Abstract:We present a computational study of reentry wave propagation using electrophysiological models of human cardiac cells and the associated magnetic field map of a human heart. We examined the details of magnetic field variation and related physiological parameters for reentry waves in two-dimensional (2-D) human atrial tissue and a three-dimensional (3-D) human ventricle model. A 3-D mesh system representing the human ventricle was reconstructed from the surface geometry of a human heart. We used existing human … Show more
“…MCG or MEG is not sensitive to the normal component of myocardial current but only sensitive to the tangential current to the thorax surface. 6 Presumably, the local current strength was underestimated because MCG omitted the normal component of myocardial currents. This factor will give a stronger signal in a practical measurement as the normal component of myocardial currents can generate the tipping magnetic field, too.…”
Section: Discussionmentioning
confidence: 99%
“…6,16 First, I simulated heart magnetic fields generated from a cyclic excitation of transmembrane potential on the myocardial surface. 16 In biomagnetism, they generally utilize equivalent current dipoles (ECD) as its sources.…”
Section: Simulation Methods For the Feasibility Testmentioning
confidence: 99%
“…Emerging studies dealing with electrophysiology (EP) in cardiology, [1][2][3][4][5] biology 6,7 and nonlinear dynamics 8,9 are reporting theoretical and experimental evidences that most of pathological cardiac conduction disorders originate from generation of reentrant sources either in ventricles or in atria. Especially, the surgical treatments for atrial fibrillation (AF) and atrial flutter are mainly based on blocking all the possible abnormal reentrant circuits on the myocardium.…”
Section: Introductionmentioning
confidence: 99%
“…Three-dimensional tissue excitation cannot be investigated by such two-dimensional measurements. 6 Non-invasively, body surface potential mapping or magnetocardiography (MCG) 16 can be applied, but the ill-posedness in inverse problems limits the accuracy of the source localization, especially for deep sources.…”
Matching the proton magnetic resonance frequency to the frequency of a periodic electrophysiological excitation of myocardium enables direct localization of the cardiac reentry by magnetic resonance imaging techniques. The feasibility of this new idea has been demonstrated by conducting a numerical simulation based on a realistic heart model and experimental parameters in SQUID-based micro-Tesla NMR.
“…MCG or MEG is not sensitive to the normal component of myocardial current but only sensitive to the tangential current to the thorax surface. 6 Presumably, the local current strength was underestimated because MCG omitted the normal component of myocardial currents. This factor will give a stronger signal in a practical measurement as the normal component of myocardial currents can generate the tipping magnetic field, too.…”
Section: Discussionmentioning
confidence: 99%
“…6,16 First, I simulated heart magnetic fields generated from a cyclic excitation of transmembrane potential on the myocardial surface. 16 In biomagnetism, they generally utilize equivalent current dipoles (ECD) as its sources.…”
Section: Simulation Methods For the Feasibility Testmentioning
confidence: 99%
“…Emerging studies dealing with electrophysiology (EP) in cardiology, [1][2][3][4][5] biology 6,7 and nonlinear dynamics 8,9 are reporting theoretical and experimental evidences that most of pathological cardiac conduction disorders originate from generation of reentrant sources either in ventricles or in atria. Especially, the surgical treatments for atrial fibrillation (AF) and atrial flutter are mainly based on blocking all the possible abnormal reentrant circuits on the myocardium.…”
Section: Introductionmentioning
confidence: 99%
“…Three-dimensional tissue excitation cannot be investigated by such two-dimensional measurements. 6 Non-invasively, body surface potential mapping or magnetocardiography (MCG) 16 can be applied, but the ill-posedness in inverse problems limits the accuracy of the source localization, especially for deep sources.…”
Matching the proton magnetic resonance frequency to the frequency of a periodic electrophysiological excitation of myocardium enables direct localization of the cardiac reentry by magnetic resonance imaging techniques. The feasibility of this new idea has been demonstrated by conducting a numerical simulation based on a realistic heart model and experimental parameters in SQUID-based micro-Tesla NMR.
“…7.13 (MathWorks Co., Natick, MA, USA). The source code of the cell model was from the CellML version and already implemented in our previous computational studies (6-8). The solution algorithm for the bidomain method was from Ashihara et al (9).…”
Although complex fractionated electrogram (CFE) is known to be a target for catheter ablation of fibrillation, its physiological meaning in fibrillation wave-dynamics remains to be clarified. We evaluated the spatiotemporal relationships among the parameters of fibrillation wave-dynamics by simulation modeling. We generated maps of CFE-cycle length (CFE-CL), local dominant frequency (LDF), wave break (WB), and phase singularity (PS) of fibrillation in 2-dimensional homogeneous bidomain cardiac modeling (1,000 × 1,000 cells ten Tusscher model). We compared spatiotemporal correlations by dichotomizing each maps into 10 × 10 lattice zones. In spatial distribution, WB and PS showed excellent correlation (R = 0.963, P < 0.001). CFE-CL had weak correlations with WB (R = 0.288, P < 0.001), PS (R = 0.313, P < 0.001), and LDF (R = -0.411, P < 0.001). However, LDF did not show correlation with PS or WB. PSs were mostly distributed at the periphery of low CFE-CL area. Virtual ablation (5% of critical mass) of CFE-CL < 100 ms terminated fibrillation at 14.3 sec, and high LDF ablation (5% of critical mass) changed fibrillation to organized tachycardia, respectively. In homogeneous 2D fibrillation modeling, CFE-CL was weakly correlated with WB, PS, and LDF, spatiotemporally. PSs are mostly positioned at the periphery of low CFE-CL areas, and virtual ablation targeting low CFE-CL regions terminated fibrillation successfully.Graphical Abstract
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