Du Dongping, Yang Hui, Ednie Andrew R, Bennett Eric S
IEEE J Biomed Health Inform. 2016 Sep;20(5):1439-52. doi: 10.1109/JBHI.2015.2458791. Epub 2015 Jul 22.
Glycan structures account for up to 35% of the mass of cardiac sodium ( Nav ) channels. To question whether and how reduced sialylation affects Nav activity and cardiac electrical signaling, we conducted a series of in vitro experiments on ventricular apex myocytes under two different glycosylation conditions, reduced protein sialylation (ST3Gal4(-/-)) and full glycosylation (control). Although aberrant electrical signaling is observed in reduced sialylation, realizing a better understanding of mechanistic details of pathological variations in INa and AP is difficult without performing in silico studies. However, computer model of Nav channels and cardiac myocytes involves greater levels of complexity, e.g., high-dimensional parameter space, nonlinear and nonconvex equations. Traditional linear and nonlinear optimization methods have encountered many difficulties for model calibration. This paper presents a new statistical metamodeling approach for efficient computer experiments and optimization of Nav models. First, we utilize a fractional factorial design to identify control variables from the large set of model parameters, thereby reducing the dimensionality of parametric space. Further, we develop the Gaussian process model as a surrogate of expensive and time-consuming computer models and then identify the next best design point that yields the maximal probability of improvement. This process iterates until convergence, and the performance is evaluated and validated with real-world experimental data. Experimental results show the proposed algorithm achieves superior performance in modeling the kinetics of Nav channels under a variety of glycosylation conditions. As a result, in silico models provide a better understanding of glyco-altered mechanistic details in state transitions and distributions of Nav channels. Notably, ST3Gal4(-/-) myocytes are shown to have higher probabilities accumulated in intermediate inactivation during the repolarization and yield a shorter refractory period than WTs. The proposed statistical design of computer experiments is generally extensible to many other disciplines that involve large-scale and computationally expensive models.
聚糖结构占心脏钠(Nav)通道质量的35%。为了探究唾液酸化减少是否以及如何影响Nav活性和心脏电信号传导,我们在两种不同的糖基化条件下,即蛋白质唾液酸化减少(ST3Gal4(-/-))和完全糖基化(对照),对心室尖部心肌细胞进行了一系列体外实验。尽管在唾液酸化减少时观察到异常电信号传导,但如果不进行计算机模拟研究,就很难更好地理解INa和AP病理变化的机制细节。然而,Nav通道和心肌细胞的计算机模型涉及更高的复杂性,例如高维参数空间、非线性和非凸方程。传统的线性和非线性优化方法在模型校准方面遇到了许多困难。本文提出了一种新的统计元建模方法,用于高效的计算机实验和Nav模型的优化。首先,我们利用分数析因设计从大量模型参数中识别控制变量,从而降低参数空间的维度。此外,我们开发了高斯过程模型作为昂贵且耗时的计算机模型的替代模型,然后确定产生最大改进概率的下一个最佳设计点。这个过程迭代直到收敛,并用实际实验数据评估和验证性能。实验结果表明,所提出的算法在模拟各种糖基化条件下Nav通道的动力学方面具有卓越的性能。因此,计算机模拟模型能更好地理解Nav通道在状态转换和分布中糖基改变的机制细节。值得注意的是,与野生型相比,ST3Gal4(-/-)心肌细胞在复极化过程中积累在中间失活状态的概率更高,且不应期更短。所提出的计算机实验统计设计通常可扩展到许多其他涉及大规模和计算昂贵模型的学科。