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Kawin Setsompop

Publications and source records attributed to Kawin Setsompop.

46 records · Page 3Linked to original sources

Accelerated spin-echo fMRI using Multisection Excitation by Simultaneous Spin-echo Interleaving (MESSI) with complex-encoded generalized SLIce Dithered Enhanced Resolution (cgSlider) Simultaneous Multi-Slice Echo-Planar Imaging

Spin-echo functional MRI (SE-fMRI) has the potential to improve spatial specificity when compared to gradient-echo fMRI. However, high spatiotemporal resolution SE-fMRI with large slice-coverage is challenging as SE-fMRI requires a long echo time (TE) to generate blood oxygenation level-dependent (BOLD) contrast, leading to long repetition times (TR). The aim of this work is to develop an acquisition method that enhances the slice-coverage of SE-fMRI at high spatiotemporal resolution. An acquisition scheme was developed entitled Multisection Excitation by Simultaneous Spin-echo Interleaving (MESSI) with complex-encoded generalized SLIce Dithered Enhanced Resolution (cgSlider). MESSI utilizes the dead-time during the long TE by interleaving the excitation and readout of two slices to enable 2x slice-acceleration, while cgSlider utilizes the stable temporal background phase in SE-fMRI to encode and decode two adjacent slices simultaneously with a phase-constrained reconstruction method. The proposed cgSlider-MESSI was also combined with Simultaneous Multi-Slice (SMS) to achieve further slice-acceleration. This combined approach was used to achieve 1.5mm isotropic whole-brain SE-fMRI with a temporal resolution of 1.5s and was evaluated using sensory stimulation and breath-hold tasks at 3T. Compared to conventional SE-SMS, cgSlider-MESSI-SMS provides four-fold increase in slice-coverage for the same TR, with comparable temporal signal-to-noise ratio. Corresponding fMRI activation from cgSlider-MESSI-SMS for both fMRI tasks were consistent with those from conventional SE-SMS. Overall, cgSlider-MESSI-SMS achieved a 32x encoding-acceleration by combining RinplanexMBxcgSliderxMESSI=4x2x2x2. High-quality, high-resolution whole-brain SE-fMRI was acquired at a short TR using cgSlider-MESSI-SMS.

physics.med-ph↗

Joint multi-contrast Variational Network reconstruction (jVN) with application to rapid 2D and 3D imaging

Purpose: To improve the image quality of highly accelerated multi-channel MRI data by learning a joint variational network that reconstructs multiple clinical contrasts jointly. Methods: Data from our multi-contrast acquisition was embedded into the variational network architecture where shared anatomical information is exchanged by mixing the input contrasts. Complementary k-space sampling across imaging contrasts and Bunch-Phase/Wave-Encoding were used for data acquisition to improve the reconstruction at high accelerations. At 3T, our joint variational network approach across T1w, T2w and T2-FLAIR-weighted brain scans was tested for retrospective under-sampling at R=6 (2D) and R=4x4 (3D) acceleration. Prospective acceleration was also performed for 3D data where the combined acquisition time for whole brain coverage at 1 mm isotropic resolution across three contrasts was less than three minutes. Results: Across all test datasets, our joint multi-contrast network better preserved fine anatomical details with reduced image-blurring when compared to the corresponding single-contrast reconstructions. Improvement in image quality was also obtained through complementary k-space sampling and Bunch-Phase/Wave-Encoding where the synergistic combination yielded the overall best performance as evidenced by exemplarily slices and quantitative error metrics. Conclusion: By leveraging shared anatomical structures across the jointly reconstructed scans, our joint multi-contrast approach learnt more efficient regularizers which helped to retain natural image appearance and avoid over-smoothing. When synergistically combined with advanced encoding techniques, the performance was further improved, enabling up to R=16-fold acceleration with good image quality. This should help pave the way to very rapid high-resolution brain exams.

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Nonlinear Dipole Inversion (NDI) enables Quantitative Susceptibility Mapping (QSM) without parameter tuning

We propose Nonlinear Dipole Inversion (NDI) for high-quality Quantitative Susceptibility Mapping (QSM) without regularization tuning, while matching the image quality of state-of-the-art reconstruction techniques. In addition to avoiding over-smoothing that these techniques often suffer from, we also obviate the need for parameter selection. NDI is flexible enough to allow for reconstruction from an arbitrary number of head orientations, and outperforms COSMOS even when using as few as 1-direction data. This is made possible by a nonlinear forward-model that uses the magnitude as an effective prior, for which we derived a simple gradient descent update rule. We synergistically combine this physics-model with a Variational Network (VN) to leverage the power of deep learning in the VaNDI algorithm. This technique adopts the simple gradient descent rule from NDI and learns the network parameters during training, hence requires no additional parameter tuning. Further, we evaluate NDI at 7T using highly accelerated Wave-CAIPI acquisitions at 0.5 mm isotropic resolution and demonstrate high-quality QSM from as few as 2-direction data.

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Fast Sub-millimeter Diffusion MRI using gSlider-SMS and SNR-Enhancing Joint Reconstruction

We evaluate a new approach for achieving diffusion MRI data with high spatial resolution, large volume coverage, and fast acquisition speed. A recent method called gSlider-SMS enables whole-brain sub-millimeter diffusion MRI with high signal-to-noise ratio (SNR) efficiency. However, despite the efficient acquisition, the resulting images can still suffer from low SNR due to the small size of the imaging voxels. This work proposes to mitigate the SNR problem by combining gSlider-SMS with a regularized SNR-enhancing reconstruction approach. Illustrative results show that, from gSlider-SMS data acquired over a span of only 25 minutes on a 3T scanner, the proposed method is able to produce 71 MRI images (64 diffusion encoding orientations with $b=$1500 s/mm$^2$, and 7 images without diffusion weighting) of the entire \emph{in vivo} human brain with nominal 0.66 mm spatial resolution. Using data acquired from 75 minutes of acquisition as a gold standard reference, we demonstrate that the proposed SNR-ehancement procedure leads to substantial improvements in estimated diffusion parameters compared to conventional gSlider reconstruction. Results also demonstrate that the proposed method has advantages relative to denoising methods based on low-rank matrix modeling. A theoretical analysis of the trade-off between spatial resolution and SNR suggests that the proposed approach has high efficiency. The combination of gSlider-SMS with advanced regularized reconstruction enables high-resolution quantitative diffusion MRI from a relatively fast acquisition.

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Highly efficient MRI through multi-shot echo planar imaging

Multi-shot echo planar imaging (msEPI) is a promising approach to achieve high in-plane resolution with high sampling efficiency and low T2* blurring. However, due to the geometric distortion, shot-to-shot phase variations and potential subject motion, msEPI continues to be a challenge in MRI. In this work, we introduce acquisition and reconstruction strategies for robust, high-quality msEPI without phase navigators. We propose Blip Up-Down Acquisition (BUDA) using interleaved blip-up and -down phase encoding, and incorporate B0 forward-modeling into Hankel structured low-rank model to enable distortion- and navigator-free msEPI. We improve the acquisition efficiency and reconstruction quality by incorporating simultaneous multi-slice acquisition and virtual-coil reconstruction into the BUDA technique. We further combine BUDA with the novel RF-encoded gSlider acquisition, dubbed BUDA-gSlider, to achieve rapid high isotropic-resolution MRI. Deploying BUDA-gSlider with model-based reconstruction allows for distortion-free whole-brain 1mm isotropic T2 mapping in about 1 minute. It also provides whole-brain 1mm isotropic diffusion imaging with high geometric fidelity and SNR efficiency. We finally incorporate sinusoidal wave gradients during the EPI readout to better use coil sensitivity encoding with controlled aliasing.

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Linear Predictability in MRI Reconstruction: Leveraging Shift-Invariant Fourier Structure for Faster and Better Imaging

Over the past several decades, many different types of computational imaging approaches have been proposed for improving MRI. In this paper, we provide an overview of methods that assume that MRI Fourier data is linearly predictable. Linear prediction is well known in signal processing and may be most recognizable for its usefulness in speech processing and spectrum estimation applications. In MRI, linear predictability implies that data can be sampled below the conventional Nyquist rate, since unmeasured data may be imputed as a shift-invariant linear combination of measured samples. Linear predictive methods include some of the earliest methods in the computational MRI reconstruction field, some of the most widely utilized computational MRI methods in modern clinical practice, and some of the most flexible and versatile modern computational imaging approaches that are enabling unprecedented new styles of data acquisition. In addition, the concept of linear predictability can be used to unify a number of more classical MRI reconstruction constraints, but without needing to make the strong assumptions of classical constrained reconstruction methods.

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High-fidelity, high-isotropic resolution diffusion imaging through gSlider acquisition with B1+ & T1 corrections and integrated ΔB0/Rx shim array

Purpose: B1+ and T1 corrections and dynamic multi-coil shimming approaches were proposed to improve the fidelity of high isotropic resolution Generalized slice dithered enhanced resolution (gSlider) diffusion imaging. Methods: An extended reconstruction incorporating B1+ inhomogeneity and T1 recovery information was developed to mitigate slab-boundary artifacts in short-TR gSlider acquisitions. Slab-by-slab dynamic B0 shimming using a multi-coil integrated ΔB0/Rx shim-array, and high in-plane acceleration (Rinplane=4) achieved with virtual-coil GRAPPA were also incorporated into a 1 mm isotropic resolution gSlider acquisition/reconstruction framework to achieve an 8-11 fold reduction in geometric distortion compared to single-shot EPI. Results: The slab-boundary artifacts were alleviated by the proposed B1+ and T1 corrections compared to the standard gSlider reconstruction pipeline for short-TR acquisitions. Dynamic shimming provided >50% reduction in geometric distortion compared to conventional global 2nd order shimming. 1 mm isotropic resolution diffusion data show that the typically problematic temporal and frontal lobes of the brain can be imaged with high geometric fidelity using dynamic shimming. Conclusions: The proposed B1+ and T1 corrections and local-field control substantially improved the fidelity of high isotropic resolution diffusion imaging, with reduced slab-boundary artifacts and geometric distortion compared to conventional gSlider acquisition and reconstruction. This enabled high-fidelity whole-brain 1 mm isotropic diffusion imaging with 64 diffusion-directions in 20 minutes using a 3T clinical scanner.

physics.med-ph↗

Highly Accelerated Multishot EPI through Synergistic Machine Learning and Joint Reconstruction

Purpose: To introduce a combined machine learning (ML) and physics-based image reconstruction framework that enables navigator-free, highly accelerated multishot echo planar imaging (msEPI), and demonstrate its application in high-resolution structural and diffusion imaging. Methods: Singleshot EPI is an efficient encoding technique, but does not lend itself well to high-resolution imaging due to severe distortion artifacts and blurring. While msEPI can mitigate these artifacts, high-quality msEPI has been elusive because of phase mismatch arising from shot-to-shot variations which preclude the combination of the multiple-shot data into a single image. We employ deep learning to obtain an interim image with minimal artifacts, which permits estimation of image phase variations due to shot-to-shot changes. These variations are then included in a Joint Virtual Coil Sensitivity Encoding (JVC-SENSE) reconstruction to utilize data from all shots and improve upon the ML solution. Results: Our combined ML + physics approach enabled Rinplane x MultiBand (MB) = 8x2-fold acceleration using 2 EPI-shots for multi-echo imaging, so that whole-brain T2 and T2* parameter maps could be derived from an 8.3 sec acquisition at 1x1x3mm3 resolution. This has also allowed high-resolution diffusion imaging with high geometric fidelity using 5-shots at Rinplane x MB = 9x2-fold acceleration. To make these possible, we extended the state-of-the-art MUSSELS reconstruction technique to Simultaneous MultiSlice (SMS) encoding and used it as an input to our ML network. Conclusion: Combination of ML and JVC-SENSE enabled navigator-free msEPI at higher accelerations than previously possible while using fewer shots, with reduced vulnerability to poor generalizability and poor acceptance of end-to-end ML approaches.

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Optimal Experiment Design for Magnetic Resonance Fingerprinting: Cramér-Rao Bound Meets Spin Dynamics

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 Cramer-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 $T_2$ maps, while keeping similar or slightly better accuracy of $T_1$ maps. Finally, as a remarkable observation, we find that the sequence of optimized acquisition parameters appears to be highly structured rather than randomly/pseudo-randomly varying as is prescribed in the conventional MR fingerprinting experiments.

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Quantitative Susceptibility Mapping using Deep Neural Network: QSMnet

Deep neural networks have demonstrated promising potential for the field of medical image reconstruction. In this work, an MRI reconstruction algorithm, which is referred to as quantitative susceptibility mapping (QSM), has been developed using a deep neural network in order to perform dipole deconvolution, which restores magnetic susceptibility source from an MRI field map. Previous approaches of QSM require multiple orientation data (e.g. Calculation of Susceptibility through Multiple Orientation Sampling or COSMOS) or regularization terms (e.g. Truncated K-space Division or TKD; Morphology Enabled Dipole Inversion or MEDI) to solve the ill-conditioned deconvolution problem. Unfortunately, they either require long multiple orientation scans or suffer from artifacts. To overcome these shortcomings, a deep neural network, QSMnet, is constructed to generate a high quality susceptibility map from single orientation data. The network has a modified U-net structure and is trained using gold-standard COSMOS QSM maps. 25 datasets from 5 subjects (5 orientation each) were applied for patch-wise training after doubling the data using augmentation. Two additional datasets of 5 orientation data were used for validation and test (one dataset each). The QSMnet maps of the test dataset were compared with those from TKD and MEDI for image quality and consistency in multiple head orientations. Quantitative and qualitative image quality comparisons demonstrate that the QSMnet results have superior image quality to those of TKD or MEDI and have comparable image quality to those of COSMOS. Additionally, QSMnet maps reveal substantially better consistency across the multiple orientations than those from TKD or MEDI. As a preliminary application, the network was tested for two patients. The QSMnet maps showed similar lesion contrasts with those from MEDI, demonstrating potential for future applications.

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