Skip to main content
. Author manuscript; available in PMC: 2016 Jun 10.
Published in final edited form as: J Psychopharmacol. 2015 Jan 13;29(2):97–115. doi: 10.1177/0269881114563634

Table 5.

The 1H-MRS studies in studies in individuals at increased risk of schizophrenia

Study Medication status MN/MF/M/HC Phenotype Field Strength Findings: Glu/Gln/Glx
MPFC Hipp Tha BG
Keshavan et al. 2009 40/0/0/46 UHR 1.5T na/na/- na/na/- na/na/-
Tandon et al. 2008 15/0/0/14 UHR 3.0T -/na/-
Stone et al. 2009 19/3/2/27 UHR 3.0T -/↑/- -/-/- ↓/-/↓
Yoo et al. 2009 22/0/0/22 UHR 1.5T na/na/- na/na/-
Lutkenhoff et al. 2010 12/0/0/21 Twins of Scz patients 3.0T ↓/na/na -/na/na
Tandon et al. 2013 23/0/0/24 Children of Scz parents 1.5T na/na/- na/na/↑ na/na/↑
Tibbo et al. 2004a 20/0/0/22 Children of Scz parents 3.0T na/na/na

1H-MRS= Proton Magnetic Resonance Spectroscopy; MN- antipsychotic naïve; M – currently taking antipsychotic medication; HC – healthy control; Scz - Schizophrenia

Tha – Thalamus; BG – Basal Ganglia; Hipp – Hippocampus; MPFC – medial prefrontal cortex (including anterior cingulated cortex; Glx – Glutamate+ glutamine; Glu – glutamate; Gln – glutamine

↑ = significantly higher in patient group;v ↓ = significantly lower level in patient group; - = no significant difference; na – not analysed; UHR – Ultra high risk for psychosis

a

Absolute values not reported but significantly increased glu:gln ration in MPFC of high risk group.