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Overestimation of minimal model glucose effectiveness in presence of insulin response is due to undermodeling
1 Department of Electronics and Informatics, University of Padova, 35131 Padova; 2 San Raffaele Scientific Institute, 20132 Milan, Italy; and 3 Hypertension-Endocrine Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892 Glucose effectiveness i...
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Published in: | American journal of physiology: endocrinology and metabolism 1998-12, Vol.275 (6), p.E1031-E1036 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 1 Department of Electronics and
Informatics, University of Padova, 35131 Padova;
2 San Raffaele Scientific
Institute, 20132 Milan, Italy; and
3 Hypertension-Endocrine Branch,
National Heart, Lung, and Blood Institute, National Institutes of
Health, Bethesda, Maryland 20892
Glucose effectiveness is an important
determinant of glucose tolerance that can be derived from minimal model
analysis of an intravenous glucose tolerance test (IVGTT). However,
recent evidence suggests that glucose effectiveness is overestimated by
minimal model analysis. Here we compare a new model-independent estimate of glucose effectiveness with the minimal model estimate by
reanalyzing published data in which insulin-dependent diabetic subjects
were each given IVGTTs under two conditions (Quon, M. J., C. Cochran,
S. I. Taylor, and R. C. Eastman.
Diabetes 43: 890-896, 1994). In
one case, a basal insulin level was maintained (BI-IVGTT). In the
second case, a dynamic insulin response was recreated (DI-IVGTT). Our
results show that minimal model glucose effectiveness is very similar
to the model-independent measurement during a BI-IVGTT but is three
times higher during a DI-IVGTT. To investigate the causes of minimal
model overestimation in the presence of a dynamic insulin response,
Monte Carlo simulation studies on a two-compartment model of glucose
kinetics with various insulin response patterns were performed. Results
suggest that minimal model overestimation is due to single-compartment
representation of glucose kinetics that results in a critical
oversimplification in the presence of increasingly dynamic insulin
secretion patterns.
intravenous glucose tolerance test; glucose kinetics |
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ISSN: | 0193-1849 1522-1555 |
DOI: | 10.1152/ajpendo.1998.275.6.E1031 |