Key result
CircAdapt parameter reduction cuts variables ~85% to enable patient-specific RV strain simulation.
Why the study?
In arrhythmogenic cardiomyopathy, personalized computational parameter estimation using the CircAdapt model is challenging due to the large number of parameters (n = 110) and complex interactions.
A novel parameter reduction framework using the CircAdapt model successfully identified a subset of 16 key parameters to estimate patient-specific right ventricular tissue abnormalities in arrhythmogenic cardiomyopathy.
Enables efficient patient-specific RV modeling in AC; leaves open validation in larger cohorts before clinical use.
Arrhythmogenic cardiomyopathy (AC) is an inherited cardiac disease, clinically characterized by life-threatening ventricular arrhythmias and progressive cardiac dysfunction. Patient-specific computational models could help understand the disease progression and may help in clinical decision-making. We propose an inverse modelling approach using the CircAdapt model to estimate patient-specific regional abnormalities in tissue properties in AC subjects. However, the number of parameters ( n = 110) and their complex interactions make personalized parameter estimation challenging. The goal of this study is to develop a framework for parameter reduction and estimation combining Morris screening, quasi-Monte Carlo (qMC) simulations and particle swarm optimization (PSO). This framework identifies the best subset of tissue properties based on clinical measurements allowing patient-specific identification of right ventricular tissue abnormalities. We applied this framework on 15 AC genotype-positive subjects with varying degrees of myocardial disease. Cohort studies have shown that atypical regional right ventricular (RV) deformation patterns reveal an early-stage AC disease. The CircAdapt model of cardiovascular mechanics and haemodynamics has already demonstrated its ability to capture typical deformation patterns of AC subjects. We, therefore, use clinically measured cardiac deformation patterns to estimate model parameters describing myocardial disease substrates underlying these AC-related RV deformation abnormalities. Morris screening reduced the subset to 48 parameters. qMC and PSO further reduced the subset to a final selection of 16 parameters, including regional tissue contractility, passive stiffness, activation delay and wall reference area. This article is part of the theme issue ‘Uncertainty quantification in cardiac and cardiovascular modelling and simulation’.
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Osta et al. (2020) studied Arrhythmogenic cardiomyopathy (n=15). Parameter subset reduction framework (CircAdapt model) vs. Full 110-parameter set was evaluated on Parameter subset reduction for patient-specific simulation of right ventricular strain. A parameter reduction framework successfully reduced CircAdapt model parameters from 110 to 16, enabling patient-specific simulation of right ventricular strain in AC mutation carriers.
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