Abstract

Parkinson’s disease (PD) is a common age-related neurodegenerative disease. Gait impairment is frequent in the later stages of PD contributing to reduced mobility and quality of life. Digital biomarkers such as gait velocity and step length are predictors of motor and cognitive decline in PD. Additional gait parameters may describe different aspects of gait and motor control in PD. Sample entropy (SampEnt), a measure of signal predictability, is a nonlinear approach that quantifies regularity of a signal. This study investigated SampEnt as a potential biomarker for PD and disease duration. Real-world gait data over a seven-day period were collected using an accelerometer (Axivity AX3, York, UK) placed on the low back and gait metrics extracted. SampEnt was determined for the stride time, with vector length and threshold parameters optimized. People with PD had higher stride time SampEnt compared to older adults, indicating reduced gait regularity. The range of SampEnt increased over 36 months for the PD group, although the mean value did not change. SampEnt was associated with dopaminergic medication dose but not with clinical motor scores. In conclusion, this pilot study indicates that SampEnt from real-world data may be a useful parameter reflecting clinical status although further research is needed involving larger populations.

Highlights

  • Advances in medicine and public health preventive strategies contribute to the increased life expectancy of an expanding world population

  • Analysis of 262,735 strides during real-world walking over a 36-month period indicated significantly lower regularity of stride time in people with Parkinson’s compared to healthy age-matched older adults

  • The novelty of this study is that we analyzed real-world gait, recorded over seven days, during a 36-month period

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Summary

Introduction

Advances in medicine and public health preventive strategies contribute to the increased life expectancy of an expanding world population. A consequence of greater longevity is increased morbidity, resulting in the loss of independent living, frailty, and mortality [1]. There are substantial health and social costs linked to the loss of independence as well as the impact on quality of life of the individual and careers. In PD, deep brain structures controlling movement degenerate and there is progressive loss of motor function. The quantitative analysis of gait may provide biomarkers of disease progression and offer insight into motor control strategies. Wearable technology, such as accelerometers, allow for monitoring of ambulatory activity in both controlled and real-world environments [4]

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