Magnetic resonance multitasking for motion-resolved quantitative cardiovascular imaging.

Quantitative cardiovascular magnetic resonance (CMR) imaging can be used to characterize fibrosis, oedema, ischaemia, inflammation and other disease conditions. However, the need to reduce artefacts arising from body motion through a combination of electrocardiography (ECG) control, respiration control, and contrast-weighting selection makes CMR exams lengthy. Here, we show that physiological motions and other dynamic processes can be conceptualized as multiple time dimensions that can be resolved via low-rank tensor imaging, allowing for motion-resolved quantitative imaging with up to four time dimensions. This continuous-acquisition approach, which we name cardiovascular MR multitasking, captures - rather than avoids - motion, relaxation and other dynamics to efficiently perform quantitative CMR without the use of ECG triggering or breath holds. We demonstrate that CMR multitasking allows for T1 mapping, T1-T2 mapping and time-resolved T1 mapping of myocardial perfusion without ECG information and/or in free-breathing conditions. CMR multitasking may provide a foundation for the development of setup-free CMR imaging for the quantitative evaluation of cardiovascular health

Cardiac cine magnetic resonance fingerprinting for combined ejection fraction, T1 and T2 quantification

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/156191/2/nbm4323_am.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/156191/1/nbm4323.pd

Accelerated partial separable model using dimension-reduced optimization technique for ultra-fast cardiac MRI

Objective. Imaging dynamic object with high temporal resolution is challenging in magnetic resonance imaging (MRI). Partial separable (PS) model was proposed to improve the imaging quality by reducing the degrees of freedom of the inverse problem. However, PS model still suffers from long acquisition time and even longer reconstruction time. The main objective of this study is to accelerate the PS model, shorten the time required for acquisition and reconstruction, and maintain good image quality simultaneously. Approach. We proposed to fully exploit the dimension reduction property of the PS model, which means implementing the optimization algorithm in subspace. We optimized the data consistency term, and used a Tikhonov regularization term based on the Frobenius norm of temporal difference. The proposed dimension-reduced optimization technique was validated in free-running cardiac MRI. We have performed both retrospective experiments on public dataset and prospective experiments on in-vivo data. The proposed method was compared with four competing algorithms based on PS model, and two non-PS model methods. Main results. The proposed method has robust performance against shortened acquisition time or suboptimal hyper-parameter settings, and achieves superior image quality over all other competing algorithms. The proposed method is 20-fold faster than the widely accepted PS+Sparse method, enabling image reconstruction to be finished in just a few seconds. Significance. Accelerated PS model has the potential to save much time for clinical dynamic MRI examination, and is promising for real-time MRI applications.Comment: 23 pages, 11 figures. Accepted as manuscript on Physics in Medicine & Biolog

Current Applications and Future Development of Magnetic Resonance Fingerprinting in Diagnosis, Characterization, and Response Monitoring in Cancer

Magnetic resonance imaging (MRI) has enabled non-invasive cancer diagnosis, monitoring, and management in common clinical settings. However, inadequate quantitative analyses in MRI continue to limit its full potential and these often have an impact on clinicians' judgments. Magnetic resonance fingerprinting (MRF) has recently been introduced to acquire multiple quantitative parameters simultaneously in a reasonable timeframe. Initial retrospective studies have demonstrated the feasibility of using MRF for various cancer characterizations. Further trials with larger cohorts are still needed to explore the repeatability and reproducibility of the data acquired by MRF. At the moment, technical difficulties such as undesirable processing time or lack of motion robustness are limiting further implementations of MRF in clinical oncology. This review summarises the latest findings and technology developments for the use of MRF in cancer management and suggests possible future implications of MRF in characterizing tumour heterogeneity and response assessment

Simultaneous Multiparametric and Multidimensional Cardiovascular Magnetic Resonance Imaging

No abstract available

MR Shuffling: Accelerated Single-Scan Multi-Contrast Magnetic Resonance Imaging

Magnetic resonance imaging (MRI) is an attractive medical imaging modality as it is non-invasive and does not involve ionizing radiation. Routine clinical MRI exams obtain MR images corresponding to different soft tissue contrast by performing multiple scans. When two-dimensional (2D) imaging is used, these scans are often repeated in other scanning planes. As a result, the number of scans comprising an MRI exam leads to prohibitively long exam times as compared to other medical imaging modalities such as computed tomography. Many approaches have been designed to accelerate the MRI acquisition while maintaining diagnostic quality.One approach is to collect multiple measurements while the MRI signal is evolving due to relaxation. This enables a reduction in scan time, as fewer acquisition windows are needed to collect the same number of measurements. However, when the temporal aspect of the acquisition is left unmodeled, artifacts are likely to appear in the reconstruction. Most often, these artifacts manifest as image blurring. The effect depends on the acquisition parameters as well as the tissue relaxation itself, resulting in spatially varying blurring. The severity of the artifacts is directly related to the level of acceleration, and thus presents a tradeoff with scan time. The effect is amplified when imaging in three dimensions, severely limiting scan efficiency. Volumetric variants would be used if not for the blurring, as they are able to reconstruct images at isotropic resolution and support mutli-planar reformatting.Another established acceleration technique, called parallel imaging, takes advantage of spatially sensitive receive coil arrays to collect multiple MRI measurements in parallel. Thus, the acquisition is shortened, and the reconstruction uses the spatial sensitivity information to recover the image. More recently, methods have been developed that leverage image structure such as sparsity and low rank to reduce the required number of samples for a well-posed reconstruction. Compressed sensing and its low rank extensions use these concepts to acquire incoherent measurements below the Nyquist rate. These techniques are especially suited to MRI, as incoherent measurements can be easily achieved through pseudo-random under-sampling. As the mechanisms behind parallel imaging and compressed sensing are fundamentally different, they can be combined to achieve even higher acceleration.This dissertation proposes accelerated MRI acquisition and reconstruction techniques that account for the temporal dynamics of the MR signal. The methods build off of parallel imaging and compressed sensing to reduce scan time and flexibly model the temporal relaxation behavior. By randomly shuffling the sampling in the acquisition stage and imposing low rank constraints in the reconstruction stage, intrinsic physical parameters are modeled and their dynamics are recovered as multiple images of varying tissue contrast. Additionally, blurring artifacts are significantly reduced, as the temporal dynamics are accounted for in the reconstruction.This dissertation first introduces T2 Shuffling, a volumetric technique that reduces blurring and reconstructs multiple T2-weighted image contrasts from a single acquisition. The method is integrated into a clinical hospital environment and evaluated on patients. Next, this dissertation develops a fast and distributed reconstruction for T2 Shuffling that achieves clinically relevant processing time latency. Clinical validation results are shown comparing T2 Shuffling as a single-sequence alternative to conventional pediatric knee MRI. Based off the compelling results, a fast targeted knee MRI using T2 Shuffling is implemented, enabling same-day access to MRI at one-third the cost compared to the conventional exam. To date, over 2,400 T2 Shuffling patient scans have been performed.Continuing the theme of accelerated multi-contrast imaging, this dissertation extends the temporal signal model with T1-T2 Shuffling. Building off of T2 Shuffling, the new method additionally samples multiple points along the saturation recovery curve by varying the repetition time durations during the scan. Since the signal dynamics are governed by both T1 recovery and T2 relaxation, the reconstruction captures information about both intrinsic tissue parameters. As a result, multiple target synthetic contrast images are reconstructed, all from a single scan. Approaches for selecting the sequence parameters are provided, and the method is evaluated on in vivo brain imaging of a volunteer.Altogether, these methods comprise the theme of MR Shuffling, and may open new pathways toward fast clinical MRI