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Association Between Enlarged Perivascular Spaces and Cognition in a Memory Clinic Population

神经心理学 认知 心理学 人口 白质疏松症 高强度 血管周围间隙 病理 医学 神经科学 磁共振成像 放射科 环境卫生
作者
Young Min Choe,Hyewon Baek,Hyo Jung Choi,Min Soo Byun,Dahyun Yi,Bo Kyung Sohn,Chul Ho Sohn,Dong Young Lee
出处
期刊:Neurology [Ovid Technologies (Wolters Kluwer)]
卷期号:99 (13): e1414-e1421
标识
DOI:10.1212/wnl.0000000000200910
摘要

Although enlarged perivascular spaces (EPVS) have been suggested as an emerging measure of small vessel disease (SVD) in the brain, their association with cognitive impairment is not yet clearly understood. We aimed to examine the relationship between each EPVS in the basal ganglia (BG-EPVS) and centrum semiovale (CSO-EPVS) with cognition in a memory clinic population.Participants with a diverse cognitive spectrum were recruited from a university hospital memory clinic. They underwent comprehensive clinical and neuropsychological assessments and brain MRI. BG-EPVS and CSO-EPVS were measured on T2-weighted MRI and then dichotomized into low and high degrees for further analyses. Other SVD markers were assessed using validated rating scales.A total of 910 participants were included in this study. A high degree of BG-EPVS was significantly associated with poorer scores on the executive function domain, but not with other cognitive domains, when age, sex, education, MRI scanner type, and cognitive diagnosis were controlled as covariates. However, the association between BG-EPVS and executive function was no longer significant after controlling for other markers of SVD, such as lacunar infarcts and periventricular white matter hyperintensities, as additional covariates. CSO-EPVS did not have a significant relationship with any cognitive scores, regardless of the covariates.Our findings from a large memory clinic population suggest that EPVS, regardless of the topographical location, may not be used as a specific SVD marker for cognitive impairment, although an apparent association was observed between a high degree of BG-EPVS and executive dysfunction before controlling other SVD markers that share a common pathophysiologic process with BG-EPVS.
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