Abstract
Our aim was to investigate the effect of GnRH-agonist (GnRH-a) induced suppression of plasma sex steroids on serum GH, insulin like growth factor-l (IGF-I) and insulin levels after an oral glucose load (OGTT) in women with polycystic ovary syndrome (PCOS). Serum insulin, GH and IGF-I levels during a 75-g 4-h OGTT were measured in 3 nonobese and 7 obese hyperandrogenic women with PCOS and normal glucose tolerance before and after 10 weeks of treatment with the GnRH-a triptorelin (3, 75 mg im every 28 days). Basal estrogen and androgen levels were also measured at time 0 of the first and the second OGTT. After the therapy serum estrogens and androgens were significantly suppressed. Body weight remained unchanged. Basal GH significantly increased after the treatment while fasting IGF-I and insulin levels decreased from (mean±SE) 349.3±31.8 to 278.7±33.2 ng/mL and from 22.4±4.1 to 18.8±4.4 µU/mL, respectively. The insulin response to OGTT (area under curve) was also reduced (from 16017±2598 to 11736±2317 µU/mL/240 min). Our results suggest that the GnRH-a induced suppression of ovary secretion may modify the serum GH and IGF-I levels and the insulin response to an OGTT in women with PCOS.
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Kazer R.R., Unterman T.G., Glick R.P. An abnormality of the growth hormone/insulin-like growth factor I axis in women with polycystic ovary syndrome. J. Clin. Endocrinol. Metab. 71: 958, 1990.
Acar B., Kadanali S. Diminished growth hormone responses to L-dopa in polycystic ovarian disease. Fertil Steril. 60: 984, 1993.
Lee E.J., Park K.H., Lee B.S., Song C.H., Lee H.C., Huh K.B. Growth hormone response to L-dopa and pyridostigmine in women with polycystic ovarian syndrome. Fertil Steril. 60: 53, 1993.
Piaditis G.P., Kounadi T.G., Rangou D.B., Trovas G.P., Kaklas N.A., Chlouverakis C.S. Dysfunction of the Growth Hormone/insulin-like growth factor-l axis in women with polycystic ovarian syndrome. Clin. Endocrinol. (Oxf.) 42: 635, 1995.
Yamashita S., Melmed S. Effects of insulin on rat anterior pituitary cells. Inhibition of growyh hormone secretion and mRNA levels. Diabetes 35: 440, 1986.
Insler V., Shohan Z., Barash A., Koistinen R., Seppala M., Hen M., Lunenfeld B., Zadik Z. Polycystic ovaries in nonobese and obese patients: possihte pathophysiological mechanism based on new interpretation of facts and findings. Hum Reprod. 8: 379, 1993.
Glass A.R. Endocrine aspects of obesity. Med. Clin. North Am. 73: 139, 1989.
Suikkari A.M., Koivisto V.A., Rutanen E.M., Yki-Jarvinen H., Karonen S.L., Seppala M. Insulin regulates the serum levels of low molecular weight insulin-like growth factor-binding protein. J. Clin. Endocrinol. Metab. 66: 266, 1988.
Berelowitz M., Szabo M., Frohman L.A., Firestone S., Chu L. Somatomedin-C mediates growth hormone negative feed-back by effects on both the hypothalamus and the pituitary. Science 212: 1279, 1981.
Namba H., Morita S., Melmed S. Insulin-like growth factor-l action on growth hormone secretion and messenger ribonucleic acid levels interaction with somatostatin. Endocrinology 124: 1794, 1989.
Adams J., Poison D.W., Franks S. Prevalence of polycystic ovaries in women with anovulation and hyrsutism. Br. Med. J. 293: 355, 1986.
Tropeano G., Lucisano A., Liberale, Barini A., Vuolo I.P., Martino G., Menini E., Dell’Acqua S. Insulin, C-peptide, androgens, and beta-endorphin response to oral glucose in patients with polycystic ovary syndrome. J. Clin. Endocrinol. Metab. 78: 305, 1994.
Urdl W. Polycystic ovarian disease: endocrinological parameters with specific reference to growth hormone and somatomedin-C. Arch. Gynecol. Obstei. 243: 13, 1988.
Daughaday W.H. Growth hormone, normal synthesis, secretion, control, and mechanism of action. In: De Groot L.J. (Ed.), Sounders. Endocrinology Vol 1. Philadelphia, 1989, p. 318.
Shibasaki T., Masuda A., Hotta M., Yamauchi N., Hizuca N., Takanu K., Demura H., Shizume K. Effects of ingestion of glucose on GH and TSH secretion: evidence for stimulation of somatostatin release from the hypothalamus by acute hyperglycemia in normal man and its impairment in acromegalyc patients. Life Sci. 44: 431, 1989.
Peiris A.N., Mueller R.A., Struve M.F., Smith G.A., Kissebah A.H. Relationship of androgenic activity to splanchnic insulin metabolism and peripheral glucose utilization in premenopausal women. J. Clin. Endocrinol. Metab. 64: 1627, 1987.
Urdl W., Desoye G., Schmon B., Hofmann H.M.N., Ralph G. Interactions between insulin and insulin-like growth factor I in the pathogenesis of polycystic ovarian disease. Ann. NY Acad. Sci. 626: 177, 1991.
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Tropeano, G., Liberale, I., Vuolo, I.P. et al. Effects of ovary suppression by a long-acting GnRH-agonist on circulating GH, insulin-like growth factor I and insulin levels in women with polycystic ovary syndrome. J Endocrinol Invest 20, 220–224 (1997). https://doi.org/10.1007/BF03346907
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DOI: https://doi.org/10.1007/BF03346907