4.4 Article

Cortical gray and white matter volume in unmedicated schizotypal and schizophrenia patients

Journal

SCHIZOPHRENIA RESEARCH
Volume 101, Issue 1-3, Pages 111-123

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.schres.2007.12.472

Keywords

MRI; schizophrenia; schizotypal personality disorder; frontal lobe volume; temporal lobe volume; cingulate gyrus; negative symptoms; gray matter volume; white matter volume

Categories

Funding

  1. NCRR NIH HHS [M01-RR00071, M01 RR000071] Funding Source: Medline
  2. NIMH NIH HHS [MH073911, MH56489, R01 MH060023-05, R01 MH073911-02, R01 MH073911, R01 MH060023, MH56606, R01 MH056606-03, R01 MH065554, R01 MH056489-02, R01 MH040071-06A2, MH60023, MH40071] Funding Source: Medline

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Magnetic resonance imaging (MRI) studies have revealed fronto-temporal cortical gray matter volume reductions in schizophrenia. However, to date studies have not examined whether age- and sex-matched unmedicated schizotypal personality disorder (SPD) patients share some or all of the structural brain-imaging characteristics of schizophrenia patients. We examined cortical gray/white matter volumes in a large sample of unmedicated schizophrenia-spectrum patients (n = 79 SPD, n = 57 schizophrenia) and 148 healthy controls. MRI images were reoriented to standard position parallel to the anterior-posterior commissure line, segmented into gray and white matter tissue types, and assigned to Brodmann areas (BAs) using a postmortem-histological atlas. Group differences in regional volume of gray and white matter in the BAs were examined with MANOVA. Schizophrenia patients had significantly reduced gray matter volume widely across the cortex but more marked in frontal and temporal lobes. SPD patients had reductions in the same regions but only about half that observed in schizophrenia and sparing in key regions including BA10. In schizophrenia, greater fronto-temporal volume loss was associated with greater negative symptom severity and in SPD, greater interpersonal and cognitive impairment. Overall, our findings suggest that increased prefrontal volume in BA10 and sparing of volume loss in temporal cortex (BAs 22 and 20) may be a protective factor in SPD which reduces vulnerability to psychosis. Published by Elsevier B.V.

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