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Improving cardiomyocyte model fidelity and utility via dynamic electrophysiology protocols and optimization algorithms

机译:通过动态电生理方案和优化算法提高心肌细胞模型的保真度和实用性

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摘要

Mathematical models of cardiac electrophysiology are instrumental in determining mechanisms of cardiac arrhythmias. However, the foundation of a realistic multiscale heart model is only as strong as the underlying cell model. While there have been myriad advances in the improvement of cellular‐level models, the identification of model parameters, such as ion channel conductances and rate constants, remains a challenging problem. The primary limitations to this process include: (1) such parameters are usually estimated from data recorded using standard electrophysiology voltage‐clamp protocols that have not been developed with model building in mind, and (2) model parameters are typically tuned manually to subjectively match a desired output. Over the last decade, methods aimed at overcoming these disadvantages have emerged. These approaches include the use of optimization or fitting tools for parameter estimation and incorporating more extensive data for output matching. Here, we review recent advances in parameter estimation for cardiomyocyte models, focusing on the use of more complex electrophysiology protocols and global search heuristics. We also discuss future applications of such parameter identification, including development of cell‐specific and patient‐specific mathematical models to investigate arrhythmia mechanisms and predict therapy strategies.
机译:心脏电生理学的数学模型在确定心律不齐的机制中起着重要作用。但是,现实的多尺度心脏模型的基础仅与基础细胞模型一样牢固。尽管细胞水平模型的改进已取得了无数进步,但模型参数的识别(例如离子通道电导和速率常数)仍然是一个具有挑战性的问题。此过程的主要局限性包括:(1)这些参数通常是根据使用标准电生理学电压钳制协议记录的数据估算得出的,而该协议并未考虑到模型构建的情况;(2)模型参数通常是手动调整以主观地匹配所需的输出。在过去的十年中,出现了旨在克服这些缺点的方法。这些方法包括使用优化或拟合工具进行参数估计,并合并更广泛的数据以进行输出匹配。在这里,我们回顾了心肌细胞模型参数估计的最新进展,重点是使用更复杂的电生理方案和全局搜索启发式方法。我们还将讨论这种参数识别的未来应用,包括开发特定于细胞和特定于患者的数学模型,以研究心律不齐的机制并预测治疗策略。

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