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Am J Physiol Regul Integr Comp Physiol 279: R1671-R1684, 2000;
0363-6119/00 $5.00
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Vol. 279, Issue 5, R1671-R1684, November 2000

Development of a compartmental model of human zinc metabolism: identifiability and multiple studies analyses

Leland V. Miller, Nancy F. Krebs, and K. Michael Hambidge

Section of Nutrition, Department of Pediatrics and Center for Human Nutrition, University of Colorado Health Sciences Center, Denver, Colorado 80262

A compartmental model of zinc metabolism has been developed from stable isotope tracer studies of five healthy adults. Multiple isotope tracers were administered orally and intravenously, and the resulting enrichment was measured in plasma, erythrocytes, urine, and feces for as long as 3 wk. Data from total zinc measurements and model-independent calculations of various steady-state parameters were also modeled with the kinetic data. A structure comprised of 14 compartments and as many as 25 unknown kinetic parameters was developed to adequately model the data from each of the individual studies. The structural identifiability of the model was established using the GLOBI2 identifiability analysis software. Numerical identifiability of parameter estimates was evaluated using statistical data provided by SAAM. A majority of the model parameters was estimated with sufficient statistical certainty to be considered well determined. After the fitting of the model and data from the individual studies using SAAM/CONSAM, results were submitted to SAAM extended multiple studies analysis for aggregation into a single set of population parameters and statistics. The model was judged to be valid based on criteria described elsewhere.

SAAM; GLOBI2; extended multiple studies analysis; isotope tracer kinetics; population studies; trace element


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