Background: Although quantitative myocardial T1 and T2 mappings are clinically used to evaluate myocardial diseases, their application needs a minimum of six breath-holds to cover three short-axis slices. The purpose of this work is to simultaneously quantify multislice myocardial T1 and T2 across three short-axis slices in one breath-hold by combining simultaneous multislice (SMS) with multimapping.
Methods: An SMS-Multimapping sequence with multiband radiofrequency (RF) excitations and Cartesian fast low-angle shot readouts was developed for data acquisition. When 3 slices are simultaneously acquired, the acceleration rate is around 12-fold, causing a highly ill-conditioned reconstruction problem. To mitigate image artifacts and noise caused by the ill-conditioning, a reconstruction algorithm based on locally low-rank and sparsity (LLRS) constraints was developed. Validation was performed in phantoms and in vivo imaging, with 20 healthy subjects and 4 patients, regarding regional mean, precision, and scan-rescan reproducibility.
Results: The phantom imaging shows that SMS-Multimapping with locally low-rank (LLRS) accurately reconstructed multislice T1 and T2 maps despite a six-fold acceleration of scan time. Healthy subject imaging shows that the proposed LLRS algorithm substantially improved image quality relative to split slice-generalized autocalibrating partially parallel acquisition. Compared with modified look-locker inversion recovery (MOLLI), SMS-Multimapping exhibited higher T1 mean (1118 ± 43 ms vs 1190 ± 49 ms, P < 0.01), lower precision (67 ± 17 ms vs 90 ± 17 ms, P < 0.01), and acceptable scan-rescan reproducibility measured by 2 scans 10-min apart (bias = 1.4 ms for MOLLI and 9.0 ms for SMS-Multimapping). Compared with balanced steady-state free precession (bSSFP) T2 mapping, SMS-Multimapping exhibited similar T2 mean (43.5 ± 3.3 ms vs 43.0 ± 3.5 ms, P = 0.64), similar precision (4.9 ± 2.1 ms vs 5.1 ± 1.0 ms, P = 0.93), and acceptable scan-rescan reproducibility (bias = 0.13 ms for bSSFP T2 mapping and 0.55 ms for SMS-Multimapping). In patients, SMS-Multimapping clearly showed the abnormality in a similar fashion as the reference methods despite using only one breath-hold.
Conclusion: SMS-Multimapping with the proposed LLRS reconstruction can measure multislice T1 and T2 maps in one breath-hold with good accuracy, reasonable precision, and acceptable reproducibility, achieving a six-fold reduction of scan time and an improvement of patient comfort.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.jocmr.2024.101125 | DOI Listing |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11663759 | PMC |
ArXiv
November 2024
Laboratoire de Neurosciences Cognitives et Computationnelles, INSERM U960.
Networks of excitatory and inhibitory (EI) neurons form a canonical circuit in the brain. Seminal theoretical results on dynamics of such networks are based on the assumption that synaptic strengths depend on the type of neurons they connect, but are otherwise statistically independent. Recent synaptic physiology datasets however highlight the prominence of specific connectivity patterns that go well beyond what is expected from independent connections.
View Article and Find Full Text PDFBMC Med Imaging
December 2024
National Engineering Research Center of Advanced Magnetic Resonance Technologies for Diagnosis and Therapy, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Background: Current mainstream cardiovascular magnetic resonance-feature tracking (CMR-FT) methods, including optical flow and pairwise registration, often suffer from the drift effect caused by accumulative tracking errors. Here, we developed a CMR-FT method based on deformable groupwise registration with a locally low-rank (LLR) dissimilarity metric to improve myocardial tracking and strain estimation accuracy.
Methods: The proposed method, Groupwise-LLR, performs feature tracking by iteratively updating the entire displacement field across all cardiac phases to minimize the sum of the patchwise signal ranks of the deformed movie.
Phys Med Biol
November 2024
Department of Pulmonary and Critical Care Medicine, General Hospital of Ningxia Medical University, Yinchuan 750004, People's Republic of China.
. Low-dose computed tomography (LDCT) is an imaging technique that can effectively help patients reduce radiation dose, which has attracted increasing interest from researchers in the field of medical imaging. Nevertheless, LDCT imaging is often affected by a large amount of noise, making it difficult to clearly display subtle abnormalities or lesions.
View Article and Find Full Text PDFbioRxiv
December 2024
Center for Neural Science, New York University, New York, NY, USA.
Neocortex-wide neural activity is organized into distinct networks of areas engaged in different cognitive processes. To elucidate the underlying mechanism of flexible network reconfiguration, we developed connectivity-constrained macaque and human whole-cortex models. In our model, within-area connectivity consists of a mixture of symmetric, asymmetric, and random motifs that give rise to stable (attractor) or transient (sequential) heterogeneous dynamics.
View Article and Find Full Text PDFbioRxiv
October 2024
Center for Magnetic Resonance Research, Radiology, Medical School, University of Minnesota, Minneapolis, Minnesota.
Purpose: to propose a two-step non-local principal component analysis (PCA) method and demonstrate its utility for denoising diffusion tensor MRI (DTI) with a few diffusion directions.
Methods: A two-step denoising pipeline was implemented to ensure accurate patch selection even with high noise levels and was coupled with data preprocessing for g-factor normalization and phase stabilization before data denoising with a non-local PCA algorithm. At the heart of our proposed pipeline was the use of a data-driven optimal shrinkage algorithm to manipulate the singular values in a way that would optimally estimate the noise-free signal.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!