measurements. A new bipolar acquisition strategy that overcomes the phase errors and provides accurate fat measurements is proposed. The technique is compared to the current clinical sequence, demonstrating its efficiency in phantoms and in-vivo experiments. The proposed acquisition technique is also applied on animal models to achieve higher spatial resolution than the current sequence. In conclusion, this dissertation describes a complete framework for accurate and precise MRI fat quantification. Novel acquisitions and reconstruction techniques that address the current challenges for fat quantification are proposed

A convex relaxation approach to fat/water separation with minimum label description

While Magnetic Resonance Imaging is capable of separating water and fat components in the body, mapping of magnetic field inhomogeneities is essential for the successful application of this process. In this study, we address the problem of field map estimation using a convex-relaxed max-flow method. We propose a novel two-stage approach that leads to the global optimum of the proposed problem. The first stage minimizes the signal residuals via a convexrelaxed minimum description length (MDL)-based approach. The MDL-based labeling model penalizes the total number of appearing labels, which helps to avoid field map errors when abrupt changes in field homogeneity exist. By exploring the whole range of possible frequency offsets, this stage ensures limiting the estimated field offset within certain boundaries where the global minimum resides. The second stage employs the output of the labeling model in a commonly used gradient-descent based method (known as IDEAL) to converge to the exact global minimum, i.e. the required value of the field offset. Experimental results for cardiac imaging, where challenging field inhomogeneities exist, showed that our method significantly outperforms over a widely-used technique for fat/water separation in terms of robustness and efficiency

Accelerated Imaging Techniques for Chemical Shift Magnetic Resonance Imaging

Chemical shift imaging is a method for the separation two or more chemical species. The cost of chemical shift encoding is increased acquisition time as multiple acquisitions are acquired at different echo times. Image acceleration techniques, typically parallel imaging, are often used to improve the spatial coverage and resolution. This thesis describes a new technique for estimating the signal to noise ratio for parallel imaging reconstructions and proposes new image reconstructions for accelerated chemical shift imaging using compressed sensing and/or parallel imaging for two applications: water-fat separation and metabolic imaging of hyperpolarized [1-13C] pyruvate. Spatially varying noise in parallel imaging reconstructions makes measurements of the signal to noise ratio, a commonly used metric for image for image quality, difficult. Existing approaches have limitations such as they are not applicable to all reconstructions, require significant computation time, or rely on repeated image acquisitions. A SNR estimation technique is proposed that does not exhibit these limitations. Water-fat imaging of highly undersampled datasets from the liver, calf, knee, and abdominal cavity are demonstrated using a customized IDEAL-SPGR pulse sequence and an integrated compressed sensing, parallel imaging, water-fat reconstruction. This method is shown to offer comparable image quality relative to fully sampled reference images for a range of acceleration factors. At high acceleration factors, this technique is shown to offer improved image quality when compared to the current standard of parallel imaging. Accelerated chemical shift imaging was demonstrated for metabolic of hyperpolarized [1-13C] pyruvate. Pyruvate, lactate, alanine, and bicarbonate images were reconstructed from undersampled datasets. Phantoms were used to validate this technique while retrospectively and prospectively accelerated 3D in vivo datasets were used to demonstrate. Alternatively, acceleration was also achieved through the use of a high performance magnetic field gradient set. This thesis addresses the inherently slow acquisition times of chemical shift imaging by examining the role compressed sensing and parallel imaging can be play in chemical shift imaging. An approach to SNR assessment for parallel imaging reconstruction is proposed and approaches to accelerated chemical shift imaging are described for applications in water-fat imaging and metabolic imaging of hyperpolarized [1-13C] pyruvate