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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2008-0801
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The Journal of Clinical Endocrinology & Metabolism Vol. 93, No. 11 4231-4237
Copyright © 2008 by The Endocrine Society

Reproducibility of the Oral Glucose Tolerance Test in Overweight Children

I. M. Libman, E. Barinas-Mitchell, A. Bartucci, R. Robertson and S. Arslanian

Divisions of Pediatric Endocrinology, Metabolism and Diabetes Mellitus, and Weight Management and Wellness (I.M.L., A.B., S.A.), Children’s Hospital of Pittsburgh, Pittsburgh, Pennsylvania 15213; and Department of Epidemiology (E.B.-M.), Graduate School of Public Health, and Center for Exercise and Health-Fitness Research (R.R.), University of Pittsburgh, Pittsburgh, Pennsylvania 15260

Address all correspondence and requests for reprints to: Ingrid M. Libman, M.D., Ph.D., Children’s Hospital of Pittsburgh, 3705 Fifth Avenue, 4th A De Soto Wing, Pittsburgh, Pennsylvania 15213. E-mail: ingrid.libman{at}chp.edu.

Objective: We examined the reproducibility of the oral glucose tolerance test (OGTT) in overweight children and evaluated distinguishing characteristics between those with concordant vs. discordant results.

Design: Sixty overweight youth (8–17 yr old) completed two OGTTs (interval between tests 1–25 d). Insulin sensitivity was assessed by the surrogate measures of fasting glucose to insulin ratio, whole-body insulin sensitivity index, and homeostasis model assessment of insulin resistance, and insulin secretion by the insulinogenic index with calculation of the glucose disposition index (GDI).

Results: Of the 10 subjects with impaired glucose tolerance (IGT) during the first OGTT only three (30%) had IGT during the second OGTT. The percent positive agreement between the first and second OGTT was low for both impaired fasting glucose and IGT (22.2 and 27.3%, respectively). Fasting blood glucose had higher reproducibility, compared with the 2-h glucose. Youth with discordant OGTTs, compared with those with concordant results, were more insulin resistant (glucose/insulin 2.7 ± 1.4 vs. 4.1 ± 1.8, P = 0.006, whole-body insulin sensitivity index of 1.3 ± 0.6 vs. 2.2 ± 1.1, P = 0.003, and homeostasis model assessment of insulin resistance 10.6± 8.1 vs. 5.7 ± 2.8, P = 0.001), had a lower GDI (0.45 ± 0.58 vs. 1.02 ± 1.0, P = 0.03), and had higher low-density lipoprotein cholesterol (117.7 ± 36.6 vs. 89.9 ± 20.1, P = 0.0005) without differences in physical characteristics.

Conclusions: Our results show poor reproducibility of the OGTT in obese youth, in particular for the 2-h plasma glucose. Obese youth who have discordant OGTT results are more insulin resistant with higher risk of developing type 2 diabetes mellitus, as evidenced by a lower GDI. The implications of this remain to be determined in clinical and research settings.




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J. Clin. Endocrinol. Metab., November 1, 2008; 93(11): 4228 - 4230.
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