Background: MR fingerprinting (MRF) is a novel method for quantitative assessment of MR relaxometry that has shown high precision and accuracy. However, the method requires data acquisition using customized, complex acquisition strategies and dedicated post processing methods thereby limiting its widespread application.
Objective: To develop a deep learning (DL) network for synthesizing MRF signals from conventional magnitude-only MR imaging data and to compare the results to the actual MRF signal acquired.
Methods: A U-Net DL network was developed to synthesize MRF signals from magnitude-only 3D -weighted brain MRI data acquired from 37 volunteers aged between 21 and 62 years of age. Network performance was evaluated by comparison of the relaxometry data ( , ) generated from dictionary matching of the deep learning synthesized and actual MRF data from 47 segmented anatomic regions. Clustered bootstrapping involving 10,000 bootstraps followed by calculation of the concordance correlation coefficient were performed for both and MRF data pairs. 95% confidence limits and the mean difference between true and DL relaxometry values were also calculated.
Results: The concordance correlation coefficient (and 95% confidence limits) for and MRF data pairs over the 47 anatomic segments were 0.8793 (0.8136-0.9383) and 0.9078 (0.8981-0.9145) respectively. The mean difference (and 95% confidence limits) were 48.23 (23.0-77.3) s and 2.02 (-1.4 to 4.8) s.
Conclusion: It is possible to synthesize MRF signals from MRI data using a DL network, thereby creating the potential for performing quantitative relaxometry assessment without the need for a dedicated MRF pulse sequence.
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http://dx.doi.org/10.3389/fradi.2024.1498411 | DOI Listing |
Front Radiol
December 2024
Department of Radiology, Mayo Clinic, Rochester, MN, United States.
Curr Issues Mol Biol
December 2024
Department of Fisheries Science, Chonnam National University, Yeosu 59626, Republic of Korea.
Myogenic regulator factors (MRFs) are essential for skeletal muscle development in vertebrates, including fish. This study aimed to characterize the role of () in muscle development in Nile tilapia by cloning from muscle tissues. To explore the function of , CRISPR/Cas9 gene editing was employed.
View Article and Find Full Text PDFJ Magn Reson Imaging
December 2024
Center of Biomedical Imaging, Department of Radiology, New York University Grossman School of Medicine, New York, New York, USA.
Background: Three-dimensional MR fingerprinting (3D-MRF) has been increasingly used to assess cartilage degeneration, particularly in the knee joint, by looking into multiple relaxation parameters. A comparable 3D-MRF approach can be adapted to assess cartilage degeneration for the hip joint, with changes to accommodate specific challenges of hip joint imaging.
Purpose: To demonstrate the feasibility and repeatability of 3D-MRF in the bilateral hip jointly we map proton density (PD), T, T, T, and ∆B in clinically feasible scan times.
ArXiv
December 2024
Center for Biomedical Imaging, Department of Radiology, NYU Grossman School of Medicine, New York, NY, USA.
We developed a new sodium magnetic resonance fingerprinting (Na MRF) method for the simultaneous mapping of and sodium density with built-in (radiofrequency transmission inhomogeneities) and corrections (frequency offsets). We based our Na MRF implementation on a 3D FLORET sequence with 23 radiofrequency pulses. To capture the complex spin dynamics of the Na nucleus, the fingerprint dictionary was simulated using the irreducible spherical tensor operators formalism.
View Article and Find Full Text PDFMol Ther Methods Clin Dev
December 2024
Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Regulatory T cells (Tregs) are promising cellular therapies to induce immune tolerance in organ transplantation and autoimmune disease. The success of chimeric antigen receptor (CAR) T cell therapy for cancer has sparked interest in using CARs to generate antigen-specific Tregs. Here, we compared CAR with endogenous T cell receptor (TCR)/CD28 activation in human Tregs.
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