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Published on: November 21, 2013
Familial leukoencephalopathy in bipolar disorder
E P Ahearn1, D C Steffens, F Cassidy
1Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, N.C., USA.
Objective:
Imaging studies of patients with bipolar disorder demonstrate changes in deep white matter and subcortical gray nuclei that are seen as focal hyperintensities on T2-weighted magnetic resonance imaging (MRI). The objective of this study was to examine MRIs in a family with a strong history of bipolar disorder to look for possible MRI abnormalities in members with and without affective illness.
Method:
The authors obtained MRIs of 21 members of a family with a strong history of bipolar disorder. Eight of the family members studied had bipolar illness, one had symptoms of bipolar disorder but did not meet full DSM-III-R criteria, two had unipolar disorder, and 10 did not have bipolar disorder.
Results:
Fifteen of the 21 family members had MRI findings, including six of 10 family members who had no affective disorder and all of those with bipolar disorder. Lesions of both white matter and subcortical gray nuclei were found.
Conclusions:
Although the clinical significance of these MRI findings is unknown, the high prevalence of MRI findings in both affected and unaffected family members suggests that MRI findings may potentially serve as a biological marker for bipolar disorder. Recent genetic studies have established a link between familial leukoencephalopathy and chromosome 19. If leukoencephalopathy appears to be related to bipolar disorder, it may allow clearer characterization of the genetics of the disorder.
Insights
Magnetic resonance imaging (MRI) revealed abnormalities in deep white matter and subcortical gray nuclei in a family with a history of bipolar disorder. These findings may indicate a potential biological marker for the disorder.
Area of Science:
- Neuroimaging
- Genetics
- Psychiatry
Background:
- Bipolar disorder is associated with observable changes in deep white matter and subcortical gray nuclei.
- These changes are often detected as focal hyperintensities on T2-weighted magnetic resonance imaging (MRI).
- Understanding the genetic underpinnings of bipolar disorder is crucial for diagnosis and treatment.
Purpose of the Study:
- To investigate potential MRI abnormalities in family members with and without bipolar disorder.
- To examine a family with a strong genetic predisposition to bipolar disorder.
- To explore the relationship between MRI findings and affective illness within families.
Main Methods:
- Acquired MRI scans from 21 members of a single family with a significant history of bipolar disorder.
- Categorized family members based on diagnosed affective disorders, including bipolar disorder, unipolar disorder, and absence of illness.
- Analyzed MRI results for the presence of lesions in white matter and subcortical gray nuclei.
Main Results:
- MRI findings were present in 15 out of 21 family members.
- Abnormalities were detected in all family members with bipolar disorder.
- Notably, MRI findings were also observed in 60% of family members without affective disorder, indicating white matter and subcortical gray nuclei lesions.
Conclusions:
- The high prevalence of MRI findings in both affected and unaffected family members suggests a potential biological marker for bipolar disorder.
- Further research into the link between leukoencephalopathy, chromosome 19, and bipolar disorder may clarify the genetic basis of the illness.
- These MRI findings, while their clinical significance is yet unknown, could aid in characterizing the genetics of bipolar disorder.
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