Associations of Vascular Risk with Cognition, Brain Glucose Metabolism, and Clinical Progression in Cognitively Intact Elders

被引:7
作者
Yu, Guang-Xiang [1 ,2 ]
Zhang, Ting [3 ,4 ]
Hou, Xiao-He [5 ]
Ou, Ya-Nan [5 ]
Hu, Hao [5 ]
Wang, Zuo-Teng [5 ]
Guo, Yu [5 ]
Xu, Wei [5 ]
Tan, Lin [5 ]
Yu, Jin-Tai [3 ,4 ]
Tan, Lan [1 ,5 ]
机构
[1] Dalian Med Univ, Qingdao Municipal Hosp, Dept Neurol, Dalian, Peoples R China
[2] Dalian Med Univ, Dept Neurol, Affiliated Hosp 1, Dalian, Peoples R China
[3] Fudan Univ, Huashan Hosp, Shanghai Med Coll, Dept Neurol, Shanghai, Peoples R China
[4] Fudan Univ, Huashan Hosp, Shanghai Med Coll, Inst Neurol, Shanghai, Peoples R China
[5] Qingdao Univ, Qingdao Municipal Hosp, Dept Neurol, 5 Donghai Middle Rd, Qingdao, Peoples R China
基金
美国国家卫生研究院; 中国国家自然科学基金; 加拿大健康研究院;
关键词
Clinical progression; cognition; dementia; FDG-PET; vascular risk; CARDIOVASCULAR RISK; ALZHEIMERS-DISEASE; IMPAIRMENT; DECLINE;
D O I
10.3233/JAD-201117
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Increasing evidence supports an important role of vascular risk in cognitive decline and dementia. Objective: This study aimed to examine whether vascular risk was associated with cognitive decline, cerebral hypometabolism, and clinical progression in cognitively intact elders. Methods: Vascular risk was assessed by the Framingham Heart Study general Cardiovascular disease (FHS-CVD) risk score. The cross-sectional and longitudinal associations of FHS-CVD risk score with cognition and brain glucose metabolism were explored using multivariate linear regression and linear mixed effects models, respectively. The risk of clinical progression conversion was assessed using Kaplan-Meier survival curves and multivariate Cox proportional hazard models. Results: A total of 491 cognitively intact elders were included from Alzheimer's Disease Neuroimaging Initiative (ADNI) database. Participants with high FHS-CVD risk scores had lower baseline Mini-Mental State Examination (MMSE) (p = 0.009), executive function (EF) (p < 0.001), memory function (MEM) (p < 0.001) scores, and F18-fluorodeoxyglucose positron emission tomography (FDG-PET) uptake (p < 0.001) than those with lowFHS-CVD risk scores. In longitudinal analyses, individuals with higher FHS-CVD risk scores had greater longitudinal declines in MMSE (p = 0.043), EF (p = 0.029) scores, and FDG-PET uptake (p = 0.035). Besides, individuals with a higher vascular risk had an increased risk of clinical progression (p = 0.004). Conclusion: These findings indicated effects of vascular risk on cognitive decline, cerebral hypometabolism, and clinical progression. Early detection and management of vascular risk factors might be useful in the prevention of dementia.
引用
收藏
页码:321 / 330
页数:10
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