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Urinary pyrimidine excretion in arginase deficiency

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Journal of Inherited Metabolic Disease

Abstract

A high-performance liquid-chromatographic method was used to separate and identify uracil, uridine, pseudouridine and orotic acid after preliminary extraction in two patients (McKusick 20780). Urinary uracil excretion was 10–35 times normal in both patients with arginase deficiency. Uridine and orotic acid, not normally detected, were excreted in large amounts and were directly influenced by protein intake. Their excretions were correlated with urinary arginine excretion. Urinary uracil levels remained consistently high and showed minimal variations with increased protein intake or urinary arginine levels.

The measurement of urinary pyrimidines appears to be useful for the detection, differential diagnosis and dietary monitoring of patients with urea cycle disorders. The data presented extends this observation to include patients with arginase deficiency.

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References

  • Batshaw, M., Brusilow, S. and Walser, M. Treatment of carbamyl phosphate synthetase deficiency with keto analogues of essential amino acids.N. Engl. J. Med. 292 (1975) 1085

    Google Scholar 

  • Benson, J. V., Jr., Gordon, M. J. and Patterson, J. A. Accelerated chromatographic analysis of amino acids in physiological fluids containing glutamine and asparagine.Anal. Biochem. 18 (1967) 228

    Google Scholar 

  • Buist, N. R. M., Kennaway, N. G., Hepburn, C. A., Stradholdm, J. J. and Ramberg, D. A. Citrullinemia: investigation and treatment over a four-year period.J. Pediatr. 85 (1974) 208

    Google Scholar 

  • Cederbaum, S. D., Shaw, K. N. F. and Valentine, M. Hyperargininemia.J. Pediatr. 90 (1977) 569

    Google Scholar 

  • Cederbaum, S. D., Shaw, K. N. F., Spector, E. B., Verity, M. A., Snodgrass, P. J. and Sugarman, G. I. Hyperargininemia with arginase deficiency.Pediatr. Res. 13 (1979) 827

    Google Scholar 

  • Evans, J. E., Tieckelmann, H., Naylor, E. W. and Guthrie, R. The measurement of urinary pyrimidine bases and nucleosides by high performance liquid chromatography.J. Chrom. (Biomed. Appl.) 163 (1979) 29

    Google Scholar 

  • Gerron, G. G., Ansley, J. D., Isaacs, J. W., Kutner, M. H. and Rudman, D. Technical pitfalls in measurement of venous plasma NH3 concentration.Clin. Chem. 22 (1976) 663

    Google Scholar 

  • Hokanson, J. T., O'Brien, W. E., Idemoto, J. and Schafer, I. A. Carrier detection in ornithine transcarbamylase deficiency.J. Pediatr. 93 (1978) 75

    Google Scholar 

  • Jacobs, H. A. M. and Olthuis, F. M. F. G. A kinetic determination of ammonia in plasma.Clin. Chim. Acta 43 (1973) 81

    Google Scholar 

  • Kesner, L. The effect of ammonia administration on orotic acid excretion in rats.J. Biol. Chem. 240 (1965) 1722

    Google Scholar 

  • Levin, B., Oberholzer, V. G. and Sinclair, L. Biochemical investigations of hyperammonemia.Lancet 2 (1969) 170

    Google Scholar 

  • Michaels, V. V. and Beaudet, A. L. Arginase deficiency in multiple tissues in argininemia.Clin. Genet. 13 (1978) 61

    Google Scholar 

  • Moedjono, S. J., Shaw, K. N. F. and Cederbaum, S. D. A chemically defined diet for the treatment of hyper-argininemia due to arginase deficiency.Pediatr. Res. 13 (1979) 423

    Google Scholar 

  • Natale, P. J. and Trembley, G. D. On the availability of intra-mitochondrial carbamyl phosphate for the extramito-chondrial biosynthesis of pyrimidines.Biochem. Biophys. Res. Commun. 37 (1969) 512

    Google Scholar 

  • Paul, T. D., Naylor, E. W. and Guthrie, R. Newborn urine screening for metabolic disease.J. Pediatr. 96 (1980) 653

    Google Scholar 

  • Qureshi, I. A., Letarte, J., Quelley, R. and Lemieux, B. Enzymologic and metabolic studies in two families affected by argininosuccinic aciduria.Pediatr. Res. 21 (1978) 256

    Google Scholar 

  • Shaw, K. N. F., Gutenstein, M., Jacobs, E. E. and Blaskovics, J. C. Biochemical screening and monitoring of patients with phenylketonuria and variant forms of hyperphenylalanemia. In Bickel, H., Hudson, F. P. and Woolf, L. I. (eds.)Phenylketonuria. George Thieme Verlag, Stuttgart, 1971, p. 163

    Google Scholar 

  • Snyderman, S. E., Sansaricq, C., Chen, W. J., Norton, P. M. and Pansalkar, S. V. Argininemia.J. Pediatr. 90 (1977) 563

    Google Scholar 

  • Snyderman, S. E., Sansaricq, C., Norton, P. M. and Goldstein, F. Argininemia treated from birth.J. Pediatr. 95 (1979) 61

    Google Scholar 

  • Statter, M., Russel, A., Abzug-Horowitz, S. and Pinon, A. Abnormal orotic acid metabolism associated with acute hyperammonemia in the rat.Biochem. Med. 9 (1974) 1

    Google Scholar 

  • Sunshine, P., Lindenbaum, J. E., Levy, H. L. and Freeman, J. M. Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.Pediatrics 50 (1972) 100

    Google Scholar 

  • Terheggen, H. G., Schwenk, A., Lowenthal, A., van Sande, M. and Colombo, J. P. Argininaemia with arginase deficiency.Lancet 2 (1969) 748

    Google Scholar 

  • Terheggen, H. G., Lowenthal, A., Lavinha, F. and Colombo, J. P. Familial hyperargininaemia.Arch. Dis. Child. 50 (1975) 57

    Google Scholar 

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Naylor, E.W., Cederbaum, S.D. Urinary pyrimidine excretion in arginase deficiency. J Inherit Metab Dis 4, 207–210 (1981). https://doi.org/10.1007/BF02263653

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