[Clinical algorithm for cerebrospinal fluid test of 14-3-3 protein in diagnosis of Creutzfeldt-Jacob disease]

Ned Tijdschr Geneeskd. 2001 Jul 28;145(30):1467-71.
[Article in Dutch]

Abstract

Objective: To study whether an algorithm that includes additional diagnostic information could increase the specificity of the 14-3-3 protein testing in patients suspected to suffer from Creutzfeldt-Jakob disease (CJD).

Design: The development of a diagnostic algorithm.

Method: The 14-3-3 protein was tested in the cerebrospinal fluid from 69 consecutive patients suspected of having CJD. On the basis of a former study and literature research, a diagnostic algorithm was constructed, which restricted the indication for performing the 14-3-3 protein test.

Results: By taking into consideration the findings of neuroimaging and routine cerebrospinal fluid examination prior to 14-3-3 testing, the specificity increased to 97% (95%-CI: 85.5-99.9) thus changing the prior probability of having CJD of 35% to a posterior probability of 75-100%, in the case of a positive test result.

Conclusion: Determining the presence of 14-3-3 protein is a highly sensitive and specific marker for sporadic CJD when used in combination with imaging and cerebrospinal fluid examination.

Publication types

  • Evaluation Study

MeSH terms

  • 14-3-3 Proteins
  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Algorithms
  • Biomarkers / cerebrospinal fluid
  • Child
  • Creutzfeldt-Jakob Syndrome / cerebrospinal fluid*
  • Creutzfeldt-Jakob Syndrome / diagnosis*
  • Diagnosis, Differential
  • Female
  • Humans
  • Immunoblotting
  • Male
  • Middle Aged
  • Sensitivity and Specificity
  • Tyrosine 3-Monooxygenase / cerebrospinal fluid*

Substances

  • 14-3-3 Proteins
  • Biomarkers
  • Tyrosine 3-Monooxygenase