Regional specificity in the neuropathologic substrates of schizophrenia - A morphometric analysis of Broca's area 44 and area 9.

被引:117
作者
Selemon, LD
Mrzljak, J
Kleinman, JE
Herman, MM
Goldman-Rakic, PS
机构
[1] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06510 USA
[2] NIMH, Clin Brain Disorders Branch, Intramural Res Program, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1001/archpsyc.60.1.69
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
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.
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页码:69 / 77
页数:9
相关论文
共 54 条
[1]   Lamina-specific alterations in the dopamine innervation of the prefrontal cortex in schizophrenic subjects [J].
Akil, M ;
Pierri, JN ;
Whitehead, RE ;
Edgar, CL ;
Mohila, C ;
Sampson, AR ;
Lewis, DA .
AMERICAN JOURNAL OF PSYCHIATRY, 1999, 156 (10) :1580-1589
[2]  
Amunts K, 1999, J COMP NEUROL, V412, P319, DOI 10.1002/(SICI)1096-9861(19990920)412:2<319::AID-CNE10>3.0.CO
[3]  
2-7
[4]   Cognitive dysmetria as an integrative theory of schizophrenia: A dysfunction in cortical subcortical-cerebellar circuitry? [J].
Andreasen, NC ;
Paradiso, S ;
O'Leary, DS .
SCHIZOPHRENIA BULLETIN, 1998, 24 (02) :203-218
[5]  
ANDREASEN NC, 1992, ARCH GEN PSYCHIAT, V49, P943
[6]  
Barch D. M., 1999, Society for Neuroscience Abstracts, V25, P1289
[7]  
BENES FM, 1991, ARCH GEN PSYCHIAT, V48, P996
[8]  
Bertolino A, 1996, AM J PSYCHIAT, V153, P1554
[9]  
Brodmann K, 1909, VERGLEICHENDE LOKALI
[10]   GLUCOSE METABOLIC-RATE IN NORMALS AND SCHIZOPHRENICS DURING THE CONTINUOUS PERFORMANCE-TEST ASSESSED BY POSITRON EMISSION TOMOGRAPHY [J].
BUCHSBAUM, MS ;
NUECHTERLEIN, KH ;
HAIER, RJ ;
WU, J ;
SICOTTE, N ;
HAZLETT, E ;
ASARNOW, R ;
POTKIN, S ;
GUICH, S .
BRITISH JOURNAL OF PSYCHIATRY, 1990, 156 :216-227