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Ruud B. van Heeswijk

Publications and source records attributed to Ruud B. van Heeswijk.

7 recordsLinked to original sources

Interlaced R2D2 DNN Series for Scalable Non-Cartesian MRI with Sensitivity Self-calibration

We introduce interlaced R2D2 (iR2D2), a DNN series paradigm for scalable image reconstruction from accelerated non-Cartesian k-space acquisitions in MRI with sensitivity map self-calibration. While unrolled DNN architectures provide robust image formation, embedding non-uniform fast Fourier transform operators within the backpropagation graph becomes impractical to train at large scale, e.g., in 2D MRI with a large number of coils, or for higher-dimensional imaging. To address this scalability challenge, we leverage the R2D2 paradigm as a learned version of the Matching Pursuit algorithm that was recently introduced in radio astronomy for fast large-scale Fourier imaging. R2D2's reconstruction is formed as a series of residual images iteratively estimated as outputs of DNN modules taking the previous iteration's data residual as input. Specific to MRI, precomputed sensitivity maps derived from undersampled data can yield an inaccurate measurement operator, which may adversely affect the performance of iterative algorithms such as R2D2. Thus, we extend the R2D2 framework to iR2D2 by introducing a bespoke interlaced architecture that alternates between two R2D2 DNN series to jointly self-calibrate sensitivity maps and form the MR image. We further enhance iR2D2 to operate as an adaptive solver governed by an error-controlled update condition that enforces a sufficient residual energy descent, a dynamic capability fundamentally incompatible with the predefined forward passes of unrolled architectures. Extensive experiments in simulation and on real data, targeting undersampled radial k-space sampling, demonstrate that iR2D2 significantly improves upon R2D2 and outperforms state-of-the-art benchmarks, delivering scalable, high-fidelity imaging with corrected sensitivity profiles.

eess.IV↗

Spatiotemporal graph neural process for reconstruction, extrapolation, and classification of cardiac trajectories

We present a probabilistic framework for modeling structured spatiotemporal dynamics from sparse observations, focusing on cardiac motion. Our approach integrates neural ordinary differential equations (NODEs), graph neural networks (GNNs), and neural processes into a unified model that captures uncertainty, temporal continuity, and anatomical structure. We represent dynamic systems as spatiotemporal multiplex graphs and model their latent trajectories using a GNN-parameterized vector field. Given the sparse context observations at node and edge levels, the model infers a distribution over latent initial states and control variables, enabling both interpolation and extrapolation of trajectories. We validate the method on three synthetic dynamical systems (coupled pendulum, Lorenz attractor, and Kuramoto oscillators) and two real-world cardiac imaging datasets - ACDC (N=150) and UK Biobank (N=526) - demonstrating accurate reconstruction, extrapolation, and disease classification capabilities. The model accurately reconstructs trajectories and extrapolates future cardiac cycles from a single observed cycle. It achieves state-of-the-art results on the ACDC classification task (up to 99% accuracy), and detects atrial fibrillation in UK Biobank subjects with competitive performance (up to 67% accuracy). This work introduces a flexible approach for analyzing cardiac motion and offers a foundation for graph-based learning in structured biomedical spatiotemporal time-series data.

cs.LG↗

Fast high-resolution metabolite mapping in the rat brain using 1H-FID-MRSI at 14.1T

Magnetic resonance spectroscopic imaging (MRSI) enables the simultaneous non-invasive acquisition of MR spectra from multiple spatial locations inside the brain. While 1H-MRSI is increasingly used in the human brain, it is not yet widely applied in the preclinical settings, mostly because of difficulties specifically related to very small nominal voxel size in the rodent brain and low concentration of brain metabolites, resulting in low signal-to-noise ratio SNR. In this context, we implemented a free induction decay 1H-MRSI sequence (1H-FID-MRSI) in the rat brain at 14.1T. We combined the advantages of 1H-FID-MRSI with the ultra-high magnetic field to achieve higher SNR, coverage and spatial resolution in the rodent brain, and developed a custom dedicated processing pipeline with a graphical user interface: MRS4Brain toolbox. LCModel fit, using the simulated metabolite basis-set and in-vivo measured MM, provided reliable fits for the data at acquisition delays of 1.3 and 0.94 ms. The resulting Cramér-Rao lower bounds were sufficiently low (<30%) for eight metabolites of interest, leading to highly reproducible metabolic maps. Similar spectral quality and metabolic maps were obtained between 1 and 2 averages, with slightly better contrast and brain coverage due to increased SNR in the latter case. Furthermore, the obtained metabolic maps were accurate enough to confirm the previously known brain regional distribution of some metabolites. The acquisitions proved high reproducibility over time. We demonstrated that the increased SNR and spectral resolution at 14.1T can be translated into high spatial resolution in 1H-FID-MRSI of the rat brain in 13 minutes, using the sequence and processing pipeline described herein. High-resolution 1H-FID-MRSI at 14.1T provided reproducible and high-quality metabolic mapping of brain metabolites with significantly reduced technical limitations.

physics.med-ph↗

Compressed Sensing with Signal Averaging for Improved Sensitivity and Motion Artifact Reduction in Fluorine-19 MRI

Fluorine-19 (19F) MRI of injected perfluorocarbon emulsions (PFCs) allows for the non-invasive quantification of inflammation and cell tracking, but suffers from a low signal-to-noise ratio and extended scan time. To address this limitation, we tested the hypothesis that a 19F MRI pulse sequence that combines a specific undersampling regime with signal averaging has increased sensitivity and robustness against motion artifacts compared to a non-averaged fully-sampled dataset, when both are reconstructed with compressed sensing. To this end, numerical simulations and phantom experiments were performed to characterize the point spread function (PSF) of undersampling patterns and the vulnerability to noise of acquisition-reconstruction strategies with paired numbers of x signal averages and acceleration factor x (NAx-AFx). At all investigated noise levels, the DSC of the acquisition-reconstruction strategies strongly depended on the regularization parameters and acceleration factor. In phantoms, motion robustness of an NA8-AF8 undersampling pattern versus NA1-AF1 was evaluated with simulated and real motions. Differences were assessed with Dice similarity coefficients (DSC), and were consistently higher for NA8-AF8 compared to NA1-AF1 strategy, for both simulated and real cyclic motions (P<0.001). Both acquisition-reconstruction strategies were validated in vivo in mice (n=2) injected with perfluoropolyether. These images displayed a sharper delineation of the liver with the NA8-AF8 strategy than with the NA1-AF1 strategy. In conclusion, we validated the hypothesis that in 19F MRI, the combination of undersampling and averaging improves both the sensitivity and the robustness against motion artifacts compared to a non-averaged fully-sampled dataset, when both are reconstructed with compressed sensing.

physics.med-ph↗

T2 Mapping from Super-Resolution-Reconstructed Clinical Fast Spin Echo Magnetic Resonance Acquisitions

Relaxometry studies in preterm and at-term newborns have provided insight into brain microstructure, thus opening new avenues for studying normal brain development and supporting diagnosis in equivocal neurological situations. However, such quantitative techniques require long acquisition times and therefore cannot be straightforwardly translated to in utero brain developmental studies. In clinical fetal brain magnetic resonance imaging routine, 2D low-resolution T2-weighted fast spin echo sequences are used to minimize the effects of unpredictable fetal motion during acquisition. As super-resolution techniques make it possible to reconstruct a 3D high-resolution volume of the fetal brain from clinical low-resolution images, their combination with quantitative acquisition schemes could provide fast and accurate T2 measurements. In this context, the present work demonstrates the feasibility of using super-resolution reconstruction from conventional T2-weighted fast spin echo sequences for 3D isotropic T2 mapping. A quantitative magnetic resonance phantom was imaged using a clinical T2-weighted fast spin echo sequence at variable echo time to allow for super-resolution reconstruction at every echo time and subsequent T2 mapping of samples whose relaxometric properties are close to those of fetal brain tissue. We demonstrate that this approach is highly repeatable, accurate and robust when using six echo times (total acquisition time under 9 minutes) as compared to gold-standard single-echo spin echo sequences (several hours for one single 2D slice).

eess.IV↗

Scalable Learning-Based Sampling Optimization for Compressive Dynamic MRI

Compressed sensing applied to magnetic resonance imaging (MRI) allows to reduce the scanning time by enabling images to be reconstructed from highly undersampled data. In this paper, we tackle the problem of designing a sampling mask for an arbitrary reconstruction method and a limited acquisition budget. Namely, we look for an optimal probability distribution from which a mask with a fixed cardinality is drawn. We demonstrate that this problem admits a compactly supported solution, which leads to a deterministic optimal sampling mask. We then propose a stochastic greedy algorithm that (i) provides an approximate solution to this problem, and (ii) resolves the scaling issues of [1,2]. We validate its performance on in vivo dynamic MRI with retrospective undersampling, showing that our method preserves the performance of [1,2] while reducing the computational burden by a factor close to 200.

eess.IV↗

Noncontrast free-breathing respiratory self-navigated coronary artery cardiovascular magnetic resonance angiography at 3 T using lipid insensitive binomial off-resonant excitation (LIBRE)

Robust and homogeneous lipid suppression is mandatory for coronary magnetic resonance angiography (MRA) since coronary arteries are commonly embedded in fat. However, effective large volume lipid suppression becomes challenging when performing radial whole-heart coronary MRA and the problem may even be exacerbated at increasing magnetic field strengths. Incomplete fat suppression also generates artifacts, and may affect advanced motion correction methods. The aim was to evaluate a recently reported lipid insensitive MRI method for self-navigated coronary MRA at 3T. Lipid insensitive binomial off resonant excitation (LIBRE) radiofrequency (RF) excitation pulses were included into a self-navigated 3D radial GRE coronary MRA sequence at 3T. LIBRE was compared against conventional fat saturation (FS) and binomial 1-180°-1 water excitation (WE). First, fat suppression of all techniques was numerically characterized using Matlab and experimentally validated in phantoms and in legs of human volunteers. Subsequently, free-breathing self-navigated coronary MRA was performed using the LIBRE pulse as well as FS and WE in ten volunteers. Results obtained in the simulations were confirmed by the experimental validations as LIBRE enabled near complete fat suppression for 3D radial imaging in vitro and in vivo. For self-navigated whole-heart coronary MRA at 3T, fat SNR was significantly attenuated using LIBRE compared with conventional FS. LIBRE increased the RCA vessel sharpness significantly (37 +/- 9% (LIBRE) vs. 29 +/- 8% (FS) and 30 +/- 8% (WE), both p<0.05) and led to a significant increase in the measured RCA vessel length to (83 +/- 31 mm (LIBRE) vs. 56 +/- 12 mm (FS) and 59 +/- 27 (WE) p<0.05). LIBRE enables robust large volume fat suppression and significantly improves coronary artery image quality at 3T compared to the use of conventional fat suppression and water excitation.

physics.med-ph↗