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Volume 53, Issue 1, Pages 12-24 (1 January 2003)


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Prefrontal–posterior parietal networks in schizophrenia: primary dysfunctions and secondary compensations

Javier QuintanaCorresponding Author Informationab, Tiffany Wongb, Elena Ortiz-Portillob, Edward Kovalika, Tom Davidsona, Stephen R Marderab, John C Mazziottacdef

Received 8 October 2001; received in revised form 16 April 2002; accepted 22 April 2002.

Abstract 

Background

Working memory (WM) deficits are well known in schizophrenia and have been associated with abnormal activation patterns of the prefrontal cortex (PFC) during cognitive performance. The magnitude and particularly the direction of the PFC activation— i.e., increased (hyperfrontality) or decreased (hypofrontality)— in schizophrenia, as well as its pathophysiological implications, remain controversial. Working memory is supported by a distributed neural network, whose main components are the PFC and the posterior parietal (PPC) cortices. Monkey studies indicate that, during WM performance, PFC functional lesions may be compensated by the PPC if task demands center mainly on anticipating responses, but not if they center on remembering cues. We hypothesized that a primarily dysfunctional PFC in schizophrenia might show hypofrontality or hyperfrontality as a result, respectively, of efficient or inefficient PPC compensation, as dictated by task demands. To test our proposition, we biased the demands of WM tasks toward anticipating responses or remembering cues and measured its impact on the PFC–PPC functional balance in a group of schizophrenic patients and one of normal control subjects.

Methods

We used functional magnetic resonance imaging to measure correlates of neuronal activity in the PFC and PPC of schizophrenic patients and control subjects performing WM tasks that either demanded information retention or allowed for response anticipation.

Results

When compared to control subjects, schizophrenic patients exhibited decreased PFC activation and increased PPC activation during anticipatory WM performance, and increased PFC activation during mnemonic WM performance.

Conclusions

In schizophrenia, a PFC dysfunction results in hypo- or hyperfrontality as a function of whether other alternate areas of a PFC–PPC network for WM are available and efficacious in supporting specific task demands.

a West Los Angeles Department of Veterans Affairs Health Care Center (JQ, EK, TD, SRM), Los Angeles, California, USA

b Department of Psychiatry (JQ, TW, EO-P, SRM), School of Medicine, University of California at Los Angeles, Los Angeles, California, USA

c Department of Neurology (JCM), School of Medicine, University of California at Los Angeles Los Angeles, California, USA

d Department of Radiology (JCM), School of Medicine, University of California at Los Angeles, Los Angeles, California, USA

e Department of Pharmacology (JCM), School of Medicine, University of California at Los Angeles Los Angeles, California, USA

f Brain Mapping Center (JCM), University of California at Los Angeles, School of Medicine, Los Angeles, California, USA

Corresponding Author InformationAddress reprint requests to Javier Quintana, M.D., Ph.D., UCLA Neuropsychiatric Institute and Hospital, 760 Westwood Plaza, Room C8-846, Los Angeles CA 90024-1759, USA.

PII: S0006-3223(02)01435-X


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