Abstract

Disturbances in the brain glutamate and GABA (γ-aminobutyric acid) homeostasis may be markers of transition to psychosis in individuals at high-risk (HR). Knowledge of GABA and glutamate levels in HR stages could give an insight into changes in the neurochemistry underlying psychosis. Studies on glutamate in HR have provided conflicting data, and GABA studies have only recently been initialized. In this meta-analysis, we compared cerebral levels of glutamate and GABA in HR individuals with healthy controls (HC). We searched Medline and Embase for articles published on 1H-MRS studies on glutamate and GABA in HR states until April 9th, 2019. We identified a total of 28 eligible studies, of which eight reported GABA (243 HR, 356 HC) and 26 reported glutamate (299 HR, 279 HC) or Glx (glutamate + glutamine) (584 HR, 632 HC) levels. Sample sizes varied from 6 to 75 for HR and 10 to 184 for HC. Our meta-analysis of 1H-MRS studies on glutamate and GABA in HR states displayed significantly lower (P = 0.0003) levels of thalamic glutamate in HR individuals than in HC and significantly higher (P = 0.001) Glx in the frontal lobe of genetic HR individuals (1st-degree relatives) than in HC. No other significant differences in glutamate and GABA levels were found. Subject numbers in the studies on glutamate as well as GABA levels were generally small and the data conflicting. Our meta-analytical findings highlight the need for larger and more homogeneous studies of glutamate and GABA in high-risk states.

Original languageEnglish
Article number215
JournalSchizophrenia Research
Volume215
Pages (from-to)38-48
Number of pages11
ISSN0920-9964
DOIs
Publication statusPublished - Jan 2020

Keywords

  • Frontal Lobe/diagnostic imaging
  • Glutamic Acid/metabolism
  • Humans
  • Prodromal Symptoms
  • Proton Magnetic Resonance Spectroscopy
  • Psychotic Disorders/diagnostic imaging
  • Risk
  • Thalamus/diagnostic imaging
  • gamma-Aminobutyric Acid/metabolism
  • Glutamate
  • 1H-MRS
  • GABA
  • UHR
  • High-risk
  • Prodromal

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