Inria, Asclepios team, Sophia-Antipolis, 06902 France.
IEEE Trans Biomed Eng. 2011 Dec;58(12):3339-49. doi: 10.1109/TBME.2011.2107513. Epub 2011 Jan 20.
Computer models of cardiac electrophysiology (EP) can be a very efficient tool to better understand the mechanisms of arrhythmias. Quantitative adjustment of such models to experimental data (personalization) is needed in order to test their realism and predictive power, but it remains challenging at the organ scale. In this paper, we propose a framework for the personalization of a 3-D cardiac EP model, the Mitchell-Schaeffer (MS) model, and evaluate its volumetric predictive power under various pacing scenarios. The personalization was performed on ex vivo large porcine healthy hearts using diffusion tensor MRI (DT-MRI) and optical mapping data. The MS model was simulated on a 3-D mesh incorporating local fiber orientations, built from DT-MRI. The 3-D model parameters were optimized using features such as 2-D epicardial depolarization and repolarization maps, extracted from the optical mapping. We also evaluated the sensitivity of our personalization framework to different pacing locations and showed results on its robustness. Further, we evaluated volumetric model predictions for various epi- and endocardial pacing scenarios. We demonstrated promising results with a mean personalization error around 5 ms and a mean prediction error around 10 ms (5% of the total depolarization time). Finally, we discussed the potential translation of such work to clinical data and pathological hearts.
计算机心脏电生理学 (EP) 模型可以成为更好地理解心律失常机制的非常有效的工具。为了测试模型的真实性和预测能力,需要对这些模型进行定量调整(个性化),但在器官尺度上仍然具有挑战性。在本文中,我们提出了一种用于个性化 3-D 心脏 EP 模型(即 Mitchell-Schaeffer 模型)的框架,并评估了其在各种起搏情况下的容积预测能力。个性化是在使用扩散张量 MRI (DT-MRI) 和光学映射数据的离体大型健康猪心脏上进行的。MS 模型在从 DT-MRI 构建的包含局部纤维方向的 3-D 网格上进行模拟。使用从光学映射中提取的 2-D 心外膜去极化和复极化图等特征来优化 3-D 模型参数。我们还评估了我们的个性化框架对不同起搏位置的敏感性,并展示了其稳健性的结果。此外,我们评估了各种心外膜和心内膜起搏情况下的容积模型预测。我们的结果显示出有希望的结果,平均个性化误差约为 5 毫秒,平均预测误差约为 10 毫秒(总去极化时间的 5%)。最后,我们讨论了将此类工作转化为临床数据和病理性心脏的潜力。