Mineralized brain vessels vary by region in Alzheimer disease
In an autopsy study of 265 decedents, vessel mineralization appeared in 58.3% of globus pallidus samples, 28.6% of posterior hippocampus samples, and 13.8% of putamen samples.
Neurobiology of Aging
In an autopsy study of 265 human decedents with Alzheimer disease neuropathology, researchers evaluated mineralized blood vessels across three brain areas. The team examined tissue from the posterior hippocampus, putamen, and globus pallidus collected across three Alzheimer's Disease Research Centers. After adjusting for demographic factors, vessel mineralization showed no association with sex, ethnicity, education, APOE ε4 status, or cerebral amyloid angiopathy. Mineralized vessels did associate with état criblé in the putamen and globus pallidus. Concomitant Lewy body disease was associated with reduced vessel mineralization in the posterior hippocampus and globus pallidus. A nominal link with a history of transient ischemic attacks did not remain significant after correction for multiple comparisons. These patterns identify vascular mineralization as a regionally selective cerebrovascular feature in Alzheimer disease.
Why it matters
Vascular mineralization represents a distinct, regionally selective facet of cerebrovascular aging that could influence vulnerability and pathological heterogeneity in neurodegenerative disease.
Caveats
The findings rely on an observational, postmortem cohort restricted to individuals with intermediate or high Alzheimer pathology, which limits conclusions about cause and effect during life.
The paper
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Louise Nicole C. Sevilla, Melanie N. Luu, Laurel A. Beckett, Lawrence S. Honig, Charles S DeCarli, David G. Coughlin, Andrew F. Teich, Dan Mungas, Lee‐Way Jin, Lorena García,University of California System · University of California Davis Medical Center
Neurobiology of Aging · 3 Sep 2026