White and gray matter alterations in bipolar I and bipolar II disorder subtypes compared with healthy controls

• Verfasst von: Thiel, Katharina [VerfasserIn]
• Verfasst von: Redlich, Ronny [VerfasserIn]
• Verfasst von: Witt, Stephanie [VerfasserIn]
• Titel: White and gray matter alterations in bipolar I and bipolar II disorder subtypes compared with healthy controls
• Titelzusatz: exploring associations with disease course and polygenic risk
• Verf.angabe: Katharina Thiel, Ronny Redlich, Stephanie Witt [und viele weitere]
• Jahr: 2024
• Umfang: 10 S.
• Illustrationen: Diagramme, Illustrationen
• Fussnoten: Online veröffentlicht: 8. Februar 2024
• Titel Quelle: Enthalten in: Neuropsychopharmacology
• Ort Quelle: London : Springer Nature, 1993
• Jahr Quelle: 2024
• Band/Heft Quelle: 49(2024), 5, Seite 814-823
• ISSN Quelle: 1740-634X
• DOI: doi:10.1038/s41386-024-01812-7
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Bipolar disorder
• Sach-SW: Diagnostic markers
• Sach-SW: Genetics research
• Sach-SW: Translational research
• K10plus-PPN: 1885011970

Abstract

Patients with bipolar disorder (BD) show alterations in both gray matter volume (GMV) and white matter (WM) integrity compared with healthy controls (HC). However, it remains unclear whether the phenotypically distinct BD subtypes (BD-I and BD-II) also exhibit brain structural differences. This study investigated GMV and WM differences between HC, BD-I, and BD-II, along with clinical and genetic associations. N = 73 BD-I, n = 63 BD-II patients and n = 136 matched HC were included. Using voxel-based morphometry and tract-based spatial statistics, main effects of group in GMV and fractional anisotropy (FA) were analyzed. Associations between clinical and genetic features and GMV or FA were calculated using regression models. For FA but not GMV, we found significant differences between groups. BD-I patients showed lower FA compared with BD-II patients (ptfce-FWE = 0.006), primarily in the anterior corpus callosum. Compared with HC, BD-I patients exhibited lower FA in widespread clusters (ptfce-FWE < 0.001), including almost all major projection, association, and commissural fiber tracts. BD-II patients also demonstrated lower FA compared with HC, although less pronounced (ptfce-FWE = 0.049). The results remained unchanged after controlling for clinical and genetic features, for which no independent associations with FA or GMV emerged. Our findings suggest that, at a neurobiological level, BD subtypes may reflect distinct degrees of disease expression, with increasing WM microstructure disruption from BD-II to BD-I. This differential magnitude of microstructural alterations was not clearly linked to clinical and genetic variables. These findings should be considered when discussing the classification of BD subtypes within the spectrum of affective disorders.