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Updated: Apr 24, 2026

Developing a Rat Model for Bipolar Disorder
Published on: May 2, 2025
Brain changes in early-onset bipolar and unipolar depressive disorders: a systematic review in children and
Gianluca Serafini1, Maurizio Pompili, Stefan Borgwardt
1Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), Section of Psychiatry, University of Genoa, IRCCS San Martino, Largo Rosanna Benzi 10, 16100, Genoa, Italy, gianluca.serafini@unige.it.
Insights
Pediatric bipolar disorder (BD) and unipolar disorder (UD) show distinct white matter (WM) and gray matter (GM) brain abnormalities. BD is linked to corpus callosum changes, while UD shows basal ganglia and hippocampus volume reductions.
Area of Science:
- Neuroscience
- Child and Adolescent Psychiatry
- Radiology
Background:
- Pediatric bipolar disorder (BD) and unipolar disorder (UD) share symptoms and functional deficits.
- Brain imaging studies investigate white matter (WM) and gray matter (GM) integrity in these disorders.
- It remains unclear if observed brain alterations are common markers or distinguishing features.
Purpose of the Study:
- To systematically review WM/GM changes in pediatric BD and UD.
- To determine if neuroimaging findings can differentiate between pediatric BD and UD.
- To synthesize current knowledge on neurodevelopmental differences in pediatric mood disorders.
Main Methods:
- Systematic literature search (1980-September 2013) for WM/GM changes in pediatric BD/UD.
- Inclusion of studies using diffusion tensor imaging (DTI) and voxel-based analysis.
- Review of 17 eligible articles from an initial 34 identified.
Main Results:
- Children and adolescents with BD showed more documented brain abnormalities than those with UD.
- Reduced basal ganglia and hippocampus volumes were more specific to pediatric UD.
- Reduced corpus callosum volume and increased deep WM hyperintensities were more specific to pediatric BD.
Conclusions:
- Pediatric BD and UD exhibit both shared and distinct WM and GM impairments.
- More WM abnormalities were reported in pediatric BD compared to UD, potentially due to fewer DTI studies in pediatric UD.
- Future longitudinal research is needed to explore diagnosis-specific neurodevelopmental changes.
Abstract:
Pediatric bipolar disorder (BD) and unipolar disorder (UD) share common symptomatic and functional impairments. Various brain imaging techniques have been used to investigate the integrity of brain white matter (WM) and gray matter (GM) in these disorders. Despite promising preliminary findings, it is still unclear whether these alterations may be considered as common trait markers or may be used to distinguish BD from UD. A systematic literature search of studies between 1980 and September 2013 which reported WM/GM changes in pediatric and adolescent BD/UD, as detected by diffusion tensor imaging and voxel-based analysis was conducted. Of the 34 articles judged as eligible, 17 fulfilled our inclusion criteria and were finally retained in this review. More abnormalities have been documented in the brains of children and adolescents with BD than UD. Reductions in the volume of basal ganglia and the hippocampus appeared more specific for pediatric UD, whereas reduced corpus callosum volume and increased rates of deep WM hyperintensities were more specific for pediatric BD. Seminal papers failed to address the possibility that the differences between unipolar and bipolar samples might be related to illness severity, medication status, comorbidity or diagnosis. UD and BD present both shared and distinctive impairments in the WM and GM compartments. More WM abnormalities have been reported in children and adolescents with bipolar disease than in those with unipolar disease, maybe as a result of a low number of DTI studies in pediatric UD. Future longitudinal studies should investigate whether neurodevelopmental changes are diagnosis-specific.
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