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Updated: May 18, 2026

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Published on: May 2, 2025
White matter pathology--an endophenotype for bipolar disorder?
Stefan Borgwardt1, Paolo Fusar-Poli
1Department of Psychiatry, University of Basel, Basel, Switzerland. stefan.borgwardt@kcl.ac.uk
White matter abnormalities may indicate a genetic risk for bipolar disorder (BD). These neuroimaging findings in high-risk individuals could serve as early markers for BD development and shared genetic factors.
Area of Science:
- Neuroscience
- Psychiatry
- Genetics
Background:
- Bipolar disorder (BD) poses significant challenges in early identification and intervention.
- Neuroimaging studies in individuals at genetic risk for BD offer a unique window into preclinical changes.
- Investigating white matter abnormalities can circumvent confounds of illness duration and medication history.
Purpose of the Study:
- To explore the role of white matter abnormalities as potential trait markers for genetic liability to bipolar disorder.
- To differentiate between trait and state markers of BD in individuals at high risk.
Main Methods:
- Neuroimaging techniques were employed to examine white matter integrity.
- Comparative analysis was conducted between subjects at high risk for BD (HR), individuals with BD, and control groups.
Main Results:
- Conflicting results exist in current literature regarding structural markers for BD genetic liability.
- White matter abnormalities were observed in HR subjects, suggesting potential genetically driven trait markers.
- Shared abnormalities between HR and BD groups indicate possible common genetic risk factors.
Conclusions:
- White matter alterations may serve as endophenotypes for bipolar disorder.
- These neurobiological markers bridge the gap between genetic susceptibility and clinical manifestation of BD.
- Distinguishing between trait and state markers is crucial for understanding BD pathogenesis.
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