Efficient algorithms for covariate analysis with dynamic data using nonlinear mixed-effects model

2020 ◽  
pp. 096228022094989
Author(s):  
Min Yuan ◽  
Zhi Zhu ◽  
Yaning Yang ◽  
Minghua Zhao ◽  
Kate Sasser ◽  
...  

Nonlinear mixed-effects modeling is one of the most popular tools for analyzing repeated measurement data, particularly for applications in the biomedical fields. Multiple integration and nonlinear optimization are the two major challenges for likelihood-based methods in nonlinear mixed-effects modeling. To solve these problems, approaches based on empirical Bayesian estimates have been proposed by breaking the problem into a nonlinear mixed-effects model with no covariates and a linear regression model without random effect. This approach is time-efficient as it involves no covariates in the nonlinear optimization. However, covariate effects based on empirical Bayesian estimates are underestimated and the bias depends on the extent of shrinkage. Marginal correction method has been proposed to correct the bias caused by shrinkage to some extent. However, the marginal approach appears to be suboptimal when testing covariate effects on multiple model parameters, a situation that is often encountered in real-world data analysis. In addition, the marginal approach cannot correct the inaccuracy in the associated p-values. In this paper, we proposed a simultaneous correction method (nSCEBE), which can handle the situation where covariate analysis is performed on multiple model parameters. Simulation studies and real data analysis showed that nSCEBE is accurate and efficient for both effect-size estimation and p-value calculation compared with the existing methods. Importantly, nSCEBE can be >2000 times faster than the standard mixed-effects models, potentially allowing utilization for high-dimension covariate analysis for longitudinal or repeated measured outcomes.

2018 ◽  
Vol 28 (12) ◽  
pp. 3568-3578
Author(s):  
Min Yuan ◽  
Xu Steven Xu ◽  
Yaning Yang ◽  
Jinfeng Xu ◽  
Xiaohui Huang ◽  
...  

Nonlinear mixed-effects modeling is a popular approach to describe the temporal trajectory of repeated measurements of clinical endpoints collected over time in clinical trials, to distinguish the within-subject and the between-subject variabilities, and to investigate clinically important risk factors (covariates) that may partly explain the between-subject variability. Due to the complex computing algorithms involved in nonlinear mixed-effects modeling, estimation of covariate effects is often time-consuming and error-prone owing to local convergence. We develop a fast and accurate estimation method based on empirical Bayes estimates from the base mixed-effects model without covariates, and simple regressions outside of the nonlinear mixed-effect modeling framework. Application of the method is illustrated using a pharmacokinetic dataset from an anticoagulation drug for the prevention of major cardiovascular events in patients with acute coronary syndrome. Both the application and extensive simulations demonstrated that the performance of this high-throughput method is comparable to the commonly used maximum likelihood estimation in nonlinear mixed-effects modeling.


2020 ◽  
Vol 39 (15) ◽  
pp. 2051-2066 ◽  
Author(s):  
Rui Wang ◽  
Ante Bing ◽  
Cathy Wang ◽  
Yuchen Hu ◽  
Ronald J. Bosch ◽  
...  

2008 ◽  
Vol 01 (02) ◽  
pp. 85-90
Author(s):  
Jian Huang ◽  
Kathleen O’Sullivan ◽  
John Levis ◽  
Elizabeth Kenny-Walsh ◽  
Orla Crosbie ◽  
...  

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