Abstract

Small vessel disease, a disorder of cerebral microvessels, is an expanding epidemic and a common cause of stroke and dementia. Despite being almost ubiquitous in brain imaging, the clinicoradiologic association of small vessel disease is weak, and the underlying pathogenesis is poorly understood. The STandards for ReportIng Vascular changes on nEuroimaging (STRIVE) criteria have standardized the nomenclature. These include white matter hyperintensities of presumed vascular origin, recent small subcortical infarcts, lacunes of presumed vascular origin, prominent perivascular spaces, cerebral microbleeds, superficial siderosis, cortical microinfarcts, and brain atrophy. Recently, the rigid categories among cognitive impairment, vascular dementia, stroke, and small vessel disease have become outdated, with a greater emphasis on brain health. Conventional and advanced small vessel disease imaging markers allow a comprehensive assessment of global brain heath. In this review, we discuss the pathophysiology of small vessel disease neuroimaging nomenclature by means of the STRIVE criteria, clinical implications, the role of advanced imaging, and future directions.

Highlights

  • There is significant variation in the epidemiology of reported that parent artery atherosclerosis resulted in 20% of single Small vessel disease (SVD) markers, the prevalence of these markers is associated with

  • Studies have suggested that SVD may lead to loss of energy-dependent long-range white matter connections, which disrupt the structure of the network

  • Small vessel disease is a rising epidemic associated with detrimental brain health

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Summary

Microbleeds New markers cSS Cortical microinfarct

T2WI/FLAIR FLAIR/Fazekas scale (0–3): Periventricular WMH: 0 1⁄4 absent; 1 1⁄4 caps or pencil-thin; 2 1⁄4 smooth halo; 3 1⁄4 irregular extending to deep WM. The STRIVE guidelines define lacunes of presumed vascular origin as round or ovoid, subcortical, fluid-filled cavities (with signal similar to that of CSF in all sequences), measuring between 3 and 15 mm in diameter, consistent with a previous, small subcortical infarct or hemorrhage located in deep gray and white matter and in a territory of perforating arteriole (Fig 2B and Online Supplemental Data).

HA predominantly affects small perforating end arteries of the deep gray
Findings
CONCLUSIONS AND FUTURE DIRECTIONS

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