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Urinary creatinine and hydroxyproline in relation to childhood malnutrition

Published online by Cambridge University Press:  09 March 2007

D. S. McLaren ,
Hermine Loshkajian  and
A. A. Kanawati
D. S. McLaren
Affiliation:
Nutrition Research Program, School of Medicine, American University of Beirut, Beirut, Lebanon
Hermine Loshkajian
Affiliation:
Nutrition Research Program, School of Medicine, American University of Beirut, Beirut, Lebanon
A. A. Kanawati
Affiliation:
Nutrition Research Program, School of Medicine, American University of Beirut, Beirut, Lebanon
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Abstract

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1. Urinary excretions of creatinine (Cre) and hydroxyproline (OHPr) were measured in two groups of children: (a) 24 h collections in male and ‘spot’ samples in female marasmic infants throughout the course of treatment, and (b) ‘spot’ samples in underprivileged pre-school children at home. Results were related to certain somatic measurements and in some instances to some dietary factors.

2. Analysis of 24 h samples taken at intervals throughout 120 d of treatment showed a steady rise towards normal levels from very low initial values of OHPr. There was no corre-lation with age or body-weight on admission, nor of OHPr excretion through recovery with increase in height. Excretion of Cre also increased during recovery but the trend was more erratic. There was no relation to initial weight deficit or age but mean Cre excretion through recovery did correlate with rate of increase in weight. Values of Cre excretion at different stages of recovery expressed in terms of weight or height differed somewhat from those reported by others. The possible significance of these findings is discussed.

3. High correlations of the OHPr index according to Whitehead (1965) determined on 6 h and 24 h collections provided evidence for the representative nature of ‘spot’ samples.

4. Partial correlation analysis of body-weight and urine volume in relation to Cre excretion (mg/24 h) showed that the former (r = 0.719) had a greater influence than the latter (r= 0.485).

5. In a subgroup of eleven marasmic infants aged 3–5 months multiple linear regression analyses of OHPr and Cre excretion on somatic and dietary factors revealed no consistent correlations.

6. Periods of lowered OHPr and Cre excretion were frequent but in only half of the instances were they related to intercurrent infection.

7. A high correlation was found between changes in excretion of OHPr and of Cre throughout recovery.

8. An appraisal was made of the OHPr index according to Whitehead (1965). On the basis of the considerable influence that age was shown to have on this index during the preschool period an OHPr index (age-adjusted) was suggested for use.

9. The OHPr index (age-adjusted) determined on ‘spot’ samples from underprivileged preschool children at home and from marasmic infants during recovery was shown to be closely correlated with a modified ‘index of thriving’ based on somatic measurements.

10. The value of Cre and OHPr determinations in the study of severely malnourished children during recovery and in the detection of mild undernutrition is discussed in the light of these experimental results.

Type
Research Article
Information
British Journal of Nutrition , Volume 24 , Issue 3 , September 1970 , pp. 641 - 651
Copyright
Copyright © The Nutrition Society 1970

References

REFERENCES

Alleyne, G. A. O. (1968). Clin. Sci. 34, 199.Google Scholar
Allison, D. J., Walker, A. & Smith, Q. T. (1966). Clinica chim. Acta 14, 729.CrossRefGoogle Scholar
Anasuya, A. & Narasinga Rao, B. S. (1966). Indian J. med. Res. 54, 849.Google Scholar
Arroyave, G. & Wilson, D. (1961). Am. J. clin. Nutr. 9, 170.CrossRefGoogle Scholar
Cranny, R. L. & Cranny, C. L. (1960). Am. J. Dis. Child. 99, 507.CrossRefGoogle Scholar
Garrow, J. S., Picou, D. & Waterlow, J. C. (1962). W. Indian med. J. 11, 217.Google Scholar
Graystone, J. A. & Cheek, D. B. (1968). In Human Growth: Body Composition, Cell Growth, Energy, and Intelligence p. 221 [Cheek, D. B., editor]. Philadelphia: Lea and Febiger.Google Scholar
Howells, G. R., Wharton, B. A. & McCance, R. A. (1967). Lancet i, 1082.CrossRefGoogle Scholar
Howells, G. R. & Whitehead, R. G. (1967). J. med. Lab. Technol. 24, 98.Google Scholar
Jelliffe, D. B. (1966). Monograph Ser. W.H.O. no. 53.Google Scholar
Kanawati, A. A., McLaren, D. S. & Abu-Jawdeh, I. (1970). Proc. int. Congr. trop. Med. Malar. VIII. Teheran, Iran 1968. (In the Press).Google Scholar
Kennedy, W. P. (1961). Archs Dis. Childh. 36, 325.CrossRefGoogle Scholar
Kivirikko, K. I., Laitinen, O. & Prockop, D. J. (1967). Analyt. Biochem. 19, 249.CrossRefGoogle Scholar
Leroy, E. C. (1967). Adv. clin. Chem. 10, 213.CrossRefGoogle Scholar
McLaren, D. S. (1966). Lancet, ii 485.CrossRefGoogle Scholar
McLaren, D. S., Kamel, W. W. & Ayyoub, N. (1965). Am. J. clin. Nutr. 17, 152.CrossRefGoogle Scholar
McLaren, D. S., Pellett, P. L. & Read, W. W. C. (1967). Lancet, i, 533.CrossRefGoogle Scholar
Mohanram, M., Anasuya, A., Narasinga Rao, B. S. & Srikantia, S. G. (1969). Lancet, i, 102.CrossRefGoogle Scholar
Picou, D., Alleyne, G. A. O. & Seakins, A. (1965). Clin. Sci. 29, 517.Google Scholar
Rutishauser, I. H. E. & McCance, R. A. (1968). Archs Dis. Childh. 43, 252.CrossRefGoogle Scholar
Rutishauser, I. H. E. & Whitehead, R. G. (1969). Br. J. Nutr. 23, 1.CrossRefGoogle Scholar
Standard, K. L., Wills, V. G. & Waterlow, J. C. (1959). Am. J. clin. Nutr. 7, 271.CrossRefGoogle Scholar
Stearns, G., Newman, K. J., McKinley, J. B. & Jeans, P. C. (1958). Ann. N. Y. Acad. Sci. 69, 857.CrossRefGoogle Scholar
Stuart, H. C. & Stevenson, S. S. (1959). In Textbook of Pediatrics 7th ed., pp. 12–61 [Nelson, W., editor]. Philadelphia: Saunders.Google Scholar
Taussky, H. H. (1956). Clinica chim. Acta 1, 210.CrossRefGoogle Scholar
Wharton, B. A., Howells, G. R. & McCance, R. A. (1967). Nature, Lond. 215, 968.CrossRefGoogle Scholar
Whitehead, R. G. (1964). Lancet, i, 250.CrossRefGoogle Scholar
Whitehead, R. G. (1965). Lancet, ii, 567.CrossRefGoogle Scholar
Whitehead, R. G. (1966). Lancet i, 203.CrossRefGoogle Scholar
Whitehead, R. G. (1967). Archs Dis. Childh. 42, 479.CrossRefGoogle Scholar
Whitehead, R. G. (1969). Lancet i, 103.Google Scholar
Younoszai, M. K., Andersen, D. W., Filer, L. J. & Fomon, S. J. (1967). Pediat. Res. 1, 266.CrossRefGoogle Scholar