Key result
Subject-specific 3D MRI heart models better match experimental VT outcomes than average-value models.
Why the study?
Computational efficiency of multi-scale digital twins for cardiac arrhythmia is hindered by equation complexity, and prediction accuracy relies on parameter calibration and intricate non-linear relations.
A computationally efficient, subject-specific 3D MRI-based digital twin pipeline accurately predicts infarct-related VT inducibility, highlighting its potential for clinical translation in VT risk assessment.
Answers are grounded in this paper and cite their sources.
May advance VT prediction in infarct models; extends preclinical digital twins but leaves human translation open.
The computational efficiency of contemporary multi-scale digital twins used to investigate cardiac arrhythmia is often hindered by the equation system complexity, while the accuracy of predictions depends on the calibration of model parameters and their intricate non-linear relation. Here we employed a robust pipeline for fast simulations of scar-related ventricular tachycardia (VT) inducibility using an efficient Lattice-Boltzmann Method with GPU-based accelerated code. We tested the pipeline on 3D digital twins built from MR images acquired in n = 8 swine with chronic infarction, by performing a subject-specific personalization of each model per tissue type (i.e., scar, border zone, and healthy) and tuning the key parameters (e.g., action potential duration, excitability, and wave speed) from recorded endocardial bipolar voltage maps and intracardiac electrograms. We first validated the VT simulation outcome by precisely replicating the stimulation protocol and pacing site used in the animal studies. Our results demonstrated very good agreement between the experiment and simulated VT outcome for personalized model parameters using subject-specific values, compared to a poor outcome when parameters were tuned from average values from all cases. Second, we performed a comprehensive in silico study where the stimulation was delivered from 10 000 virtual endocardial locations and found a strong dependence of VT (non)/-inducibility per case on the stimulation site. Simulating 10 s of sustained VT induced on a 3D model comprising 1.2 million cubic voxels (0.7 mm edge size) took 30 min on a laptop using GPU, underlying the computational tractability of our pipeline and its potential clinical translation to predict infarct-related VT risk.
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Padilla et al. (2026) studied Chronic infarction and scar-related ventricular tachycardia (n=8). Subject-specific personalization of 3D MRI-based heart models vs. Models tuned from average values from all cases was evaluated on Ventricular tachycardia (VT) simulation outcome agreement with experiment. Subject-specific personalization of 3D MRI-based heart models demonstrated very good agreement between experimental and simulated VT outcomes compared to models tuned from average values.
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