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Volume 53, Issue 1, Pages 25-38 (1 January 2003)


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Prefrontal cortex dysfunction mediates deficits in working memory and prepotent responding in schizophrenia

William M PerlsteinabcdCorresponding Author Information, Neha K Dixita, Cameron S Carterd, Douglas C Nolle, Jonathan D Cohenf

Received 2 May 2002; received in revised form 9 August 2002; accepted 22 August 2002.

Abstract 

Background

Schizophrenic patients show deficits in working memory (WM) and inhibition of prepotent responses. We examined brain activity while subjects performed tasks that placed demands on WM and overriding prepotent response tendencies, testing predictions that both processes engage overlapping prefrontal cortical (PFC) regions and that schizophrenic patients show reduced PFC activity and performance deficits reflecting both processes.

Methods

Functional magnetic resonance imaging data were acquired while 16 schizophrenic and 15 healthy subjects performed the N-Back task that varied WM load and a version of the AX-CPT that required overriding a prepotent response tendency.

Results

Both tasks engaged overlapping cortical networks (e.g., bilateral dorsolateral PFC, Broca’s area, parietal cortex). Increased WM load monotonically increased activity; preparation to override a prepotent response produced greater and more enduring activity. Group differences on each task emerged in a right dorsolateral PFC region: schizophrenic subjects showed lesser magnitude increases under conditions of high WM and prepotent response override demands, with concomitant performance impairments.

Conclusions

Schizophrenic patients exhibit PFC-mediated deficits in WM and preparation to override prepotent responses. Findings are consistent with the operation of a single underlying PFC-mediated cognitive control mechanism and with physiologic dysfunction of the dorsolateral PFC in schizophrenic patients reflecting impairments in this mechanism.

a Clinical and Health Psychology (WMP, NKD), Gainesville, Florida, USA

b Psychiatry (WMP), Gainesville, Florida, USA

c McKnight Brain Institute (WMP), University of Florida, Gainesville, Florida, USA

d Department of Psychiatry (WMP, CSC), University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA

e Department of Biomedical Engineering (DCN), University of Michigan, Ann Arbor, Michigan, USA

f Department of Psychology (JDC), Princeton University, Princeton, New Jersey, USA

Corresponding Author InformationAddress reprint requests to Dr. W.M. Perlstein, Department of Clinical and Health Psychology, HSC Box 100165, University of Florida, Gainesville FL 32610, USA.

PII: S0006-3223(02)01675-X


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