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Alfio Quarteroni

Publications and source records attributed to Alfio Quarteroni.

At least 19 recordsLinked to original sources

Cardiocirculatory Computational Models for the Study of Hypertension

In this work, we develop patient-specific cardiocirculatory models with the aim of building Digital Twins for hypertension. In particular, in our pathophysiology-based framework, we consider both 0D cardiocirculatory models and a 3D-0D electromechanical model. The 0D model, which consists of an RLC circuit, is studied in two variants, with and without capillaries. The 3D-0D model consists of a three-dimensional electromechanical model of the left ventricle, coupled with a 0D model for the external blood circulation: this representation enables the assessment of additional quantities related to ventricular deformation and stress, and offers a more detailed representation compared to a fully 0D model. Sensitivity analysis is performed on the 0D model, with both a mono- and a multi-parametric approach, in order to identify the parameters that most influence the model outputs and guide the calibration process. We studied three different scenarios, corresponding to systemic, pulmonary and renovascular hypertension, each in three nuances of severity. To maintain a fair comparison among the models, a parameter calibration strategy is developed; the outputs of the 0D model with capillaries are utilized to enhance the 3D-0D model. The results demonstrate that the 3D-0D model yields an accurate representation of cardiocirculatory dynamics in the presence of hypertension; this model represents a powerful step toward digital twins for real-time hypertension control, providing refined and clinically meaningful insights beyond those achievable with 0D models alone.

math.NA

Improvements on uncertainty quantification with variational autoencoders

Inverse problems aim to determine model parameters of a mathematical problem from given observational data. Neural networks can provide an efficient tool to solve these problems. In the context of Bayesian inverse problems, Uncertainty Quantification Variational AutoEncoders (UQ-VAE), a class of neural networks, approximate the posterior distribution mean and covariance of model parameters. This allows for both the estimation of the parameters and their uncertainty in relation to the observational data. In this work, we propose a novel loss function for training UQ-VAEs, which includes, among other modifications, the removal of a sample mean term from an already existing one. This modification improves the accuracy of UQ-VAEs, as the original theoretical result relies on the convergence of the sample mean to the expected value (a condition that, in high dimensional parameter spaces, requires a prohibitively large number of samples due to the curse of dimensionality). Avoiding the computation of the sample mean significantly reduces the training time in high dimensional parameter spaces compared to previous literature results. Under this new formulation, we establish a new theoretical result for the approximation of the posterior mean and covariance for general mathematical problems. We validate the effectiveness of UQ-VAEs through three benchmark numerical tests: a Poisson inverse problem, a non affine inverse problem and a 0D cardiocirculatory model, under the two clinical scenarios of systemic hypertension and ventricular septal defect. For the latter case, we perform forward uncertainty quantification.

math.NA

Influence of cellular mechano-calcium feedback in numerical models of cardiac electromechanics

Multiphysics and multiscale mathematical models enable the non-invasive study of cardiac function. These models often rely on simplifying assumptions that neglect certain biophysical processes to balance fidelity and computational cost. In this work, we propose an eikonal-based framework that incorporates mechano-calcium feedback -- the effect of mechanical deformation on calcium-troponin buffering -- while introducing only negligible computational overhead. To assess the impact of mechano-calcium feedback at the organ level, we develop a bidirectionally coupled cellular electromechanical model and integrate it into two cardiac multiscale frameworks: a monodomain-driven model that accounts for geometric feedback on electrophysiology and the proposed eikonal-based approach, which instead neglects geometric feedback. By ensuring consistent cellular model calibration across all scenarios, we isolate the role of mechano-calcium feedback and systematically compare its effects against models without it. Our results indicate that, under baseline conditions, mechano-calcium feedback has minimal influence on overall cardiac function. However, its effects become more pronounced in altered force generation scenarios, such as inotropic modulation. Furthermore, we demonstrate that the eikonal-based framework, despite omitting other types of mechano-electric feedback, effectively captures the role of mechano-calcium feedback at significantly lower computational costs than the monodomain-driven model, reinforcing its utility in computational cardiology.

math.NA

Combining physics-based and data-driven models: advancing the frontiers of research with Scientific Machine Learning

Scientific Machine Learning (SciML) is a recently emerged research field which combines physics-based and data-driven models for the numerical approximation of differential problems. Physics-based models rely on the physical understanding of the problem, subsequent mathematical formulation, and numerical approximation. Data-driven models instead aim to extract relations between input and output data without arguing any causality principle underlining the available data distribution. In recent years, data-driven models have been rapidly developed and popularized. Such a diffusion has been triggered by a huge availability of data, increasingly cheap computing power, and the development of powerful ML algorithms. SciML leverages the physical awareness of physics-based models and the efficiency of data-driven algorithms. With SciML, we can inject physics and mathematical knowledge into ML algorithms. Yet, we can rely on data-driven algorithms' capability to discover complex and nonlinear patterns from data and improve the descriptive capacity of physics-based models. After recalling the mathematical foundations of digital modelling and ML algorithms and presenting the most popular ML architectures, we discuss the great potential of a broad variety of SciML strategies in solving complex problems governed by PDEs. Finally, we illustrate the successful application of SciML to the simulation of the human cardiac function, a field of significant socioeconomic importance that poses numerous challenges on both the mathematical and computational fronts. Despite the robustness and accuracy of physics-based models, certain aspects, such as unveiling constitutive laws for cardiac cells and myocardial material properties, as well as devising efficient reduced order models to dominate the extraordinary computational complexity, have been successfully tackled by leveraging data-driven models.

math.NA

SEIHRDV: a multi-age multi-group epidemiological model and its validation on the COVID-19 epidemics in Italy

We propose a novel epidemiological model, referred to as SEIHRDV, for the numerical simulation of the COVID-19 epidemic, which we validate using data from Italy starting in September 2020. SEIHRDV features the following compartments: Susceptible (S), Exposed (E), Infectious (I), Healing (H), Recovered (R), Deceased (D) and Vaccinated (V). The model is age-stratified, as it considers the population split into 15 age groups. Moreover, it takes into account 7 different contexts of exposition to the infection (family, home, school, work, transport, leisure, other contexts), which impact on the transmission mechanism. Thanks to these features, the model can address the analysis of the epidemics and the efficacy of non-pharmaceutical interventions, as well as possible vaccination strategies and the introduction of the Green Pass, a containment measure introduced in Italy in 2021. By leveraging on the SEIHRDV model, we successfully analyzed epidemic trends during the COVID-19 outbreak from September 2020 to July 2021. The model proved instrumental in conducting comprehensive what-if studies and scenario analyses tailored to Italy and its regions. Furthermore, SEIHRDV facilitated accurate forecasting of the future potential trajectory of the epidemic, providing critical information for informed decision making and public health strategies.

q-bio.PE

Defining myocardial fiber bundle architecture in atrial digital twins

A key component in developing atrial digital twins (ADT) - virtual representations of patients' atria - is the accurate prescription of myocardial fibers which are essential for the tissue characterization. Due to the difficulty of reconstructing atrial fibers from medical imaging, a widely used strategy for fiber generation in ADT relies on mathematical models. Existing methodologies utilze semi-automatic approaches, are tailored to specific morphologies, and lack rigorous validation against imaging fiber data. In this study, we introduce a novel atrial Laplace-Dirichlet-Rule-Based Method (LDRBM) for prescribing highly detailed myofiber orientations and providing robust regional annotation in bi-atrial morphologies of any complexity. The robustness of our approach is verified in eight extremely detailed bi-atrial geometries, derived from a sub-millimiter Diffusion-Tensor-Magnetic-Resonance Imaging (DTMRI) human atrial fiber dataset. We validate the LDRBM by quantitatively recreating each of the DTMRI fiber architectures: a comprehensive comparison with DTMRI ground truth data is conducted, investigating differences between electrophysiology (EP) simulations provided by either LDRBM and DTMRI fibers. Finally, we demonstrate that the novel LDRBM outperforms current state-of-the-art fiber models, confirming the exceptional accuracy of our methodology and the critical importance of incorporating detailed fiber orientations in EP simulations. Ultimately, this work represents a fundamental step toward the development of physics-based digital twins of the human atria, establishing a new standard for prescribing fibers in ADT.

physics.med-ph

Physics-informed Neural Network Estimation of Material Properties in Soft Tissue Nonlinear Biomechanical Models

The development of biophysical models for clinical applications is rapidly advancing in the research community, thanks to their predictive nature and their ability to assist the interpretation of clinical data. However, high-resolution and accurate multi-physics computational models are computationally expensive and their personalisation involves fine calibration of a large number of parameters, which may be space-dependent, challenging their clinical translation. In this work, we propose a new approach which relies on the combination of physics-informed neural networks (PINNs) with three-dimensional soft tissue nonlinear biomechanical models, capable of reconstructing displacement fields and estimating heterogeneous patient-specific biophysical properties. The proposed learning algorithm encodes information from a limited amount of displacement and, in some cases, strain data, that can be routinely acquired in the clinical setting, and combines it with the physics of the problem, represented by a mathematical model based on partial differential equations, to regularise the problem and improve its convergence properties. Several benchmarks are presented to show the accuracy and robustness of the proposed method and its great potential to enable the robust and effective identification of patient-specific, heterogeneous physical properties, s.a. tissue stiffness properties. In particular, we demonstrate the capability of the PINN to detect the presence, location and severity of scar tissue, which is beneficial to develop personalised simulation models for disease diagnosis, especially for cardiac applications.

cs.LG

Two new calibration techniques of lumped-parameter mathematical models for the cardiovascular system

Cardiocirculatory mathematical models serve as valuable tools for investigating physiological and pathological conditions of the circulatory system. To investigate the clinical condition of an individual, cardiocirculatory models need to be personalized by means of calibration methods. In this study we propose a new calibration method for a lumped-parameter cardiocirculatory model. This calibration method utilizes the correlation matrix between parameters and model outputs to calibrate the latter according to data. We test this calibration method and its combination with L-BFGS-B (Limited memory Broyden - Fletcher - Goldfarb - Shanno with Bound constraints) comparing them with the performances of L-BFGS-B alone. We show that the correlation matrix calibration method and the combined one effectively reduce the loss function of the associated optimization problem. In the case of in silico generated data, we show that the two new calibration methods are robust with respect to the initial guess of parameters and to the presence of noise in the data. Notably, the correlation matrix calibration method achieves the best results in estimating the parameters in the case of noisy data and it is faster than the combined calibration method and L-BFGS-B. Finally, we present real test case where the two new calibration methods yield results comparable to those obtained using L-BFGS-B in terms of minimizing the loss function and estimating the clinical data. This highlights the effectiveness of the new calibration methods for clinical applications.

math.NA

Robust radial basis function interpolation based on geodesic distance for the numerical coupling of multiphysics problems

Multiphysics simulations frequently require transferring solution fields between subproblems with non-matching spatial discretizations, typically using interpolation techniques. Standard methods are usually based on measuring the closeness between points by means of the Euclidean distance, which does not account for curvature, cuts, cavities or other non-trivial geometrical or topological features of the domain. This may lead to spurious oscillations in the interpolant in proximity to these features. To overcome this issue, we propose a modification to rescaled localized radial basis function (RL-RBF) interpolation to account for the geometry of the interpolation domain, by yielding conformity and fidelity to geometrical and topological features. The proposed method, referred to as RL-RBF-G, relies on measuring the geodesic distance between data points. RL-RBF-G removes spurious oscillations appearing in the RL-RBF interpolant, resulting in increased accuracy in domains with complex geometries. We demonstrate the effectiveness of RL-RBF-G interpolation through a convergence study in an idealized setting. Furthermore, we discuss the algorithmic aspects and the implementation of RL-RBF-G interpolation in a distributed-memory parallel framework, and present the results of a strong scalability test yielding nearly ideal results. Finally, we show the effectiveness of RL-RBF-G interpolation in multiphysics simulations by considering an application to a whole-heart cardiac electromecanics model.

math.NA

A reduced order model for domain decompositions with non-conforming interfaces

In this paper, we propose a reduced-order modeling strategy for two-way Dirichlet-Neumann parametric coupled problems solved with domain-decomposition (DD) sub-structuring methods. We split the original coupled differential problem into two sub-problems with Dirichlet and Neumann interface conditions, respectively. After discretization by, e.g., the finite element method, the full-order model (FOM) is solved by Dirichlet-Neumann iterations between the two sub-problems until interface convergence is reached. We then apply the reduced basis (RB) method to obtain a low-dimensional representation of the solution of each sub-problem. Furthermore, we apply the discrete empirical interpolation method (DEIM) at the interface level to achieve a fully reduced-order representation of the DD techniques implemented. To deal with non-conforming FE interface discretizations, we employ the INTERNODES method combined with the interface DEIM reduction. The reduced-order model (ROM) is then solved by sub-iterating between the two reduced-order sub-problems until the convergence of the approximated high-fidelity interface solutions. The ROM scheme is numerically verified on both steady and unsteady coupled problems, in the case of non-conforming FE interfaces.

math.NA

An electromechanics-driven fluid dynamics model for the simulation of the whole human heart

We introduce a multiphysics and geometric multiscale computational model, suitable to describe the hemodynamics of the whole human heart, driven by a four-chamber electromechanical model. We first present a study on the calibration of the biophysically detailed RDQ20 activation model (Regazzoni et al., 2020) that is able to reproduce the physiological range of hemodynamic biomarkers. Then, we demonstrate that the ability of the force generation model to reproduce certain microscale mechanisms, such as the dependence of force on fiber shortening velocity, is crucial to capture the overall physiological mechanical and fluid dynamics macroscale behavior. This motivates the need for using multiscale models with high biophysical fidelity, even when the outputs of interest are relative to the macroscale. We show that the use of a high-fidelity electromechanical model, combined with a detailed calibration process, allows us to achieve remarkable biophysical fidelity in terms of both mechanical and hemodynamic quantities. Indeed, our electromechanical-driven CFD simulations - carried out on an anatomically accurate geometry of the whole heart - provide results that match the cardiac physiology both qualitatively (in terms of flow patterns) and quantitatively (when comparing in silico results with biomarkers acquired in vivo). We consider the pathological case of left bundle branch block, and we investigate the consequences that an electrical abnormality has on cardiac hemodynamics thanks to our multiphysics integrated model. The computational model that we propose can faithfully predict a delay and an increasing wall shear stress in the left ventricle in the pathological condition. The interaction of different physical processes in an integrated framework allows us to faithfully describe and model this pathology, by capturing and reproducing the intrinsic multiphysics nature of the human heart.

math.NA

An integrated heart-torso electromechanical model for the simulation of electrophysiogical outputs accounting for myocardial deformation

When generating in-silico clinical electrophysiological outputs, such as electrocardiograms (ECGs) and body surface potential maps (BSPMs), mathematical models have relied on single physics, i.e. of the cardiac electrophysiology (EP), neglecting the role of the heart motion. Since the heart is the most powerful source of electrical activity in the human body, its motion dynamically shifts the position of the principal electrical sources in the torso, influencing electrical potential distribution and potentially altering the EP outputs. In this work, we propose a computational model for the simulation of ECGs and BSPMs by coupling a cardiac electromechanical model with a model that simulates the propagation of the EP signal in the torso, thanks to a flexible numerical approach, that simulates the torso domain deformation induced by the myocardial displacement. Our model accounts for the major mechano-electrical feedbacks, along with unidirectional displacement and potential couplings from the heart to the surrounding body. For the numerical discretization, we employ a versatile intergrid transfer operator that allows for the use of different Finite Element spaces to be used in the cardiac and torso domains. Our numerical results are obtained on a realistic 3D biventricular-torso geometry, and cover both cases of sinus rhythm and ventricular tachycardia (VT), solving both the electromechanical-torso model in dynamical domains, and the classical electrophysiology-torso model in static domains. By comparing standard 12-lead ECG and BSPMs, we highlight the non-negligible effects of the myocardial contraction on the EP-outputs, especially in pathological conditions, such as the VT.

math.NA

lifex-cfd: an open-source computational fluid dynamics solver for cardiovascular applications

Computational fluid dynamics (CFD) is an important tool for the simulation of the cardiovascular function and dysfunction. Due to the complexity of the anatomy, the transitional regime of blood flow in the heart, and the strong mutual influence between the flow and the physical processes involved in the heart function, the development of accurate and efficient CFD solvers for cardiovascular flows is still a challenging task. In this paper we present lifex-cfd, an open-source CFD solver for cardiovascular simulations based on the lifex finite element library, written in modern C++ and exploiting distributed memory parallelism. We model blood flow in both physiological and pathological conditions via the incompressible Navier-Stokes equations, accounting for moving cardiac valves, moving domains, and transition-to-turbulence regimes. In this paper, we provide an overview of the underlying mathematical formulation, numerical discretization, implementation details and examples on how to use lifex-cfd. We verify the code through rigorous convergence analyses, and we show its almost ideal parallel speedup. We demonstrate the accuracy and reliability of the numerical methods implemented through a series of idealized and patient-specific vascular and cardiac simulations, in different physiological flow regimes. The lifex-cfd source code is available under the LGPLv3 license, to ensure its accessibility and transparency to the scientific community, and to facilitate collaboration and further developments.

physics.flu-dyn

Discontinuous Galerkin Methods for Fisher-Kolmogorov Equation with Application to $α$-Synuclein Spreading in Parkinson's Disease

This spreading of prion proteins is at the basis of brain neurodegeneration. This paper deals with the numerical modelling of the misfolding process of $α$-synuclein in Parkinson's disease. We introduce and analyze a discontinuous Galerkin method for the semi-discrete approximation of the Fisher-Kolmogorov (FK) equation that can be employed to model the process. We employ a discontinuous Galerkin method on polygonal and polyhedral grids (PolyDG) for space discretization, to accurately simulate the wavefronts typically observed in the prionic spreading and we prove stability and a priori error estimates. Next, we use a Crank-Nicolson scheme to advance in time. For the numerical verification of our numerical model, we first consider a manufactured solution, and then we consider a case with wavefront propagation in two-dimensional polygonal grids. Next, we carry out a simulation of $α$-synuclein spreading in a two-dimensional brain slice in the sagittal plane with a polygonal agglomerated grid that takes full advantage of the flexibility of PolyDG approximation. Finally, we present a simulation in a three-dimensional geometry reconstructed from magnetic resonance images of a patient's brain.

math.NA

A staggered-in-time and non-conforming-in-space numerical framework for realistic cardiac electrophysiology outputs

Computer-based simulations of non-invasive cardiac electrical outputs, such as electrocardiograms and body surface potential maps, usually entail severe computational costs due to the need of capturing fine-scale processes and to the complexity of the heart-torso morphology. In this work, we model cardiac electrical outputs by employing a coupled model consisting of a reaction-diffusion model - either the bidomain model or the most efficient pseudo-bidomain model - on the heart, and an elliptic model in the torso. We then solve the coupled problem with a segregated and staggered in-time numerical scheme, that allows for independent and infrequent solution in the torso region. To further reduce the computational load, main novelty of this work is in introduction of an interpolation method at the interface between the heart and torso domains, enabling the use of non-conforming meshes, and the numerical framework application to realistic cardiac and torso geometries. The reliability and efficiency of the proposed scheme is tested against the corresponding state-of-the-art bidomain-torso model. Furthermore, we explore the impact of torso spatial discretization and geometrical non-conformity on the model solution and the corresponding clinical outputs. The investigation of the interface interpolation method provides insights into the influence of torso spatial discretization and of the geometrical non-conformity on the simulation results and their clinical relevance.

math.NA

lifex-ep: a robust and efficient software for cardiac electrophysiology simulations

Simulating the cardiac function requires the numerical solution of multi-physics and multi-scale mathematical models. This underscores the need for streamlined, accurate, and high-performance computational tools. Despite the dedicated endeavors of various research teams, comprehensive and user-friendly software programs for cardiac simulations are still in the process of achieving full maturity within the scientific community. This work introduces lifex-ep, a publicly available software for numerical simulations of the electrophysiology activity of the cardiac muscle, under both physiological and pathological conditions. lifex-ep employs the monodomain equation to model the heart's electrical activity. It incorporates both phenomenological and second-generation ionic models. These models are discretized using the Finite Element method on tetrahedral or hexahedral meshes. Additionally, lifex-ep integrates the generation of myocardial fibers based on Laplace-Dirichlet Rule-Based Methods, previously released in Africa et al., 2023, within lifex-fiber. This paper provides a concise overview of the mathematical models and numerical methods underlying lifex-ep, along with comprehensive implementation details and instructions for users. lifex-ep features exceptional parallel speedup, scaling efficiently when using up to thousands of cores, and its implementation has been verified against an established benchmark problem for computational electrophysiology. We showcase the key features of lifex-ep through various idealized and realistic simulations. lifex-ep offers a user-friendly and flexible interface. lifex-ep provides easy access to cardiac electrophysiology simulations for a wide user community. It offers a computational tool that integrates models and accurate methods for simulating cardiac electrophysiology within a high-performance framework, while maintaining a user-friendly interface.

math.NA

Real-time whole-heart electromechanical simulations using Latent Neural Ordinary Differential Equations

Cardiac digital twins provide a physics and physiology informed framework to deliver predictive and personalized medicine. However, high-fidelity multi-scale cardiac models remain a barrier to adoption due to their extensive computational costs and the high number of model evaluations needed for patient-specific personalization. Artificial Intelligence-based methods can make the creation of fast and accurate whole-heart digital twins feasible. In this work, we use Latent Neural Ordinary Differential Equations (LNODEs) to learn the temporal pressure-volume dynamics of a heart failure patient. Our surrogate model based on LNODEs is trained from 400 3D-0D whole-heart closed-loop electromechanical simulations while accounting for 43 model parameters, describing single cell through to whole organ and cardiovascular hemodynamics. The trained LNODEs provides a compact and efficient representation of the 3D-0D model in a latent space by means of a feedforward fully-connected Artificial Neural Network that retains 3 hidden layers with 13 neurons per layer and allows for 300x real-time numerical simulations of the cardiac function on a single processor of a standard laptop. This surrogate model is employed to perform global sensitivity analysis and robust parameter estimation with uncertainty quantification in 3 hours of computations, still on a single processor. We match pressure and volume time traces unseen by the LNODEs during the training phase and we calibrate 4 to 11 model parameters while also providing their posterior distribution. This paper introduces the most advanced surrogate model of cardiac function available in the literature and opens new important venues for parameter calibration in cardiac digital twins.

math.NA

Preserving the positivity of the deformation gradient determinant in intergrid interpolation by combining RBFs and SVD: application to cardiac electromechanics

The accurate robust and efficient transfer of the deformation gradient tensor between meshes of different resolution is crucial in cardiac electromechanics simulations. We present a novel method that combines rescaled localized Radial Basis Function (RBF) interpolation with Singular Value Decomposition (SVD) to preserve the positivity of the determinant of the deformation gradient tensor. The method involves decomposing the evaluations of the tensor at the quadrature nodes of the source mesh into rotation matrices and diagonal matrices of singular values; computing the RBF interpolation of the quaternion representation of rotation matrices and the singular value logarithms; reassembling the deformation gradient tensors at quadrature nodes of the destination mesh, to be used in the assembly of the electrophysiology model equations. The proposed method overcomes limitations of existing interpolation methods, including nested intergrid interpolation and RBF interpolation of the displacement field, that may lead to the loss of physical meaningfulness of the mathematical formulation and then to solver failures at the algebraic level, due to negative determinant values. The proposed method enables the transfer of solution variables between finite element spaces of different degrees and shapes and without stringent conformity requirements between different meshes, enhancing the flexibility and accuracy of electromechanical simulations. Numerical results confirm that the proposed method enables the transfer of the deformation gradient tensor, allowing to successfully run simulations in cases where existing methods fail. This work provides an efficient and robust method for the intergrid transfer of the deformation gradient tensor, enabling independent tailoring of mesh discretizations to the particular characteristics of the physical components concurring to the of the multiphysics model.

math.NA