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Background: Despite its potential to improve the assessment of cardiovascular diseases, four-dimensional (4D) flow cardiovascular magnetic resonance (CMR) is hampered by long scan times. 4D flow CMR is conventionally acquired with three motion encodings and one reference encoding, as the three-dimensional velocity data are obtained by subtracting the phase of the reference from the phase of the motion encodings. In this study, we aim to use deep learning to predict the reference encoding from the three motion encodings for cardiovascular 4D flow.
Methods: A U-Net was trained with adversarial learning (U-Net) and with a velocity frequency-weighted loss function (U-Net) to predict the reference encoding from the three motion encodings obtained with a non-symmetric velocity-encoding scheme. Whole-heart 4D flow datasets from 126 patients with different types of cardiomyopathies were retrospectively included. The models were trained on 113 patients with a 5-fold cross-validation, and tested on 13 patients. Flow volumes in the aorta and pulmonary artery, mean and maximum velocity, total and maximum turbulent kinetic energy at peak systole in the cardiac chambers and main vessels were assessed.
Results: Three-dimensional velocity data reconstructed with the reference encoding predicted by deep learning agreed well with the velocities obtained with the reference encoding acquired at the scanner for both models. U-Net performed more consistently throughout the cardiac cycle and across the test subjects, while U-Net performed better for systolic velocities. Comprehensively, the largest error for flow volumes, maximum and mean velocities was -6.031% for maximum velocities in the right ventricle for the U-Net, and -6.92% for mean velocities in the right ventricle for U-Net. For total turbulent kinetic energy, the highest errors were in the left ventricle (-77.17%) for the U-Net, and in the right ventricle (24.96%) for the U-Net, while for maximum turbulent kinetic energy were in the pulmonary artery for both models, with a value of -15.5% for U-Net and 15.38% for the U-Net.
Conclusion: Deep learning-enabled referenceless 4D flow CMR permits velocities and flow volumes quantification comparable to conventional 4D flow. Omitting the reference encoding reduces the amount of acquired data by 25%, thus allowing shorter scan times or improved resolution, which is valuable for utilization in the clinical routine.
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http://dx.doi.org/10.1016/j.jocmr.2025.101920 | DOI Listing |
Cell Rep
September 2025
Molecular Neurobiology Laboratory, Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA. Electronic address:
The neural circuits that transmit the sense of pain and how pain is encoded by these circuits are still poorly understood.Mechanical allodynia is a prominent form of chronic pain characterized by painful responses to innocuous touch that develops as a consequence of nerve damage and inflammation. Here, we show that alterations to the normal log-normal distribution of neuronal activity and structure of neural correlations between neurons in the dorsal column nuclei (DCN) constitute a signature feature of mechanical allodynia, with the transmission of "allodynic" light touch information to the thalamus by somatostatin-positive projection neurons in the DCN being essential for its expression and development.
View Article and Find Full Text PDFAm J Med Genet A
September 2025
Division of Clinical and Metabolic Genetics, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Most complex V subunits are nuclear encoded and so far, were not found in association with recognized Mendelian disorders. ATP5PO is a candidate gene for complex V mitochondrial disease. It encodes the oligomycin sensitivity-conferring protein (OSCP), an essential component of the "stalk" region that links the F1 and F0 domains of the ATP synthase complex.
View Article and Find Full Text PDFMissing genotypes reduce statistical power and hinder genome-wide association studies. While reference-based methods are popular, they struggle in complex regions and under population mismatch. Existing reference-free deep learning models show promise in addressing this issue but often fail to impute rare variants in small datasets.
View Article and Find Full Text PDFMagn Reson Med
September 2025
School of Biomedical Engineering & State Key Laboratory of Advanced Medical Materials and Devices, ShanghaiTech University, Shanghai, China.
Purpose: To develop a rapid 2D free-running myocardial mapping technique that is robust to through-plane respiratory motion.
Methods: A free-running golden angle radial sequence consisting of encoding and self-navigated auto motion calibration (SNAC) was developed. The encoding adopted inversion recovery (IR) prepared interleaved multi-slice acquisition with optimized inter-slice gap to ensure a uniform excitation of the middle slice regardless of through-plane respiratory motion.
J Cardiovasc Magn Reson
September 2025
Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM), University of Leeds, Leeds, UK. Electronic address:
Background: Cardiac diffusion tensor imaging (cDTI) is sensitive to imaging parameters including the number of unique diffusion encoding directions (ND) and number of repetitions (NR; analogous to number of signal averages or NSA). However, there is no clear guidance for optimising these parameters in the clinical setting.
Methods: Spin echo cDTI data with 2 order motion compensated diffusion encoding gradients were acquired in ten healthy volunteers on a 3T MRI scanner with different diffusion encoding schemes in pseudo-randomised order.