Reduced white matter integrity and verbal fluency impairment in young adults with bipolar disorder: a diffusion

Isabelle E Bauer1, Austin Ouyang2, Benson Mwangi1

  • 1University of Texas Health Science Center at Houston, Department of Psychiatry and Behavioral Sciences, 77054 Houston, TX, United States.

Abstract

Insights

Bipolar disorder (BD) is linked to white matter (WM) abnormalities, affecting cognitive functions like verbal fluency. Diffusion tensor imaging revealed specific WM alterations associated with these cognitive deficits in BD patients.

Area of Science:

  • Neuroimaging
  • Psychiatry
  • Cognitive Neuroscience

Background:

  • Bipolar disorder (BD) is clinically associated with white matter (WM) microstructural abnormalities.
  • The biological mechanisms underlying these WM changes and their impact on cognition remain unclear.

Purpose of the Study:

  • To investigate WM microstructural alterations in bipolar disorder patients using diffusion tensor imaging (DTI).
  • To explore the relationship between these WM abnormalities and cognitive functioning in BD.

Main Methods:

  • 49 adult BD patients and 28 healthy controls underwent DTI.
  • Tract-based spatial statistics (TBSS) analyzed WM coherence (fractional anisotropy - FA) and axonal integrity (mean, axial, radial diffusivity - MD, AD, RD).
  • Cognitive performance was assessed using the Brief Assessment of Cognition for Affective disorders (BAC-A).

Main Results:

  • BD patients showed poorer verbal fluency and altered FA, RD, and MD values in specific WM tracts, including the internal capsule and corpus callosum.
  • Increased FA in the left inferior fronto-occipital fasciculus (IFOF) and forceps minor correlated with better verbal fluency.
  • Altered RD in the corticospinal tract and forceps minor was linked to reduced visuomotor abilities.

Conclusions:

  • WM microstructural alterations (FA, RD, MD) and verbal fluency deficits may serve as neural and cognitive markers for BD.
  • Abnormal radial diffusivity (RD) suggests potential demyelination contributing to cognitive impairments in bipolar disorder.