4.6 Article

Neuropathologic scales of cerebrovascular disease associated with diffusion changes on MRI

期刊

ACTA NEUROPATHOLOGICA
卷 144, 期 6, 页码 1117-1125

出版社

SPRINGER
DOI: 10.1007/s00401-022-02465-w

关键词

Cerebrovascular disease; Neuropathology; Imaging; Diffusion MRI

资金

  1. NIH [R01 NS097495, U01 AG06786, R01 AG56366, R01 AG054449, R01 AG075802, U19 AG069701, P50 AG16574, R37 AG11378, R01 AG41851]
  2. Gerald and Henrietta Rauenhorst Foundation
  3. Alzheimer's Drug Discovery Foundation (ADDF)
  4. Alexander Family Alzheimer's Disease Research Professorship of the Mayo Foundation
  5. Elsie and Marvin Dekelboum Family Foundation
  6. Schuler Foundation
  7. Opus building NIH Grant [C06 RR018898]
  8. Rochester Epidemiology Project [R01 AG34676]
  9. Liston Award

向作者/读者索取更多资源

This study evaluated the association between neuroimaging measures of cerebrovascular disease (CVD) and neuropathologic CVD scales, finding that dMRI could serve as a meaningful surrogate for CVD assessment and suggesting the development of better quantitative measures using dMRI.
Summarizing the multiplicity and heterogeneity of cerebrovascular disease (CVD) features into a single measure has been difficult in both neuropathology and imaging studies. The objective of this work was to evaluate the association between neuroimaging surrogates of CVD and two available neuropathologic CVD scales in those with both antemortem imaging CVD measures and postmortem CVD evaluation. Individuals in the Mayo Clinic Study of Aging with MRI scans within 5 years of death (N = 51) were included. Antemortem CVD measures were computed from diffusion MRI (dMRI), FLAIR, and T2* GRE imaging modalities and compared with postmortem neuropathologic findings using Kalaria and Strozyk Scales. Of all the neuroimaging measures, both regional and global dMRI measures were associated with Kalaria and Strozyk Scales (p < 0.05) and modestly correlated with global cognitive performance. The major conclusions from this study were: (i) microstructural white matter injury measurements using dMRI may be meaningful surrogates of neuropathologic CVD scales, because they aid in capturing diffuse (and early) changes to white matter and secondary neurodegeneration due to lesions; (ii) vacuolation in the corpus callosum may be associated with white matter changes measured on antemortem dMRI imaging; (iii) Alzheimer's disease neuropathologic change did not associate with neuropathologic CVD scales; and (iv) future work should be focused on developing better quantitative measures utilizing dMRI to optimally assess CVD-related neuropathologic changes.

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