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White Matter Abnormalities in Bipolar II and Unipolar Depression - Evidence from Fixel-Based Analysis.
Idy W Y Chou1, Anna Manelis2, Holly A Swartz2
1Department of Psychiatry, The Chinese University of Hong Kong.
Bipolar II disorder (BD-II) and unipolar depression (UD) share white matter (WM) integrity deficits, but BD-II shows more widespread abnormalities. Illness duration and depressive episodes in BD-II correlate with specific WM changes, suggesting distinct neurobiological mechanisms.
Area of Science:
- Neuroimaging
- Psychiatry
- Neuroscience
Background:
- Diagnosing bipolar II disorder (BD-II) during depressive episodes is challenging, impacting clinical outcomes.
- A lack of BD-II-specific neuroimaging studies hinders understanding of its pathophysiology.
- This study investigates white matter (WM) integrity differences between BD-II and unipolar depression (UD).
Purpose of the Study:
- To compare WM integrity in individuals with BD-II, UD, and healthy controls (HC) using fixel-based analysis (FBA).
- To identify shared and distinct WM abnormalities between BD-II and UD.
- To explore the relationship between illness characteristics and WM alterations in BD-II.
Main Methods:
- Fixel-based analysis (FBA) was used to compare fibre density (FD), fibre cross-section (FC), and fibre density and cross-section (FDC) in 72 WM tracts.
- Participants included 33 individuals with BD-II, 50 with UD, and 51 HC.
- Sensitivity analyses examined unmedicated participants and the impact of medication status.
Main Results:
- Both BD-II and UD groups exhibited reduced FD in left parieto-occipito-pontine (POPT) and striato-occipital (ST-OCC) tracts.
- BD-II showed significantly lower FD than UD in the left arcuate fascicle (AF) and bilateral superior longitudinal fasciculi I and II (SLF-I and II).
- In BD-II, longer illness duration correlated with reduced FD, while more depressive episodes correlated with higher FDC.
Conclusions:
- Shared and distinct WM abnormalities exist in BD-II and UD, particularly in tracts relevant to visuomotor and executive functions.
- BD-II demonstrates more extensive WM alterations compared to UD.
- Findings suggest potential degenerative (illness duration) and compensatory (depressive episodes) neurobiological mechanisms in BD-II, warranting longitudinal investigation.
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