help button home button Endocrine Society JCEM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit a related Letter to the Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email 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 Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hardin, D. S.
Right arrow Articles by Seilheimer, D. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hardin, D. S.
Right arrow Articles by Seilheimer, D. K.
The Journal of Clinical Endocrinology & Metabolism Vol. 86, No. 9 4424-4428
Copyright © 2001 by The Endocrine Society


Other Original Articles

Growth Hormone Decreases Protein Catabolism in Children with Cystic Fibrosis

Dana S. Hardin, Kenneth J. Ellis, Maynard Dyson, Julie Rice, Ruth McConnell and Dan K. Seilheimer

University of Texas Southwestern Medical School (D.S.H., J.R.), Dallas, Texas 75390; Texas Children’s Hospital/Baylor College of Medicine (D.S.H., K.J.E., R.M., D.K.S.), Houston, Texas 77030; and Cook Children’s Hospital (M.D.), Fort Worth, Texas 76104

Address all correspondence and requests for reprints to: Dana S. Hardin, M.D., Associate Professor of Pediatrics, Pediatric Endocrinology, University of Texas Southwestern Medical School, 5323 Harry Hines Boulevard, G2.234, Dallas, Texas 75390-9063. E-mail: dana.hardin{at}utsouthwestern.edu

Abstract

Despite aggressive nutritional therapy, low body weight and protein catabolism are common problems in children with cystic fibrosis. Previous studies by our group and others have demonstrated improvement in both height and weight in children with cystic fibrosis who were treated with human recombinant GH, and our group has recently documented improved clinical status and lean tissue mass as well. The purpose of this report is to summarize our findings of the effect of GH on whole body protein kinetics in cystic fibrosis and to relate these findings to changes in TNF-{alpha} levels.

We conducted a 1-yr study of 19 prepubertal children with cystic fibrosis (age 7–12 yr, all <94% of ideal body weight). Ten children were randomly assigned to take daily injections of GH (0.3 mg/kg·wk), and nine were randomly assigned to be controls. Baseline results from the subjects with cystic fibrosis were compared with results obtained from nine age- and gender-matched healthy children. Whole body protein turnover was measured at baseline and every 6 months using the stable isotope [1-13C]leucine and mass spectrometric analysis.

Leucine rate of appearance, a measure of protein catabolism, was similar in both cystic fibrosis subgroups at baseline and was significantly higher than in the control children without cystic fibrosis. Treatment with GH resulted in a significantly lower leucine rate of appearance, as well as significantly lower leucine oxidation. The rate of protein synthesis, as calculated from these numbers, actually decreased in the cystic fibrosis subgroup. TNF-{alpha} levels were higher in both cystic fibrosis subgroups than in controls and correlated with leucine rate of appearance.

The results of this study suggest that one reason GH improves body weight and lean tissue mass is due to improved whole body protein catabolism and improved efficiency of whole body protein kinetics.




This article has been cited by other articles:


Home page
PediatricsHome page
D. Schnabel, C. Grasemann, D. Staab, H. Wollmann, F. Ratjen, and for the German Cystic Fibrosis Growth Hormone Stud
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Metabolic and Respiratory Effects of Growth Hormone in Children With Cystic Fibrosis
Pediatrics, June 1, 2007; 119(6): e1230 - e1238.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
R. M. Aris, P. A. Merkel, L. K. Bachrach, D. S. Borowitz, M. P. Boyle, S. L. Elkin, T. A. Guise, D. S. Hardin, C. S. Haworth, M. F. Holick, et al.
Guide to Bone Health and Disease in Cystic Fibrosis
J. Clin. Endocrinol. Metab., March 1, 2005; 90(3): 1888 - 1896.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
P. B. Soeters, M. C. G. van de Poll, W. G. van Gemert, and C. H. C. Dejong
Amino Acid Adequacy in Pathophysiological States
J. Nutr., June 1, 2004; 134(6): 1575S - 1582S.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
D. Darmaun, V. Hayes, D. Schaeffer, S. Welch, and N. Mauras
Effects of Glutamine and Recombinant Human Growth Hormone on Protein Metabolism in Prepubertal Children with Cystic Fibrosis
J. Clin. Endocrinol. Metab., March 1, 2004; 89(3): 1146 - 1152.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 2001 by The Endocrine Society