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mvLognCorrEst:一个用于从多元对数正态分布中抽样和从不完全相关矩阵中估计相关性的 R 包。

mvLognCorrEst: an R package for sampling from multivariate lognormal distributions and estimating correlations from uncomplete correlation matrix.

机构信息

Electrical, Computer and Biomedical Engineering, University of Pavia, Pavia, Italy.

Electrical, Computer and Biomedical Engineering, University of Pavia, Pavia, Italy; Systems Forecasting UK Ltd, Lancaster, UK.

出版信息

Comput Methods Programs Biomed. 2023 Jun;235:107517. doi: 10.1016/j.cmpb.2023.107517. Epub 2023 Mar 31.

Abstract

BACKGROUND AND OBJECTIVE

Pharmacometrics (PMX) is a quantitative discipline which supports decision-making processes in all stages of drug development. PMX leverages Modeling and Simulations (M&S), which represents a powerful tool to characterize and predict the behavior and the effect of a drug. M&S-based methods, such as Sensitivity Analysis (SA) and Global Sensitivity Analysis (GSA), are gaining interest in PMX as they allow the evaluation of model-informed inference quality. Simulations should be correctly designed to obtain reliable results. Neglecting correlations between model parameters can significantly alter the results of simulations. However, the introduction of a correlation structure between model parameters can cause some issues. Sampling from a multivariate lognormal distribution, which is the typically distribution assumed for PMX model parameters, is not straightforward when a correlation structure is introduced. Indeed, correlations need to respect some constraints which depend by the CVs (i.e., coefficients of variation) of lognormal variables. In addition, when correlation matrices have some unspecified values, they should be properly fixed preserving the positive semi-definiteness of the correlation structure. In this paper, we present mvLognCorrEst, an R package developed to address these issues.

METHODS

The proposed sampling strategy was based on reconducting the extraction from the multivariate lognormal distribution of interest to the underlying Normal distribution. However, with high lognormal CVs, a positive semi-definite Normal covariance matrix cannot be obtained due to the violation of some theoretical constraints. In these cases, the Normal covariance matrix was approximated to its nearest positive definite matrix using Frobenius norm as matrix distance. For the estimation of unknown correlations terms, the graph theory was used to represent the correlation structure as weighed undirected graph. Plausible value ranges for the unspecified correlations were derived considering the paths between variables. Then, their estimation was performed by solving a constrained optimization problem.

RESULTS

Package functions are presented and applied on a real case study, that is the GSA of a PMX model that has been recently developed to support preclinical oncological studies.

CONCLUSIONS

mvLognCorrEst package is an R tool to support simulation-based analysis for which sampling from multivariate lognormal distributions with correlated variables and/or estimation of partially defined correlation matrix are required.

摘要

背景与目的

药物计量学(PMX)是一门定量学科,支持药物开发各个阶段的决策过程。PMX 利用建模和模拟(M&S),这是一种强大的工具,可以描述和预测药物的行为和效果。基于模拟的方法,如敏感性分析(SA)和全局敏感性分析(GSA),在 PMX 中越来越受到关注,因为它们允许评估基于模型的推断质量。为了获得可靠的结果,模拟应该正确设计。忽略模型参数之间的相关性会显著改变模拟结果。然而,引入模型参数之间的相关结构可能会导致一些问题。从多元对数正态分布中进行抽样,这是 PMX 模型参数通常假设的分布,当引入相关结构时并不简单。实际上,相关性需要满足一些依赖于对数正态变量的变异系数(即变异系数)的约束。此外,当相关矩阵具有一些未指定的值时,它们应该被正确固定,以保持相关结构的正半定。在本文中,我们提出了 mvLognCorrEst,这是一个为解决这些问题而开发的 R 包。

方法

所提出的抽样策略基于重新从感兴趣的多元对数正态分布中提取到基本正态分布。然而,对于高对数正态变异系数,由于违反了一些理论约束,无法获得正半定正态协方差矩阵。在这些情况下,使用 Frobenius 范数作为矩阵距离,将正态协方差矩阵近似为其最近的正定矩阵。对于未知相关项的估计,使用图论将相关结构表示为加权无向图。考虑变量之间的路径,为未指定的相关项推导了合理的可能值范围。然后,通过求解约束优化问题来进行它们的估计。

结果

介绍了包函数,并将其应用于一个实际案例研究,即最近开发的支持临床前肿瘤学研究的 PMX 模型的 GSA。

结论

mvLognCorrEst 包是一个 R 工具,用于支持基于模拟的分析,需要从具有相关变量的多元对数正态分布中进行抽样和/或估计部分定义的相关矩阵。

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