CSF lactate dehydrogenase activity in patients with Creutzfeldt-Jakob disease exceeds that in other dementias

Dement Geriatr Cogn Disord. 2004;17(3):204-6. doi: 10.1159/000076357. Epub 2004 Jan 20.

Abstract

The diagnosis of Creutzfeldt-Jakob disease (CJD) is still made by exclusion of other dementias. We now evaluated lactate dehydrogenase (LDH) in the cerebrospinal fluid (CSF) as a possible additional diagnostic tool. CSF LDH levels of patients with CJD (n = 26) were compared with those in other dementias (n = 28). LDH isoenzymes were determined in a subset (n = 9). Total LDH and isoenzyme LDH-1 were significantly higher, whereas the fractions of LDH-2 and LDH-3 were significantly lower in CJD patients. We conclude that in addition to established CSF parameters, LDH and its isoenzymes might serve as a further help to discriminate between CJD and other dementias.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Creutzfeldt-Jakob Syndrome / cerebrospinal fluid*
  • Creutzfeldt-Jakob Syndrome / enzymology*
  • Dementia / cerebrospinal fluid*
  • Dementia / enzymology*
  • Diagnosis, Differential
  • Female
  • Humans
  • Isoenzymes / cerebrospinal fluid
  • L-Lactate Dehydrogenase / cerebrospinal fluid*
  • Male
  • Middle Aged
  • Psychiatric Status Rating Scales

Substances

  • Isoenzymes
  • L-Lactate Dehydrogenase