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Jacques Ohayon

Publications and source records attributed to Jacques Ohayon.

3 recordsLinked to original sources

AI-enabled cardiac shape reconstruction from routine magnetic resonance imaging

Computational models of cardiac structure and function are increasingly central to the development of subject-specific cardiac digital twins, enabling improved characterization of contractile dysfunction, pathological remodeling, and electrical abnormalities. A critical prerequisite for these models is the accurate reconstruction of three-dimensional (3D) cardiac anatomy from medical imaging. Multi-planar magnetic resonance imaging, particularly when combined with artificial intelligence, offers a clinically feasible alternative to conventional reconstruction techniques. In this study, we present a neural field-based reconstruction framework that recovers 3D cardiac geometries from sparse planar contour data by learning continuous shape representations. Reconstruction performance was evaluated using complementary in-silico and in vivo datasets spanning variations in sampling density and geometric complexity. Across both datasets, reconstructed meshes closely matched reference geometries, demonstrating that the neural field approach faithfully captures cardiac planar contours. Compared with traditional local interpolation methods, the proposed framework exhibited improved geometric fidelity in anatomically challenging regions, including the left ventricular apex and basal segments, particularly under sparse sampling conditions. Collectively, these findings demonstrate that neural field-based reconstruction provides a robust and efficient pathway for multi-planar cardiac shape recovery, with particular relevance for AI-driven modeling pipelines and data-limited settings such as small-animal and time-resolved cardiac imaging.

physics.med-ph

A pseudo active kinematic constraint for a biological living soft tissue: an effect of the collagen network

Recent studies in mammalian hearts show that left ventricular wall thickening is an important mechanism for systolic ejection and that during contraction the cardiac muscle develops significant stresses in the muscular cross-fiber direction. We suggested that the collagen network surrounding the muscular fibers could account for these mechanical behaviors. To test this hypothesis we develop a model for large deformation response of active, incompressible, nonlinear elastic and transversely isotropic living soft tissue (such as cardiac or arteries tissues) in which we include a coupling effect between the connective tissue and the muscular fibers. Then, a three-dimensional finite element formulation including this internal pseudo-active kinematic constraint is derived. Analytical and finite element solutions are in a very good agreement. The numerical results show this wall thickening effect with an order of magnitude compatible with the experimental observations.

math.AP

The motility of normal and cancer cells in response to the combined influence of substrate rigidity and anisotropic microstructure

Cell adhesion and migration are strongly influenced by extracellular matrix (ECM) architecture and rigidity, but little is known about the concomitant influence of such environmental signals to cell responses, especially when considering cells of similar origin and morphology, but exhibiting a normal or cancerous phenotype. Using micropatterned polydimethylsiloxane substrates (PDMS) with tuneable stiffness (500kPa, 750kPa, 2000kPa) and topography (lines, pillars or unpatterned), we systematically analyse the differential response of normal (3T3) and cancer (SaI/N) fibroblastic cells. Our results demonstrate that both cells exhibit differential morphology and motility responses to changes in substrate rigidiy and microtopography. 3T3 polarization and spreading are influenced by substrate microtopography and rigidity. The cells exhibit a persistent type of migration, which depends on the substrate anisotropy. In contrast, the dynamic of SaI/N spreading is strongly modified by the substrate topography but not by substrate rigidity. SaI/N morphology and migration seem to escape from extracellular cues: the cells exhibit uncorrelated migration trajectories and a large dispersion of their migration speed, which increases with substrate rigidity.

q-bio.CB