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Similar grey matter abnormalities in 22q11.2DS and chronic schizophrenia: a voxel-based morphometry study
Marianna Frascarelli1, Tommaso Accinni1, Antonino Buzzanca1
1Department of Human Neurosciences, Sapienza University of Rome, Italy.
Individuals with 22q11.2 Deletion Syndrome (22q11.2DS) and schizophrenia share common grey matter loss in the left medial frontal gyrus. This finding highlights 22q11.2DS as a model for studying schizophrenia neuroanatomy.
Area of Science:
- Neuroscience
- Genetics
- Psychiatry
Background:
- 22q11.2 Deletion Syndrome (22q11.2DS) is a key genetic model for schizophrenia research.
- Investigating neuroanatomical differences in 22q11.2DS is crucial for understanding schizophrenia.
- Comparing 22q11.2DS, chronic schizophrenia, and healthy controls provides valuable insights.
Purpose of the Study:
- To compare neuroanatomical characteristics in 22q11.2DS and schizophrenia.
- To identify shared brain structural abnormalities between 22q11.2DS and schizophrenia.
- To utilize 22q11.2DS as a biological model for studying schizophrenia.
Main Methods:
- Voxel-Based Morphometry (VBM) was used to analyze grey matter volumes.
- The study included individuals with chronic schizophrenia (SCZ>10), recent-onset schizophrenia (SCZ≤10), 22q11.2DS patients (DEL), and healthy controls (HCs).
- Global intelligence (IQ) was assessed for all participants.
Main Results:
- A significant reduction in grey matter volume was observed in the left medial frontal gyrus in both schizophrenia patients and 22q11.2DS patients compared to controls.
- The 22q11.2DS group showed distinct grey matter differences in the right lingual gyrus compared to the chronic schizophrenia group.
- Grey matter abnormalities were extensive in the 22q11.2DS group.
Conclusions:
- A common area of grey matter loss in the left medial frontal gyrus exists between idiopathic schizophrenia and 22q11.2DS.
- This finding supports the utility of 22q11.2DS as a neurobiological model for schizophrenia.
- Further research with larger samples is warranted to confirm these neuroanatomical findings.
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