Apolipoprotein E4 Allele and Gait Performance in Mild Cognitive Impairment: Results From the Gait and Brain Study

被引:25
|
作者
Sakurai, Ryota [1 ,2 ,3 ]
Montero-Odasso, Manuel [1 ,2 ,4 ]
机构
[1] Lawson Hlth Res Inst, Parkwood Inst, Gait & Brain Lab, London, ON, Canada
[2] Univ Western Ontario, Schulich Sch Med & Dent, Div Geriatr Med, Dept Med, London, ON, Canada
[3] Tokyo Metropolitan Inst Gerontol, Tokyo, Japan
[4] Univ Western Ontario, Dept Epidemiol & Biostat, London, ON, Canada
基金
加拿大健康研究院;
关键词
Apolipoprotein E; Gait variability; Cognition; Mild cognitive impairment; Longitudinal study; ALZHEIMERS-DISEASE; E GENOTYPE; PHYSICAL FUNCTION; APOE GENOTYPE; MOTOR CORTEX; FOLLOW-UP; RISK; VARIABILITY; DECLINE; ASSOCIATION;
D O I
10.1093/gerona/glx075
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
Background: The apolipoprotein E polymorphism epsilon 4 allele (ApoE4) and gait impairment are both known risk factors for developing cognitive decline and dementia. However, it is unclear the interrelationship between these factors, particularly among older adults with mild cognitive impairment (MCI) who are considered as prodromal for Alzheimer's disease. This study aimed to determine whether ApoE4 carrier individuals with MCI may experience greater impairment in gait performance. Methods: Fifty-six older adults with MCI from the "Gait and Brain Study" who were identified as either ApoE4 carriers (n = 20) or non-ApoE4 carriers (n = 36) with 1 year of follow-up were included. Gait variability, the main outcome variable, was assessed as stride time variability with an electronic walkway. Additional gait variables and cognitive performance (mini-mental state examination [MMSE] and Montreal Cognitive Assessment [MoCA]) were also recorded. Covariates included age, sex, education level, body mass index, and number of comorbidities. Results: Baseline characteristics were similar for both groups. Repeated measures analysis of covariance showed that gait stride time and stride length variabilities significantly increased in ApoE4 carriers but was maintained in the non-ApoE4 carriers. Similarly, ApoE4 carriers showed greater decrease in MMSE score at follow-up. Conclusions: In this sample of older adults with MCI, the presence of at least one copy of ApoE4 was associated with the development of both increased gait variability and cognitive decline during 1 year of follow-up. ApoE4 genotype might be considered as a potential mediator of decline in mobility function in MCI; future studies with larger samples are needed to confirm our preliminary findings.
引用
收藏
页码:1676 / 1682
页数:7
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