Disease progression in bipolar disorder in relation to white matter microstructure: A comprehensive approach based on staging models

• Published in: European Psychiatry
• Main Authors: Katharina Thiel, Kira Flinkenflügel, Dominik Grotegerd, Christoph Jurischka, Julia Hubbert, Tim Hahn, Elisabeth J. Leehr, Hannah Meinert, Elisabeth Schrammen, Florian Thomas-Odenthal, Paula Usemann, Lea Teutenberg, Benjamin Straube, Nina Alexander, Hamidreza Jamalabadi, Andreas Jansen, Frederike Stein, Michael Bauer, Andrea Pfennig, Eva Mennigen, Philipp Kanske, Katharina Förster, Igor Nenadić, Tilo Kircher, Susanne Meinert, Udo Dannlowski
• Format: Article
• Language: English
• Published: Cambridge University Press 2025-01-01
• Subjects: bipolar disorder; diffusion tensor imaging; neuroprogression; staging; white matter microstructure
• Online Access: https://www.cambridge.org/core/product/identifier/S0924933825101053/type/journal_article
• ISSN: 0924-9338; 1778-3585

Abstract Background Bipolar disorder (BD) is assumed to follow a progressive course, conceptualized through staging models. It is unclear whether white matter (WM) microstructure abnormalities, central to BD pathophysiology, parallel this development throughout disease progression. This study explored the link between WM and disease progression in BD, using a comprehensive approach based on clinical staging models. Methods This cross-sectional diffusion tensor-imaging study included 153 BD patients and 153 healthy controls (HCs) matched for age, sex, and study site. Using tract-based spatial statistics (TBSS), we examined associations between WM integrity and three criteria: (1) number of manic episodes, (2) remission quality between episodes, and (3) inter-episode global functioning. Results Analyses revealed significant fractional anisotropy (FA) differences between early and late stages of BD based on the number of manic episodes (p tfce-FWE = 0.003), but not on remission quality (p tfce-FWE = 0.075). However, compared to HC, BD patients with persistent symptoms between episodes showed more widespread FA differences (p tfce-FWE < 0.001) than those with stable remission (p tfce-FWE = 0.031). Regression analyses indicated a positive association between global functioning and FA in euthymic BD patients (ptfce-FWE < 0.001). Conclusions Results indicated more severe WM disruptions in patients at advanced stages compared to earlier stages of the disease. While these findings may imply changes occurring with disease progression, the cross-sectional design cannot rule out that they instead reflect stable clinical subtypes of varying severity. The results highlight the clinical relevance of WM alterations and the need for longitudinal studies to better understand the neurobiology and complexity of BD.