Regional neural dysfunctions in chronic schizophrenia studied with positron emission tomography.

 

Authors

Kim JJ. Mohamed S. Andreasen NC. O'Leary DS. Watkins GL. Boles
Ponto LL. Hichwa RD.
 
Institution
Mental Health Clinical Research Center, Department of Psychiatry, University of Iowa Hospital, College of Medicine, Iowa City, USA.
 
Title
Regional neural dysfunctions in chronic schizophrenia studied with positron emission tomography.

Source

American Journal of Psychiatry. 157(4):542-8, 2000 Apr.
 
Abstract
OBJECTIVE: Whether chronicity of illness produces progressive neural
abnormality is an important question in current schizophrenia research.
Positron emission tomography (PET) offers an opportunity to visualize and
measure blood flow in vivo to address this issue. The authors previously
compared healthy volunteers with neuroleptic-naive patients experiencing
their first episode of schizophrenia and reported that abnormalities in blood
flow, including lower flow in prefrontal regions and higher flow in the
thalamus and cerebellum, are present at the early stage of schizophrenic
illness. The goal of the present study was to measure blood flow with PET in
patients with chronic schizophrenia. METHOD: PET was used to examine regional
cerebral blood flow (rCBF) in 30 patients with chronic schizophrenia and 30
normal comparison subjects. To determine if the patterns of flow abnormality
in the patients with chronic schizophrenia were similar to those of patients
experiencing their first episode of schizophrenia, the same cognitive
condition was examined as in the earlier study. The patients with chronic
schizophrenia in the current study had been neuroleptic-free for at least 3
weeks. RESULTS: As in the authors' previous study, the chronically ill
patients showed lower flow in prefrontal areas and higher flow in thalamic
and cerebellar regions than normal comparison subjects, suggesting that a
similar neural dysfunction occurs in both first-episode and chronic
schizophrenia. CONCLUSIONS: rCBF abnormalities in patients with chronic
schizophrenia are not due to chronicity of illness or the effects of
medication. These results provide evidence that the primary neural
abnormalities in schizophrenia may occur in cortical, cerebellar, and
thalamic regions and that the dysfunction in these regions may explain the
"loosening of associations" that Bleuler considered to be the fundamental
cognitive phenotype of schizophrenia. These abnormalities can be
reconceptualized as "cognitive dysmetria."

 

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