PARK7 and nucleoside diphosphate kinase A as plasma markers for the early diagnosis of stroke

Clin Chem. 2005 Nov;51(11):2043-51. doi: 10.1373/clinchem.2005.053942. Epub 2005 Sep 1.

Abstract

Background: Plasma markers for stroke could be useful in diagnosis and prognosis and in prediction of response of stroke patients to therapy. PARK7 and nucleoside diphosphate kinase A (NDKA) are increased in human postmortem cerebrospinal fluid (CSF), a model of global brain insult, suggesting that measurement in CSF and, more importantly, in plasma may be useful as a biomarker of stroke.

Methods: We used ELISA to measure PARK7 and NDKA in plasma in 3 independent European and North American retrospective studies encompassing a total of 622 stroke patients and 165 control individuals.

Results: Increases in both biomarkers were highly significant, with sensitivities of 54%-91% for PARK7 and 70%-90% for NDKA and specificities of 80%-97% for PARK7 and 90%-97% for NDKA. The concentrations of both biomarkers increased within 3 h of stroke onset.

Conclusions: PARK7 and NDKA may be useful plasma biomarkers for the early diagnosis of stroke. In addition, this study demonstrated the utility of analysis of postmortem CSF proteins as a first step in the discovery of plasma markers of ischemic brain injury.

Publication types

  • Multicenter Study

MeSH terms

  • Biomarkers / blood
  • Biomarkers / cerebrospinal fluid
  • Cohort Studies
  • Enzyme-Linked Immunosorbent Assay
  • Europe
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • NM23 Nucleoside Diphosphate Kinases
  • North America
  • Nucleoside-Diphosphate Kinase / blood*
  • Nucleoside-Diphosphate Kinase / cerebrospinal fluid
  • Oncogene Proteins / blood*
  • Oncogene Proteins / cerebrospinal fluid
  • Plasma
  • Protein Deglycase DJ-1
  • Proteome / analysis
  • Sensitivity and Specificity
  • Stroke / blood
  • Stroke / cerebrospinal fluid
  • Stroke / diagnosis*

Substances

  • Biomarkers
  • Intracellular Signaling Peptides and Proteins
  • NM23 Nucleoside Diphosphate Kinases
  • Oncogene Proteins
  • Proteome
  • Nucleoside-Diphosphate Kinase
  • PARK7 protein, human
  • Protein Deglycase DJ-1