Meal and oral glucose tests for assessment of β-cell function:: modeling analysis in normal subjects

被引:250
作者
Mari, A
Schmitz, O
Gastaldelli, A
Oestergaard, T
Nyholm, B
Ferrannini, E
机构
[1] CNR, Inst Syst Sci & Biomed Engn, LADSEB, I-35127 Padua, Italy
[2] Univ Pisa, Dept Internal Med, I-56126 Pisa, Italy
[3] Univ Pisa, CNR, Inst Clin Physiol, I-56126 Pisa, Italy
[4] Aarhus Univ Hosp, Dept Med Endocrinol & Diabet M, DK-8000 Aarhus, Denmark
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2002年 / 283卷 / 06期
关键词
insulin secretion; glucose-induced insulin release; potentiation of glucose-induced insulin release; insulin sensitivity;
D O I
10.1152/ajpendo.00093.2002
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
We investigated beta-cell function and its relationship to insulin sensitivity in 17 normal volunteers. For insulin secretion (derived by C-peptide deconvolution), a mathematical model was applied to 24-h triple-meal tests (MT) as well as oral glucose tolerance tests (OGTT); insulin sensitivity was assessed by the euglycemic insulin clamp technique. The beta-cell model featured a glucose concentration-insulin secretion dose response (characterized by secretion at 5 mM glucose and slope), a secretion component proportional to the glucose concentration derivative, and a time-dependent potentiation factor (modulating the dose response and accounting for effects of sustained hyperglycemia and incretins). The beta-cell dose-response functions estimated from the whole 24-h MT, the first 2 h of the MT, and the OGTT differed systematically, because a different potentiation factor was involved. In fact, potentiation was higher than average during meals (1.6 +/- 0.1-fold during the first meal) and had a different time course in the MT and OGTT. However, if potentiation was accounted for, the 24- and 2-h MT and the OGTT yielded similar dose responses, and most beta-cell function parameters were intercorrelated (r = 0.50-0.86, P less than or equal to 0.05). The potentiation factor was found to be related to plasma glucose-dependent insulin-releasing polypeptide concentrations (r = 0.49, P < 0.0001). Among β-cell function parameters, only insulin secretion at 5 mM glucose from MT correlated inversely with insulin sensitivity (24- h MT: r = -0.74, P < 0.001; 2-h MT: r = -0.52, P < 0.05), whereas the dose-response slope and the OGTT parameters did not. In nine other subjects, reproducibility of model parameters was evaluated from repeated MTs. Coefficients of variation were generally ∼20%, but the derivative component was less reproducible. We conclude that our model for the multiple MT yields useful information on β-cell function, particularly with regard to the role of potentiation. With cautious interpretation, a 2-h MT or a standard OGTT can be used as surrogates of 24- h tests in assessing spontaneous β-cell function.
引用
收藏
页码:E1159 / E1166
页数:8
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