Cerebral perfusion features linking subclinical cardiac and aortic dysfunction to vascular brain injury.

Publication Type Academic Article
Authors Zhang Y, Hughes T, Zhang W, Glodzik L, Dolui S, Goulart T, Nation D, Mahar A, Norling A, Lipsitz L, Mittleman M, Ma Y
Journal Alzheimers Dement
Volume 22
Issue 8
Pagination e71756
Date Published 08/01/2026
ISSN 1552-5279
Keywords Cerebrovascular Circulation
Abstract INTRODUCTION: Subclinical cardiovascular remodeling may impair cerebral hemodynamics and contribute to dementia, but the perfusion features linking subclinical cardiovascular dysfunction to cerebrovascular injury remain unclear. METHODS: We studied 1748 UK Biobank participants with cardiac magnetic resonance imaging (MRI), arterial spin labeling (ASL) MRI, and structural brain MRI. Six cardiac MRI biomarkers were analyzed individually and as a composite score. Cerebral perfusion was assessed by cerebral blood flow (CBF) and arterial transit time (ATT). RESULTS: Greater subclinical cardiac and aortic dysfunction was associated with lower CBF and prolonged ATT. Participants with low CBF and prolonged ATT had the greatest white matter hyperintensity (WMH) burden, equivalent to 5.5 years of age-related accumulation. CBF and ATT jointly mediated 53% of the association between subclinical cardiac and aortic dysfunction and WMH burden. DISCUSSION: Impaired cerebral perfusion, captured by lower perfusion volume and delayed perfusion timing, may be a mechanism linking subclinical cardiovascular dysfunction to brain vascular injury.
DOI 10.1002/alz.71756
PubMed ID 42625496
PubMed Central ID PMC13494673
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