LINEAR MIXED-EFFECT MULTIVARIATE ADAPTIVE REGRESSION SPLINES APPLIED TO NONLINEAR PHARMACOKINETICS DATA

Abstract

In a frequently performed pharmacokinetics study, different subjects are given different doses of a drug. After each dose is given, drug concentrations are observed according to the same sampling design. The goal of the experiment is to obtain a representation for the pharmacokinetics of the drug, and to determine if drug concentrations observed at different times after a dose are linear in respect to dose. The goal of this paper it to obtain a representation for concentration as a function of time and dose, which (a) makes no assumptions on the underlying pharmacokinetics of the drug; (b) takes into account the repeated measure structure of the data; and (c) detects nonlinearities in respect to dose. To address (a) we use a multivariate adaptive regression splines representation (MARS), which we recast into a linear mixed-effects model, addressing (b). To detect nonlinearity we describe a general algorithm that obtains nested (mixed-effect) MARS representations. In the pharmacokinetics application, the algorithm obtains representations containing time, and time and dose, respectively, with the property that the bases functions of the first representation are a subset of the second. Standard statistical model selection criteria are used to select representations linear or nonlinear in respect to dose. The method can be applied to a variety of pharmacokinetics (and pharmacodynamic) preclinical and phase I–III trials. Examples of applications of the methodology to real and simulated data are reported.

Work supported by NIH Grant GM 51197 and GM 57193.

Keywords:

• Response-surface
• MARS
• Mixed-effect
• Nested models
• Growth curve
• Nonlinear systems

Acknowledgments

Notes

Work supported by NIH Grant GM 51197 and GM 57193.