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NeuroImage
Volume 35, Issue 3, 15 April 2007, Pages 1181-1191
 
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doi:10.1016/j.neuroimage.2007.01.008    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2007 Elsevier Inc. All rights reserved.

Grey matter correlates of early psychotic symptoms in adolescents at enhanced risk of psychosis: A voxel-based study

Michael D. SpencerCorresponding Author Contact Information, a, E-mail The Corresponding Author, T. William J. Moorheada, Andrew M. McIntosha, Andrew C. Stanfielda, Walter J. Muira, Peter Hoarea, David G.C. Owensa, Stephen M. Lawriea and Eve C. Johnstonea

aDivision of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, EH10 5HF, UK

Received 13 November 2006; 
revised 12 January 2007; 
accepted 12 January 2007. 
Available online 25 January 2007.

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Abstract

A three-fold enhanced risk of schizophrenia is conferred by learning disability. Here we use voxel-based morphometry (VBM) to investigate grey matter correlates of early psychotic and related symptoms in 137 adolescents at enhanced risk of this disorder because of intellectual disability. Anxiety, hallucinations, incoherence of speech and delusions were assessed at clinical interview, and VBM was used to examine linear associations between symptom severity and grey matter density (GMD). We found significant correlations between anxiety and GMD in the right dorsomedial thalamic nucleus, left parahippocampal gyrus and left hippocampus. Incoherence of speech was associated with GMD in the left cerebellar hemisphere. Gender-separate analysis demonstrated correlations between anxiety and GMD in the right dorsomedial thalamic nucleus of males and the right pulvinar nucleus of females, hallucinations and GMD in the right STG of males, delusions and GMD in the left middle temporal gyrus (MTG) of females, and incoherence of speech and GMD in the right MTG of males and both cerebellar hemispheres and right inferior temporal gyrus of females. Findings are consistent with symptom–structure associates previously reported in populations with schizophrenia or at enhanced genetic risk, and suggest an anatomical basis for the psychopathology found in this young nonclinical population.

Article Outline

Introduction
Materials and methods
Participants
Image acquisition
Voxel-based morphometry
Statistical analysis
Results
Participant characteristics
VBM analysis of male and female participants combined (n = 137)
VBM analysis of male participants alone (n = 85)
VBM analysis of female participants alone (n = 52)
Normality of distribution and exclusion of outliers
Effects of age and gender
Discussion
Conclusion
Acknowledgements
References




NeuroImage
Volume 35, Issue 3, 15 April 2007, Pages 1181-1191
 
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