Background
Dilated perivascular spaces (PVS) in the brain are associated with greater arterial pulsatility. We hypothesized that PVS identify individuals at higher risk of systemic and cerebral vascular events.
Methods
Stroke-free participants in the population-based Northern Manhattan Study had brain MRI performed, and were followed for myocardial infarction, any stroke, and death. Imaging analyses distinguished PVS from lesions presumably ischemic (LPI). PVS were further subdivided into lesions with diameter of ≤ 3 mm (small PVS) and > 3 mm (large PVS). We calculated relative rates of events with Poisson models, and hazard ratios (HR) with Cox proportional models.
Results
NOMAS participants who had MRI data available for review (n=1228; 59% women, 65% Hispanic, mean age 71 ± 9 years) were followed for an average of 9 ± 2 years. Participants in the highest tertile of the small PVS score had higher relative rate of all death (1.38, 1.01–1.91), vascular death (1.87, 1.12–3.14), myocardial infarction (2.08, 1.01–4.31), any stroke (1.79, 1.03–3.11), and any vascular event (1.74, 1.18–2.56). After adjusting for confounders there was a higher risk of vascular death (HR 1.06, 1.01–1.11), myocardial infarction (HR 2.22, 1.12–4.42), and any vascular events (HR 1.04, 1.01–1.08) with a higher small PVS scores.
Conclusions
In this multi-ethnic, population-based study, participants with a high burden of SPVS had increased risk of vascular events. By gaining pathophysiological insight into the mechanism of PVS dilatation, we may be able to propose novel therapies to better prevent vascular disorders in the population.