Abstract
Growth hormone (GH) secretion disorders have been reported in poorly controlled type I diabetes mellitus patients. Our work was aimed to evaluate GH secretion in 9 type I young diabetes mellitus patients as well as the low molecular weight IGF-binding protein secretion (IGFBP-1) in 5 of them. The patients did not show any signs of malnutrition or neurovascular complications, neither were they on any medication except for insulin. The study protocol included blood samples collection during a 24-h period for measurement of glucose, glycated hemoglobin, GHIGF-I and IGFBP-1 levels under two situations: on poor glycemic control and after 2–3 months on better control through systematic diet, low in carbohydrates and increase in insulin dosage. GH secretion data were analyzed by Cluster algorithm for pulsatility parameters; for rhythm assessment Cosinor method was used. The first study (poor control) reported significant increase of GH maximal and incremental amplitude and duration pulse values, when compared to the second study (better control). Mean 24-h secretion values as well mean GH for interpulse intervals (valleys) decreased, although not statistically significant. The fraction of pulsatile GH/24 h GH did not change significantly with better glycemic control. No changes in pulse frequency were observed. Mean IGF-I concentrations were significantly higher when patients were on better glycemic control. An ultradian variation for GH secretion was noticed in the first study (poor control) and a circadian variation in the second one (better control). IGFBP-1 analysis showed significant decrease of the mean 24-h values under better glycemic control. Linear regression analysis demonstrated a correlation between IGFBP-1 levels and fasting glucose levels. A circadian variation was present in IGFBP-1 secretion, irrespective of glycemic control. Therefore, we concluded that for type I diabetic patients: 1. GH secretion is increased on poor control, through maximal, incremental amplitude and pulse duration values; 2. IGFBP-1 values were significantly reduced and IGF-1 levels significantly higher after better glycemic control; 4. GH ultradian secretion is reported on poor control, and circadian on the better one, 5. IGFBP-1 circadian secretion occurred irrespective of glycemic control.
Similar content being viewed by others
References
Hayford J.T., Danney M.M., Hendrix J.A., Thompson R.G. Integrated concentrations of growth hormone in juvenile diabetes. Diabetes 29: 391, 1980.
Amiel S.A., Sherwin R.S., Hintz R.L, Gertner J.M., Press M., Tamborlane W.V. Effect of diabetes and its control on insulin-like growth factors in the young subject with type I Diabetes. Diabetes 33: 1175, 1984.
Asplin C.M., Faria A.C.S., Carlsen E.C, Vaccaro V.A., Barr R.E., Iranmesh A., Lee M.M., Veldhuis J.D., Evans W.S. Alterations in the pulsatile mode of growth hormone release in men and women with insulin-dependent diabetes mellitus. J. Clin. Endocrinol. Metab. 69: 239, 1989.
Underwoood L.E., D’Ercole A.J., Clemmons D.R., Van Wyk J.J. Paracrine functions of somatomedins. Clin. Endocrinol. Metab. 15: 59, 1986.
Hall K., Lunding G., Póvoa C Serum levels of the low molecular weight form of insulin-like growth factor binding protein in healthy subjects and patients with growth hormone deficiency acromegaly and anorexia nervosa. Acta Endocrinol. (Copenh.) 118: 321, 1988.
Póvoa C.I, Enberg G., Jörnvall H., Hall K. Isolation and characterization of a somatomedin-binding protein from mid-term human aminiotic fluid. Eur. J. Biochem. 114: 199, 1984.
Baxter R.C, Cowell C.T. Diurnal rhythm of growth hormone independent binding protein for insulin-like growth factors in human plasma. J. Clin. Endocrinol. Metab. 65: 432, 1987.
Holly J.M.P., Biddlecombe R.A., Dunger D.B., Edge J.A., Amiel S.A., Howell R., Chard T., Ress L.H., Wass J.A.H. Circadian variation of GH-independent IGF-binding protein in diabetes mellitus and its relationship to insulin. A new role for insulin? Clin. Endocrinol. (Oxf.) 29: 667, 1988.
Brismar K., Gutniak M., Póvoa G., Werner S., Hall K. Insulin regulates the 35 kD IGF binding protein in patients with diabetes mellitus. J. Endocrinol. Invest. 11: 599, 1988.
Suikkari A.M., Koivisto V.A., Rutauen E.M., Yki-Jarvinen H., Karonen S.L., Seppala M. Insulin regulates the serum of low molecular weight insulin-like growth factor-binding protein. J. Clin. Endocrinol. Metab. 66: 266, 1988.
Hansen A.P. Serum growth patterns in juvenile diabetes. Dan. Med. Bull. 19 (Suppl. 1): 1, 1972.
Evans W.S., Christiansen E., Faria A.C.S., Parish E., Asplin CM. Pulsatile growth hormone secretion in insulin dependent diabetes mellitus. Proc. of the 69th Annual Meeting of the Endocrine Society, Abstract n. 231, 1987.
Lanes R., Recker B., Fort P., Lifshitz F. Impaired somatomedin generation test in children with insulin dependent diabetes mellitus. Diabetes 334: 156, 1985.
Veldhuis J., Johnson M.L. Clustel Analysis: a simple, versatile and robust algorithm for endocrine pulse detection. Am. J. Physiol. 250 (Endocrinol. Metab. 13): E486, 1986.
Nelson W., Tong Y.L., Lee J.K. Halberg F. Methods for cosinor — Rhytmometry. Chronobiologia 6: 305, 1979.
Tanner J.M. Growth at adolescence, 2nd ed. C arles C. Thomas Springfield, 1962.
Hartman M.L., Veldluis J.D., Vance M.L., Faria A.C.S., Furlanetto R.W., Thorner M.O. Somatotropin pulse frequency and basal concentrations are increased in acromegaly and are reduced by successful therapy. J. Clin. Endocrinol. Metab. 70: 1375, 1990.
Würzburger M.I., Prelevic G.M., Sönken P.H., Peric L, Till S., Morris R.W. The effects of improved blood glucose on growth hormone and cortisol secretion in insulin-dependent diabetes mellitus. Clin. Endocrinol. (Oxf.) 32: 787,1990.
Malone J.I. Growth and sexual maturation in children with insulin-dependent diabetes mellitus. Curr. Opin. Pediatr. 5: 494, 1993.
Cohen H.N., Paterson K.R., Wallace A.M. Dissociation of adrenarche and gonadarche in diabetes mellitus. Clin Endocrinol (Oxf.) 20: 717, 1984.
Cotterill A.M., Cowell CT., Baxta R.C., Mc Neil D., Silinik M. Regulation of the growth hormone-independent growth factor-binding protein in children. J. Clin. Endocrinol. Metab. 67: 882, 1988.
Plotsky P.M., Vale W. Patterns of growth hormone releasing factor and somatostatin into the hypophysial — portal circulation of the rat. Science 230: 461, 1985.
Tannenbaum G.S., Ling N. The interelationship of growth hormone (GH) — releasing factor and somatostatin in generation of the ultradian rhythm of GH secretion. Endocrinology 115: 1952, 1984.
Frohman L.A., Jansson J.O. Growth hormone releasing hormone. Endocr. Rev. 7: 223, 1986.
Schaper R.C., De Groot J., Roelse H., Reitsma W.D., Wluiter W.J., Doorenbos H. Effects acute elevation of blood glucose and non-esterified fatty acids levels on growth hormone-releasing hormone-stimulated growth hormone secretion in type diabetes mellitus. Acta Endocrinol. (Copenh.) 122: 27, 1990.
Press M., Tamborlane W.V., Thorner M.O., Vale W., Rivier J., Gertner J.M., Sherwin R.S. Pituitary response to growth hormone-releasing factor in diabetes. Failure of glucose mediated suppression. Diabetes 33: 804, 1984.
Masuda A., Shibasaki T., Nakahara N. The effect of glucose on growth hormone (GH) — releasing hormone-mediate GH secretion in man. J. Clin. Endocrinol. Metab. 60: 523, 1985.
Berelowitz M., Szabo M., Frohman L.A., Firestone S., Chu L, Hintz R.L. Somatomedin-C mediates growth hormone negative feedback by effects on both the hypothalamus and pituitary. Science 212: 1279, 1981.
Hall K., Johansson B.L, Póvoa G., Thalme B. Serum levels of insulin-like gowth factor (IGF) I, II and IGF binding protein in diabetic adolescents treated with continuous sub cutaneous insulin infusion. J. Int. Med. 225: 273, 1989.
Holly J.M.P. The physiologycal role of IGFBP-1. Acta. Endocrinol. (Copenh.) 124: 55, 1991.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Salgado, L.R., Semer, M., Nery, M. et al. Effect of glycemic control on growth hormone and IGFBP-1 secretion in patients with type I diabetes mellitus. J Endocrinol Invest 19, 433–440 (1996). https://doi.org/10.1007/BF03349888
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF03349888