arXiv subjects

Alexis Leconte

Publications and source records attributed to Alexis Leconte.

6 recordsLinked to original sources

arXiv2026

ULMShare: A Large-Scale In Vivo Ultrasound Localization Microscopy Dataset for Microvascular Imaging

Ultrasound Localization Microscopy (ULM) enables microscopic imaging of the cerebral microvasculature in vivo, but relies on a multi-stage processing pipeline in which acquisition settings and reconstruction processes strongly influence the final output. Existing public datasets remain sparse, restricting rigorous evaluation and slowing progress in algorithm development, including emerging machine-learning approaches, which by design require large quantities of data to be robust and reliable. We introduce \textbf{ULMShare}, an open-access dataset of 99 whole-brain transcranial ULM acquisitions from 61 healthy mice (36 females, 22 males, 3 unknown; mean age: $8.2 \pm 5.5$ weeks; mean weight: $17.7 \pm 4.2$ g), for a total of 30TB of raw data. The dataset spans three experimental procedures, multiple injection and anesthesia protocols, two ultrasound probes, and different imaging planes and orientations. Each acquisition includes raw ultrasonic data, detailed metadata, an illustrative reconstruction and the corresponding microbubble trajectories. Alongside the data, we report vascular saturation, Fourier Ring Correlation, and track-length statistics, plus expert visual gradings. ULMShare provides a broad, standardized and publicly available resource for method development, validation, and benchmarking. The full dataset is available on the Federated Research Data Repository and additional resources are hosted on the ULMShare Github repository.

physics.med-ph↗

arXiv2025

The-Bodega: A Matlab Toolbox for Biologically Dynamic Microbubble Simulations on Realistic Hemodynamic Microvascular Graphs

The-Bodega is a Matlab-based toolbox for simulating ground-truth datasets for Ultrasound Localization Microscopy (ULM)-a super resolution imaging technique that resolves microvessels by systematically tracking microbubbles flowing through the microvasculature. The-Bodega enables open-source simulation of stochastic microbubble dynamics through anatomically complex vascular graphs and features a quasi-automated pipeline for generating ground-truth ultrasound data from simple vascular inputs. It incorporates sequential Monte Carlo simulations augmented with Poiseuille flow distributions and dynamic pulsatile flow. A key novelty of our framework is its flexibility to accommodate arbitrary vascular architectures and benchmark common ULM algorithms, such as Fourier Ring Correlation and Singular Value Decomposition (SVD) spatiotemporal filtering, on realistic hemodynamic digital phantoms. The-Bodega supports consistent microbubble-to-ultrasound simulations across domains ranging from mouse brains to human hearts and automatically leverages available CPU/GPU parallelization to improve computational efficiency. We demonstrate its versatility in applications including image quality assessment, motion artifact analysis, and the simulation of novel ULM modalities, such as capillary imaging, myocardial reconstruction under beating heart motion, and simulating neurovascular evoked responses.

physics.med-ph↗

arXiv2024

Functional Assessment of Cerebral Capillaries using Single Capillary Reporters in Ultrasound Localization Microscopy

The brain's microvascular cerebral capillary network plays a vital role in maintaining neuronal health, yet capillary dynamics are still not well understood due to limitations in existing imaging techniques. Here, we present Single Capillary Reporters (SCaRe) for transcranial Ultrasound Localization Microscopy (ULM), a novel approach enabling non-invasive, whole-brain mapping of single capillaries and estimates of their transit-time as a neurovascular biomarker. We accomplish this first through computational Monte Carlo and ultrasound simulations of microbubbles flowing through a fully-connected capillary network. We unveil distinct capillary flow behaviors which informs methodological changes to ULM acquisitions to better capture capillaries in vivo. Subsequently, applying SCaRe-ULM in vivo, we achieve unprecedented visualization of single capillary tracks across brain regions, analysis of layer-specific capillary heterogeneous transit times (CHT), and characterization of whole microbubble trajectories from arterioles to venules. Lastly, we evaluate capillary biomarkers using injected lipopolysaccharide to induce systemic neuroinflammation and track the increase in SCaRe-ULM CHT, demonstrating the capability to detect subtle capillary functional changes. SCaRe-ULM represents a significant advance in studying microvascular dynamics, offering novel avenues for investigating capillary patterns in neurological disorders and potential diagnostic applications.

physics.med-ph↗

arXiv2024

3D transcranial Dynamic Ultrasound Localization Microscopy in the mouse brain using a Row-Column Array

The role of brain hemodynamics in neurodegenerative diseases cannot be fully assessed using existing imaging technologies. Recently, 2D Dynamic Ultrasound Localization Microscopy (DULM) has allowed for the quantitative mapping of the pulsatile flow at sub-wavelength resolution. However, to obtain accurate velocity estimates, 3D imaging is more adapted, especially for complex vascularized organs like the brain. 3D+t DULM is achievable using matrix array probes, but suffers from limitations in terms of cost, device complexity associated with the high channel count, and operating frequencies. Alternatively, Row Column Arrays (RCA) can reduce the number of elements while maintaining a large field of view and high frame rate. Herein, we demonstrate the feasibility of performing 3D+t blood flow measurements in the mouse brain using an RCA and a DULM sequence with a high spatiotemporal resolution. Transcranial images of anesthetized mice (n=7) were acquired at a volume rate of 750 Hz using 42 tilted plane waves. After microbubbles localization and tracking, super-resolved dynamic density and velocity maps of the 3D brain vascular network were obtained. Cortical vessels were segmented and pulsatility in the arteries was significantly higher than in veins for all mice, in accordance with the literature. Our results demonstrate the feasibility and reproducibility of achieving high spatiotemporal resolution volumes of the mouse brain vasculature with DULM using a RCA.

physics.med-ph↗

arXiv2023

Equivalent-Time-Active-Cavitation-Imaging Enables Vascular-Resolution Blood-Brain-Barrier-Opening-Therapy Planning

Linking cavitation and anatomy was found to be important for predictable outcomes in Focused-Ultrasound Blood-Brain-Barrier-Opening and requires high resolution cavitation mapping. However, cavitation mapping techniques for planning and monitoring of therapeutic procedures either 1) do not leverage the full resolution capabilities of ultrasound imaging or 2) place strong constraints on the length of the therapeutic pulse. This study aimed to develop a high-resolution technique that could resolve vascular anatomy in the cavitation map. Herein, we develop BP-ETACI, derived from bandpass sampling and dual-frequency contrast imaging at 12.5 MHz to produce cavitation maps prior and during blood-brain barrier opening with long therapeutic bursts using a 1.5-MHz focused transducer in the brain of C57BL/6 mice. The BP-ETACI cavitation maps were found to correlate with the vascular anatomy in ultrasound localization microscopy vascular maps and in histological sections. Cavitation maps produced from non-blood-brain-barrier disrupting doses showed the same cavitation-bearing vasculature as maps produced over entire blood-brain-barrier opening procedures, allowing use for 1) monitoring FUS-BBBO, but also for 2) therapy planning and target verification. BP-ETACI is versatile, created high resolution cavitation maps in the mouse brain and is easily translatable to existing FUS-BBBO experiments. As such, it provides a means to further study cavitation phenomena in FUS-BBBO.

physics.med-ph↗

arXiv2023

A Tracking prior to Localization workflow for Ultrasound Localization Microscopy

Ultrasound Localization Microscopy (ULM) has proven effective in resolving microvascular structures and local mean velocities at sub-diffraction-limited scales, offering high-resolution imaging capabilities. Dynamic ULM (DULM) enables the creation of angiography or velocity movies throughout cardiac cycles. Currently, these techniques rely on a Localization-and-Tracking (LAT) workflow consisting in detecting microbubbles (MB) in the frames before pairing them to generate tracks. While conventional LAT methods perform well at low concentrations, they suffer from longer acquisition times and degraded localization and tracking accuracy at higher concentrations, leading to biased angiogram reconstruction and velocity estimation. In this study, we propose a novel approach to address these challenges by reversing the current workflow. The proposed method, Tracking-and-Localization (TAL), relies on first tracking the MB and then performing localization. Through comprehensive benchmarking using both in silico and in vivo experiments and employing various metrics to quantify ULM angiography and velocity maps, we demonstrate that the TAL method consistently outperforms the reference LAT workflow. Moreover, when applied to DULM, TAL successfully extracts velocity variations along the cardiac cycle with improved repeatability. The findings of this work highlight the effectiveness of the TAL approach in overcoming the limitations of conventional LAT methods, providing enhanced ULM angiography and velocity imaging.

physics.med-ph↗