Abstract

A novel identification algorithm using a deep learning approach was developed in this study to classify neurodegenerative diseases (NDDs) based on the vertical ground reaction force (vGRF) signal. The irregularity of NDD vGRF signals caused by gait abnormalities can indicate different force pattern variations compared to a healthy control (HC). The main purpose of this research is to help physicians in the early detection of NDDs, efficient treatment planning, and monitoring of disease progression. The detection algorithm comprises a preprocessing process, a feature transformation process, and a classification process. In the preprocessing process, the five-minute vertical ground reaction force signal was divided into 10, 30, and 60 s successive time windows. In the feature transformation process, the time–domain vGRF signal was modified into a time–frequency spectrogram using a continuous wavelet transform (CWT). Then, feature enhancement with principal component analysis (PCA) was utilized. Finally, a convolutional neural network, as a deep learning classifier, was employed in the classification process of the proposed detection algorithm and evaluated using leave-one-out cross-validation (LOOCV) and k-fold cross-validation (k-fold CV, k = 5). The proposed detection algorithm can effectively differentiate gait patterns based on a time–frequency spectrogram of a vGRF signal between HC subjects and patients with neurodegenerative diseases.

Highlights

  • Amyotrophic lateral sclerosis (ALS), Huntington’s disease (HD), and Parkinson’s disease (PD), as neurodegenerative diseases (NDDs), are defined as diseases caused by the progressive death of neurons in different regions of the nervous system, through the loss of structure and function of neurons [1]

  • This study used a time–frequency spectrogram based on a vertical ground reaction force (vGRF) signal to implement a novel AI-based NDD detection algorithm

  • The ability to distinguish between the gait phenomena of NDD patients and a healthy control (HC) was achieved through pattern visualization and the recognition of the time–frequency spectrogram

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Summary

Introduction

Amyotrophic lateral sclerosis (ALS), Huntington’s disease (HD), and Parkinson’s disease (PD), as NDDs, are defined as diseases caused by the progressive death of neurons in different regions of the nervous system, through the loss of structure and function of neurons [1]. PD is the second most prevalent NDD, with a prevalence of 0.3% in the general population, ~1% in the elderly over 60 years old, and ~3% in those aged 80 years old or more [2]. The median age at onset is 60 years, and the average time it takes for the disease to progress, from the diagnosis to death, is approximately 15 years [2]. Men show a 1.5–2 times greater prevalence of this disease and incidence compared to women [2]. ALS is the third most prevalent NDD and the most common motor neuron disease, with an estimated annual incidence of 1.9 people out of 100,000 per year [4,5]. As NDDs mainly affect people in their middle to late years of life, the incidence is expected to increase with the an increasingly aging population. In 2030, 1 out of every 5 Americans will be over the age of

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