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Event-related fMRI of word classification and successful word recognition in subjects at genetically enhanced risk of schizophrenia

Published online by Cambridge University Press:  29 June 2006

MARIE-CLAIRE WHYTE
Affiliation:
Division of Psychiatry, University of Edinburgh, UK
HEATHER C. WHALLEY
Affiliation:
Division of Psychiatry, University of Edinburgh, UK
ENRICO SIMONOTTO
Affiliation:
Division of Psychiatry, University of Edinburgh, UK Invivo Diagnostic Imaging, Orlando, FL, USA
SUSANNA FLETT
Affiliation:
School of Philosophy, Psychology and Language Sciences, University of Edinburgh, UK
RICHARD SHILLCOCK
Affiliation:
School of Philosophy, Psychology and Language Sciences, University of Edinburgh, UK
IAN MARSHALL
Affiliation:
Division of Medical Physics, University of Edinburgh, UK
NIGEL H. GODDARD
Affiliation:
Centre for Functional Imaging Studies (CFIS), Division of Informatics, University of Edinburgh, UK
EVE C. JOHNSTONE
Affiliation:
Division of Psychiatry, University of Edinburgh, UK
STEPHEN M. LAWRIE
Affiliation:
Division of Psychiatry, University of Edinburgh, UK

Abstract

Background. Verbal declarative memory is a core deficit in schizophrenia patients, seen to a lesser extent in unaffected biological relatives. Neuroimaging studies suggest volumetric differences and aberrant function in prefrontal and temporal regions in schizophrenia patients compared to controls. These deficits are also reflected in the small number of similar investigations in unaffected biological relatives. However, it is unclear the extent to which dysfunction is genetically mediated or a feature of the established illness.

Method. Event-related blood-oxygen-level-dependent (BOLD) functional magnetic resonance imaging (fMRI) was used to measure brain activation in 68 biological relatives of schizophrenia patients (of whom 27 experienced transient or isolated psychotic symptoms) and 21 controls during verbal classification and recognition.

Results. During word classification, the high-risk group showed a greater response relative to controls in the right inferior frontal gyrus. During correct recognition (relative to correct rejection), the high-risk group showed significantly greater response relative to controls in the right cerebellum. When the high-risk group was split into those with (HR+) and without (HR−) psychotic symptoms, the increased response in the right inferior frontal gyrus was only seen when the HR+ were compared to controls. The greater cerebellar response was seen when both HR groups were compared to controls.

Conclusions. Activation increases in the right inferior frontal gyrus and cerebellum in high-risk subjects compared to controls during a relatively low-load memory task are likely to represent compensation for genetically mediated abnormalities. This is consistent with a leftward shift of the inverted ‘U’ load–response model of cognitive function in schizophrenia.

Type
Original Article
Copyright
2006 Cambridge University Press

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