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Arterial Spin Labeling Hemodynamic Indices Relate to Cognitive and Small Vessel Disease Trajectories Over 11 Years

Sep 2026 · Stroke · 0 citations · 32 references
Medicine

TL;DR

ASL-sCoV may serve as an important hemodynamic measure for identifying perfusion deficits tied to SVD burden and progression and could provide substantial insight into the longitudinal clinical consequences of SVD.

Abstract

Background: Hemodynamic insufficiency may contribute to the development of neuroimaging signs of cerebral small vessel disease (SVD). The arterial spin-labeling (ASL) spatial coefficient of variation (ASL-sCoV) is a proxy marker of arterial transit time and may better capture SVD-related hemodynamic disturbances compared to ASL-derived cerebral blood flow (CBF). We investigated ASL-derived hemodynamic indices in relation to cognition and neuroimaging markers of SVD over an 11-year follow-up period. Methods: Participants without dementia or stroke were enrolled in the Vanderbilt Memory and Aging Project, a longitudinal observational cohort study in Nashville, TN. Participants underwent serial multimodal 3T brain magnetic resonance imaging to quantify SVD burden and neuropsychological assessment from 2012–2024 (4.9±3.5 years mean follow-up). Pseudo-continuous ASL assessed CBF and ASL-sCoV in total gray matter. Baseline ASL-sCoV and CBF were individually related to the cross-sectional burden and longitudinal trajectory of each SVD neuroimaging marker [white matter hyperintensities (WMHs), enlarged perivascular spaces (ePVS), cerebral microbleeds, and lacunar infarcts] and cognitive performances using linear and linear mixed effects regression models. Models were adjusted for demographics, cognitive status, Framingham Stroke Risk Profile (minus age), apolipoprotein E-ε4 status, intracranial volume (for SVD outcomes), and follow-up time (for longitudinal models). Results: Among participants (n=667, 68±9 years, 18% mild cognitive impairment, 51% female), higher ASL-sCoV was cross-sectionally associated with SVD markers, including WMHs and ePVS (pFDR-values<0.006). Higher baseline ASL-sCoV was associated with a faster longitudinal increase in the burden of WMHs (pFDR=0.03) and accelerated decline in executive function, information processing, language, and visuospatial performances (p-values<0.05). Gray matter CBF was not associated with SVD burden or cognition cross-sectionally (pFDR-values>0.05) or longitudinally (pFDR-values>0.06). Conclusions: ASL-sCoV may serve as an important hemodynamic measure for identifying perfusion deficits tied to SVD burden and progression. Readily derived from existing ASL datasets, ASL-sCoV could provide substantial insight into the longitudinal clinical consequences of SVD.

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