van Veluw · Stroke 2022 · narrative review · n=?

Neuropathology of Vascular Brain Health: Insights From Ex Vivo Magnetic Resonance Imaging-Histopathology Studies in Cerebral Small Vessel Disease.

Cited 62 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

Narrative review summarizing ex vivo MRI-histopathology literature without systematic search methodology or original clinical data.

PubMed 35000425 · doi:10.1161/STROKEAHA.121.032608 · record verified 2026-08-30

What was done

This narrative review synthesized published research on ex vivo magnetic resonance imaging (MRI) and histopathological evaluation of postmortem human brain tissue in sporadic cerebral small vessel disease (SVD). It examined histopathologic substrates—principally cerebral amyloid angiopathy and arteriolosclerosis, alongside coexisting Alzheimer disease pathology—underlying macroscopic MRI-detectable parenchymal brain abnormalities, while evaluating the technical strengths and limitations of ex vivo imaging methods.

What was found

The abstract reports conceptual and methodological overviews without numerical data or statistical measures. It notes that while in vivo MRI detects gross parenchymal consequences of SVD, postmortem ex vivo MRI co-registered with histopathology allows direct visualization and localized characterization of underlying microvascular changes and secondary tissue injury.

Why it matters

Understanding the exact pathological correlates of neuroimaging markers improves the biological interpretation of MRI in vascular cognitive impairment and dementia research. Ex vivo MRI bridges the resolution gap between macroscopic in vivo neuroimaging and microscopic tissue pathology.

Limits

The paper is a non-systematic narrative review without quantitative synthesis, formal study quality assessment, or sample size reporting. The underlying methodologies rely on postmortem tissue, which is constrained by end-stage disease bias, postmortem interval artifacts, tissue fixation effects, and an inability to track active longitudinal dynamics in living humans.

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