Abstract
Nonlinear mixed effects models are widely used to describe longitudinal data to improve the efficiency of drug development process or increase the understanding of the studied disease. In such settings, the appropriateness of the modeling assumptions is critical in order to draw correct conclusions and must be carefully assessed for any substantial violations. Here, we propose a new method for structure model assessment, based on assessment of bias in conditional weighted residuals (CWRES). We illustrate this method by assessing prediction bias in two integrated models for glucose homeostasis, the integrated glucose-insulin (IGI) model, and the integrated minimal model (IMM). One dataset was simulated from each model then analyzed with the two models. CWRES outputted from each model fitting were modeled to capture systematic trends in CWRES as well as the magnitude of structural model misspecifications in terms of difference in objective function values (ΔOFVBias). The estimates of CWRES bias were used to calculate the corresponding bias in conditional predictions by the inversion of first-order conditional estimation method’s covariance equation. Time, glucose, and insulin concentration predictions were the investigated independent variables. The new method identified correctly the bias in glucose sub-model of the integrated minimal model (IMM), when this bias occurred, and calculated the absolute and proportional magnitude of the resulting bias. CWRES bias versus the independent variables agreed well with the true trends of misspecification. This method is fast easily automated diagnostic tool for model development/evaluation process, and it is already implemented as part of the Perl-speaks-NONMEM software.
Highlights
Nonlinear mixed effects (NLME) models are currently advocated to maximize the utilization of gained information throughout all the phases of drug development
We present a new method based on conditional weighted residuals (CWRES) modeling to assess structural assumptions as prediction bias in NLME models developed for continuous data, by back-extrapolating a CWRES-based bias using the first-order conditional estimation (FOCE) approximation
When either of the two data sets was analyzed with the integrated glucose-insulin (IGI) model or data simulated by the integrated minimal model (IMM) was analyzed by the IMM, ΔOFVBias was non-significant for both dependent variable (DV)
Summary
Nonlinear mixed effects (NLME) models are currently advocated to maximize the utilization of gained information throughout all the phases of drug development. These models are adopted for reducing sample size, calculating study power, confirming drug effects, selecting doses, and optimizing trial design as well as supporting final/interim analysis decisions [1]. In such settings, the appropriateness of the modeling assumptions is critical in order to draw correct.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.