Proton magnetic resonance spectroscopy (1H-MRS) of hippocampus, basal ganglia, and vermis of cerebellum in schizophrenia associated with idiopathic unconjugated hyperbilirubinemia (Gilbert's syndrome)

J Psychiatr Res. 2005 Jan;39(1):29-34. doi: 10.1016/j.jpsychires.2004.05.003.

Abstract

Objective: Whether patients with schizophrenia-associated idiopathic unconjugated hyperbilirubinemia (Gilbert's syndrome, GS) have specific changes in brain metabolism was examined in this study.

Method: This study applied proton magnetic resonance spectroscopy (1H-MRS) to the hippocampus, basal ganglia, and vermis of the cerebellum of schizophrenic patients with GS (n=15) or without GS (n=15), all diagnosed according to DSM-IV criteria, and healthy subjects (n=15).

Results: In the hippocampus, schizophrenic patients with GS showed a significant decrease of N-acetyl aspartate/creatine-phosphocreatinine (NAA/Cr) and myoinositol/creatine-phosphocreatinine (mI/Cr) ratios compared to healthy subjects and schizophrenic patients without GS, while schizophrenic patients without GS showed only a significant decrease of NAA/Cr compared to healthy subjects. In the basal ganglia, schizophrenic patients with GS showed a significant decrease of ml/Cr compared to schizophrenic patients without GS and healthy subjects, and schizophrenic patients with GS showed a significant decrease of NAA/Cr compared to healthy subjects. In the vermis of the cerebellum, schizophrenic patients with GS showed only a significant decrease of ml/Cr compared to healthy subjects, although schizophrenic patients without GS did not show a significant decrease of ml/Cr compared to healthy subjects.

Conclusion: The findings suggest that schizophrenia with GS is a more severe sub-type with regard to brain metabolism.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Basal Ganglia / metabolism*
  • Basal Ganglia / pathology
  • Case-Control Studies
  • Cerebellum / metabolism*
  • Cerebellum / pathology
  • Female
  • Gilbert Disease / complications*
  • Gilbert Disease / psychology*
  • Hippocampus / metabolism*
  • Hippocampus / pathology
  • Humans
  • Magnetic Resonance Spectroscopy / methods
  • Male
  • Protons
  • Schizophrenia / diagnosis*
  • Schizophrenia / etiology*

Substances

  • Protons