Literature DB >> 8475214

A computerized magnetic resonance imaging study of corpus callosum morphology in schizophrenia.

P W Woodruff1, G D Pearlson, M J Geer, P E Barta, H D Chilcoat.   

Abstract

The hypothesis tested was that, in schizophrenia, corpus callosum size would be reduced, particularly in the region responsible for communication between both temporal lobes. This is supported by knowledge of: (a) anatomical homotopicity and functional specialization of fibres within the corpus callosum; (b) evidence linking structural and functional deficits of the corpus callosum and left temporal lobe with schizophrenia; and (c) that temporal lobe neuronal fibres pass through the middle region of the corpus callosum. Brain area and corpus callosum areas, widths and length were measured on mid-sagittal MRI scans using a computer outlining method. Scans from 30 schizophrenics and 44 normal subjects were compared. Mid-sagittal brain area, corpus callosum area, length and anterior widths were reduced in the schizophrenic group compared with controls. A significant area difference between schizophrenics and controls was seen in the mid-corpus callosum which communicates between the temporal lobes, including the superior temporal gyri. In schizophrenics, corpus callosum area reduction was not accounted for by brain area shrinkage alone. Differences between the two groups were accounted for by comparisons between males only. These findings support the hypothesis and the possibility that localized abnormalities of bilaterally connected brain regions might have secondary effects on their homotopically distributed fibres within the corpus callosum.

Entities:  

Mesh:

Year:  1993        PMID: 8475214     DOI: 10.1017/s0033291700038836

Source DB:  PubMed          Journal:  Psychol Med        ISSN: 0033-2917            Impact factor:   7.723


  19 in total

Review 1.  MRI anatomy of schizophrenia.

Authors:  R W McCarley; C G Wible; M Frumin; Y Hirayasu; J J Levitt; I A Fischer; M E Shenton
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2.  Neural activity in speech-sensitive auditory cortex during silence.

Authors:  M D Hunter; S B Eickhoff; T W R Miller; T F D Farrow; I D Wilkinson; P W R Woodruff
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3.  Corpus callosal area differences and gender dimorphism in neuroleptic-naïve, recent-onset schizophrenia and healthy control subjects.

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Review 4.  The relations between neuroscience and human behavioral science.

Authors:  F Strumwasser
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5.  A four-dimensional probabilistic atlas of the human brain.

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Journal:  J Am Med Inform Assoc       Date:  2001 Sep-Oct       Impact factor: 4.497

6.  Abnormalities of the corpus callosum in non-psychotic high-risk offspring of schizophrenia patients.

Authors:  Alan N Francis; Tejas S Bhojraj; Konasale M Prasad; Shreedhar Kulkarni; Debra M Montrose; Shaun M Eack; Matcheri S Keshavan
Journal:  Psychiatry Res       Date:  2010-12-09       Impact factor: 3.222

7.  Fronto-temporal dysfunction in schizophrenia: A selective review.

Authors:  John P John
Journal:  Indian J Psychiatry       Date:  2009 Jul-Sep       Impact factor: 1.759

8.  Anatomical characteristics of the corpus callosum and clinical correlates in schizophrenia.

Authors:  C Colombo; A Bonfanti; S Scarone
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1994       Impact factor: 5.270

9.  A longitudinal study of the corpus callosum in chronic schizophrenia.

Authors:  Serge A Mitelman; Yekaterina K Nikiforova; Emily L Canfield; Erin A Hazlett; Adam M Brickman; Lina Shihabuddin; Monte S Buchsbaum
Journal:  Schizophr Res       Date:  2009-08-26       Impact factor: 4.939

10.  Lack of normal gender differences of the perigenual cingulate gyrus in schizophrenia spectrum disorders. A magnetic resonance imaging study.

Authors:  Tsutomu Takahashi; Michio Suzuki; Shi-Yu Zhou; Hirofumi Hagino; Yasuhiro Kawasaki; Ikiko Yamashita; Shigeru Nohara; Kazue Nakamura; Hikaru Seto; Masayoshi Kurachi
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2004-10       Impact factor: 5.270

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