Cystatin C predicts cognitive decline in multiple system atrophy: A 1-year prospective cohort study

被引:3
作者
Zhang, Lingyu [1 ,2 ]
Li, Ruicen [1 ]
Hou, Yanbing [2 ]
Cao, Bei [2 ]
Wei, Qianqian [2 ]
Ou, Ruwei [2 ]
Liu, Kuncheng [2 ]
Lin, Junyu [2 ]
Yang, Tianmi [2 ]
Xiao, Yi [2 ]
Huang, Wenxia [1 ]
Shang, Huifang [2 ]
机构
[1] Sichuan Univ, West China Hosp, Hlth Management Ctr, Gen Practice Med Ctr, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Rare Dis Ctr, Dept Neurol,Lab Neurodegenerat Disorders, Chengdu, Peoples R China
关键词
multiple system atrophy; cystatin C; cognitive decline; prospective study; movement disorder; PARKINSONS-DISEASE; IMPAIRMENT; VALIDATION; STATEMENT; PATHOLOGY;
D O I
10.3389/fnagi.2022.1069837
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
BackgroundAccumulating evidence has suggested that cystatin C is associated with cognitive impairment in patients with neurodegenerative diseases. However, the association between cystatin C and cognitive decline in patients with multiple system atrophy (MSA) remains largely unknown. ObjectivesThe objective was to determine whether cystatin C was independently associated with cognitive decline in patients with early-stage MSA. MethodsPatients with MSA underwent evaluation at baseline and the 1-year follow-up. Cognitive function was evaluated with Montreal cognitive assessment (MoCA). Changes in the MoCA score and the absolute MoCA score at the 1-year assessment were considered the main cognitive outcome. The cystatin C concentrations in patients with MSA and age, sex, and body mass index matched-healthy controls (HCs) were measured. A multiple linear regression model was used to test the association between cystatin C and cognitive decline. ResultsA total of 117 patients with MSA and 416 HCs were enrolled in the study. The cystatin C levels were significantly higher in patients with MSA than in HCs (p < 0.001). Cystatin C levels were negatively correlated with MoCA score at baseline and at 1-year follow-up. Multiple linear regression model adjusted for potential confounders showed that baseline cystatin C levels were significantly associated with the MoCA score (p = 0.004) or change in the MoCA score (p = 0.008) at 1-year follow-up. ConclusionOur results suggested that cystatin C may serve as a potential biomarker of cognitive decline in patients with early-stage MSA.
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页数:8
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