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Does the Brain Matter? Cortical Alterations in Pediatric Bipolar Disorder: A Critical Review of Structural and
Mario Luciano1, Matteo Di Vincenzo1, Emiliana Mancuso1
1Department of Psychiatry, University of Campania "L. Vanvitelli", Naples, Italy.
Insights
Pediatric bipolar disorder (PBD) is linked to brain structure and function changes, including reduced gray matter and altered circuitry. These neuroimaging findings offer insights into PBD
Area of Science:
- Neuroscience
- Child and Adolescent Psychiatry
- Neuroimaging
Background:
- Pediatric bipolar disorder (PBD) causes significant psychosocial impairment, high service utilization, and frequent relapses.
- Neuroimaging offers a window into neurodevelopmental processes and potential biomarkers for PBD.
- Understanding brain correlates is crucial for targeted interventions.
Approach:
- Systematic review of neuroimaging studies on PBD in individuals aged 0-18 years.
- Searched PubMed, ISI Web of Knowledge, and PsychINFO databases.
- Included studies using structural/functional MRI comparing PBD patients with healthy controls.
Key Points:
- PBD patients exhibit structural alterations, including reduced gray matter and cortical thinning in frontal, parietal, and occipital regions.
- Functional neuroimaging shows altered frontolimbic engagement and frontostriatal hyperactivation.
- Brain connectivity studies suggest less efficient communication between cognitive and emotional regions in PBD.
Conclusions:
- Neuroimaging reveals distinct structural and functional brain abnormalities in pediatric bipolar disorder.
- These findings highlight the neurobiological underpinnings of PBD.
- Further research can inform the development of targeted, developmentally sensitive treatments.
Abstract:
Pediatric bipolar disorder (PBD) is associated with significant psychosocial impairment, high use of mental health services and a high number of relapses and hospitalization. Neuroimaging techniques provide the opportunity to study the neurodevelopmental processes underlying PBD, helping to identify the endophenotypic markers of illness and early biological markers of PBD. The aim of the study is to review available studies assessing structural and functional brain correlates associated with PBD. PubMed, ISI Web of Knowledge and PsychINFO databases have been searched. Studies were included if they enrolled patients aged 0-18 years with a main diagnosis of PBD according to ICD or DSM made by a mental health professional, adopted structural and/or functional magnetic resonance as the main neuroimaging method, were written in English and included a comparison with healthy subjects. Of the 400 identified articles, 46 papers were included. Patients with PBD present functional and anatomic alterations in structures normally affecting regulations and cognition. Structural neuroimaging revealed a significant reduction in gray matter, with cortical thinning in bilateral frontal, parietal and occipital cortices. Functional neuroimaging studies reported a reduced engagement of the frontolimbic and hyperactivation of the frontostriatal circuitry. Available studies on brain connectivity in PBD patients potentially indicate less efficient connections between regions involved in cognitive and emotional functions. A greater functional definition of alteration in brain functioning of PBD patients will be useful to set up a developmentally sensitive targeted pharmacological and nonpharmacological intervention.
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