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Risk Factors for Decline in Gait Speed During Walking While Talking in Older Adults

Overview
Journal Gait Posture
Specialty Orthopedics
Date 2022 May 20
PMID 35594829
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Abstract

Background & Aims: Slow gait speed during Walking While Talking (walking while reciting alternate letters of the alphabet; WWT) is associated with an increased risk of developing dementia and falls. The aim of this study was to examine longitudinal changes in WWT-speed and to identify risk factors that may modify the rate of change in WWT-speed.

Methods: A total of 431 older participants (55.7% female; M Age=76.8 ± 6.4 years; mean follow up 2.1 ± 1.8 years) enrolled in the Central Control of Mobility in Aging study were examined. WWT-speed (cm/s) was measured with a computerized walkway. The following baseline measures were examined as risk factors: demographics [age, sex, education], medical illnesses [hypertension, diabetes, cardiac arrhythmias, history of stroke, Parkinson's disease, kidney disease, arthritis], cognitive functions [global cognition, executive function, processing speed], physical and sensory functions [unipedal stance time, gait speed during single task walking, visual acuity], psychological variables [depression, anxiety] and falls. Linear mixed effect models were used to examine 1) change in WWT-speed over time, and 2) risk factors associated with change in WWT-speed over time.

Results: WWT-speed declined in an accelerating non-linear fashion over time after adjusting for baseline age, sex and education. The rate of decline in WWT-speed was modified by older age (b -0.16 95%CI -0.22, -0.09), poorer balance (b -1.73 95%CI -2.57, -0.90), and faster gait speed during single task walking (b -0.06 95%CI -0.08, -0.04).

Significance: This study identified fixed and modifiable risk factors of faster decline in WWT-speed over time in community-residing older adults.

Citing Articles

White Matter Hyperintensities Are Associated with Slower Gait Speed in Older Adults without Dementia.

Vazquez J, Verghese J, Barzilai N, Milman S, Blumen H Neurodegener Dis. 2024; 1-9.

PMID: 39025052 PMC: 11747921. DOI: 10.1159/000538944.

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