Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Dec 1:12:597799.
doi: 10.3389/fnagi.2020.597799. eCollection 2020.

New Insights in Addressing Cerebral Small Vessel Disease: Association With the Deep Medullary Veins

Affiliations

New Insights in Addressing Cerebral Small Vessel Disease: Association With the Deep Medullary Veins

Zhihua Xu et al. Front Aging Neurosci. .

Abstract

Objective: To assess the suitability of deep medullary vein visibility in susceptibility weighted imaging-magnetic resonance imaging studies as a method for the diagnosis and evaluation of cerebral small vessel disease progression.

Methods: A total of 92 patients with CSVD were enrolled and baseline clinical and imaging data were reviewed retrospectively. Neuroimaging biomarkers of CSVD including high-grade white matter hyperintensity (HWMH), cerebral microbleed (CMB), enlarged perivascular space (PVS), and lacunar infarct (LI) were identified and CSVD burden was calculated. Cases were grouped accordingly as mild, moderate, or severe. The DMV was divided into six segments according to the regional anatomy. The total DMV score (0-18) was calculated as the sum of the six individual segmental scores, which ranged from 0 to 3, for a semi-quantitative assessment of the DMV based on segmental continuity and visibility.

Results: The DMV score was independently associated with the presence of HWMH, PVS, and LI (P < 0.05), but not with presence and absence of CMB (P > 0.05). Correlation between the DMV score and the CSVD burden was significant (P < 0.05) [OR 95% C.I., 1.227 (1.096-1.388)].

Conclusion: The DMV score was associated with the presence and severity of CSVD.

Keywords: cerebral microbleed; cerebral small vessel disease; deep medullary vein; lacunar infarct; perivascular space; white matter hyperintensity.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Flowchart of enrollment of study patients.
FIGURE 2
FIGURE 2
Deep medullary veins scoring system. (A,E) A score of 0 is assigned for each continuous and prominently visible vein. (B,F) A score of 1 indicates that the vein is continuous and with unequivocal visibility, but at least one vein has inhomogeneous signal. (C,G) A score of 2 indicates that at least one vein is not continuous and with faint visibility, presenting with spot-like hypointensity. (D,H) A score of 3 is assigned if the DMV is not visible.

References

    1. Amin Al Olama A., Wason J. M. S., Tuladhar A. M. (2020). Simple MRI score aids prediction of dementia in cerebral small vessel disease. Neurology 94 e1294–e1302. - PMC - PubMed
    1. Chen X., Wei L., Wang J., Shan Y., Cai W., Men X., et al. (2020). Decreased visible deep medullary veins is a novel imaging marker for cerebral small vessel disease. Neurol. Sci. 41 1497–1506. 10.1007/s10072-019-04203-9 - DOI - PubMed
    1. Chung C. P., Hu H. H. (2010). Pathogenesis of leukoaraiosis: role of jugular venous reflux. Med. Hypothes. 75 85–90. 10.1016/j.mehy.2010.01.042 - DOI - PubMed
    1. Dolui S., Tisdall D., Vidorreta M., Jacobs D. R., Nasrallah I. M., Bryan R. N., et al. (2019). Characterizing a perfusion-based periventricular small vessel region of interest. Neuroimage Clin. 23:101897. 10.1016/j.nicl.2019.101897 - DOI - PMC - PubMed
    1. Duan Y., Xu Z., Li H., Cai X., Chang C., Yang B. (2018). Prominent deep medullary veins: a predictive biomarker for stroke risk from transient ischemic attack? Acta Radiol. 59 606–611. 10.1177/0284185117726813 - DOI - PubMed