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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2007-2837
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The Journal of Clinical Endocrinology & Metabolism Vol. 93, No. 7 2633-2638
Copyright © 2008 by The Endocrine Society

Absence of an Acute Insulin Response Predicts Onset of Type 2 Diabetes in a Caucasian Population with Impaired Glucose Tolerance

G. Nijpels, W. Boorsma, J. M. Dekker, F. Hoeksema, P. J. Kostense, L. M. Bouter and R. J. Heine

EMGO Institute (G.N., W.B., J.M.D., F.H., P.J.K., L.M.B., R.J.H.) and Departments of General Practice (G.N.), Clinical Epidemiology and Biostatistics (P.J.K.), and Endocrinology/Diabetes Center (R.J.H.), Vrije Universiteit Medical Center, 1081 BT Amsterdam, the Netherlands

Address all correspondence and requests for reprints to: Prof. G. Nijpels, Department of General Practice, Vrije Universiteit Medical Center, van der Boechorststraat 7, 1081 BT Amsterdam. E-mail: g.nijpels{at}vumc.nl.

Context: In persons with impaired glucose tolerance (IGT), both impaired insulin secretion and insulin resistance contribute to the conversion to type 2 diabetes mellitus (T2DM). However, few studies have used criterion standard measures to asses the predictive value of impaired insulin secretion and insulin resistance for the conversion to T2DM in a Caucasian IGT population.

Objectives: The objective of the study was to determine the predictive value of measures of insulin secretion and insulin resistance derived from a hyperglycemic clamp, including the disposition index, for the development of T2DM in a Caucasian IGT population.

Design, Setting, and Participants: The population-based Hoorn IGT study consisted of 101 Dutch IGT subjects (aged < 75 yr), with mean 2-h plasma glucose values, of two separate oral glucose tolerance tests, between 8.6 and 11.1 mmol/liter. A hyperglycemic clamp at baseline was performed to assess first-phase and second-phase insulin secretion and insulin sensitivity. During follow-up, conversion to T2DM was assessed by means of 6-monthly fasting glucose levels and yearly oral glucose tolerance tests.

Results: The cumulative incidence of T2DM was 34.7%. Hazard ratio for T2DM development adjusted for age, sex, and body mass index was 5.74 [95% confidence interval (CI) 2.60–12.67] for absence of first insulin peak, 1.58 (95% CI 0.60–4.17) for lowest vs. highest tertile of insulin sensitivity, and 1.78 (95% CI 0.65–4.88) for lowest vs. highest tertile of the disposition index.

Conclusions: In these Caucasian persons with IGT, the absence of the first insulin peak was the strongest predictor of T2DM.







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