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NIMROD:一个用于在基于常微分方程的具有随机效应模型中通过后验的正态逼近进行推理的程序。

NIMROD: a program for inference via a normal approximation of the posterior in models with random effects based on ordinary differential equations.

机构信息

Univ. Bordeaux, ISPED, Centre INSERM U897-Epidemiologie-Biostatistique, F-33000 Bordeaux, France.

出版信息

Comput Methods Programs Biomed. 2013 Aug;111(2):447-58. doi: 10.1016/j.cmpb.2013.04.014. Epub 2013 Jun 10.

DOI:10.1016/j.cmpb.2013.04.014
PMID:23764196
Abstract

Models based on ordinary differential equations (ODE) are widespread tools for describing dynamical systems. In biomedical sciences, data from each subject can be sparse making difficult to precisely estimate individual parameters by standard non-linear regression but information can often be gained from between-subjects variability. This makes natural the use of mixed-effects models to estimate population parameters. Although the maximum likelihood approach is a valuable option, identifiability issues favour Bayesian approaches which can incorporate prior knowledge in a flexible way. However, the combination of difficulties coming from the ODE system and from the presence of random effects raises a major numerical challenge. Computations can be simplified by making a normal approximation of the posterior to find the maximum of the posterior distribution (MAP). Here we present the NIMROD program (normal approximation inference in models with random effects based on ordinary differential equations) devoted to the MAP estimation in ODE models. We describe the specific implemented features such as convergence criteria and an approximation of the leave-one-out cross-validation to assess the model quality of fit. In pharmacokinetics models, first, we evaluate the properties of this algorithm and compare it with FOCE and MCMC algorithms in simulations. Then, we illustrate NIMROD use on Amprenavir pharmacokinetics data from the PUZZLE clinical trial in HIV infected patients.

摘要

基于常微分方程 (ODE) 的模型是描述动力系统的常用工具。在生物医学科学中,每个个体的数据可能较为稀疏,通过标准的非线性回归难以精确估计个体参数,但通常可以从个体间的变异性中获得信息。这使得混合效应模型成为估计群体参数的自然选择。尽管最大似然法是一种有价值的方法,但由于可识别性问题,贝叶斯方法更受欢迎,因为贝叶斯方法可以灵活地纳入先验知识。然而,来自 ODE 系统和随机效应的困难的结合带来了一个主要的数值挑战。通过对后验进行正态近似来找到后验分布的最大值 (MAP),可以简化计算。在这里,我们介绍了 NIMROD 程序(基于常微分方程的具有随机效应的模型中的正态近似推断),用于 ODE 模型中的 MAP 估计。我们描述了特定的实现功能,如收敛标准和留一交叉验证的近似,以评估模型拟合质量。在药代动力学模型中,我们首先在模拟中评估该算法的性质,并将其与 FOCE 和 MCMC 算法进行比较。然后,我们将 NIMROD 用于 HIV 感染患者的 PUZZLE 临床试验中的氨普那韦药代动力学数据。

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