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The Journal of Clinical Endocrinology & Metabolism Vol. 84, No. 12 4426-4430
Copyright © 1999 by The Endocrine Society


Special Articles

Somatostatin Infusion Withdrawal: Studies in Normal Children and in Children with Growth Hormone Deficiency

Marco Cappa, Antonello E. Rigamonti, Carla Bizzarri, Ottavia Porzio, Patrizia Civolani, Silvano G. Cella, Sandro Loche and Eugenio E. Müller

Divisione di Pediatria (M.C., C.B., O.P.), Ospedale Bambino Gesù, IRCCS, 00050 Roma, Italy; Dipartimento di Farmacologia, Chemioterapia e Tossicologia Medica (A.E.R., S.G.C., E.E.M.), Università di Milano, Milan 20129, Italy; and Servizio di Endocrinologia Pediatrica (P.C., S.L.), Ospedale Microcitemico, 09100 Cagliari, Italy

Address correspondence and requests for reprints to: Eugenio E. Müller, Dipartmento di Farmacologia, Universitá Degli Studi di Milano, Via Vanvitelli, 32, Milan 20129, Italy.

Withdrawal of a somatostatin infusion (SSIW) is followed by a rebound rise of GH in both animals and normal adult men, a phenomenon likely mediated by endogenous GHRH function. In the present study, we have evaluated the GH response to SSIW in a group of 28 prepubertal children (18 boys and 10 girls; aged 3.7–11.1 yr). Six children had GH deficiency [GHD; GH responses to pyridostigmine (PD)+GHRH and to clonidine <20 and <7 µg/L, respectively], 4 children had GH neurosecretory dysfunction (GHND; GH responses to PD+GHRH and to clonidine >=20 and >7 µg/L, respectively; mean integrated nighttime GH concentrations <3 µg/L), and 18 children were short normal children [normal controls (NC)]. All children received a constant infusion of SS at the dose of 3 µg/Kg·h for 90 min.

SSIW elicited a clear-cut GH rise in NC children (13.7 ± 1.0 µg/L), but not in GH-deficient children, regardless of the underlying etiology (GHD, 1.6 ± 0.4 µg/L; GHND, 2.4 ± 0.3 µg/L). The GH response to SSIW was similar between GHD and GHND children. There was no overlapping of the maximum SSIW-stimulated GH peaks between NC and GHD or GHND children.

In conclusion, we have demonstrated that SSIW elicits a significant GH rise in NC children, but not in GH-deficient children, regardless of the underlying etiology (GHD or GHND). This resulted in complete discrimination of NC from GHD or GHND children. Were these present findings confirmed on a larger number of children, SSIW, because of its testing efficaciousness and safety, procedural simplicity, and economy holds promise of being a useful diagnostic tool for GH-dependent growth disorders.




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