A minimal mathematical model of calcium homeostasis

被引:41
作者
Raposo, JF
Sobrinho, LG
Ferreira, HG
机构
[1] Portuguese Canc Inst, Dept Endocrinol, P-1099023 Lisbon, Portugal
[2] Univ Porto, Abel Salazars Inst Biomed Sci, P-4099003 Oporto, Portugal
[3] Univ Nova Lisboa, Dept Chem, P-2829516 Caparica, Portugal
[4] Univ Nova Lisboa, Fac Sci & Technol, P-2829516 Caparica, Portugal
关键词
D O I
10.1210/jc.2002-011870
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A mathematical model of calcium homeostasis is presented in which the controlling factors are the plasma concentrations of calcium, PTH, and calcitriol, and the effector organs are the parathyroids, bone, kidney, and intestine. Other factors can be added as the need arises. The model is aimed at simulating what happens in a single individual, but its parameters and variables were adjusted to the corresponding published average values. Simulations of published observations in humans undergoing the infusion of calcium or its chelators are presented. With a single exception, these simulations provided a good fit to the data. The response of the system to extrinsic perturbations was characterized by simulating chronic infusions of calcium, PTH, and calcitriol. Finally, the steady state response to perturbations in some of its parameters (the secretory mass of the parathyroids and the affinity and/or sensitivity of the calcium, PTH, and calcitriol receptors) and to renal failure were also investigated in an attempt to analyze the pathogenesis of clinical hypo- or hypercalcemias. In its present form the model cannot be used to base clinical decisions in individual cases. However, it requires modest computational resources, and clinicians with a modest mathematical background can manipulate it. It is a useful tool for the analysis of general mechanisms of the diseases of calcium metabolism and for the design of clinical experiments aimed at characterizing these diseases. The model can also be the core of future autoadaptive extensions to be used in individual patients.
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页码:4330 / 4340
页数:11
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