The association between simple reaction time variability and gait variability: The Tasmanian Study of Cognition and Gait

被引:7
|
作者
Jayakody, Oshadi [1 ,2 ]
Breslin, Monique [1 ]
Beare, Richard [3 ,4 ]
Siejka, Timothy P. [5 ]
Gujjari, Siddhanth [6 ]
Srikanth, Velandai K. [1 ,3 ]
Blumen, Helena M. [2 ]
Callisaya, Michele L. [1 ,3 ]
机构
[1] Univ Tasmania, Menzies Inst Med Res, Hobart, Tas, Australia
[2] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[3] Monash Univ, Cent Clin Sch, Peninsula Clin Sch, Melbourne, Vic, Australia
[4] Royal Childrens Hosp, Murdoch Childrens Res Inst, Dev Imaging, Melbourne, Vic, Australia
[5] Alfred Hlth, Melbourne, Vic, Australia
[6] Monash Hlth, Monash Med Ctr, Melbourne, Vic, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Gait; Double support time variability; Reaction time variability; Cognition; Brain structure; INTRAINDIVIDUAL VARIABILITY; PERFORMANCE VARIABILITY; OLDER-PEOPLE; FALLS; FLUCTUATIONS; RISK; AGE;
D O I
10.1016/j.gaitpost.2021.07.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Introduction: Greater double support time (DST) variability is associated with falls and memory decline. The underlying neurophysiological mechanisms of DST variability are poorly understood. Simple reaction time (SRT) variability, a measure of attention-processing speed is associated with falls and dementia and, may underlie greater DST variability. The aims of this study were to examine the association between SRT and DST variability and if SRT variability mediates the associations between poorer cognition/brain structure and DST variability. Methods: Participants (n = 408) were community-dwelling older people without dementia (mean age 72.0 +/- 7.0). DST variability was the standard deviation (SD) of DST, assessed with a walkway and averaged across steps of 6 walks. SRT variability was the SD of a button pressing task in response to a visual stimulus. Executive function and processing speed were assessed with neuropsychological tests. Magnetic Resonance Imaging was used to obtain cortical thickness (total and in frontal regions) and cerebral small vessel disease (cSVD). Multivariable linear regression models were used to examine the association between SRT and DST variability and if SRT variability mediated any associations of cognition/brain structure with DST variability. Results: Greater SRT variability was associated with greater DST variability (p = 0.002). SRT variability partially mediated the association between poorer executive function and greater DST variability. Smaller mean thickness in orbitofrontal regions and greater cSVD burden were only associated with DST variability (p < 0.05), not with SRT variability (p > 0.05). Conclusions: Greater SRT variability, which may occur due to inefficient executive functioning, could be an underlying neurophysiological mechanism of greater DST variability.
引用
收藏
页码:206 / 210
页数:5
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