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Original Studies |
Diabetes Research Laboratory (C.M., D.T.F.), School of Kinesiology, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada; and Brigham and Womens Hospital (A.D.), Boston, Massachusetts 02115
Address correspondence and requests for reprints to: Diane T. Finegood, Ph.D., School of Kinesiology, Simon Fraser University, Room K9625, Burnaby, British Columbia V5A 1S6, Canada. E-mail: finegood{at}sfu.ca
The minimal-model method allows for estimation of insulin sensitivity (SI = P3/P2) and glucose effectiveness (SG = P1) from the time course of glucose and insulin after a glucose bolus. We previously demonstrated that the minimal-model results in overestimates of SG in subjects with normal insulin secretory function. To determine whether overestimation of SG has an impact on estimation of SI, we examined model estimation of SI when SG was constrained to levels below that found by the regular minimal-model fit. Fifty-six glucose tolerance tests from lean and obese women, with and without polycystic ovary syndrome, were used. SI ranged from 0.222.6 x 10-4 min-1/(µU/mL), and SG ranged from 0.83.8 x 10-2 min-1 for the standard minimal-model fits. Constraining SG to as low as 40% of the unconstrained value resulted in a 4-fold increase in P2 and P3, but only a 3% reduction in SI. We conclude that estimation of the insulin sensitivity index is independent of errors in minimal-model-derived estimates of glucose effectiveness.
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