Skip to main content
Log in

Stable isotope dilution analysis ofN-acetylaspartic acid in CSF, blood, urine and amniotic fluid: Accurate postnatal diagnosis and the potential for prenatal diagnosis of canavan disease

  • Published:
Journal of Inherited Metabolic Disease

Summary

A sensitive and selective analytical technique is described for the determination ofN-acetylaspartic acid in body fluids using stable isotope dilution in combination with positive chemical ionization mass spectrometry with selected ion monitoring.

Control mean and ranges have been established: in urine 19.5 and 6.6–35.4 µmol/mmol creat.; in plasma 0.44 and 0.17–0.81 µmol/L; in cerebrospinal fluid 1.51 and 0.25–2.83 µmol/L; and in amniotic fluid 1.27 and 0.30–2.55 µmol/L.

In a patient with Canavan disease,N-acetylaspartic acid concentration was elevated 80-fold in urine and 20-fold in plasma compared to the control means. A subsequent pregnancy of the mother was monitored and theN-acetylaspartic acid concentration in the amniotic fluid was within the control range and a healthy child was born.

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

References

  • Buchanan, D. S. and Davis, R. L. Spongy degeneration of the nervous system: a report of 4 cases with a review of the literature.Neurology 15 (1965) 207–222

    PubMed  CAS  Google Scholar 

  • Canavan, M. M. Schilder's encephalites peri-axialis diffusa. Report of a case in a child aged sixteen and one-half months.Arch. Neurol. Psychiatry (Chicago) 25 (1931) 299–308

    Google Scholar 

  • Divry, P., Vianey-Liaud, C., Gay, C., Macabeo, V., Rapin, F. and Echenne, B.N-Acetylaspartic aciduria; report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophy.J. Inher. Metab. Dis. 11 (1988) 307–308

    Article  PubMed  CAS  Google Scholar 

  • Echenne, B., Divry, P. and Vianey-Liaud, C. Spongy degeneration of the neuraxis (Canavan-Van Bogaert Disease) andN-acetylaspartic aciduria.Neuropediatrics 20 (1989) 79–81

    Article  PubMed  CAS  Google Scholar 

  • Elpeleg, O. N., Amir, N., Barash, V., Glick, B., Gross-Tsur, V., Shachar, E., Shapira, Y. and Tzelnik, N. Canavan disease andN-acetylaspartic aciduria.Neuropediatrics 20 (1989) 238

    Article  PubMed  CAS  Google Scholar 

  • Hagenfeldt, L., Bollgren, I. and Venizelos, N.N-Acetylaspartic aciduria due to aspartoacylase deficiency — a new aetiology of childhood leukodystrophy.J. Inher. Metab. Dis. 10 (1987) 135–141

    Article  PubMed  CAS  Google Scholar 

  • Jakobs, C., Ten Brink, H. J. and Stellaard, F. Prenatal diagnosis of inherited metabolic disorders by quantitation of characteristic metabolites in amniotic fluid: Facts and future.Prenat. Diag. 10 (1990) 265–271

    Article  CAS  Google Scholar 

  • Kvittingen, E. A., Guldal, G., Borsing, S., Skalpe, I. O., Stokke, O. and Jellum, E.N-Acetylaspartic aciduria in a child with a progressive cerebral atrophy.Clin. Chim. Acta 158 (1986) 217–227

    Article  PubMed  CAS  Google Scholar 

  • Matalon, R., Michals, K. M., Sebesta, D., Deanching, M., Gashkoff, P. and Casanova, J. Aspartoacylase deficiency andN-acetylaspartic aciduria in patients with Canavan Disease.Am. J. Hum. Gen. 29 (1988) 463–471

    CAS  Google Scholar 

  • Matalon, R., Kaul, R., Casanova, J., Michals, K., Johnson, A., Rapin, I., Gashkoff, P. and Deanching, M. Aspartoacylase deficiency: the enzyme defect in Canavan Disease.J. Inher. Metab. Dis. 12 (1989) 329–331

    Article  PubMed  Google Scholar 

  • Ozand, P. T., Gascon, G. G. and Dhalla, M. Aspartoacylase deficiency and Canavan Disease in Saudi Arabia.Am. J. Med. Gen. 35 (1990) 266–268

    Article  CAS  Google Scholar 

  • Sweetman, L. Prenatal diagnosis of the organic acidurias.J. Inher. Metab. Dis. 7 (Suppl. 1) (1984) 18–22

    Article  PubMed  Google Scholar 

  • Van Bogaert, L. and Bertrand, I.Spongy Degeneration of Brain in Infancy, North Holland Publishing Co., Amsterdam, 1967, pp. 3–132

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jakobs, C., ten Brink, H.J., Langelaar, S.A. et al. Stable isotope dilution analysis ofN-acetylaspartic acid in CSF, blood, urine and amniotic fluid: Accurate postnatal diagnosis and the potential for prenatal diagnosis of canavan disease. J Inherit Metab Dis 14, 653–660 (1991). https://doi.org/10.1007/BF01799929

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01799929

Keywords

Navigation