Enlarged Perivascular Spaces Are Negatively Associated With Montreal Cognitive Assessment Scores in Older Adults

被引:10
作者
Libecap, Timothy J. [1 ]
Zachariou, Valentinos [1 ]
Bauer, Christopher E. [1 ]
Wilcock, Donna M. [2 ,3 ]
Jicha, Gregory A. [3 ,4 ]
Raslau, Flavius D. [5 ]
Gold, Brian T. [1 ,3 ,6 ]
机构
[1] Univ Kentucky, Coll Med, Dept Neurosci, Lexington, KY 40536 USA
[2] Univ Kentucky, Coll Med, Dept Physiol, Lexington, KY USA
[3] Univ Kentucky, Coll Med, Sanders Brown Ctr Aging, Lexington, KY 40504 USA
[4] Univ Kentucky, Coll Med, Dept Neurol, Lexington, KY USA
[5] Univ Kentucky, Coll Med, Dept Radiol, Lexington, KY USA
[6] Univ Kentucky, Coll Med, Magnet Resonance Imaging & Spect Ctr, Lexington, KY 40536 USA
关键词
enlarged perivascular spaces-ePVS; cerebral small vessel disease; Montreal Cognitive Assessment-MoCA; neuroimaging biomarkers; white matter hyperintensities-WMH; SMALL VESSEL DISEASE; VIRCHOW-ROBIN SPACES; MENTAL-STATE-EXAMINATION; WHITE-MATTER; ASSESSMENT MOCA; CEREBRAL MICROBLEEDS; VASCULAR CONTRIBUTIONS; MRI; IMPAIRMENT; DEMENTIA;
D O I
10.3389/fneur.2022.888511
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Emerging evidence suggests that enlarged perivascular spaces (ePVS) may be a clinically significant neuroimaging marker of global cognitive function related to cerebral small vessel disease (cSVD). We tested this possibility by assessing the relationship between ePVS and both a standardized measure of global cognitive function, the Montreal Cognitive Assessment (MoCA), and an established marker of cSVD, white matter hyperintensity volume (WMH) volume. One hundred and eleven community-dwelling older adults (56-86) underwent neuroimaging and MoCA testing. Quantification of region-specific ePVS burden was performed using a previously validated visual rating method and WMH volumes were computed using the standard ADNI pipeline. Separate linear regression models were run with ePVS as a predictor of MoCA scores and whole brain WMH volume. Results indicated a negative association between MoCA scores and both total ePVS counts (P <= 0.001) and centrum semiovale ePVS counts (P <= 0.001), after controlling for other relevant cSVD variables. Further, WMH volumes were positively associated with total ePVS (P = 0.010), basal ganglia ePVS (P <= 0.001), and centrum semiovale ePVS (P = 0.027). Our results suggest that ePVS burden, particularly in the centrum semiovale, may be a clinically significant neuroimaging marker of global cognitive dysfunction related to cSVD.
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页数:10
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