MRI Lesion Load of Cerebral Small Vessel Disease and Cognitive Impairment in Patients With CADASIL

被引:13
作者
Shi, YuZhi [1 ]
Li, ShaoWu [2 ]
Li, Wei [1 ]
Zhang, Chen [1 ]
Guo, LiYing [1 ]
Pan, YunZhu [1 ]
Zhou, XueMei [1 ]
Wang, XinGao [1 ]
Niu, Songtao [1 ]
Yu, XueYing [1 ]
Tang, HeFei [1 ]
Chen, Bin [1 ]
Zhang, ZaiQiang [1 ]
机构
[1] Capital Med Univ, Beijing Tiantan Hosp, Dept Neurol, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Neurosurg Inst, Dept Funct Neuroimaging, Beijing, Peoples R China
关键词
cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy; cognitive impairment; total small vessel disease score; cerebral atrophy; small vessel disease; WHITE-MATTER HYPERINTENSITIES; DEMENTIA; DECLINE; INFARCTS; ATROPHY; MEMORY;
D O I
10.3389/fneur.2018.00862
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and objective: Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the best known and the most common monogenic small vessel disease (SVD). Cognitive impairment is an inevitable feature of CADASIL. Total SVD score and global cortical atrophy (GCA) scale were found to be good predictors of poor cognitive performance in community-dwelling adults. We aimed to estimate the association between the total SVD score, GCA scale and the cognitive performance in patients with CADASIL. Methods: We enrolled 20 genetically con fi rmed CADASIL patients and 20 controls matched by age, gender, and years of education. All participants underwent cognitive assessments to rate the global cognition and individual domain of executive function, information processing speed, memory, language, and visuospatial function. The total SVD score and GCA scale were rated. Results: The CADASIL group performed worse than the controls on all cognition measures. Neither global cognition nor any separate domain of cognition was signi fi cantly different among patients grouped by total SVD score. Negative correlations between the GCA score and cognitive performance were observed. Approximately 40% of the variance was explained by the total GCA score in the domains of executive function, information processing speed, and language. The super fi cial atrophy score was associated with poor performance in most of the domains of cognition. Adding the super fi cial atrophy score decreased the prediction power of the deep atrophy score on cognitive impairment alone. Conclusions: The GCA score, not the total SVD score, was signi fi cantly associated with poor cognitive performance in patients with CADASIL. Adding the super fi cial atrophy score attenuated the prediction power of the deep atrophy score on cognitive impairment alone.
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