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Updated: Oct 19, 2025

Patient-specific Modeling of the Heart: Estimation of Ventricular Fiber Orientations
Published on: January 8, 2013
Multiparameter optimization of nonuniform passive diffusion properties for creating coarse-grained equivalent models
Éric Irakoze1, Vincent Jacquemet1
1Pharmacology and Physiology Department, Institute of Biomedical Engineering, Université de Montréal, Montreal, QC, H3T 1J4, Canada; Hôpital Du Sacré-Cœur de Montréal, Research Center, 5400 Boul. Gouin Ouest, Montreal, QC, H4J 1C5, Canada.
Abstract:
The arrhythmogenic role of discrete cardiac propagation may be assessed by comparing discrete (fine-grained) and equivalent continuous (coarse-grained) models. We aim to develop an optimization algorithm for estimating the smooth conductivity field that best reproduces the diffusion properties of a given discrete model. Our algorithm iteratively adjusts local conductivity of the coarse-grained continuous model by simulating passive diffusion from white noise initial conditions during 3-10 ms and computing the root mean square error with respect to the discrete model. The coarse-grained conductivity field was interpolated from up to 300 evenly spaced control points. We derived an approximate formula for the gradient of the cost function that required (in two dimensions) only two additional simulations per iteration regardless of the number of estimated parameters. Conjugate gradient solver facilitated simultaneous optimization of multiple conductivity parameters. The method was tested in rectangular anisotropic tissues with uniform and nonuniform conductivity (slow regions with sinusoidal profile) and random diffuse fibrosis, as well as in a monolayer interconnected cable model of the left atrium with spatially-varying fibrosis density. Comparison of activation maps served as validation. The results showed that after convergence the errors in activation time were < 1 ms for rectangular geometries and 1-3 ms in the atrial model. Our approach based on the comparison of passive properties (<10 ms simulation) avoids performing active propagation simulations (>100 ms) at each iteration while reproducing activation maps, with possible applications to investigating the impact of microstructure on arrhythmias.
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