Volume 47, Issue 10 , Pages 1125-1132, October 2008
Global and Temporal Cortical Folding in Patients With Early-Onset Schizophrenia
Abstract
Objective
Adult-onset schizophrenia has repeatedly been associated with disturbances in the temporal lobes and alterations in cortical folding, which are thought to reflect neurodevelopmental impairment. Early-onset schizophrenia (EOS; onset before 18 years) is considered to involve even more pronounced neurodevelopmental deviance across a wide range of brain structural measures. We hypothesized that overall alteration of cortical folding also applies to EOS, and EOS involves prominent structural aberrations in superior temporal and collateral sulci.
Method
Magnetic resonance T1 images of 51 patients with EOS and 59 healthy participants were investigated. A fully automated method was applied to the images to extract, label, and measure the sulcus area in the whole cortex. Cortical folding was assessed by computing global sulcal indices (the ratio between total sulcal area and total outer cortex area) for each hemisphere and local sulcal indices (the ratio between the area of labeled sulcus and total outer cortex area in the corresponding hemisphere) for superior temporal and collateral sulci.
Results
Relative to healthy individuals, patients with EOS had significantly lower global sulcal indices in both hemispheres and a lower local sulcal index in the left collateral sulcus.
Conclusions
Reduced hemispheric sulcation appears to be a feature of schizophrenia, irrespective of age at onset. Structural aberration involving the left collateral sulcus may contribute to neurobiological substrate of EOS.
Key Words: adolescent development , cerebral cortex , magnetic resonance imaging , schizophrenia , temporal lobe
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This work was supported in part by a grant (PSYMARKER/APV05137LSA) from the National Agency for Research, France, and the study in the U.K. was supported by NARSAD. Dr. Penttilä received personal grants from the Finnish Cultural Foundation and the Sigrid Jusélius Foundation, Finland. Dr. Paillère-Martinot was supported by an AP-HP/INSERM Interface Research grant 2003. The authors acknowledge Professor André Syrota for support and the Association of European Psychiatrists (AEP), Neuroimaging Section.
PII: S0890-8567(08)60097-0
doi:10.1097/CHI.0b013e3181825aa7
© 2008 American Academy of Child and Adolescent Psychiatry. Published by Elsevier Inc. All rights reserved.
Volume 47, Issue 10 , Pages 1125-1132, October 2008
