ArticleThe AAPS journal2020
Saddle-Reset for Robust Parameter Estimation and Identifiability Analysis of Nonlinear Mixed Effects Models.
Article in The AAPS journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Development and comparison of model-integrated evidence approaches for bioequivalence studies with pharmacokinetic end points.CPT: pharmacometrics & systems pharmacology · 2024Article
- Evaluation of model-integrated evidence approaches for pharmacokinetic bioequivalence studies using model averaging methods.CPT: pharmacometrics & systems pharmacology · 2024Article
- Assessment of frequency response techniques in diagnosing polymer electrolyte membrane fuel cells.iScience · 2024Article
- Fractal Kinetic Implementation in Population Pharmacokinetic Modeling.Pharmaceutics · 2023Article
- Metaheuristics for pharmacometrics.CPT: pharmacometrics & systems pharmacology · 2021Review
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Authors and funding
4 authors.
Funding
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Abstract
Parameter estimation of a nonlinear model based on maximizing the likelihood using gradient-based numerical optimization methods can often fail due to premature termination of the optimization algorithm. One reason for such failure is that these numerical optimization methods cannot distinguish between the minimum, maximum, and a saddle point; hence, the parameters found by these optimization algorithms can possibly be in any of these three stationary points on the likelihood surface. We have found that for maximization of the likelihood for nonlinear mixed effects models used in pharmaceutical development, the optimization algorithm Broyden-Fletcher-Goldfarb-Shanno (BFGS) often terminates in saddle points, and we propose an algorithm, saddle-reset, to avoid the termination at saddle points, based on the second partial derivative test. In this algorithm, we use the approximated Hessian matrix at the point where BFGS terminates, perturb the point in the direction of the eigenvector associated with the lowest eigenvalue, and restart the BFGS algorithm. We have implemented this algorithm in industry standard software for nonlinear mixed effects modeling (NONMEM, version 7.4 and up) and showed that it can be used to avoid termination of parameter estimation at saddle points, as well as unveil practical parameter non-identifiability. We demonstrate this using four published pharmacometric models and two models specifically designed to be practically non-identifiable.
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Registered trials
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