Changes in body composition and muscle protein degradation during nutritional supplementation in nutritionally growth-retarded children with cystic fibrosis

Journal of Pediatric Gastroenterology and Nutrition

Volumn 2, Issue 3, 1983, Pages 439-446

  Shepherd, R W ^a,b   Thomas, B J ^a,b   Bennett, D ^a,b   Cooksley, W ^b   Ward, L C ^a,b  

^a ROYAL CHILDREN'S HOSPITAL   (Australia)

^b UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Cystic fibrosis; Growth retardation; Nutritional supplementation

Indexed keywords

MUSCLE PROTEIN; POTASSIUM 40; RADIOISOTOPE;

BODY COMPOSITION; CASE REPORT; CHILD; CONGENITAL DISORDER; CONTROLLED STUDY; CYSTIC FIBROSIS; DIAGNOSIS; GROWTH RETARDATION; HUMAN; MUSCLE; NUTRITIONAL DEFICIENCY; PROTEIN DEGRADATION;

ADOLESCENT; BODY COMPOSITION; BODY WEIGHT; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; DIETARY PROTEINS; ENERGY INTAKE; FEMALE; FOOD, FORTIFIED; GROWTH DISORDERS; HUMANS; MALE; METHYLHISTIDINES; MUSCLE PROTEINS;

EID: 0020965040     PISSN: 02772116     EISSN: 15364801     Source Type: Journal    
DOI: 10.1097/00005176-198302030-00008     Document Type: Article

References (32)

1. Chase WP, Long MA, Lavin MH, Cystic fibrosis and malnutrition. J Pediatr 1979:95:337-46.
2. Phelan P, Landau L, Improved survival of patients with cystic fibrosis. Med JAttst 1979;1:261-4.
3. Kraemer R, Rudeberg A, Hadorn B, Rossi E, Relative underweight in cystic fibrosis and its prognostic value. Acta Paediatr Scand 1978;67:33-7.
4. Bankier A, Allan J, Phelan PD, Death from cystic fibrosis [Abstract]. Aust Paediatr J 1980:16:128.
5. Miller M, Ward L, Thomas BJ, Cooksley WGE, Shepherd RW, Altered body composition and muscle protein degradation in children with cystic fibrosis. Am J Clin Nutr 1982;36:492-9.
6. Shepherd RW, Cooksley WGE, Cooke WDD. Improved growth and clinical nutritional and respiratory changes in response to nutritional therapy in cystic fibrosis. J Pediatr 1980;97:351-7.
7. Pierson RN, Lin DWY, Phillips RA, Total body potassium in health: Effects of age, sex, height and fat. Am J Physiol 1974;226:206-12.
8. Hansen JD, Freesemann C, Moddie AD, Evans DE, What does nutritional growth retardation imply. Pediatrics 1971;47:499-504.
9. Taussig LM, Kattwinkel J, Friedewald WT, di Sant’Agnese PA, A new prognostic score and clinical evaluation system for cystic fibrosis. J Pediatr 1973;83:380-6.
10. Thomas S, Corden M, Metric tables of composition of Australian food. Commonwealth Department of Health, Food and Nutrition Section. Canberra: Australian Government Publishing, 1977.
11. Kuo PT, Huang N, The effect of medium chain triglycerides upon fat absorption and plasma lipid depot fat of children with cystic fibrosis of the pancreas. J Clin Invest 1965;44:1924-33.
12. Imondey A, Stradley R, Utilization of enzymatically hydro-lysed protein and crystalline amino acid diets by rats with exocrine pancreatic insufficiency. J Nutr 1974;104:793-801.
13. National Health and Medical Research Council. Heights and masses of Australian infants and children. Sydney: National Health and Medical Research Council, 1973.
14. Brook CGD. Determination of body composition of children from skinfold measurements. Arch Dis Child 1971;46: 182-7.
15. Picou D, Reeds PJ, Jackson A, Poulter N, The measurement of muscle mass in children using 15N creatine. Pediatr Res 1976:10:184-88.
16. Forbes GB, Schultz F, Caferelli G, Effects of body size on potassium 40 measurement in the whole body counter (tilt-chair technique). Health Phys 1968;15:435-42.
17. Ward LC, Buttery PJ, N-methylhistidine-An index of the true rate of myofibrillar degradation? An appraisal. Life Sci 1978;23:1103-16.
18. Tomas FM, Ballard FJ, Pope LM, Age dependent changes in the rate of myofibrillar protein degradation in humans as assessed by 3-methylhistidine and creatinine excretion. Clin Sci 1979:56:341-46.
19. Ward LC, Miller MN, Hawgood S, A simple and rapid high performance thin-layer chromatographic method for quantification of 3-methylhistidine. J Chromatogr 1981:223: 417-20.
20. Garrow JS, Fletcher K, Halliday D, Body composition in severe infantile malnutrition. J Clin Invest 1965;44:417-23.
21. Alleyne GAO, Halliday D, Waterlow JC, Nichols BC, Chemical composition of organs of children who died from malnutrition. Br J Nutr 1969;23:783-9.
22. Cahill GF, Starvation in man. N Engl J Med 1970;282: 668-73.
23. Waterlow JC, Alleyne GAO. Protein malnutrition in children. Adv Protein Chem 1971;25:117-20.
24. Picou D, Taylor-Roberts T, The measurement of total protein synthesis and catabolism and nitrogen turnover in infants in different nutritional states receiving different amounts of dietary protein. Clin Sci 1969;36:283-9.
25. Nagabhusan VS, Rao N, Studies on 3-methylhistidine metabolism in children with protein-energy malnutrition. Am J Clin Nutr 1978;31:1322-7.
26. Yassa JG, Prosser R, Dodge JA, Effects of an artificial diet on growth of patients with cystic fibrosis. Arch Dis Child 1978;53:777-83.
27. Berry HK, Kellogg FW, Hunt WM, Ingberg RC, Richter L, Gutjar C, Dietary supplement and nutrition in children with cystic fibrosis. Am J Dis Child 1975;129:165-71.
28. Allan JD, Mason A, Moss AD, Nutritional supplementation in treatment of cystic fibrosis of the pancreas. Am J Dis Child 1973;126:122-6.
29. Gow R, Bradbear R, Francis P, Shepherd RW, Comparative study of varying regimens to improve steatorrhoea and crea-torrhoea in cystic fibrosis. Lancet 1981;2:1071-4.
30. Adeniyi-Jones S, Suskind R, Polombo J, Pena-Cruz V, Khaw KJ, Whole body and muscle protein turnover in malnourished cystic fibrous fibrosis patients [Abstract], Pediatr Res 1979;13:394.
31. Dooley RR, Moss AJ, Wright PM, Hassakis PC, Norethan-drolone in cystic fibrosis of the pancreas. J Pediatr 1969;74:95-97.
32. Keens TG, Krastins IRB, Wannamaker EM, et al. Ventilatory muscle endurance training in normal subjects and patients with CF. Am Rev Respir Dis 1977.116:853-8.