Prevalence of large cavum septi pellucidi in ultra high-risk individuals and patients with psychotic disorders

Tsutomu Takahashi, Alison R. Yung, Murat Yücel, Stephen J. Wood, Lisa J. Phillips, Ian H. Harding, Bridget Soulsby, Patrick D. McGorry, Michio Suzuki, Dennis Velakoulis, Christos Pantelis

    Research output: Contribution to journalArticlepeer-review

    Abstract

    An increased prevalence of large cavum septum pellucidum (CSP), a marker of midline neurodevelopmental abnormality, has been reported in schizophrenia. However, not all studies have been able to replicate this finding and very few studies have been conducted in large samples. In the current study, magnetic resonance imaging was used to assess the presence of an abnormal CSP in 162 patients with first-episode psychosis (FEP), 89 patients with chronic schizophrenia, 135 ultra high-risk (UHR) individuals, and 87 controls. The prevalence of a large CSP (> 5.6 mm) did not differ between the groups (9.3% of the FEP patients, 11.2% of the chronic schizophrenia patients, 11.1% of the UHR individuals, and 11.5% of the controls). The length of the CSP was not associated with sulcal morphology of the anterior cingulate cortex (ACC), suggesting different biological processes responsible for the CSP enlargement versus ACC folding. These findings suggest that the CSP is not a neurodevelopmental marker of psychosis and cast doubt over the notion that it plays a major role in the neurobiology of psychosis. © 2008 Elsevier B.V. All rights reserved.
    Original languageEnglish
    Pages (from-to)236-244
    Number of pages8
    JournalSchizophrenia Research
    Volume105
    Issue number1-3
    DOIs
    Publication statusPublished - Oct 2008

    Keywords

    • Affective psychosis
    • Cavum septum pellucidum
    • High-risk
    • Magnetic resonance imaging
    • Neurodevelopment
    • Schizophrenia

    Fingerprint

    Dive into the research topics of 'Prevalence of large cavum septi pellucidi in ultra high-risk individuals and patients with psychotic disorders'. Together they form a unique fingerprint.

    Cite this