Skip to main content
Log in

Peritoneal dialysis in maple-syrup-urine disease: Studies on branched-chain amino and keto acids

  • Original Investigations
  • Published:
European Journal of Pediatrics Aims and scope Submit manuscript

Abstract

We report biochemical data on a child with MSUD who underwent peritoneal dialysis for severe metabolic imbalance. In confirmation of earlier data, the BCKA/BCAA ratios in blood had been found to be fairly stable in this patient during long-term dietary therapy.

The child became comatose at comparatively low levels of leucine and KICA (ca. 2 mM each). At this time the blood/cerebrospinal fluid ratio for BCAA's and BCKA's was markedly diminished. During peritoneal dialysis, peritoneal clearance was highest for KIVA, but less for MEVA and BCAA's (40–50% or urea clearance), and least for the allegedly most toxic metabolite, KICA. The differences for BCKA's may be due to their differential protein binding. Given these individual differences, 1.8 to 8.7 initial plasma volumes were cleared in 14h with 24.21 of dialysis fluid. In the same time, urinary excretion of BCAA's and BCKA's was much less efficient.

The data are discussed with regard to the pathobiochemical significance of high tissue levels of branched chain acids. A quantitative comparison between peritoneal dialysis and exchange transfusion is not yet possible.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

BCAA's :

branched-chain α-amino acids

BCKA's :

branched-chain α-keto acids

KICA :

α-keto-isocaproic acid

KIVA :

α-keto-isovalerio acid

MEVA :

α-keto-β-methyl-n-valeric acid

MSUD :

maple syrup urine disease

References

  1. Astine, J., Froye, E., Luciani, J.-M., Bellet, H., de Bornier, P. M., Brunel, D.: Leucinose néo-natale d'évolution favorable. Problèmes évolutives et thérapeutiques. Ann. Pédiat. 24, 605–610 (1977)

    Google Scholar 

  2. Benson, J. V., Cormick, J., Patterson, J. A.: Accelerated chromatography of aminoacids associated with phenylketonuria, leucinosis (maple syrup urine disease) and other inborn errors of metabolism. Anal. Biochem. 18, 481–492 (1967)

    Google Scholar 

  3. Boen, S. T.: Peritoneal dialysis in clinical medicine. Springfield, Ill.: Thomas 1964

    Google Scholar 

  4. Bulla, M.: Dialyse im Kindesalter. Stuttgart: Enke 1977

    Google Scholar 

  5. Dancis, J., Hutzler, J., Lewitz, M.: Metabolism of the white blood cells in maple syrup urine disease. Biochim. Biophys. Acta 43, 342–343 (1960)

    Google Scholar 

  6. Dent, C. E., Westall, R. G.: Studies in maple syrup urine disease. Arch. Dis. Child. 36, 259–268 (1961)

    Google Scholar 

  7. Dreyfus, P. M., Prensky, A. L.: Further observations on the biochemical lesion in maple syrup urine disease. Nature 214, 276 (1967)

    Google Scholar 

  8. Gaull, G. E.: Pathogenesis of maple syrup urine disease: Observation during dietary management and treatment of coma by peritoneal dialysis. Biochem. Med. 3, 130–149 (1969)

    Google Scholar 

  9. Gaull, G. E., Tallan, H. H., Lajtha, A., Rassin, D. K.: Pathogenesis of brain dysfunction in inborn errors of amino acid metabolism. In: Biology of brain dysfunction, Vol. 3, G. E. Gaull (ed.). New York, London: Plenum 1975

    Google Scholar 

  10. Hammersen, G., Wille, L., Schmidt, H., Lutz, P., Bickel, H.: Maple syrup urine disease: Treatment of the acutely ill newborn. Eur. J. Pediatr. 129, 157–165 (1978)

    Google Scholar 

  11. Harris, R. J.: Infection in maple-syrup urine disease. Lancet 1971 II, 813–814

    Google Scholar 

  12. Humoller, F. L., Mahler, D. J., Parker, M. M.: Distribution of amino acids between plasma and spinal fluid. Int. J. Neuropsych. 2, 293–297 (1966)

    Google Scholar 

  13. Lancaster, G., Mamer, O. A., Scriver, C. R.: Branched-chain alpha-keto acids isolated as oxime derivatives: Relationship to the corresponding hydroxy acids and amino acids in maple syrup urine disease. Metabolism 23, 257–265 (1974)

    Google Scholar 

  14. Langenbeck, U., Hoinowski, A., Mantel, K., Mehring, H.-U.: Quantitative gaschromatography and single-ion detection of aliphatic α-keto acids from urine as their o-trimethylsilyl quinoxalinol derivatives. J. Chromatogr. 143, 39–50 (1977)

    Google Scholar 

  15. Langenbeck, U., Matthaei, D.: Unpublished observations, 1979

  16. Langenbeck, U., Wendel, U., Luthe, H.: Renal clearance of branched-chain 2-oxo-acids in maple syrup urine disease. J. Clin. Chem. Clin. Biochem. 17, 176–177 (1979)

    Google Scholar 

  17. Langenbeck, U., Wendel, U., Mench-Hoinowski, A., Kuschel, D., Becker, K., Przyrembel, H., Bremer, H. J.: Correlations between branched-chain amino acids and branched-chain α-keto acids in blood in maple syrup urine disease. Clin. Chim. Acta 88, 283–291 (1978)

    Google Scholar 

  18. Rapoport, S. J.: Blood-brain barrier in physiology and medicine. New York: Raven Press 1976

    Google Scholar 

  19. Rey, F., Rey, J., Cloup, M., Féron, J.-F., Doré, F., Labrune, B., Frézal, J.: Traitement d'urgence d'une forme aigue de leucinose par dialyse peritoneale. Arch. Franç. Pédiat. 26, 133–137 (1969)

    Google Scholar 

  20. Sallan, S. E., Cottom, D.: Peritoneal dialysis in maple syrup urine disease. Lancet 1969 II, 1423–1424

    Google Scholar 

  21. Saudubray, J.-M., Fournet, J.-P., Cloup, M.: Intérêt de la dialyse péritonéale dans le traitement d'urgence des maladies métaboliques d'origine constitutionelle révélées dans la période néo-natale. Ann. Méd. interne 122, 1279–1283 (1971)

    Google Scholar 

  22. Schauder, P., Matthaei, D., Scheler, F., Mench-Hoinowski, A., Langenbeck, U.: Blood levels of branched-chain α-keto acids in uremia: therapeutic implication. Klin. Wochenschr. 57, 825–830 (1979)

    Google Scholar 

  23. Schuchmann, L., Witt, I., Schulz, P., Schuhmacher, H., Rüdiger, H. W.: Multiple exchange transfusions as treatment during the acute period in maple syrup urine disease. Helv. Paediat. Acta 27, 449–456 (1972)

    Google Scholar 

  24. Scriver, C. R., Rosenberg, L. E.: Amino acid metabolism and its disorders, pp. 54–56. Philadelphia: Saunders 1973

    Google Scholar 

  25. Snyderman, S. E., Norton, P. M., Roitman, E., Holt, L. E., Jr.: Maple syrup urine disease with particular reference to dieto-therapy. Pediatrics 34, 454–472 (1964)

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

With support of the Landesamt für Forschung des Ministeriums für Wissenschaft und Forschung des Landes Nordrhein-Westfalen. U.L. was supported by Deutsche Forschungsgemeinschaft, Bad Godesberg, G.F.R. (DFG La 201, Schwerpunkt “Biochemische Humangenetik” and SFB 33 “Nervensystem und biologische Information”)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wendel, U., Becker, K., Przyrembel, H. et al. Peritoneal dialysis in maple-syrup-urine disease: Studies on branched-chain amino and keto acids. Eur J Pediatr 134, 57–63 (1980). https://doi.org/10.1007/BF00442404

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00442404

Key words

Navigation