Tips for the choice of initial estimates in NONMEM.
10.12793/tcp.2016.24.3.119
- Author:
Seunghoon HAN
1
;
Sangil JEON
;
Dong Seok YIM
Author Information
1. Department of Clinical Pharmacology and Therapeutics, Seoul St. Mary's Hospital, Seoul 06591, Korea. waystolove@catholic.ac.kr
- Publication Type:Review
- Keywords:
NONMEM;
initial estimate;
pharmacometrics;
pharmacokinetic-pharmacodynamic model
- MeSH:
Physiology
- From:Translational and Clinical Pharmacology
2016;24(3):119-123
- CountryRepublic of Korea
- Language:English
-
Abstract:
The importance of precise information and knowledge on the initial estimates (IEs) in modeling has not been paid its due attention so far. By focusing on the IE, this tutorial may serve as a practical guide for beginners in pharmacometrics. A 'good' set of IEs rather than arbitrary values is required because the IEs where NONMEM kicks off its estimation may influence the subsequent objective function minimization. To provide NONMEM with acceptable IEs, modelers should understand the exact meaning of THETA, OMEGA and SIGMA based on physiology. In practice, problems related to the value of the IE are more likely to occur for THETAs rather than the random-effect terms. Because it is almost impossible for a modeler to give a precise IE for OMEGAs at the beginning, it may be a good practice to start at relatively small IEs for them. NONMEM may fail to converge when too small IEs are provided for residual error parameters; thus, it is recommended to give sufficiently large values for them. The understandings on the roles, meanings and implications of IEs even help modelers in troubleshooting situations which frequently occur over the whole modeling process.
