Brain white matter extracellular free-water increases are related to reduced neurocognitive function in systemic

Xing Qian1, Fang Ji1, Kwun Kei Ng1

  • 1Centre for Sleep and Cognition.

Abstract

Insights

Systemic lupus erythematosus (SLE) patients show increased brain white matter free water (FW), linked to poorer sustained attention. This suggests neuroinflammation or microvascular issues, potentially influenced by glucocorticoid use.

Area of Science:

  • Neuroimaging
  • Rheumatology
  • Neurology

Background:

  • Systemic lupus erythematosus (SLE) is associated with brain white matter (WM) microstructural changes.
  • Conventional diffusion MRI struggles to distinguish tissue alterations from free water (FW) changes in SLE.
  • Understanding WM changes is crucial for assessing neurocognitive deficits in SLE.

Purpose of the Study:

  • To differentiate WM tissue microstructure changes from extracellular FW volume in SLE patients.
  • To investigate the relationship between WM FW changes and neurocognitive function in SLE.
  • To explore potential underlying mechanisms like neuroinflammation and microvascular disruption.

Main Methods:

  • Cross-sectional study comparing 20 SLE patients and 61 healthy controls (HCs).
  • Diffusion MRI with a Free Water imaging (FWI) method to assess WM microstructure and FW volume.
  • Computerized neuropsychological assessments to evaluate neurocognitive performance, particularly sustained attention.

Main Results:

  • SLE patients exhibited significantly higher WM extracellular FW compared to HCs.
  • No significant differences were found in FW-corrected tissue microstructure or structural connectivity metrics between groups.
  • Increased WM extracellular FW in SLE patients correlated with poorer sustained attention and higher cumulative glucocorticoid dose.

Conclusions:

  • Elevated WM extracellular FW in SLE patients, even with inactive disease, may indicate microvascular degradation or neuroinflammation.
  • The findings highlight the potential impact of cumulative glucocorticoid therapy on WM FW.
  • FWI offers a valuable approach to characterize WM pathology in SLE and its neurocognitive consequences.