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- ItemInversion-recovery MR elastography of the human brain for improved stiffness quantification near fluid-solid boundaries(New York, NY [u.a.] : Wiley-Liss, 2021) Lilaj, Ledia; Herthum, Helge; Meyer, Tom; Shahryari, Mehrgan; Bertalan, Gergely; Caiazzo, Alfonso; Braun, Jürgen; Fischer, Thomas; Hirsch, Sebastian; Sack, IngolfPurpose: In vivo MR elastography (MRE) holds promise as a neuroimaging marker. In cerebral MRE, shear waves are introduced into the brain, which also stimulate vibrations in adjacent CSF, resulting in blurring and biased stiffness values near brain surfaces. We here propose inversion-recovery MRE (IR-MRE) to suppress CSF signal and improve stiffness quantification in brain surface areas. Methods: Inversion-recovery MRE was demonstrated in agar-based phantoms with solid-fluid interfaces and 11 healthy volunteers using 31.25-Hz harmonic vibrations. It was performed by standard single-shot, spin-echo EPI MRE following 2800-ms IR preparation. Wave fields were acquired in 10 axial slices and analyzed for shear wave speed (SWS) as a surrogate marker of tissue stiffness by wavenumber-based multicomponent inversion. Results: Phantom SWS values near fluid interfaces were 7.5 ± 3.0% higher in IR-MRE than MRE (P =.01). In the brain, IR-MRE SNR was 17% lower than in MRE, without influencing parenchymal SWS (MRE: 1.38 ± 0.02 m/s; IR-MRE: 1.39 ± 0.03 m/s; P =.18). The IR-MRE tissue–CSF interfaces appeared sharper, showing 10% higher SWS near brain surfaces (MRE: 1.01 ± 0.03 m/s; IR-MRE: 1.11 ± 0.01 m/s; P <.001) and 39% smaller ventricle sizes than MRE (P <.001). Conclusions: Our results show that brain MRE is affected by fluid oscillations that can be suppressed by IR-MRE, which improves the depiction of anatomy in stiffness maps and the quantification of stiffness values in brain surface areas. Moreover, we measured similar stiffness values in brain parenchyma with and without fluid suppression, which indicates that shear wavelengths in solid and fluid compartments are identical, consistent with the theory of biphasic poroelastic media. © 2021 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals LLC on behalf of International Society for Magnetic Resonance in Medicine
- ItemMultiscale Coupling of One-dimensional Vascular Models and Elastic Tissues(Dordrecht [u.a.] : Springer Science + Business Media B.V, 2021) Heltai, Luca; Caiazzo, Alfonso; Müller, Lucas O.We present a computational multiscale model for the efficient simulation of vascularized tissues, composed of an elastic three-dimensional matrix and a vascular network. The effect of blood vessel pressure on the elastic tissue is surrogated via hyper-singular forcing terms in the elasticity equations, which depend on the fluid pressure. In turn, the blood flow in vessels is treated as a one-dimensional network. Intravascular pressure and velocity are simulated using a high-order finite volume scheme, while the elasticity equations for the tissue are solved using a finite element method. This work addresses the feasibility and the potential of the proposed coupled multiscale model. In particular, we assess whether the multiscale model is able to reproduce the tissue response at the effective scale (of the order of millimeters) while modeling the vasculature at the microscale. We validate the multiscale method against a full scale (three-dimensional) model, where the fluid/tissue interface is fully discretized and treated as a Neumann boundary for the elasticity equation. Next, we present simulation results obtained with the proposed approach in a realistic scenario, demonstrating that the method can robustly and efficiently handle the one-way coupling between complex fluid microstructures and the elastic matrix. © 2021, The Author(s).
- ItemReconstruction of flow domain boundaries from velocity data via multi-step optimization of distributed resistance(Berlin : Weierstraß-Institut für Angewandte Analysis und Stochastik, 2022) Pártl, Ondřej; Wilbrandt, Ulrich; Mura, Joaquín; Caiazzo, AlfonsoWe reconstruct the unknown shape of a flow domain using partially available internal velocity measurements. This inverse problem is motivated by applications in cardiovascular imaging where motion-sensitive protocols, such as phase-contrast MRI, can be used to recover three-dimensional velocity fields inside blood vessels. In this context, the information about the domain shape serves to quantify the severity of pathological conditions, such as vessel obstructions. We consider a flow modeled by a linear Brinkman problem with a fictitious resistance accounting for the presence of additional boundaries. To reconstruct these boundaries, we employ a multi-step gradient-based variational method to compute a resistance that minimizes the difference between the computed flow velocity and the available data. Afterward, we apply different post-processing steps to reconstruct the shape of the internal boundaries. To limit the overall computational cost, we use a stabilized equal-order finite element method. We prove the stability and the well-posedness of the considered optimization problem. We validate our method on three-dimensional examples based on synthetic velocity data and using realistic geometries obtained from cardiovascular imaging.
- ItemDisplacement and pressure reconstruction from magnetic resonance elastography images: Application to an in silico brain model(Berlin : Weierstraß-Institut für Angewandte Analysis und Stochastik, 2022) Galarce Marín, Felipe; Tabelow, Karsten; Polzehl, Jörg; Papanikas, Christos Panagiotis; Vavourakis, Vasileios; Lilaj, Ledia; Sack, Ingolf; Caiazzo, AlfonsoThis paper investigates a data assimilation approach for non-invasive quantification of intracranial pressure from partial displacement data, acquired through magnetic resonance elastography. Data assimilation is based on a parametrized-background data weak methodology, in which the state of the physical system tissue displacements and pressure fields is reconstructed from partially available data assuming an underlying poroelastic biomechanics model. For this purpose, a physics-informed manifold is built by sampling the space of parameters describing the tissue model close to their physiological ranges, to simulate the corresponding poroelastic problem, and compute a reduced basis. Displacements and pressure reconstruction is sought in a reduced space after solving a minimization problem that encompasses both the structure of the reduced-order model and the available measurements. The proposed pipeline is validated using synthetic data obtained after simulating the poroelastic mechanics on a physiological brain. The numerical experiments demonstrate that the framework can exhibit accurate joint reconstructions of both displacement and pressure fields. The methodology can be formulated for an arbitrary resolution of available displacement data from pertinent images. It can also inherently handle uncertainty on the physical parameters of the mechanical model by enlarging the physics-informed manifold accordingly. Moreover, the framework can be used to characterize, in silico, biomarkers for pathological conditions, by appropriately training the reduced-order model. A first application for the estimation of ventricular pressure as an indicator of abnormal intracranial pressure is shown in this contribution.
- ItemMultiscale coupling of one-dimensional vascular models and elastic tissues(Berlin : Weierstraß-Institut für Angewandte Analysis und Stochastik, 2021) Heltai, Luca; Caiazzo, Alfonso; Müller, Lucas O.We present a computational multiscale model for the efficient simulation of vascularized tissues, composed of an elastic three-dimensional matrix and a vascular network. The effect of blood vessel pressure on the elastic tissue is surrogated via hyper-singular forcing terms in the elasticity equations, which depend on the fluid pressure. In turn, the blood flow in vessels is treated as a one-dimensional network. The pressure and velocity of the blood in the vessels are simulated using a high-order finite volume scheme, while the elasticity equations for the tissue are solved using a finite element method. This work addresses the feasibility and the potential of the proposed coupled multiscale model. In particular, we assess whether the multiscale model is able to reproduce the tissue response at the effective scale (of the order of millimeters) while modeling the vasculature at the microscale. We validate the multiscale method against a full scale (three-dimensional) model, where the fluid/tissue interface is fully discretized and treated as a Neumann boundary for the elasticity equation. Next, we present simulation results obtained with the proposed approach in a realistic scenario, demonstrating that the method can robustly and efficiently handle the one-way coupling between complex fluid microstructures and the elastic matrix.