Microstructural Bias in the Assessment of Periventricular Flow as Revealed in Postmortem Brains

Sihui Li1, Ruike Chen1, Zuozhen Cao1

  • 1Key Laboratory for Biomedical Engineering of Ministry of Education, Department of Biomedical Engineering, College of Biomedical Engineering & Instrument Science, Zhejiang University, 38 Zheda Rd, Hangzhou, China.

Radiology
|September 16, 2025
PubMed

Insights

Diffusion tensor imaging analysis along the perivascular space (DTI-ALPS) may be influenced by brain microstructure. Correcting for this bias reduced its correlation with Alzheimer disease markers in living individuals.

Area of Science:

  • Neuroimaging
  • Neurology
  • Biomedical Engineering

Background:

  • Diffusion tensor imaging analysis along the perivascular space (DTI-ALPS) is a proposed method for assessing global glymphatic activity.
  • The influence of fiber microstructure on DTI-ALPS measurements in neurologic diseases remains unclear.
  • Alzheimer disease (AD) is a neurodegenerative disorder characterized by amyloid-beta (Aβ) pathology.

Purpose of the Study:

  • To investigate the impact of fiber microstructure on DTI-ALPS in postmortem brains with and without AD.
  • To evaluate a corrected ALPS index in living participants to minimize microstructural bias.

Main Methods:

  • Postmortem human brains (Aβ-positive and Aβ-negative) underwent DTI-ALPS analysis.
  • Microstructural asymmetries were compared between pathologic groups and correlated with age.
  • A corrected ALPS index was applied to in vivo data from the Alzheimer's Disease Neuroimaging Initiative (ADNI) and compared among diagnostic groups.

Main Results:

  • Microstructural asymmetry of projection fibers was higher in Aβ-negative than Aβ-positive postmortem brains.
  • Association fiber asymmetry correlated negatively with age in postmortem samples.
  • In ADNI data, the corrected ALPS showed reduced correlation with cognitive scores and AD biomarkers compared to uncorrected ALPS.

Conclusions:

  • Microstructural asymmetry in DTI-ALPS is associated with Aβ pathology and age.
  • Minimizing microstructural bias in ALPS measurements may reduce its association with in vivo AD markers.
  • Further research is needed to refine DTI-ALPS for accurate glymphatic assessment in neurodegenerative diseases.