We measured N-acetylaspartate and its precursor/product N-acetylaspartyl-gl
utamate (NAAG) in urine of patients with Canavan disease using capillary zo
ne electrophoresis. Abnormal levels of NAAG were found in 32 of 43 patients
examined. Elevated NAAG was also present in the CSF of one patient. Given
that NAAG may interfere with N-methyl-D-aspartate receptor function, the oc
currence of high levels of NAAG in patients' urine conceivably represents a
participating factor in the pathogenesis of Canavan disease.
Conclusion The biochemical role of N-acetylaspartylglutamate and its relati
onship to glutamatergic function may be relevant to the pathogenesis of Can
avan disease.