MODEL PARAMETER-ESTIMATION AND ANALYSIS - UNDERSTANDING PARAMETRIC STRUCTURE

被引:3
作者
LI, HM
WATANABE, K
AUSLANDER, D
SPEAR, RC
机构
[1] UNIV CALIF BERKELEY,DEPT MECH ENGN,BERKELEY,CA 94720
[2] UNIV CALIF BERKELEY,SCH PUBL HLTH,BERKELEY,CA 94720
关键词
BENZENE; PHARMACOKINETIC MODELS; PARAMETER ESTIMATION; MONTE CARLO SIMULATIONS; PARAMETRIC ANALYSIS;
D O I
10.1007/BF02368226
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
We developed three algorithms to facilitate an analysis of the parameter combinations (PASS points) that fit experimental data to a desired degree of accuracy. The clustering algorithm separates PASS points into clusters (PASS clusters) as a preliminary step for the following geometrical parametric analyses. The PASS region reconstruction algorithm defines the space of a PASS cluster to allow further parametric structural analysis. The feasible parameter space expansion algorithm-produces a complete PASS duster to be used for model predictions to evaluate the effects of variability and uncertainty. These algorithms are demonstrated using two pharmacokinetic models; a single compartment model for procainamide and a three-compartment physiologically based model for benzene. We found a more thorough representation of the parameter space than previously considered. Thus, we obtained model predictions that describe better the variability in population responses. In addition, we also parametrically identified a subpopulation that may have a higher risk for cancer.
引用
收藏
页码:97 / 111
页数:15
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