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Insulin sensitivity by oral glucose minimal models: validation against clamp
被引:93
|作者:
Dalla Man, C
Yarasheski, KE
Caumo, A
Robertson, H
Toffolo, G
Polonsky, KS
Cobelli, C
机构:
[1] Univ Padua, Dept Informat Engn, I-35131 Padua, Italy
[2] Washington Univ, Sch Med, Div Endocrinol Metab & Lipid Res, St Louis, MO USA
[3] Ist Sci San Raffaele, Milan, Italy
来源:
关键词:
insulin resistance;
oral glucose tolerance test;
meal;
insulin action;
tracer kinetics;
D O I:
10.1152/ajpendo.00076.2005
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Measuring insulin sensitivity in the presence of physiological changes in glucose and insulin concentrations, e. g., during a meal or OGTT, is important to better understand insulin resistance in a variety of metabolic conditions. Recently, two oral minimal models have been proposed to measure overall insulin sensitivity (S-I) and its selective effect on glucose disposal (S-I(*)) from oral tests. S-I and S-I(*) have been successfully validated against multiple tracer meal estimates, but validation against euglycemic hyperinsulinemic clamp estimates is lacking. Here, we do so in 21 subjects who underwent both a multiple-tracer OGTT and a labeled euglycemic hyperinsulinemic clamp. Correlation between minimal-model S-I, S-I(*) and corresponding clamp estimates S-I(*clamp), S-I(*clamp) was satisfactory, respectively r = 0.81, P < 0.001, and r = 0.71, P < 0.001. SI was significantly lower than S I clamp (8.08 +/- 0.89 vs. 13.66 +/- 1.69 10(-4) dl.kg(-1).min(-1) per mu U/ml, P = 0.0002), whereas S-I(*) and S-I(*clamp) were very similar (8.17 +/- 1.59 vs. 8.84 +/- 1.39 10(-4) dl.kg(-1).min(-1) per mu U/ml, P = 0.52). These results add credibility to the oral minimal-model method as a simple and reliable physiological tool to estimate S-I and S-I(*), also in large-scale clinical trials.
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页码:E954 / E959
页数:6
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