Efficient Computational Modeling of Human Ventricular Activation and Its Electrocardiographic Representation: A Sensitivity Study

Jonathan P. Cranford, Thomas J. O’Hara, Christopher T. Villongco, Omar M. Hafez, Robert C. Blake, Joseph Loscalzo, Jean Luc Fattebert, David F. Richards, Xiaohua Zhang, James N. Glosli, Andrew D. McCulloch, David E. Krummen, Felice C. Lightstone, Sergio E. Wong

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Patient-specific models of the ventricular myocardium, combined with the computational power to run rapid simulations, are approaching the level where they could be used for personalized cardiovascular medicine. A major remaining challenge is determining model parameters from available patient data, especially for models of the Purkinje-myocardial junctions (PMJs): the sites of initial ventricular electrical activation. There are no non-invasive methods for localizing PMJs in patients, and the relationship between the standard clinical ECG and PMJ model parameters is underexplored. Thus, this study aimed to determine the sensitivity of the QRS complex of the ECG to the anatomical location and regional number of PMJs. The QRS complex was simulated using an image-based human torso and biventricular model, and cardiac electrophysiology was simulated using Cardioid. The PMJs were modeled as discrete current injection stimuli, and the location and number of stimuli were varied within initial activation regions based on published experiments. Results indicate that the QRS complex features were most sensitive to the presence or absence of four “seed” stimuli, and adjusting locations of nearby “regional” stimuli provided finer tuning. Decreasing number of regional stimuli by an order of magnitude resulted in virtually no change in the QRS complex. Thus, a minimal 12-stimuli configuration was identified that resulted in physiological excitation, defined by QRS complex feature metrics and ventricular excitation pattern. Overall, the sensitivity results suggest that parameterizing PMJ location, rather than number, be given significantly higher priority in future studies creating personalized ventricular models from patient-derived ECGs.

Original languageEnglish
Pages (from-to)447-467
Number of pages21
JournalCardiovascular Engineering and Technology
Volume9
Issue number3
DOIs
StatePublished - Sep 15 2018
Externally publishedYes

Funding

We thank the Lawrence Livermore National Laboratory (LLNL) Computing Grand Challenge Program for the computational resources that enabled this work. We thank William D. Krauss at LLNL for his technical consultations on visualization and Erik W. Draeger at LLNL for contributing post-processing scripts for ECG generation. Seg3D software used in this study is supported by the National Institute of General Medical Sciences of the National Institutes of Health under grant number P41 GM103545-18. We thank the Blender Foundation (https://www.blender.org/foundation/) for creating superb technical software that we used for visualization of our ventricular activation timing maps. We thank the Laboratory Directed Research and Development (LDRD) program at Lawrence Livermore National Laboratory under the National Nuclear Security Administration (NNSA) for their support of this work, project numbers 15-SI-002 and 13-ERD-035. Financial support to O.M.H. from Department of Energy Computational Science Graduate Fellowship (CSGF) grant DE-FG02-97ER25308 is gratefully acknowledged, as well as to C.T.V. from National Institutes of Health, National Heart, Lung, and Blood Institute (NHLBI) Ruth L. Kirschstein National Research Service Award under Institutional T32 Research Training grant 5 T32 HL 7444-32. Support was provided to J.L. from National Institute of Health grants HL61795, HG007690, and GM107618. Support was provided to A.D.M. by National Institutes of Health grants including the National Biomedical Computation Resource (P41 GM103426), U01 grants HL122199 and HL126273, R01 grants HL105242 and HL111197, and a subaward of U54 HL119893. Support to D.E.K. was provided by the University of California San Diego Clinical Translational Research Institute (CTRI) Galvanizing Engineering in Medicine (GEM) grant. This work was performed under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344. We thank the Lawrence Livermore National Laboratory (LLNL) Computing Grand Challenge Program for the computational resources that enabled this work. We thank William D. Krauss at LLNL for his technical consultations on visualization and Erik W. Draeger at LLNL for contributing post-processing scripts for ECG generation. Seg3D software used in this study is supported by the National Institute of General Medical Sciences of the National Institutes of Health under grant number P41 GM103545-18. We thank the Blender Foundation (https://www.blender. org/foundation/) for creating superb technical software that we used for visualization of our ventricular activation timing maps. We thank the Laboratory Directed Research and Development (LDRD) program at Lawrence Livermore National Laboratory under the National Nuclear Security Administration (NNSA) for their support of this work, project numbers 15-SI-002 and 13-ERD-035. Financial support to O.M.H. from Department of Energy Computational Science Graduate Fellowship (CSGF) grant DE-FG02-97ER25308 is gratefully acknowledged, as well as to C.T.V. from National Institutes of Health, National Heart, Lung, and Blood Institute (NHLBI) Ruth L. Kirschstein National Research Service Award under Institutional T32 Research Training grant 5 T32 HL 7444-32. Support was provided to J.L. from National Institute of Health grants HL61795, HG007690, and GM107618. Support was provided to A.D.M. by National Institutes of Health grants including the National Biomedical Computation Resource (P41 GM103426), U01 grants HL122199 and HL126273, R01 grants HL105242 and HL111197, and a subaward of U54 HL119893. Support to D.E.K. was provided by the University of California San Diego Clinical Translational Research Institute (CTRI) Galvanizing Engineering in Medicine (GEM) grant. This work was performed under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344. This is LLNL report LLNL-JRNL-723037.

FundersFunder number
Department of Energy Computational ScienceDE-FG02-97ER25308
National Biomedical Computation Resource
National Institute of Health
National Institutes of HealthP41 GM103545-18, U54 HL119893
U.S. Department of Energy
National Heart, Lung, and Blood Institute5 T32 HL 7444-32, GM107618, HL61795, HL126273, U01HL122199
National Human Genome Research InstituteHG007690
National Institute of General Medical Sciences
National Institute for Occupational Safety and HealthHL105242, HL111197, P41 GM103426
National Nuclear Security Administration13-ERD-035, 15-SI-002
Lawrence Livermore National LaboratoryDE-AC52-07NA27344
Office of Extramural Research, National Institutes of Health
Laboratory Directed Research and Development

    Keywords

    • Bundle branch block
    • Computational electrophysiology
    • Electrocardiogram
    • Human ventricular excitation
    • Patient-specific modeling
    • Sensitivity analysis

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