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Case report: bipolar disorder as the first manifestation of CADASIL
Soyeon Park, Boram Park, Min Kyung Koh
1Department of Psychiatry, University of Ulsan College of Medicine, Asan Medical Center, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 136-736, Korea. jooyh@amc.seoul.kr.
Insights
This study reports a rare case of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) initially presenting as bipolar disorder. This highlights the importance of considering organic causes for late-onset mood changes.
Area of Science:
- Neurology
- Psychiatry
- Genetics
Background:
- Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) is a genetic cerebrovascular disorder.
- It typically manifests with migraines, strokes, cognitive decline, and mood disturbances.
Observation:
- A 53-year-old woman presented with late-onset mania and personality changes.
- Neuropsychological testing showed impaired attention and executive function, with cognitive rigidity.
- MRI findings were consistent with CADASIL, confirmed by NOTCH3 mutation testing.
Findings:
- This case represents the first documented instance of bipolar disorder as the initial presentation of CADASIL.
- Atypical antipsychotics were effective in managing manic symptoms and behavioral control.
Implications:
- Late-onset personality changes or chronic irritability warrant consideration of organic causes like CADASIL.
- Further research is needed to elucidate the relationship between cerebral lesions and psychiatric symptoms in CADASIL.
Background:
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited cerebrovascular disease, clinically characterized by variable manifestations of migraine, recurrent transient ischemic attack or lacunar strokes, cognitive decline, and mood disturbances. However, manic episodes have rarely been documented as an initial symptom of CADASIL and bipolar disorder presenting as the first manifestation in CADASIL has not been reported previously from evaluations by psychiatrists or psychological testing by psychologists.
Case Presentation:
A 53 year old woman developed symptoms of mania in her 50s leading to a personality change involving a continuously labile mood and irritability over a number of years. Neuropsychological testing revealed an intact memory, but impairment in attention and executive function. In the Rorschach test, she showed a high level of cognitive rigidity. Magnetic resonance imaging findings were very consistent with a diagnosis of CADASIL, which was confirmed by genetic testing for NOTCH3 mutations. Atypical antipsychotics proved to be helpful in treating her manic symptoms and for behavior control.
Conclusion:
We present a novel case of CADASIL that first presented as bipolar disorder. We contend that when patients show a late onset personality change or chronically irritable mood that deteriorates over many years, an organic cause such as CADASIL must be considered. Further studies are needed to better understand the exact impacts of cerebral tissue lesions and psychiatric symptoms in CADASIL patients.
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