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Quantifying the uncertainty in model parameters using Gaussian process-based Markov chain Monte Carlo in cardiac electrophysiology

机译:基于高斯过程的Markov Chain Monte Carlo在心脏电生理学中量化模型参数的不确定性

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Model personalization requires the estimation of patient-specific tissue properties in the form of model parameters from indirect and sparse measurement data. Moreover, a low-dimensional representation of the parameter space is needed, which often has a limited ability to reveal the underlying tissue heterogeneity. As a result, significant uncertainty can be associated with the estimated values of the model parameters which, if left unquantified, will lead to unknown variability in model outputs that will hinder their reliable clinical adoption. Probabilistic estimation of model parameters, however, remains an unresolved challenge. Direct Markov Chain Monte Carlo (MCMC) sampling of the posterior distribution function (pdf) of the parameters is infeasible because it involves repeated evaluations of the computationally expensive simulation model. To accelerate this inference, one popular approach is to construct a computationally efficient surrogate and sample from this approximation. However, by sampling from an approximation, efficiency is gained at the expense of sampling accuracy. In this paper, we address this issue by integrating surrogate modeling of the posterior pdf into accelerating the Metropolis-Hastings (MH) sampling of the exact posterior pdf. It is achieved by two main components: (1) construction of a Gaussian process (GP) surrogate of the exact posterior pdf by actively selecting training points that allow for a good global approximation accuracy with a focus on the regions of high posterior probability; and (2) use of the GP surrogate to improve the proposal distribution in MH sampling, in order to improve the acceptance rate. The presented framework is evaluated in its estimation of the local tissue excitability of a cardiac electrophysiological model in both synthetic data experiments and real data experiments. In addition, the obtained posterior distributions of model parameters are interpreted in relation to the factors contributing to parameter uncertainty, including different low-dimensional representations of the parameter space, parameter non-identifiability, and parameter correlations. (C) 2018 Elsevier B.V. All rights reserved.
机译:模型个性化需要从间接和稀疏测量数据的模型参数形式估计患者特异性组织特性。此外,需要参数空间的低维表示,这通常具有揭示潜在的组织异质性的有限能力。结果,显着的不确定性可以与模型参数的估计值相关联,如果留下无关,将导致模型输出中未知的可变性,这将阻碍其可靠的临床采用。然而,模型参数的概率估计仍然是一个尚未解决的挑战。 Direct Markov链蒙特卡罗(MCMC)参数后部分布函数(PDF)的采样是不可行的,因为它涉及对计算昂贵的模拟模型的重复评估。为了加速这一推理,一种流行的方法是从该近似构建计算上有效的代理和样本。然而,通过从近似抽样,效率以采样精度为代价而获得。在本文中,我们通过将后部PDF的代理建模集成到加速精确后部PDF的大都会 - 黑斯汀(MH)采样来解决这个问题。它通过两个主要成分实现:(1)通过主动选择允许良好的全球近似精度的培训点来构造精确的后验PDF的高斯过程(GP)代理,其重点是高后概率的区域; (2)使用GP代理改善MH采样中的提案分布,以提高验收率。在合成数据实验和实际数据实验中估算了所呈现的框架。另外,所获得的模型参数的后部分布是关于有助于参数不确定性的因素的关于,包括参数空间,参数不可识别性和参数相关的不同低维表示。 (c)2018 Elsevier B.v.保留所有权利。

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