 |
 |

Regional Specificity in the Neuropathologic Substrates of Schizophrenia
A Morphometric Analysis of Broca's Area 44 and Area 9
Lynn D. Selemon, PhD;
Jasna Mrzljak, MD;
Joel E. Kleinman, MD, PhD;
Mary M. Herman, MD;
Patricia S. Goldman-Rakic, PhD
Arch Gen Psychiatry. 2003;60:69-77.
Background Numerous recent studies of postmortem schizophrenic brains have reported the presence of structural abnormalities in the dorsolateral prefrontal cortex (dlPFC) that are consistent with a reduction of neuropil. Ventrolateral prefrontal areas have been studied less extensively, and therefore it is not clear whether these cortices exhibit pathologic abnormalities of the same type and magnitude. Because thought disturbances in schizophrenic patients involve language processing, we have performed a morphometric analysis of Broca's area in the ventral frontal lobe.
Methods Neuronal and glial density and somal size were assessed via stereologic cell counting in postmortem samples of Broca's area 44 in 9 schizophrenic patients and 14 normal controls. Cell density was reexamined in dorsolateral prefrontal area 9 as an internal control.
Results We did not detect abnormalities in overall or laminar neuronal density, glial density, cortical thickness, or somal size in area 44 of schizophrenic patients. In contrast, neuronal density in area 9 exhibited a 12% increase in the schizophrenic cohort, replicating previous findings. In addition, there was a significant effect of disease on laminar neuronal density in area 9, with neuronal density tending to be higher (7%-29%) in all layers.
Conclusions The absence of significant cytoarchitectonic abnormalities in Broca's area in the same brains in which the dlPFC exhibited an increase in neuronal density suggests that the neuropil deficit is a regionally specific pathologic finding in schizophrenia and indicates that the dlPFC is a particularly vulnerable target of the disease process.
From the Department of Neurobiology, Yale University School of Medicine, New Haven, Conn (Drs Selemon, Mrzljak, and Goldman-Rakic); and Clinical Brain Disorders Branch, National Institute of Mental Health, Intramural Research Program, National Institutes of Health, Bethesda, Md (Drs Kleinman and Herman).
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES
 |
Lifespan Alterations of Basal Dendritic Trees of Pyramidal Neurons in the Human Prefrontal Cortex: A Layer-Specific Pattern
Petanjek et al.
Cereb Cortex 2008;18:915-929.
ABSTRACT
| FULL TEXT
Disturbed Structural Connectivity in Schizophrenia Primary Factor in Pathology or Epiphenomenon?
Konrad and Winterer
Schizophr Bull 2008;34:72-92.
ABSTRACT
| FULL TEXT
Dysfunctional and Compensatory Prefrontal Cortical Systems, Genes and the Pathogenesis of Schizophrenia
Tan et al.
Cereb Cortex 2007;17:i171-i181.
ABSTRACT
| FULL TEXT
The Consortium on the Genetics of Schizophrenia: Neurocognitive Endophenotypes
Gur et al.
Schizophr Bull 2007;33:49-68.
ABSTRACT
| FULL TEXT
Dysfunctional Prefrontal Regional Specialization and Compensation in Schizophrenia
Tan et al.
Am. J. Psychiatry 2006;163:1969-1977.
ABSTRACT
| FULL TEXT
Anomalies of asymmetry of pyramidal cell density and structure in dorsolateral prefrontal cortex in schizophrenia
CULLEN et al.
Br. J. Psychiatry 2006;188:26-31.
ABSTRACT
| FULL TEXT
fMRI Study of Maintenance and Manipulation Processes Within Working Memory in First-Episode Schizophrenia
Tan et al.
Am. J. Psychiatry 2005;162:1849-1858.
ABSTRACT
| FULL TEXT
Mapping Cortical Thickness and Gray Matter Concentration in First Episode Schizophrenia
Narr et al.
Cereb Cortex 2005;15:708-719.
ABSTRACT
| FULL TEXT
|