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Midline Brain Abnormalities Across Psychotic and Mood Disorders
Ramón Landin-Romero, Benedikt L Amann1, Salvador Sarró2
1FIDMAG Germanes Hospitalàries Research Foundation, Barcelona, Spain; CIBERSAM, Madrid, Spain; benedikt.amann@gmail.com.
Patients with psychotic and mood disorders show higher rates of midline brain abnormalities, including cavum septum pellucidum and absent adhesio interthalamica. This suggests a potential shared neurodevelopmental origin for these conditions.
Area of Science:
- Neuroscience
- Psychiatry
- Neuroimaging
Background:
- Schizophrenia is associated with midline brain structure abnormalities.
- Cavum septum pellucidum (CSP) and absent adhesio interthalamica (AAI) are key midline abnormalities.
- Previous research has not extensively studied these abnormalities across multiple psychiatric diagnoses.
Purpose of the Study:
- To investigate the prevalence of CSP and AAI in a large, multidiagnostic patient sample.
- To compare the prevalence of these abnormalities between patients with various psychotic and mood disorders and healthy controls.
Main Methods:
- Assessed CSP and AAI in 639 patients with schizophrenia, delusional disorder, schizoaffective disorder, bipolar disorder, major depressive disorder, or first-episode psychosis/mania/depression.
- Compared findings with 223 healthy controls.
- Utilized logistic regression to calculate odds ratios (OR) for the presence of abnormalities.
Main Results:
- Patients with psychotic or mood disorders exhibited significantly increased prevalence of both CSP (OR=2.1) and AAI (OR=2.6).
- The combined presence of CSP and AAI was also significantly higher in patients (OR=3.8).
- These increased prevalences were observed across most studied disorders, even after controlling for confounding factors.
Conclusions:
- Midline brain abnormalities are generally more prevalent in patients with mood and psychotic disorders.
- The nonspecificity of these findings suggests a potential shared neurodevelopmental etiology underlying these diverse psychiatric conditions.
- Further research into neurodevelopmental factors is warranted to understand the shared pathophysiology.
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