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Journal of Clinical Endocrinology & Metabolism Vol. 73, No. 5 964-968
doi:10.1210/jcem-73-5-964
Copyright © 1991 by the Endocrine Society.
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Abnormal Regulation of Insulin-Like Growth Factor Binding Proteins in Adolescents with Insulin-Dependent Diabetes*

JENNIFER A. BATCH, ROBERT C. BAXTER and GEORGE WERTHER

Department of Endocrinology Royal Children's Hospital Melbourne, Australia
Department of Endocrinology, Royal Prince Alfred Hospital Sydney, Australia

Address all correspondence and requests for reprints to: Dr. Jennifer Batch, Department of Paediatrics, Addenbrooke's Hospital, Cambridge, United Kingdom CB2 2QQ.

We have measured fasting 0800 h insulin-like growth factor binding proteins (IGFBP)-1 and IGFBP-3, in 52 diabetic adolescents and 74 puberty-matched control subjects with short stature and normal hormonal status. We have also measured overnight hourly profiles of IGFBP-1, glucose, free insulin, and GH in 12 of the diabetic adolescents. With advancing age and pubertal status, IGFBP-1 declined and IGFBP-3 increased significantly in the control, but not the diabetic group. Fasting IGFBP-1 levels were elevated 4-fold compared to controls. Median IGFBP-3 was significantly lower in the diabetic compared to the control group in pubertal stages III and V. Elevated IGFBP-1 was significantly correlated with metabolic control in poorly controlled subjects (mean 12-month glycosylated haemoglobin > 8.5%). In the overnight profiles, mean hourly IGFBP-1 was inversely related to insulin, but not glucose. As free insulin levels declined, IGFBP-1 rose, associated with rising predawn blood sugars. The integrated 3-h IGFBP-1 value (0500–0800 h) was significantly correlated with the corresponding glucose integrated value. IGFBP-1 area under the curve for the whole overnight profile was significantly correlated with glycosylated hemoglobin in 11 of the 12 subjects. IGFBP-1 from diabetic adolescents has been shown to inhibit IGF-I bioactivity. We postulate that IGFBP-1 may have a role in growth impairment of poorly controlled diabetes and may contribute to the dawn phenomenon.

* This work was supported by the National Health and Medical Research Council of Australia.

Received September 4, 1990.




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