Mathematical modelling of the intravenous glucose tolerance test

被引:208
作者
De Gaetano, A
Arino, O
机构
[1] Univ Cattolica Sacro Cuore, CNR, Ctr Fisiopatol Shock, I-00168 Rome, Italy
[2] Lab Math Appl, UPRES A 5033 IPRA, Pau, France
关键词
glucose; insulin; dynamical systems; differential equations; delay;
D O I
10.1007/s002850050007
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several attempts at building a satisfactory model of the glucose-insulin system are recorded in the literature. The minimal model, which is the model currently mostly used in physiological research on the metabolism of glucose, was proposed in the early eighties for the interpretation of the glucose and insulin plasma concentrations following the intravenous glucose tolerance test. It is composed of two parts: the first consists of two differential equations and describes the glucose plasma concentration time-course treating insulin plasma concentration as a known forcing function; the second consists of a single equation and describes the time course of plasma insulin concentration treating glucose plasma concentration as a known forcing function. The two parts are to be separately estimated on the available data. In order to study glucose-insulin homeostasis as a single dynamical system, a unified model would be desirable. To this end, the simple coupling of the original two parts of the minimal model is not appropriate, since it can be shown that, for commonly observed combinations of parameter values, the coupled model would not admit an equilibrium and the concentration of active insulin in the "distant" compartment would be predicted to increase without bounds. For comparison, a simple delay-differential model is introduced, is demonstrated to be globally asymptotically stable around a unique equilibrium point corresponding to the pre-bolus conditions, and is shown to have positive and bounded solutions for all times. The results of fitting the delay-differential model to experimental data from ten healthy volunteers are also shown. It is concluded that a global unified model is both theoretically desirable and practically usable, and that any such model ought to undergo formal analysis to establish its appropriateness and to exclude conflicts with accepted physiological notions.
引用
收藏
页码:136 / 168
页数:33
相关论文
共 30 条
[1]   MODEL STUDIES OF BLOOD-GLUCOSE REGULATION [J].
ACKERMAN, E ;
GATEWOOD, LC ;
ROSEVEAR, JW ;
MOLNAR, GD .
BULLETIN OF MATHEMATICAL BIOPHYSICS, 1965, 27 :21-&
[2]  
[Anonymous], 1981, SEMIDYNAMICAL SYSTEM
[3]  
Bergman RN, 1979, AM J PHYSIOL, V236, P667
[4]   COEFFICIENTS OF NORMAL BLOOD GLUCOSE REGULATION [J].
BOLIE, VW .
JOURNAL OF APPLIED PHYSIOLOGY, 1961, 16 (05) :783-&
[5]   INSULIN SENSITIVITY AND B-CELL RESPONSIVENESS TO GLUCOSE DURING LATE PREGNANCY IN LEAN AND MODERATELY OBESE WOMEN WITH NORMAL GLUCOSE-TOLERANCE OR MILD GESTATIONAL DIABETES [J].
BUCHANAN, TA ;
METZGER, BE ;
FREINKEL, N ;
BERGMAN, RN .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1990, 162 (04) :1008-1014
[6]   NORMALIZATION OF INSULIN SENSITIVITY IN THE OBESE PATIENT AFTER STABLE WEIGHT-REDUCTION WITH BILIOPANCREATIC DIVERSION [J].
CASTAGNETO, M ;
DEGAETANO, A ;
MINGRONE, G ;
TACCHINO, R ;
NANNI, G ;
CAPRISTO, E ;
BENEDETTI, G ;
TATARANNI, PA ;
GRECO, AV .
OBESITY SURGERY, 1994, 4 (02) :161-168
[7]   CONTROL OF BLOOD GLUCOSE IN NORMAL AND IN DIABETIC SUBJECTS - STUDIES BY COMPARTMENTAL ANALYSIS AND DIGITAL COMPUTER TECHNICS [J].
CERESA, F ;
GHEMI, F ;
MARTINI, PF ;
MARTINO, P ;
SEGRE, G ;
VITELLI, A .
DIABETES, 1968, 17 (09) :570-&
[8]   INSULIN RESISTANCE - A MULTIFACETED SYNDROME RESPONSIBLE FOR NIDDM, OBESITY, HYPERTENSION, DYSLIPIDEMIA, AND ATHEROSCLEROTIC CARDIOVASCULAR-DISEASE [J].
DEFRONZO, RA ;
FERRANNINI, E .
DIABETES CARE, 1991, 14 (03) :173-194
[9]   INSULIN RESISTANCE, HYPERINSULINEMIA, AND CORONARY-ARTERY DISEASE - A COMPLEX METABOLIC WEB [J].
DEFRONZO, RA .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1992, 20 :S1-S16
[10]  
DEFRONZO RA, 1979, AM J PHYSIOL, V237, P214