Literature DB >> 29107004

Extending existing structural identifiability analysis methods to mixed-effects models.

David L I Janzén1, Mats Jirstrand2, Michael J Chappell3, Neil D Evans3.   

Abstract

The concept of structural identifiability for state-space models is expanded to cover mixed-effects state-space models. Two methods applicable for the analytical study of the structural identifiability of mixed-effects models are presented. The two methods are based on previously established techniques for non-mixed-effects models; namely the Taylor series expansion and the input-output form approach. By generating an exhaustive summary, and by assuming an infinite number of subjects, functions of random variables can be derived which in turn determine the distribution of the system's observation function(s). By considering the uniqueness of the analytical statistical moments of the derived functions of the random variables, the structural identifiability of the corresponding mixed-effects model can be determined. The two methods are applied to a set of examples of mixed-effects models to illustrate how they work in practice.
Copyright © 2017 Elsevier Inc. All rights reserved.

Keywords:  Input-Output form approach; Mixed-Effects modelling; Structural identifiability; Taylor series expansion approach

Mesh:

Year:  2017        PMID: 29107004     DOI: 10.1016/j.mbs.2017.10.009

Source DB:  PubMed          Journal:  Math Biosci        ISSN: 0025-5564            Impact factor:   2.144


  1 in total

1.  Analysis of cellular kinetic models suggest that physiologically based model parameters may be inherently, practically unidentifiable.

Authors:  Liam V Brown; Mark C Coles; Mark McConnell; Alexander V Ratushny; Eamonn A Gaffney
Journal:  J Pharmacokinet Pharmacodyn       Date:  2022-08-06       Impact factor: 2.410

  1 in total

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