Back to Search Start Over

Performance comparison of various maximum likelihood nonlinear mixed-effects estimation methods for dose-response models

Authors :
Plan, Elodie
Maloney, Alan
Mentré, France
Karlsson, Mats
Bertrand, Julie
Department of Pharmaceutical Biosciences
Uppsala University
Exprimo NV
Exprimo
Modèles et méthodes de l'évaluation thérapeutique des maladies chroniques (U738 / UMR_S738)
Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM)
E.L. Plan was supported by UCB Pharma, Belgium
Source :
European Journal of Clinical Pharmacology, European Journal of Clinical Pharmacology, Springer Verlag, 2012, 14 (3), pp.420-32. ⟨10.1208/s12248-012-9349-2⟩
Publication Year :
2012
Publisher :
HAL CCSD, 2012.

Abstract

International audience; Estimation methods for nonlinear mixed-effects modelling have considerably improved over the last decades. Nowadays, several algorithms implemented in different software are used. The present study aimed at comparing their performance for dose-response models. Eight scenarios were considered using a sigmoid E(max) model, with varying sigmoidicity and residual error models. One hundred simulated datasets for each scenario were generated. One hundred individuals with observations at four doses constituted the rich design and at two doses, the sparse design. Nine parametric approaches for maximum likelihood estimation were studied: first-order conditional estimation (FOCE) in NONMEM and R, LAPLACE in NONMEM and SAS, adaptive Gaussian quadrature (AGQ) in SAS, and stochastic approximation expectation maximization (SAEM) in NONMEM and MONOLIX (both SAEM approaches with default and modified settings). All approaches started first from initial estimates set to the true values and second, using altered values. Results were examined through relative root mean squared error (RRMSE) of the estimates. With true initial conditions, full completion rate was obtained with all approaches except FOCE in R. Runtimes were shortest with FOCE and LAPLACE and longest with AGQ. Under the rich design, all approaches performed well except FOCE in R. When starting from altered initial conditions, AGQ, and then FOCE in NONMEM, LAPLACE in SAS, and SAEM in NONMEM and MONOLIX with tuned settings, consistently displayed lower RRMSE than the other approaches. For standard dose-response models analyzed through mixed-effects models, differences were identified in the performance of estimation methods available in current software, giving material to modellers to identify suitable approaches based on an accuracy-versus-runtime trade-off.

Details

Language :
English
ISSN :
00316970 and 14321041
Database :
OpenAIRE
Journal :
European Journal of Clinical Pharmacology, European Journal of Clinical Pharmacology, Springer Verlag, 2012, 14 (3), pp.420-32. ⟨10.1208/s12248-012-9349-2⟩
Accession number :
edsair.od......2592..94304441cce84e2b67511cd39c3e5f46