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Corpus callosum development in childhood-onset schizophrenia
Audrey Keller1, Neal O Jeffries, Jonathan Blumenthal
1Child Psychiatry Branch, National Institute of Mental Health, Building 10, Room 3N 202, 10 Center Drive MSC 1600, Bethesda, MD 20892-1600, USA.
Childhood-onset schizophrenia (COS) patients show a declining splenial area, unlike healthy individuals. This brain difference in the corpus callosum may indicate later visual cortex changes in schizophrenia.
Area of Science:
- Neuroscience
- Developmental Psychology
- Psychiatry
Background:
- Schizophrenia is associated with corpus callosum (CC) abnormalities and altered interhemispheric communication.
- Childhood-onset schizophrenia (COS) represents a severe, continuous form of the disorder.
- Previous research indicates CC size differences between schizophrenia patients and controls.
Purpose of the Study:
- To examine corpus callosum area in childhood-onset schizophrenia (COS) at initial presentation and prospectively through adolescence.
- To investigate developmental trajectories of CC subregions in COS.
- To correlate CC development with other abnormalities in COS.
Main Methods:
- Acquired 113 MRI scans from 55 COS patients and 110 scans from 56 age/gender-matched healthy volunteers (ages 8-24).
- Obtained baseline and follow-up scans at ~2-year intervals.
- Calculated midsagittal areas of the total CC and seven subregions using automated software; analyzed data with mixed-effects models.
Main Results:
- No initial diagnostic differences in CC area were observed.
- Longitudinally, COS patients exhibited a different developmental trajectory for the splenium compared to controls.
- The splenial area significantly decreased in COS patients starting around age 22, even after adjusting for total brain volume.
Conclusions:
- Patients with schizophrenia demonstrate a divergent developmental trajectory for the splenial area, showing a decline in COS.
- This finding may suggest anticipated late-onset occipital and extrastriate alterations in brain regions affected by schizophrenia.
- Further replication is needed to confirm these developmental changes.
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