arXiv subjects

Martijn Froeling

Publications and source records attributed to Martijn Froeling.

5 recordsLinked to original sources

arXiv2026

An in vivo validation dataset for dynamic volumetric MRI

Dynamic volumetric MRI provides valuable information on in vivo motion and biomechanics, with applications spanning cardiac, musculoskeletal, or pulmonary imaging, amongst others. Developing reconstruction methods for time-resolved volumetric MRI is challenging due to the inherently slow acquisition process of MRI, which makes it an active area of research. However, in vivo validation of these methods remains challenging due to the lack of publicly available datasets with fully sampled ground-truth images. Here, we present a publicly available in vivo dataset designed to facilitate the development and validation of dynamic volumetric MRI reconstruction algorithms. Controlled and repeatable deformations of the muscles in the thigh were induced using a pneumatic pressure cuff, enabling the acquisition of both undersampled dynamic data and fully sampled validation images. The dataset comprises multichannel undersampled k-space data from nine healthy volunteers across four different dynamic deformations, with fully sampled validation data for one deformation. Additionally, an anatomical reference scan and muscle segmentation masks are provided for each subject. To illustrate a possible image reconstruction and validation approach, a binning-based reconstruction was performed on the undersampled data from six dynamic repetitions. The resulting images were consistent with the corresponding fully sampled validation images. This dataset offers possibilities for validating and advancing time-resolved volumetric MRI reconstruction methods.

physics.med-ph↗

arXiv2025

Quasi-static in vivo elastography from internal displacement information only

As disease often alters the structural properties of soft tissue, noninvasive elastography techniques have emerged to quantitatively assess in vivo mechanical properties. Magnetic Resonance Elastography (MRE) based on dynamic deformations is the standard technique for imaging mechanical properties, but the viscoelastic nature of soft tissue makes the results dependent on the actuation frequency, which can be limiting. In this proof-of-principle study we propose a noise robust framework for reconstructing relative stiffness properties from quasi-static in vivo displacement fields captured on a physiological time scale. The acquisition is performed using a pneumatic pressure cuff to induce tissue deformation in a controlled manner. The reconstruction does not require boundary information which is generally hard to access in vivo nor spatial derivatives of displacement fields that are known to amplify noise. The validity of our framework is corroborated with in silico experiments on a numerical phantom. In vivo experiments on the thigh of a volunteer demonstrate the repeatability of the method. As an application, the quantitative change in muscle stiffness during isometric knee flexion is investigated which yielded physiologically meaningful results.

physics.med-ph↗

arXiv2025

Millennium Pathways for Tractography: 40 grand challenges to shape the future of tractography

In the spirit of the historic Millennium Prize Problems that heralded a new era for mathematics, the newly formed International Society for Tractography (IST) has launched the Millennium Pathways for Tractography, a community-driven roadmap designed to shape the future of the field. Conceived during the inaugural Tract-Anat Retreat, this initiative reflects a collective vision for advancing tractography over the coming decade and beyond. The roadmap consists of 40 grand challenges, developed by international experts and organized into seven categories spanning three overarching themes: neuroanatomy, tractography methods, and clinical applications. By defining shared short-, medium-, and long-term goals, these pathways provide a structured framework to confront fundamental limitations, promote rigorous validation, and accelerate the translation of tractography into a robust tool for neuroscience and medicine. Ultimately, the Millennium Pathways aim to guide and inspire future research and collaboration, ensuring the continued scientific and clinical relevance of tractography well into the future.

physics.med-ph↗

arXiv2023

A three-dimensional MR-STAT protocol for high-resolution multi-parametric quantitative MRI

Magnetic Resonance Spin Tomography in Time-Domain (MR-STAT) is a multiparametric quantitative MR framework, which allows for simultaneously acquiring quantitative tissue parameters such as T1, T2 and proton density from one single short scan. A typical 2D MR-STAT acquisition uses a gradient-spoiled, gradient-echo sequence with a slowly varying RF flip-angle train and Cartesian readouts, and the quantitative tissue maps are reconstructed by an iterative, model-based optimization algorithm. In this work, we design a 3D MR-STAT framework based on previous 2D work, in order to achieve better image SNR, higher though-plan resolution and better tissue characterization. Specifically, we design a 7-minute, high-resolution 3D MR-STAT sequence, and the corresponding two-step reconstruction algorithm for the large-scale dataset. To reduce the long acquisition time, Cartesian undersampling strategies such as SENSE are adopted in our transient-state quantitative framework. To reduce the computational burden, a data splitting scheme is designed for decoupling the 3D reconstruction problem into independent 2D reconstructions. The proposed 3D framework is validated by numerical simulations, phantom experiments and in-vivo experiments. High-quality knee quantitative maps with 0.8 x 0.8 x 1.5mm3 resolution and bilateral lower leg maps with 1.6mm isotropic resolution can be acquired using the proposed 7-minute acquisition sequence and the 3-minute-per-slice decoupled reconstruction algorithm. The proposed 3D MR-STAT framework could have wide clinical applications in the future.

physics.med-ph↗

arXiv2019

On the sensitivity of the diffusion MRI signal to brain activity in response to a motor cortex paradigm

Diffusion functional MRI (dfMRI) is a promising technique to map functional activations by acquiring diffusion-weighed spin-echo images. In previous studies, dfMRI showed higher spatial accuracy at activation mapping compared to classic functional MRI approaches. However, it remains unclear whether dfMRI measures result from changes in the intra-/extracellular environment, perfusion and/or T2 values. We designed an acquisition/quantification scheme to disentangle such effects in the motor cortex during a finger tapping paradigm. dfMRI was acquired at specific diffusion weightings to selectively suppress perfusion and free-water diffusion, then times series of the apparent diffusion coefficient (ADC-fMRI) and of the perfusion signal fraction (IVIM-fMRI) were derived. ADC-fMRI provided ADC estimates sensitive to changes in perfusion and free-water volume, but not to T2/T2* values. With IVIM-fMRI we isolated the perfusion contribution to ADC, while suppressing T2 effects. Compared to conventional gradient-echo BOLD fMRI, activation maps obtained with dfMRI and ADC-fMRI had smaller clusters, and the spatial overlap between the three techniques was below 50%. Increases of perfusion fractions were observed during task in both dfMRI and ADC-fMRI activations. Perfusion effects were more prominent with ADC-fMRI than with dfMRI but were significant in less than 25% of activation ROIs. Taken together, our results suggest that the sensitivity to task of dfMRI derives from a decrease of hindered diffusion and an increase of the pseudo-diffusion signal fraction, leading to different, more confined spatial activation patterns compared to classic functional MRI.

physics.med-ph↗