Increased platelet glycogen sysnthase kinase 3beta in first-episode psychosis

Schizophr Res. 2018 May:195:402-405. doi: 10.1016/j.schres.2017.08.062. Epub 2017 Sep 6.

Abstract

Past studies have linked intracellular pathways related to psychotic disorders to the GSK3B enzyme. This study aimed to investigate GSK3B protein expression and phosphorylation in drug-naïve first-episode psychosis patients (n=43) at baseline and following symptom remission, and in healthy controls (n=77). At baseline GSK3B total level was higher in patients (p<0.001). In schizophrenia spectrum patients (n=25) GSK3B total and phosphorylated levels were higher than in controls and patients with other non-affective psychotic disorders (n=18) (p<0.001; p=0.027; p=0.05 respectively). No enzyme changes were found after clinical remission. The implication of this finding for the biology of psychoses warrants further studies to clarify whether increased GSK3B may be useful as a biomarker for psychosis in general, and schizophrenia in particular.

Keywords: Antipsychotic treatment; First-episode psychosis; GSK3B; Non-affective psychosis; Schizophrenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Glycogen Synthase Kinase 3 beta / blood*
  • Humans
  • Male
  • Phosphorylation
  • Psychotic Disorders / blood*
  • Schizophrenia / blood*
  • Statistics, Nonparametric
  • Young Adult

Substances

  • GSK3B protein, human
  • Glycogen Synthase Kinase 3 beta