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PMID: 12668360 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Abnormal fMRI response of the dorsolateral prefrontal cortex in cognitively intact siblings of patients with schizophrenia.

The American journal of psychiatry ·Vol. 160 ·No. 4 ·2003-04-00 ·Pages 709-19

Callicott JH, Egan MF, Mattay VS, Bertolino A, Bone AD, Verchinksi B, Weinberger DR

Abstract

The identification of neurobiological intermediate phenotypes may hasten the search for susceptibility genes in complex psychiatric disorders such as schizophrenia. Earlier family studies have suggested that deficits in executive cognition and working memory may be related to genetic susceptibility for schizophrenia, but the biological basis for this behavioral phenotype has not been identified. The authors used functional magnetic resonance imaging (fMRI) during performance of the N-back working memory task to assess working memory-related cortical physiology in nonschizophrenic, cognitively intact siblings of patients with schizophrenia. They compared 23 unaffected siblings of schizophrenic patients to 18 matched comparison subjects. As a planned replication, they studied another 25 unaffected siblings and 15 comparison subjects. In both cohorts, there were no group differences in working memory performance. Nevertheless, both groups of siblings showed an exaggerated physiological response in the right dorsolateral prefrontal cortex that was qualitatively similar to results of earlier fMRI studies of patients with schizophrenia. These fMRI data provide direct evidence of a primary physiological abnormality in dorsolateral prefrontal cortex function in individuals at greater genetic risk for schizophrenia, even in the absence of a manifest cognitive abnormality. This exaggerated fMRI response implicates inefficient processing of memory information at the level of intrinsic prefrontal circuitry, similar to earlier findings in patients with schizophrenia. These data predict that inheritance of alleles that contribute to inefficient prefrontal information processing will increase risk for schizophrenia.

MeSH Terms
Adult Catechol O-Methyltransferase/genetics Cognition/physiology Cognition Disorders/diagnosis,genetics Cohort Studies Female Functional Laterality/genetics,physiology Genetic Predisposition to Disease/genetics Humans Magnetic Resonance Imaging/statistics & numerical data Male Memory/physiology Neuropsychological Tests Phenotype Polymorphism, Genetic Prefrontal Cortex/physiology Risk Factors Schizophrenia/diagnosis,genetics Schizophrenic Psychology Siblings
Chemicals
Catechol O-Methyltransferase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Callicott Joseph H
Clinical Brain Disorders Branch, IRP, NIMH, NIH, Bethesda, MD 20982-1389, USA. [email protected]
Egan Michael F
Mattay Venkata S
Bertolino Alessandro
Bone Ashley D
Verchinksi Beth
Weinberger Daniel R
Article Info
Journal
The American journal of psychiatry
Abbr.
Am J Psychiatry
ISSN
0002-953X
Published
2003-04-00
Pages
709-19
Language
English
Region
United States
NLM ID
0370512
Subset
IM
Corrections
ErratumIn
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