When models are used to measure or predict physiological variables and para
meters in a given individual, the experiments needed are often complex and
costly. A valuable solution for improving their cost effectiveness is repre
sented by population models. A widely used population model in insulin secr
etion studies is the one proposed by Van Cauter et al. (Diabetes 41:368-377
, 1992), which determines the parameters of the two compartment model of C-
peptide kinetics in a given individual from the knowledge of his/her age, s
ex, body surface area, and health condition (i.e., normal, obese, diabetic)
. This population model was identified from the data of a large training se
t (more than 200 subjects) via a deterministic approach. This approach, whi
le sound in terms of providing a point estimate of C-peptide kinetic parame
ters in a given individual, does not provide a measure of their precision.
In this paper, by employing the same training set of Van Cauter et al., we
show that the identification of the population model into a Bayesian framew
ork (by using Markov chain Monte Carlo) allows, at the individual level, th
e estimation of point values of the C-peptide kinetic parameters together w
ith their precision. A successful application of the methodology is illustr
ated in the estimation of C-peptide kinetic parameters of seven subjects (n
ot belonging to the training set used for the identification of the populat
ion model) for which reference values were available thanks to an independe
nt identification experiment. (C) 2000 Biomedical Engineering Society. [S00
90-6964(00)00907-3].