PEDIATRICS Vol. 39 No. 6 June 1967, pp. 844-852
This Article
Right arrow Full Text (PDF)
Right arrow P3Rs: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when P3Rs are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Root, A. W.
Right arrow Articles by Eberlein, W. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Root, A. W.
Right arrow Articles by Eberlein, W. R.

THE PLASMA GROWTH HORMONE RESPONSE TO INSULIN-INDUCED HYPOGLYCEMIA IN CHILDREN WITH RETARDATION OF GROWTH

Allen W. Root M.D.1, Robert L. Rosenfield M.D.1, Alfred M. Bongiovanni M.D.1, and Walter R. Eberlein M.D.1

1 The Department of Pediatrics, University of Pennsylvania School of Medicine and the Children's Hospital of Philadelphia, Philadelphia

The response of plasma growth hormone (HGH) concentration to insulin-induced hypoglycemia has been assessed in children with growth disturbances of varied etiology. In normal children and in patients with genetic short stature, constitutional delay in growth and development, Down's syndrome, Turner's syndrome, and glucocorticoid-induced growth retardation, plasma HGH concentration increased several fold following the administration of insulin.

In patients with hypopituitarism of unknown etiology and in four of six patients with hypopituitarism secondary to a craniopharyngioma, HGH concentration did not increase significantly in response to the hypoglycemic stimulus. In two patients with hypopituitarism secondary to craniopharyngioma, low concentrations of HGH were detectable but did not increase in response to the hypoglycemic state. Remnants of autonomously functioning pituitary tissue most probably explain this observation. Normal HGH responsivenesss was observed in children with vasopressin sensitive diabetes insipidus.

Three children with hypothyroidism had abnormal HGH responsiveness, which improved following restoration of the euthyroid state. Pituitary and/or hypothalamic myxedema may be responsible for the decreased responsiveness.

It is suggested that the control of growth hormone secretion in the young, growing child differs quantitatively from that of the adult subject.

Submitted on November 4, 1966
Accepted on January 3, 1967




This article has been cited by other articles:


Home page
PediatricsHome page
F. B. Diamond, E. V. Jorgensen, A. W. Root, D. I. Shulman, J. P. Sy, S. L. Blethen, and B. B. Bercu
The Role of Serial Sampling in the Diagnosis of Growth Hormone Deficiency
Pediatrics, August 1, 1998; 102(2): 521 - 524.
[Abstract] [Full Text]