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White matter abnormalities in children with and at risk for bipolar disorder
Jean A Frazier1, Janis L Breeze, George Papadimitriou
1Department of Psychiatry, Harvard Medical School, Boston, USA. jfrazier@challiance.org
Insights
Children with bipolar disorder (BPD) show white matter (WM) abnormalities, specifically reduced fractional anisotropy (FA) in key brain tracts. These WM differences in the superior longitudinal fasciculus I (SLF I) may be a trait marker for BPD risk.
Area of Science:
- Neuroimaging
- Child Psychiatry
- Neuroscience
Background:
- White matter (WM) abnormalities may precede the onset of bipolar disorder (BPD) in children.
- Diffusion tensor magnetic resonance imaging (DT-MRI) is a key tool for assessing WM integrity.
Purpose of the Study:
- To investigate potential WM abnormalities in children with BPD compared to healthy controls (HC) and at-risk children (AR-BPD).
- To identify if observed WM differences represent trait-based markers or disease-state indicators in pediatric BPD.
Main Methods:
- DT-MRI scans were performed on children with BPD (n=10), HC (n=8), and AR-BPD (n=7).
- Fractional anisotropy (FA) values were compared between groups to identify significant differences (p < 0.05).
Main Results:
- Children with BPD exhibited reduced FA in bilateral superior longitudinal fasciculus I (SLF I) compared to HC.
- Reduced FA was also observed in the cingulate-paracingulate WM (CG-PAC(WM)) and corpus callosum in the BPD group.
- Both BPD and AR-BPD groups showed reduced FA in bilateral SLF I compared to HC.
Conclusions:
- Reduced FA in bilateral SLF I in both BPD and AR-BPD groups may indicate a trait-based marker or endophenotype for BPD.
- Decreased FA in the right and left CG-PAC(WM) in the BPD group compared to others may suggest a disease-state finding.
Objectives:
Diffusion tensor magnetic resonance imaging (DT-MRI) assesses the integrity of white matter (WM) tracts in the brain. Children with bipolar disorder (BPD) may have WM abnormalities that precede illness onset. To more fully examine this possibility, we scanned children with DSM-IV BPD and compared them to healthy peers and children at risk for BPD (AR-BPD), defined as having a first-degree relative with the disorder.
Methods:
Ten children with BPD, eight healthy controls (HC), and seven AR-BPD, similar in age, had MRI scans on a 1.5 Tesla GE scanner, including a standard DT-MRI sequence (T2-EPI) with 25 axial slices. Fractional anisotropy (FA) values were compared between groups to determine regions of significant difference (p < 0.05).
Results:
Compared to HC, children with BPD had decreased FA in right and left superior frontal tracts, including the superior longitudinal fasciculus I (SLF I) and the cingulate-paracingulate WM (CG-PAC(WM)). In addition, the BPD group had reduced FA in left orbital frontal WM and the right corpus callosum body. Compared to AR-BPD, children with BPD showed reduced FA in the right and left CG-PAC(WM). Both the BPD and AR-BPD groups showed reduced FA relative to HC in bilateral SLF I.
Conclusions:
The bilateral SLF I finding in both the BPD and AR-BPD groups may represent a trait-based marker or endophenotype of the disorder. The finding of decreased FA in the right and left CG-PAC(WM) in children with BPD compared to the other two groups may represent a disease-state related finding.
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