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PMID: 9545997 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

MRI study of cavum septi pellucidi in schizophrenia, affective disorder, and schizotypal personality disorder.

The American journal of psychiatry ·Vol. 155 ·No. 4 ·1998-04-00 ·Pages 509-15

Kwon JS, Shenton ME, Hirayasu Y, Salisbury DF, Fischer IA, Dickey CC, Yurgelun-Todd D, Tohen M, Kikinis R, Jolesz FA, McCarley RW

Abstract

A cavum between the septi pellucidi may reflect neurodevelopmental anomalies in midline structures of the brain. The authors examined cavum septi pellucidi in subjects with schizophrenia, affective disorder, and schizotypal personality disorder and in normal subjects. Thirty schizophrenic patients (15 chronic, 15 first-episode), 16 patients with affective disorder (first-episode), 21 patients with schizotypal personality disorder, and 46 normal subjects were evaluated with magnetic resonance imaging. Cavum septi pellucidi was assessed by counting the number of 1.5-mm slices containing cavum septi pellucidi. The presence or absence of cavum septi pellucidi did not differentiate among groups. However, the prevalence of abnormal cavum septi pellucidi (i.e., cavum septi pellucidi contained on four or more slices) was 30.4% for schizophrenic patients (36.4% for chronic, 25.0% for first-episode), 20.0% for patients with affective disorder, 18.8% for patients with schizotypal personality disorder, and 10.3% for normal subjects. When the authors used the Nopoulos et al. criteria for rating cavum septi pellucidi, which omitted borderline cases with cavum septi pellucidi on three slices, the prevalence of abnormal cavum septi pellucidi increased to 35.0% for schizophrenia (40.0% for chronic, 30.0% for first-episode), 25.0% for affective disorder, 27.3% for schizotypal personality disorder, and 13.0% for normal subjects. There was a statistically significant difference in ratings between schizophrenic and normal subjects. The results suggest that alterations in midline structures during the course of neurodevelopment may play a role in the pathogenesis of schizophrenia.

MeSH Terms
Adult Chronic Disease Hippocampus/anatomy & histology Humans Magnetic Resonance Imaging Male Middle Aged Mood Disorders/diagnosis,pathology Psychiatric Status Rating Scales/statistics & numerical data Schizophrenia/diagnosis,etiology,pathology Schizotypal Personality Disorder/diagnosis,pathology Septum Pellucidum/abnormalities,pathology Temporal Lobe/anatomy & histology
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Kwon J S
Department of Psychiatry (116A), VA Medical Center-Brockton/West Roxbury, Harvard Medical School, MA, USA.
Shenton M E
Hirayasu Y
Salisbury D F
Fischer I A
Dickey C C
Yurgelun-Todd D
Tohen M
Kikinis R
Jolesz F A
McCarley R W
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Article Info
Journal
The American journal of psychiatry
Abbr.
Am J Psychiatry
ISSN
0002-953X
Published
1998-04-00
Pages
509-15
Language
English
Region
United States
NLM ID
0370512
PMCID
PMC2826366
Subset
IM
Grants
NIMH NIH HHS · R01 MH040799 · United States
NIMH NIH HHS · MH-40799 · United States
NIMH NIH HHS · MH-50747 · United States
NIMH NIH HHS · K05 MH070047 · United States
NIMH NIH HHS · R01 MH050740 · United States
NIMH NIH HHS · K02 MH001110-10 · United States
NIMH NIH HHS · MH-01110 · United States
NIMH NIH HHS · K05 MH070047-06 · United States
NIMH NIH HHS · R01 MH050740-14 · United States
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