Association of MRI-Visible Perivascular Spaces With Longitudinal Cognitive Decline Over a Decade
Kyoko Kohno1,2, Yunyi Sun1,3, James D LeFevre1
1Vanderbilt Memory and Alzheimer's Center, Vanderbilt University School of Medicine, Nashville, TN.
Neurology
|April 24, 2026
Summary
Higher basal ganglia perivascular spaces (PVS) burden is linked to long-term cognitive decline, particularly in executive function and visuospatial skills. This finding highlights PVS as a key marker for age-related cognitive impairment.
Area of Science:
- Neurology
- Radiology
- Gerontology
Background:
- Cerebral small vessel disease (SVD) is a primary cause of vascular dementia.
- Perivascular spaces (PVS) visualized by MRI are an emerging SVD marker.
- Previous research indicated PVS's cross-sectional association with cognitive decline.
Purpose of the Study:
- To investigate the role of PVS as a unique marker of longitudinal cognitive decline.
- To assess the independent contribution of PVS to cognitive changes over time.
- To characterize the clinical relevance of PVS in aging.
Main Methods:
- Longitudinal observational study (Vanderbilt Memory and Aging Project) with 750 participants.
- 3T MRI at baseline to quantify SVD markers including PVS volume fraction.
- Deep learning algorithm used for PVS segmentation.
- Serial neuropsychological testing over an 11-year follow-up.
- Linear mixed-effects models used for statistical analysis, adjusting for covariates.
Main Results:
- Higher basal ganglia PVS burden was associated with worse longitudinal performance in multiple cognitive domains.
- Independent associations were observed for executive function and visuospatial skills (Hooper Visual Organization Test).
- PVS remained a significant predictor even when compared head-to-head with other SVD markers.
Conclusions:
- Basal ganglia PVS burden independently predicts longitudinal decline in executive function and visuospatial skills.
- PVS emerges as a significant marker for domain-specific cognitive decline in aging.
- Findings support PVS's role in vascular contributions to cognitive impairment over time.
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