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Published on: December 2, 2015
Psychosocial functioning in offspring of parents with bipolar disorder
Tolulope Bella1, Tina Goldstein, David Axelson
1Department of Psychiatry, Western Psychiatric Institute and Clinic, University of Pittsburgh Medical Center, Pittsburgh, PA, USA. bellatt2002@yahoo.com
Insights
Children with parents who have bipolar disorder show psychosocial functioning impairments. These issues are linked to parental functioning and the child's own psychopathology, not solely genetics.
Area of Science:
- Child and Adolescent Psychiatry
- Psychosocial Functioning
- Genetic Risk Factors
Background:
- Offspring of parents with bipolar disorder (BP) have an increased risk for psychopathology.
- Psychosocial functioning in these offspring is not well-understood.
Purpose of the Study:
- To compare the psychosocial functioning of children with parents with bipolar disorder, other psychopathology, or no psychopathology.
Main Methods:
- Utilized data from the Pittsburgh Bipolar Offspring Study (BIOS).
- Compared three groups: offspring of BP probands (n=388), other psychopathology probands (n=132), and healthy probands (n=118).
- Assessed psychosocial functioning using A-LIFE, CBCL, and CGAS.
Main Results:
- Offspring of BP probands showed impaired psychosocial functioning compared to offspring of healthy probands.
- These impairments were generally greater than in offspring of non-BP psychopathology probands.
- After adjusting for parental functioning and child's psychopathology, differences diminished.
Conclusions:
- Psychosocial impairments in offspring of BP parents are largely explained by parental functioning and the child's own psychopathology.
- Interventions targeting parental and child psychopathology may mitigate long-term functional impairment risks.
- Cross-sectional data limits causal inference.
Background:
Offspring of parents with bipolar disorder are at increased risk for a range of psychopathology, including bipolar disorder. It is not clear if they also have impairments in their psychosocial functioning.
Methods:
We compared the psychosocial functioning of three groups of children enrolled in the Pittsburgh Bipolar Offspring Study (BIOS): offspring of probands with bipolar disorder (n=388), offspring of probands with other types of psychopathology (n=132), and offspring of healthy probands (n=118). Psychosocial functioning was assessed at study intake using the schedule of the Adolescent Longitudinal Interval Follow-Up Evaluation (A-LIFE), the Child Behavior Check List (CBCL) and the Children's Global Assessment Scale (CGAS).
Results:
Offspring of probands with bipolar disorder exhibited impairments in various aspects of psychosocial functioning. On all measures, they had worse functioning in comparison with offspring of healthy probands. Offspring of probands with bipolar disorder generally exhibited more impairment than offspring of probands with nonbipolar psychopathology. After adjusting for proband parent functioning and the child's Axis I psychopathology, functioning of offspring of probands with bipolar disorder was similar to that of offspring of healthy probands.
Limitations:
Data are cross-sectional and therefore do not allow for causal conclusions about the association between parental psychopathology, child psychopathology and offspring psychosocial functioning.
Conclusions:
Offspring of parents with bipolar disorder exhibit impairments in psychosocial functioning which appear largely attributable to proband parent functional impairment and the child's own psychopathology. As such, interventions to improve parental functioning, as well as early interventions to treat the child's psychopathology may help reduce the risk for long-term functional impairment in offspring.
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