Integrated mathematical model to assess beta-cell activity during the oral glucose test

被引:50
作者
Thomaseth, K [1 ]
KautzkyWiller, A [1 ]
Ludvik, B [1 ]
Prager, R [1 ]
Pacini, G [1 ]
机构
[1] UNIV VIENNA, MED CLIN 3, DEPT ENDOCRINOL & METAB, A-1090 VIENNA, AUSTRIA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1996年 / 270卷 / 03期
关键词
insulin; C-peptide; islet amyloid polypeptide; compartmental modeling; splines; model identification; parameter estimation; insulin resistance;
D O I
10.1152/ajpendo.1996.270.3.E522
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A model describing beta-cell secretion during an oral glucose tolerance test (OGTT) is introduced. The aim was to quantify beta-cell activity in different pathologies by analyzing peripheral concentration data of insulin, C-peptide, and islet amyloid polypeptide (IAPP). Insulin appearance in periphery is given by the fraction of C-peptide secretion, CPS(t), which accounts for liver degradation. A novelty of this study is the inclusion of IAPP delivery assumed proportional to CPS(t). Although IAPP fractional clearance is estimated in every subject, the clearances of insulin and C-peptide are assigned from a wide set of previous independent studies. Sensitivity analysis was performed to quantify the ''error'' in the estimated variables due to these assignments. All parameters relating to beta-cell secretion increased in the glucose-intolerant states [integrated CPS(t) = 56 +/- 8 nmol/l in 180 min vs. 32 +/- 3 of controls, P < 0.05; total IAPP delivery = 83 +/- 21 pmol/l in 180 min vs. 41 +/- 6, P < 0.05]. Elevated plasma IAPP concentration of the patients was due to augmented secretion since IAPP clearance was found to be even slightly greater than in controls (0.053 +/- 0.011 vs. 0.034 +/- 0.004 min(-1)) and markedly lower than that of insulin (0.14 +/- 0.02, P < 0.01). In conclusion, the model introduced here allows the characterization of beta-cell secretory parameters during a simple test such as OGTT.
引用
收藏
页码:E522 / E531
页数:10
相关论文
共 29 条
[1]  
[Anonymous], 1983, MATH MODELING METABO
[2]   PHYSIOLOGIC EVALUATION OF FACTORS CONTROLLING GLUCOSE-TOLERANCE IN MAN - MEASUREMENT OF INSULIN SENSITIVITY AND BETA-CELL GLUCOSE SENSITIVITY FROM THE RESPONSE TO INTRAVENOUS GLUCOSE [J].
BERGMAN, RN ;
PHILLIPS, LS ;
COBELLI, C .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (06) :1456-1467
[3]   ISLET AMYLOID - AN ENIGMA OF TYPE-2 DIABETES [J].
CLARK, A .
DIABETES-METABOLISM REVIEWS, 1992, 8 (02) :117-132
[4]   ON OPTIMALITY OF THE IMPULSE INPUT FOR LINEAR-SYSTEM IDENTIFICATION [J].
COBELLI, C ;
THOMASETH, K .
MATHEMATICAL BIOSCIENCES, 1988, 89 (02) :127-133
[5]   INSULIN-SECRETION AND HEPATIC EXTRACTION IN HUMANS BY MINIMAL MODELING OF C-PEPTIDE AND INSULIN KINETICS [J].
COBELLI, C ;
PACINI, G .
DIABETES, 1988, 37 (02) :223-231
[6]  
de Boor C., 1978, PRACTICAL GUIDE SPLI, DOI DOI 10.1007/978-1-4612-6333-3
[7]  
FERRANNINI E, 1987, Diabetes Metabolism Reviews, V3, P365
[8]  
HARRTER E, 1990, LANCET, V335, P854
[9]  
HARRTER E, 1991, DIABETOLOGIA, V34, P52
[10]   ELEVATED HEPATIC INSULIN EXTRACTION IN ESSENTIAL-HYPERTENSION [J].
KAUTZKYWILLER, A ;
PACINI, G ;
WEISSEL, M ;
CAPEK, M ;
LUDVIK, B ;
PRAGER, R .
HYPERTENSION, 1993, 21 (05) :646-653