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Neurostructural Differences Associated With Prodromal Mania Symptoms in Children
Camille Archer1, Amy Milewski1, Hee Jung Jeong2
1Department of Psychology, Vanderbilt University, Nashville, Tennessee, USA.
Insights
Children with early mania symptoms show reduced gray matter volume, indicating smaller overall brain size. These brain structure differences may help identify youth at risk for bipolar disorder.
Area of Science:
- Neuroscience
- Child Psychiatry
- Developmental Psychology
Background:
- Prodromal mania symptoms in children predict future bipolar disorder.
- Neurostructural correlates of early mania symptoms are not well understood.
Purpose of the Study:
- Investigate the association between prodromal mania symptoms and brain structure in a large pediatric cohort.
- Examine concurrent and longitudinal associations between mania symptoms and gray matter volume.
Main Methods:
- Analyzed data from 10,662 children (9-10 years old) from the Adolescent Brain Cognitive Development (ABCD) Study.
- Utilized structural equation modeling to assess brain structure and mania symptoms.
- Controlled for age, sex, socioeconomic status, and medication use.
Main Results:
- Baseline mania symptoms correlated with reduced gray matter volume in cortical and subcortical areas (global effect).
- The association between mania symptoms and gray matter volume was linked to smaller overall brain size.
- Brain volume at baseline did not predict future mania symptoms at follow-up.
Conclusions:
- Findings support structural differences seen in adults with bipolar disorder.
- Refines understanding of neurostructural links to childhood prodromal mania.
- Potential to improve early identification and intervention for at-risk youth.
Introduction:
Prodromal symptoms of mania in children are predictive of the later development of bipolar disorder; yet, the neurostructural correlates of these early symptoms remain poorly understood. This study aimed to investigate the association between prodromal mania symptoms and brain structure in a large cohort of children.
Methods:
We analyzed data from 10,662 nine- to 10-year-old children from the Adolescent Brain Cognitive Development (ABCD) Study, employing structural equation modeling to examine the concurrent and longitudinal associations between prodromal mania symptoms and cortical and subcortical gray matter volume.
Results:
After adjusting for multiple comparisons and controlling for age, sex, scanner model, socioeconomic status, and medication use, we found that baseline mania symptoms were associated with reduced gray matter volume across both cortical and subcortical areas, suggesting a global effect. These findings were further supported by the loss of these effects when total intracranial volume was included as an additional covariate, suggesting that smaller overall brain size, rather than specific regional effects, is related to prodromal mania symptoms. Lastly, longitudinal analyses revealed that brain volume at baseline did not predict prodromal mania symptoms at the second-year follow-up.
Conclusion:
Our results support the structural differences observed in adults with bipolar disorder in prior work and refine our understanding of the neurostructural correlates of prodromal mania symptoms in children. These findings could enhance early identification and intervention efforts for youth at risk of developing bipolar disorder.
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