Physical activity complexity, cognition, and risk of cognitive impairment and dementia in the Baltimore Longitudinal Study of Aging

IF 4.9 Q1 CLINICAL NEUROLOGY
Yurun Cai, Junhong Zhou, Paul W. Scott, Qu Tian, Amal A. Wanigatunga, Lewis Lipsitz, Eleanor M. Simonsick, Susan M. Resnick, Luigi Ferrucci, Dianxu Ren, Jennifer H. Lingler, Jennifer A. Schrack
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引用次数: 0

Abstract

INTRODUCTION

Studies on physical activity (PA) and dementia mainly focus on activity quantity or intensity. Yet PA requires neuro-coordination of movement, and it is unclear whether complexity of daily activity varies by cognitive status. Thus, we examined the association between PA complexity, using multiscale entropy, and cognitive function, mild cognitive impairment (MCI), and dementia in older adults in the Baltimore Longitudinal Study of Aging (BLSA).

METHODS

A total of 637 older adults (age 73.9 ± 11.3 years) in the BLSA completed a 7-day wrist-worn accelerometer assessment and neuropsychological tests from 2015 to 2020. Using logistic regression and structural equation modeling, we examined cross-sectional associations of PA complexity with MCI/dementia and cognition. Cross-lagged panel models (CLPMs) were used to assess bidirectional associations at baseline and 2-year follow-up. Multivariable models were adjusted for age, sex, race, education years, body mass index, and comorbidities.

RESULTS

Participants in the lowest tertile of PA complexity had over double the odds of MCI/dementia (odds ratio = 2.63, 95% confidence interval [CI]: 1.02 to 6.79, p = 0.045) compared to those in the highest tertile in the fully adjusted model. Structural equation modeling showed that PA complexity was associated with global cognitive function (standardized B [SB] = 0.102, 95% CI: 0.033 to 0.171, p = 0.004), executive function (SB = 0.119, 95% CI: 0.049 to 0.189, p = 0.001), and visuospatial ability (SB = 0.096, 95% CI: 0.026 to 0.167, p = 0.008). CLPMs showed bidirectional associations between lower PA complexity and poorer executive function.

DISCUSSION

Lower complexity of accelerometry-detected movement is associated with poorer cognition and higher risk of MCI/dementia. Future studies should explore whether low PA complexity is an early indicator of dementia.

Highlights

  • Prior studies mainly focused on quantity or intensity of physical activity.
  • Poorer cognitive function was associated with lower complexity of daily activity.
  • Lower complexity of physical activity may be an early indicator of dementia.

Abstract Image

巴尔的摩老龄化纵向研究中的身体活动复杂性、认知和认知障碍和痴呆的风险
体力活动(PA)与痴呆的研究主要集中在运动量或强度上。然而,PA需要运动的神经协调,并且尚不清楚日常活动的复杂性是否因认知状态而异。因此,我们在巴尔的摩老龄化纵向研究(BLSA)中使用多尺度熵来研究老年人的认知功能、轻度认知障碍(MCI)和痴呆之间的关系。方法2015 - 2020年,BLSA共有637名老年人(73.9±11.3岁)完成了为期7天的腕带加速度计评估和神经心理测试。使用逻辑回归和结构方程模型,我们研究了PA复杂性与MCI/痴呆和认知的横断面关联。交叉滞后面板模型(clpm)用于评估基线和2年随访时的双向关联。多变量模型根据年龄、性别、种族、受教育年限、体重指数和合并症进行调整。结果:在完全调整后的模型中,PA复杂性最低分位数的参与者患MCI/痴呆的几率是最高分位数参与者的两倍多(优势比= 2.63,95%可信区间[CI]: 1.02至6.79,p = 0.045)。结构方程模型显示,PA复杂性与整体认知功能(标准化B [SB] = 0.102, 95% CI: 0.033 ~ 0.171, p = 0.004)、执行功能(SB = 0.119, 95% CI: 0.049 ~ 0.189, p = 0.001)和视觉空间能力(SB = 0.096, 95% CI: 0.026 ~ 0.167, p = 0.008)相关。低PA复杂度与较差的执行功能之间存在双向关联。加速度计检测到的运动复杂性较低与认知能力较差和MCI/痴呆风险较高相关。未来的研究应该探索低PA复杂性是否是痴呆的早期指标。先前的研究主要集中在体力活动的数量或强度上。较差的认知功能与较低的日常活动复杂性有关。较低的体力活动复杂性可能是痴呆症的早期指标。
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来源期刊
CiteScore
10.10
自引率
2.10%
发文量
134
审稿时长
10 weeks
期刊介绍: Alzheimer''s & Dementia: Translational Research & Clinical Interventions (TRCI) is a peer-reviewed, open access,journal from the Alzheimer''s Association®. The journal seeks to bridge the full scope of explorations between basic research on drug discovery and clinical studies, validating putative therapies for aging-related chronic brain conditions that affect cognition, motor functions, and other behavioral or clinical symptoms associated with all forms dementia and Alzheimer''s disease. The journal will publish findings from diverse domains of research and disciplines to accelerate the conversion of abstract facts into practical knowledge: specifically, to translate what is learned at the bench into bedside applications. The journal seeks to publish articles that go beyond a singular emphasis on either basic drug discovery research or clinical research. Rather, an important theme of articles will be the linkages between and among the various discrete steps in the complex continuum of therapy development. For rapid communication among a multidisciplinary research audience involving the range of therapeutic interventions, TRCI will consider only original contributions that include feature length research articles, systematic reviews, meta-analyses, brief reports, narrative reviews, commentaries, letters, perspectives, and research news that would advance wide range of interventions to ameliorate symptoms or alter the progression of chronic neurocognitive disorders such as dementia and Alzheimer''s disease. The journal will publish on topics related to medicine, geriatrics, neuroscience, neurophysiology, neurology, psychiatry, clinical psychology, bioinformatics, pharmaco-genetics, regulatory issues, health economics, pharmacoeconomics, and public health policy as these apply to preclinical and clinical research on therapeutics.
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