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Research Article Free access | 10.1172/JCI107276

Responsiveness of Growth Hormone-Deficient Children to Human Growth Hormone EFFECT OF REPLACEMENT THERAPY FOR ONE YEAR

Daniel Rudman, Joseph H. Patterson, and Donna L. Gibbas

Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322

Department of Biochemistry, Emory University School of Medicine, Atlanta, Georgia 30322

Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia 30322

Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Find articles by Rudman, D. in: PubMed | Google Scholar

Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322

Department of Biochemistry, Emory University School of Medicine, Atlanta, Georgia 30322

Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia 30322

Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Find articles by Patterson, J. in: PubMed | Google Scholar

Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322

Department of Biochemistry, Emory University School of Medicine, Atlanta, Georgia 30322

Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia 30322

Clinical Research Facility, Emory University Hospital, Atlanta, Georgia 30322

Find articles by Gibbas, D. in: PubMed | Google Scholar

Published May 1, 1973 - More info

Published in Volume 52, Issue 5 on May 1, 1973
J Clin Invest. 1973;52(5):1108–1112. https://doi.org/10.1172/JCI107276.
© 1973 The American Society for Clinical Investigation
Published May 1, 1973 - Version history
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Abstract

Previous studies have shown that growth hormone (GH)-deficient children are more responsive to exogenous human growth hormone (HGH) than non-GH-deficient children. In six GH-deficient children, velocity of linear growth was less than 2.5 cm/yr. By the metabolic balance study technique, anabolic responses (increments in elemental balances) were measured to a 7 day course of 0.0532 U HGH/kg body weight (BW)3/4 per day (dose B) and to 0.168 U/kg BW3/4 per day (dose C). They were then treated for 1 yr with HGH at a dose intermediate between B and C. Velocity of linear growth accelerated to 15-25 cm/yr for the first 4-7 mo, then declined to 0-8 cm/yr. At 12 mo, responsiveness to doses B and C was measured again; the responses were only 20-60% as great as before treatment. After 3 mo without HGH treatment, responsiveness to the anabolic effects of doses B and C returned to the magnitudes observed before treatment. A low titer of plasma antibodies to HGH was detected in two of the six children at the end of the year's treatment; these titers showed little change after 3 mo without HGH. Thus the hyperresponsiveness of GH-deficient subjects to exogenous HGH, compared to non-GH-deficient individuals, declines during long-term HGH treatment and is restored by 3 mo interruption of treatment. These changes in peripheral responsiveness may be related to the decline in velocity of linear growth which occurs after 4-7 mo of continuous treatment.

When HGH was withdrawn after 12 mo, all six patients exhibited negative balances of N, P, Na, and K and loss of BW. Ratios of elemental balances showed about half the weight loss to represent protoplasm, and about half extracellular fluid. These observations indicate a role of GH in the continuing regulation of nitrogen and mineral metabolism in addition to its function as a growth-promoting hormone.

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