Correlations between immune and metabolic serum markers and schizophrenia/bipolar disorder polygenic risk score in first-episode psychosis

Early Interv Psychiatry. 2020 Aug;14(4):507-511. doi: 10.1111/eip.12906. Epub 2019 Nov 21.

Abstract

Aims: There is a strong interest in identifying the biological mechanisms involved in the genetic risk for psychotic disorders. In this study, we evaluated the correlation between serum concentrations of specific molecular markers and the genetic component for schizophrenia and bipolar disorder.

Methods: We analysed the association between the polygenic risk score (PRS) and the serum levels of different inflammatory/metabolic markers in a sample of 81 first-episode psychosis patients (FEP) with a diagnosis of schizophrenia or bipolar disorder and 33 controls.

Results: A positive correlation of schizophrenia and bipolar disorder PRS with the inflammatory marker C-C Motif Chemokine Ligand 4 serum concentration (ρ = 0.42, P = 1.56 × 10-04 and ρ = 0.40, P = 1.65 × 10-03 , respectively) and a negative correlation with the serum ghrelin content (ρ = - 0.35, P = 4.27 × 10-03 and ρ = - 0.45, P = 6.05 × 10-04 , respectively) were observed.

Conclusion: These findings provide new insight into the biological underpinnings of the PRS component, thus supporting a role of the genetic liability on the inflammatory and metabolic alterations that characterize psychosis onset.

Keywords: first episode psychosis; inflammation; metabolism; polygenic risk score.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / blood
  • Bipolar Disorder / blood*
  • Case-Control Studies
  • Chemokine CCL4 / blood*
  • Female
  • Ghrelin / blood*
  • Humans
  • Male
  • Multifactorial Inheritance
  • Risk Factors
  • Schizophrenia / blood*
  • Young Adult

Substances

  • Biomarkers
  • Chemokine CCL4
  • Ghrelin