GAIT-CKD (Gait Analysis using Artificial Intelligence for digital Therapeutics of patients with Chronic Kidney Disease): design and methods

Article information

Korean J Nephrol. 2024;.j.krcp.23.273
Publication date (electronic) : 2024 August 22
doi : https://doi.org/10.23876/j.krcp.23.273
1Department of Internal Medicine, Hallym University Chuncheon Sacred Heart Hospital, Chuncheon, Republic of Korea
2Division of AI Convergence, College of Infomation Science, Hallym University, Chuncheon, Republic of Korea
3Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA
4Cerebrovascular Disease Research Center, Hallym University, Chuncheon, Republic of Korea
5BI Team, HEALTH-BRIDGE COM, Seoul, Republic of Korea
6School of Integrated Technology, Gwangju Institute of Science and Technology, Gwangju, Republic of Korea
7Department of Neurology, Kangdong Sacred Heart Hospital, Seoul, Republic of Korea
8Department of Psychiatry, Hallym University Chuncheon Sacred Heart Hospital, Chuncheon, Republic of Korea
9Department of Emergency Medicine, Hallym University Chuncheon Sacred Heart Hospital, Chuncheon, Republic of Korea
Correspondence: Hyunsuk Kim Department of Internal Medicine, Hallym University Chuncheon Sacred Heart Hospital, 77 Sakju-ro, Chuncheon 24253, Republic of Korea. E-mail: nephrokim@hallym.ac.kr
*Youngjin Song and In cheol Jeong contributed equally to this study as co-first authors.
Received 2023 October 22; Revised 2024 January 31; Accepted 2024 February 13.

Abstract

Background

Digital therapeutics are emerging as treatments for diseases and disabilities. In chronic kidney disease (CKD), gait is a potential biomarker for health status and intervention effectiveness. This study aims to analyze gait characteristics in CKD patients, providing baseline data for digital therapeutics development.

Methods

At baseline and after an 8-week intervention, we performed bioimpedance analysis measurements, the Timed Up and Go, Tinetti, and grip strength tests, and gait analysis in 217 healthy individuals and 276 patients with CKD. Demographic and clinical information was collected, including underlying diseases and medications, laboratory tests, and quality of life satisfaction surveys. Gait analysis was performed using skeleton data, which involved acquiring three-dimensional skeleton data of a walker using a single Kinect sensor. The performance of an artificial intelligence-based classification model in distinguishing between healthy individuals and those with CKD was then investigated. Simultaneously, inertia measurement unit analysis was conducted using measurements taken from the wrist and waist.

Results

Most subjects received a health intervention via an app, and their gait was assessed for improvements after an 8-week period. Incidents such as falls, fractures, hospitalizations, and deaths will be investigated in years 1 and 3.

Conclusion

This study confirmed that the gaits of healthy individuals and CKD patients were different, and the effect of the 8-week app-based health intervention will be analyzed. The study will yield important baseline data for creating digital therapeutics for CKD patients’ diet/exercise in the future.

Introduction

Digital therapeutics represent a novel approach to patient management and treatment. They are defined as therapeutic interventions that utilize software programs to manage patients’ medical conditions [1]. With the rapid digital transformation of medical systems worldwide, digital therapeutics are garnering increasing attention. They are a form of digital technology with a proven treatment effect, designed to directly treat and manage patients’ diseases and disabilities. Since the U.S. Food and Drug Administration approved ‘reSET’ for the management of substance use disorder in 2017, a variety of digital therapeutics have emerged and are now widely used in the clinical field [2].

Currently, digital therapeutics are being utilized in a variety of prospects, including hypertension, diabetes, and even oncology. Several studies have reported that digital therapeutics demonstrate economic benefits in the management of hypertension and diabetes [3,4]. In the field of oncology, digital therapeutics have shown effectiveness in patient management.

Gait involves numerous physical systems, including the cardiovascular, pulmonary, neurological, and musculoskeletal systems [5]. Some research has observed gait disturbances in chronic diseases such as chronic obstructive pulmonary disease and chronic kidney disease (CKD). Additionally, gait disturbances can serve as a predictor for cardiovascular disease [68]. From a neurological perspective, gait function demonstrates a correlation with neurological diseases such as cerebral palsy and Parkinson disease. This correlation extends to fundamental areas such as cognitive function, and gait function can be utilized as a significant factor in confirming these diseases [911]. Gait speed can also be useful in screening for sarcopenia [12]. Another report suggests that sarcopenia is associated with cognitive impairment, which may be attributed to a slower gait speed [13]. Therefore, gait can be considered a significant biomarker, indicative of an individual’s health status.

Globally, CKD has a prevalence of 13.4%, necessitating renal replacement therapy for millions of patients. CKD imposes a significant burden on global health and mobility, primarily due to its impact on cardiovascular risk and end-stage kidney disease. Additionally, the rise in diabetes, hypertension, obesity, and aging patients contributes to an increase in CKD cases. To manage the economic burden of the growing number of CKD patients, it is crucial to enhance disease surveillance and prevention [14,15].

Patients undergoing hemodialysis who are unable to walk or can only walk slowly have higher mortality and hospitalization rates than those who can walk normally [5]. Dialysis patients often exhibit gait disturbances due to metabolic factors that contribute to muscle loss. There are also observable changes in the brain area that controls motor function, leading to walking disorders [7]. Furthermore, these gait disturbances can contribute to falls, which are associated with increased mortality and morbidity, and pose an economic burden on society.

As CKD advances, there is a higher rate of muscle loss, which is associated with increased disability in daily life and a reduction in walking speed. This muscle loss has also been linked to a higher rate of vascular calcification and vascular access failure in patients undergoing hemodialysis [16].

We hypothesized that gait can serve as a proxy indicator of patients’ disease status (e.g., sarcopenia or CKD) and that health interventions for those patients will improve gait. Thus, our interventions have the therapeutic goal of improving gait parameters. We will also conduct bioelectrical impedance analysis (BIA) measurements to analyze changes in muscle mass.

Increasingly many researchers are interested in identifying ways to improve gait abnormalities in CKD patients, particularly in light of studies indicating that musculoskeletal health is linked to kidney function. However, few studies have specifically investigated abnormal gait in CKD patients. Nonetheless, interventions that have an impact on gait—including exercise, nutritional support, and the management of underlying conditions—may exert a beneficial effect on CKD patients’ physical function and quality of life.

CKD exerts substantial negative impacts on the structure, activity, and function of bone and skeletal muscle, reducing the quality of life of CKD patients and making a contribution to morbidity and mortality. Exercise has positive effects on the metabolism and function of muscle and bone, which has prompted suggestions that regular physical exercise could serve as a therapeutic modality for patients with muscle and bone-related disorders [17]. Muscle weakness can contribute to gait abnormalities, including slower walking speed, changes in stride length, and impaired balance. CKD patients might also develop peripheral neuropathy as a result of metabolic imbalances and uremic toxins. Neuropathy can affect motor and sensory nerves; this can impair gait through poor coordination, muscle weakness, and changes in sensations [18]. Abnormal gait in CKD patients could potentially be improved indirectly through the treatment of complications such as peripheral neuropathy and the management of factors contributing to wasting and muscle weakness. Chu and McAdams-DeMarco [19], in this context, pointed out that exercise training, in addition to cognitive training, can lead to better quality of life and long-term health outcomes.

In CKD patients, gait parameters can be improved through regular exercise—in particular, balance exercises and resistance training—since these activities have positive impacts on coordination, balance, and muscle strength. Sufficient protein intake and nutritional support may avert muscle wasting and weakness, which could also lead to improved gait in patients with CKD.

The aim of this study is to compare the gait of patients with CKD to that of healthy individuals in order to identify any distinctive features of pathologic gait in CKD patients. We conducted an intervention targeting pathologic gait through lifestyle modifications, such as dietary changes and exercise interventions, and we will conduct long-term follow-up to determine whether these can lead to improvements. Ultimately, we plan to use gait as a baseline measure and biomarker for diagnosis and treatment within the realm of digital therapeutics.

Methods

This study received approval from the Institutional Review Board at Hallym University Chuncheon Sacred Heart Hospital (No. 2022-06-009). All participants provided informed consent.

Subjects (chronic kidney disease patients and healthy individuals) and the study protocol

To investigate the characteristics of pathological gait in patients with CKD, we recruited 300 CKD patients and 220 individuals from a non-CKD healthy population. The healthy population was defined as those who do not currently have acute or chronic diseases or take regular medications, including for hypertension and diabetes, and have no noteworthy medical history in our hospital’s electronic medical records. We excluded those who were unable to walk, had pacemakers, or declined health intervention services. Consequently, 276 CKD patients and 217 individuals from the healthy population were included in this study. In both groups, skeletal and inertial measurement unit (IMU) measurements were conducted as the primary examination.

For CKD patients, we collected information on age, sex, primary renal disease and the length of ESRD. The CKD patient group underwent a primary workup that included a complete blood count (CBC), routine chemistry, bone mineral density (BMD), BIA, and a handgrip test. The healthy individuals, meanwhile, received a primary workup consisting of BIA and a handgrip test.

Both groups participated in an 8-week health intervention, after which they were retested using skeleton and IMU measurements, similar to the primary examination. Concurrently, as part of a secondary evaluation, CKD patients underwent testing for CBC, routine chemistry, BIA, and handgrip strength, while the control group was tested for BIA and handgrip strength (Fig. 1).

Figure 1.

Participants (CKD patients and healthy individuals) and study protocol.

BMD, bone mineral density; BIA, bioelectrical impedance analysis; CBC, complete blood count; CKD, chronic kidney disease; IMU, inertial measurement unit.

Structure of the gait analysis room

Tests were carried out in the gait analysis room established at Hallym University Chuncheon Sacred Heart Hospital. The laboratory measured 9 × 4 m and was equipped with Azure Kinect cameras (Microsoft Corp.) centrally positioned for recording inspections. A rectangular line was delineated with tape to guide subjects in their walking patterns as per the instructions. The laboratory was staffed with three inspectors and a nurse, who were responsible for conducting tests and managing any unforeseen circumstances.

Initially, the subjects completed a 10-step walk, followed by a 6-m walk. This 6-m walk was performed twice in total. Gait data was collected during the middle of these walks, specifically excluding the acceleration and deceleration phases. In addition, the Timed Up and Go (TUG) test and Tinetti test, which are widely used in studies of walking and falls, were conducted as performance-oriented mobility assessments [20,21]. Participants engaged in activities such as sitting on chairs, rising to their feet, following walking instructions, or standing with their eyes closed. Their stability or instability during these tasks was then scored. Based on these tests, we categorized participants into high-risk fall groups. Additionally, while the participants were performing these tasks, we collected data on their walking patterns (Fig. 2).

Figure 2.

Structure of the gait analysis room.

TUG, Timed Up and Go test. Azure Kinect, Microsoft Corp.

Skeleton analysis and artificial intelligence models

We used Azure Kinect and its software development kit to acquire RGB images and depth data [22]. This equipment enables us to capture three-dimensional (3D) skeleton information from subjects. We have also implemented an automatic quality inspection framework to filter out noisy data automatically. Furthermore, by using 3D skeleton refining tool, we were able to generate refined skeleton data, as depicted in Fig. 3A [23].

Figure 3.

Skeleton analysis and artificial intelligence (AI) models.

(A) Methods of skeleton analysis. (B) AI algorithm.

CKD, chronic kidney disease; GRU, gated recurrent unit; RNN, recurrent neural network; SDK, software development kit. Azure Kinect, Microsoft Corp.

While participants walked, between 80 and 120 frames of skeleton data were collected at a speed of 20 to 25 frames per second. The gait parameters were then extracted from this joint three-axis data. The organization of the gait parameter, based on the joint three-axis data, is displayed in Table 1. Our gait analysis provides a total of 44 parameters, including movements of the head, spine, hip, knee, and foot joints. The skeleton data were analyzed using various artificial intelligence (AI) classification models, including GRU (gated recurrent unit) and RNN (recurrent neural network), to distinguish the healthy population and CKD patients. The derived data were then compared with diagnostic labels, which were based on medical diagnostic data. The analysis was conducted using accuracy, sensitivity, specificity, precision, recall, and F1 score, metrics that have proven accurate in previous studies [24]. Ultimately, our goal is to develop a model capable of distinguishing between patients with CKD and those without, by analyzing the gait parameters of each subject.

Gait parameters in skeleton analysis

Inertial measurement unit analysis and artificial intelligence models

Before the walk test, subjects were equipped with devices to collect IMU data. This process involved gathering information from the three-axis gyroscope and three-axis accelerometer, and applying a pre-processing technique to eliminate noise using digital filter algorithms. Only data collected during the walking phase were used in the study, excluding measurements taken before the walk commenced and after it had ceased.

1) Inertial measurement unit data selection and preprocessing method

In this study, three-axis acceleration data and three-axis gyroscope data were generated as input to the model. Only the IMU data measured during 10-second walking and 6-meter walking were analyzed. Data that were missing due to errors at the time of measurement or were determined unsuitable for analysis were excluded. The data measured at 50 Hz by IMU were segmented into 3-second windows (150 samples) to generate the data, and the windows were slid by 12 samples. Windows with missing data (missing packets due to communication problems) were not used for segmentation. There were 7 labels: 0 for patients without CKD, 1 to 5 according to CKD stage, and 6 for hemodialysis or peritoneal dialysis.

All data were normalized using the standard scale, with missing data excluded. Subjects in each class were divided into a training set and a testing set, and the model’s generalization performance was evaluated on a subject-by-subject basis. Furthermore, after the window split, the ratio of training sets to testing sets in each class was approximately 8:2, as shown in Fig. 4A.

Figure 4.

Inertial measurement unit (IMU) analysis and artificial intelligence (AI) models.

(A) IMU data segmentation. (B) AI model and architecture of analysis.

CNN, convolutional neural network; 1D, one-dimensional.

2) Methods and architecture of artificial intelligence model analysis

The CKD classification network consists of a one-dimensional (1D) convolutional neural network (CNN). Four distinct models were developed for each sensor placement site (wrist, waist) and each gait measurement method, with training subsequently conducted. The 1D CNN model is structured with feature extraction part, which is composed of convolution layers, and classification part, which is composed of fully connected layers. The information gleaned from the feature extraction is then relayed to the classifier, which consists of dense layers and a softmax layer. In the context of CNN, the input signal is processed as a time series signal, necessitating the use of a 1D convolution operation. This operation is employed to analyze the characteristics of the gait signal (Fig. 4B). We split the training and validation sets using a stratified approach and used k-fold cross-validation to evaluate performance comprehensively in a way that does not depend on specific targets. Specifically, when this method is practically applied, 1) a developed model with training data will be fine-tuned with a validation set to strengthen the model, or 2) a model will be learned with not only training data but also all datasets.

Protocol of the bioelectrical impedance analysis measurement

Subjects were instructed to consume meals 2 hours before BIA measurement to prevent interference from digestion. For dialysis patients, BIA measurements were performed within 10 to 30 minutes after dialysis. Once subjects arrived to the gait analysis room, they were instructed to stand for 5 minutes with light clothes and BIA was measured using the 790 device (InBody) in an upright position. They underwent BIA measurements with the same machine before and after the health intervention.

Protocol of the health intervention program

The protocol of the planned health intervention program is shown in Fig. 5.

Figure 5.

Protocol of the health intervention program.

EMR, electronic medical record; PHR, personal health record.

Personal health information was gathered using smartphone applications, and Health Cube (Health Bridge) models were employed to assess the health status of members. Following an 8-week healthcare intervention service, the performance of the intervention was managed. Additionally, life logs, including diet photos, exercise details, health coaching records, and self-reported health information, were collected. The detailed methods are described below.

Health cube classification

We divided the participants into 27 categories based on their classification of physical activity (high, medium, and low), disease (hyperlipidemia, diabetes, and hypertension), and weight (normal, obese, and underweight). The health goal was set to be one level higher than the subject’s current health status, and exercise and nutritional management were implemented.

Eight-week health intervention

Using the developed app, strength training and aerobic exercise were performed once or twice a week and nutrition was appropriately managed, depending on the subject’s Health Cube classification and health goal. We analyzed and provided customized health coaching to subjects based on their activity, step count, InBody diagnosis results, and meal photos.

Study variables

The variables collected in this study included the following: the appendicular skeletal muscle index (ASMI), which was obtained using BIA to determine sarcopenia, and a handgrip test (Table 2). Sarcopenia was categorized into three stages based on the criteria outlined in Table 3. Probable sarcopenia was identified by criterion 1. The diagnosis was confirmed by additional documentation of criterion 2. If criteria 1, 2 and 3 are all met, sarcopenia was considered severe (Table 3) [25]. To align the gait analysis with existing test methods, we conducted 10-second walk, 6-meter walk, TUG, and Tinetti tests. Blood and urine tests were performed for patients, and electronic medical records were reviewed to investigate medication use and disease codes for all subjects. Additionally, BMD was measured using a dual X-ray absorptiometry scan for patients only (Table 2).

Types and definitions of collected variables

Definitions of sarcopenia

Gait analysis schedule

The detailed schedule for gait analysis was as follows. Initially, the patient was escorted to the examination room, where they took a 10-minute rest, provided their informed consent, and completed a health-related survey and BIA study. Subsequently, after donning IMU sensor, their gait was measured (Table 4).

Time sequence of gait analysis

Outcome measurements

All CKD subjects in this study are regular outpatients at Hallym University Chuncheon Sacred Heart Hospital. Therefore, any incidents of falls, fractures, hospitalizations, and deaths will be confirmed at the 1- and 3-year marks. Laboratory tests will be conducted during each outpatient visit (every 1 to 6 months). Additionally, BMD tests will be performed annually.

Results

Baseline characteristics of the participants

Out of 493 participants, 217 did not have any disease including CKD, while 276 did. The age and sex of the two groups were not matched, as the study’s aim was to gather data on both normal and pathological gait. The CKD group was older (CKD, 65 years vs. normal, 38 years) and had a higher proportion of men than the normal population (CKD, 157 [64.3%] vs. normal, 87 [35.7%]). The mean BMI was higher in the CKD group than in the normal control group (CKD, 24.98 kg/m2 vs. normal, 23.63 kg/m2). The ASMI was not significantly different between the two groups, but the prevalence of sarcopenia was higher in the CKD group (CKD, 73 [26.5%] vs. normal, 31 [14.3%]). As anticipated, the CKD group had a higher number of slower TUG subjects (those who took 10 seconds or longer to perform the test; CKD, 204 [73.9%] vs. normal, 129 [59.4%]) and exhibited weaker hand grip strength compared to the normal population (CKD, 204 [73.9%] vs. normal, 129 [59.4%]). In the Tinetti test, a biomarker for balance and falls, the CKD group had a higher number of subjects at risk (Table 5).

Baseline characteristics of the subjects

We enrolled numerous young people to collect normal gait, and we plan to perform 1:1 matching by age and sex in the future for additional analyses to confirm differences with CKD patients.

Discussion

As society continues to age, the incidence of fall accidents is on the rise, leading to a significant economic burden globally. Consequently, there is a growing demand for technology that can prevent such accidents [26]. Falls can be attributed to a variety of factors, including muscle loss, balance impairment, nutritional deficiencies, comorbidities, and medication. Notably, gait plays a substantial role in the occurrence of falls [27,28].

Gait disorders can negatively impact numerous areas, such as patient quality of life, long-term survival, and the occurrence of additional complications, including falls [29,30]. In the realm of modern medicine, where there is an increasing focus on quality of life and daily health care, gait is emerging as a crucial factor [31]. Various factors, including aging, cognitive impairment, dementia, sarcopenia, and musculoskeletal disorders, are involved in gait disorders in complex, mutually interdependent ways [32].

Gait analysis and interventions to improve gait have been researched in various medical fields, including sports medicine, pediatrics, orthopedics, and neurology, as well as in the context of sarcopenia. However, there has not been extensive research or standardization related to gait analysis and interventions specifically tailored for CKD patients, including those with ESRD. Nonetheless, it is reasonable to hypothesize that gait performance could be indirectly improved by addressing underlying factors, such as CKD complications, nutritional deficiencies, and muscle weakness, through physical therapy, exercise, and other strategies for disease management. However, further studies investigating gait analysis and interventions specifically developed for CKD patients are necessary in order to develop more targeted strategies.

Previous studies have underscored the significance of walking and suggested the necessity for quantitative standards for walking data, to facilitate the analysis of walking disorders [33,34]. Therefore, this study conducted a gait analysis, utilizing patient skeleton and IMU data, to lay the groundwork for future research into gait disorders. The hope is that this analysis will offer a scientific foundation for a clinical comprehension of patients’ pathological gait mechanisms, and supply objective, quantifiable data for evaluation.

We also encourage lifestyle modifications in all subjects through the use of a smartphone application. The data collected will be subsequently utilized for gait analysis via ontology-based analysis. This will aid us in gaining a precise understanding of gait, provided that the subjects incorporate the use of IMU into their daily routines.

However, when analyzing gait, the presence of numerous confounding factors must be kept in mind. Gait can be affected by orthopedic problems, cognitive and neurologic disorders, medication, and nutritional status, as well as by demographic characteristics such as sex and age. Nonetheless, gait has the potential to serve as a biomarker for digital therapeutics because it can be measured longitudinally at regular intervals and is linked to an individual’s health status. A limitation of our study, though, is that it was not feasible to perform BMD measurements in individuals with normal clinical profiles, although these people could have underlying health problems.

Our study not only aims to evaluate gait disorders through gait analysis but also to utilize baseline data in the development of digital therapeutics. Despite the rapid growth of the digital therapeutic market, gait remains a highly attractive area of focus [26,27]. However, as previously mentioned, numerous factors influence walking, and there are insufficient standards for gait analysis data, particularly for CKD subjects, that can differentiate between normal and pathological gaits. Consequently, there is a growing demand and investment for large-scale clinical data and AI learning data by group. We also plan to conduct a subgroup analysis matched for age and sex.

Thus, in this study, we conducted health interventions on subjects using patient medical data. The aim was to establish AI learning data capable of distinguishing between normal and abnormal walking patterns. Throughout this process, we also collected data on the subjects’ daily activities.

We also aim to assess the efficacy of health interventions utilizing AI models, drawing on historical data. Over the course of follow-up, our goal is to analyze both normal and pathological gait in Koreans, as well as falls, hospitalization rates, and mortality following the display of pathological gait. Ultimately, we intend to use the gait itself, along with related elements, as digital biomarkers. We will then apply this data to the development of digital therapeutics, which can predict high-risk fall groups, prevent falls, and aid in the rehabilitation of CKD patients (Fig. 6).

Figure 6.

Study background and overview of the GAIT-CKD (Gait Analysis using Artificial Intelligence for digital Therapeutics of patients with Chronic Kidney Disease) study.

CKD, chronic kidney disease; CVD, cardiovascular disease; DTx, digital therapeutics; EMR, electronic medical record; PACS, picture archiving and communication system.

In conclusion, gait serves as a significant biomarker in the progression of CKD and can be utilized as an assessment variable after health interventions. Through this study, we aim to differentiate between pathologic and normal gait, and ascertain whether the stage of CKD can be determined by gait. Additionally, we will explore the potential of gait as a diagnostic and therapeutic biomarker for digital therapeutics. This will be achieved by examining the prevalence of hard outcomes based on patients’ gait and observing any improvements in their gait following our health intervention.

Notes

Conflicts of interest

All authors have no conflicts of interest to declare.

Funding

This research was supported by a grant from the National Research Foundation of Korea (grant number: NRF-2021R1I1A3057140), Korean government (MSIT) (No. 2022R1A5A8019303), Korea Technology and Information Promotion Agency for SMEs, funded by the Ministry of SMEs and Startups, Republic of Korea (grant number: S3368443), and the Korean Nephrology Research Foundation (FMC, 2022).

Data sharing statement

The data presented in this study are available upon reasonable request from the corresponding author.

Authors’ contributions

Conceptualization: HK

Formal analysis: YS, ICJ

Investigation: SR, Sunghan Lee, JK, SJ, SP, MK, WL, OR, YK, Sanggyu Lee, MA

Writing–original draft: YS, ICJ

Writing–review and editing: HK

All authors have read and agreed to the published version of the manuscript.

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Article information Continued

Figure 1.

Participants (CKD patients and healthy individuals) and study protocol.

BMD, bone mineral density; BIA, bioelectrical impedance analysis; CBC, complete blood count; CKD, chronic kidney disease; IMU, inertial measurement unit.

Figure 2.

Structure of the gait analysis room.

TUG, Timed Up and Go test. Azure Kinect, Microsoft Corp.

Figure 3.

Skeleton analysis and artificial intelligence (AI) models.

(A) Methods of skeleton analysis. (B) AI algorithm.

CKD, chronic kidney disease; GRU, gated recurrent unit; RNN, recurrent neural network; SDK, software development kit. Azure Kinect, Microsoft Corp.

Figure 4.

Inertial measurement unit (IMU) analysis and artificial intelligence (AI) models.

(A) IMU data segmentation. (B) AI model and architecture of analysis.

CNN, convolutional neural network; 1D, one-dimensional.

Figure 5.

Protocol of the health intervention program.

EMR, electronic medical record; PHR, personal health record.

Figure 6.

Study background and overview of the GAIT-CKD (Gait Analysis using Artificial Intelligence for digital Therapeutics of patients with Chronic Kidney Disease) study.

CKD, chronic kidney disease; CVD, cardiovascular disease; DTx, digital therapeutics; EMR, electronic medical record; PACS, picture archiving and communication system.

Table 1.

Gait parameters in skeleton analysis

Gait parameter Definition
Velocity Walking speed
Stride average Average of the distance between two successive placements of the same foot
Stride unbalance Differences of stride length
Max front spine Maximum forward/backward bending of the waist
Min front spine Minimum forward/backward bending of the waist
Front spine Average forward/backward bending of the waist
Max side spine Maximum left/right bending of the waist
Min side spine Minimum left/right bending of the waist
Side spine Average left/right bending of the waist
Max left knee Maximum left knee flexion
Min left knee Minimum left knee flexion
Left knee Average left knee flexion
Max light knee Maximum right knee flexion
Min right knee Minimum right knee flexion
Right knee Average right knee flexion
Max left hip Maximum left hip flexion
Min left hip Minimum left hip flexion
Left hip Average left hip flexion
Max right hip Maximum right hip flexion
Min right hip Minimum right hip flexion
Right hip Average right hip flexion
Left swing time The time from toe off to heel strike of the left foot
Left stance time Time of the left foot first touches the ground and ends when the left foot leaves the ground
Right swing time The time from toe off to heel strike of the right foot
Right stance time Time of the right foot first touches the ground and ends when the right foot leaves the ground
Height Distance from head to feet measured when walking
Left knee height Average height of the left knee observed when walking
Right knee height Average height of the right knee observed when walking
Max left knee height Maximum height of the left knee observed when walking
Max right knee height Maximum height of the right knee observed when walking
Min left knee height Maximum height of the left knee observed when walking
Min right knee height Maximum height of the right knee observed when walking
Max left foot side Maximum length of left foot off center to the left or right
Max right foot side Maximum length of right foot off center to the left or right
Min left foot side Minimum length of left foot off center to the left or right
Min right foot side Minimum length of right foot off center to the left or right
Max left foot head diff Maximum front/back length of head and left foot
Max right foot head diff Maximum front/back length of head and right foot
Min left foot head diff Minimum front/back length of head and left foot
Min right foot head diff Minimum front/back length of head and right foot
Max left hip side Maximum length by which the left pelvis deviates to the left/right
Min left hip side Minimum length by which the left pelvis deviates to the left/right
Max right hip side Maximum length by which the right pelvis deviates to the left/right
Min right hip side Minimum length by which the right pelvis deviates to the left/right

diff, difference.

Table 2.

Types and definitions of collected variables

Assessment Test Category Collected data
Explanatory note
Patients Normal Example Reference Unit
Sarcopenia diagnosis Epidemiology Inbody: ASMI Yes Yes 6.3 7.0 in male and 5.7 in female kg/m2
Handgrip Yes Yes 23 20–64 kg/m2
Gait analysis Skeleton and IMU measurements (2 turns, total 3 times) Yes Yes
Timed Up and Go test Yes Yes 15 10 sec
Tinetti test Yes Yes 20 25–28, low; 19–24, moderate; >19, high
Diagnosis Laboratory test Hemoglobin, BUN/Cr Yes No 12/20/0.1 12–14, 20/1.0 mg/dL
EMR Medication Yes Yes Amlodipine
EMR Disease code Yes Yes N189
PACS BMD Yes No Image Below –1.0
T and Z score

ASMI, appendicular skeletal muscle index; BMD, bone mineral density; BUN, blood urea nitrogen; Cr, creatinine; EMR, electronic medical record; IMU, inertial measurement unit; PACS, picture archiving and communication system.

Table 3.

Definitions of sarcopenia

Sarcopenia criterion Positive
1. Muscle mass: ASMI <7.0 kg/m2 in male and 5.7 kg/m2 in female
2. Muscle strength: hand grip <27 kg in male and <16 kg in female
3. Performance TUG ≥20 sec or gait speed <0.8 m/sec

ASMI, appendicular skeletal muscle index; TUG, Timed Up and Go test.

Table 4.

Time sequence of gait analysis

No. Diagnosis category Time (min)
1 Enter (if patient, 10-min rest) 10
2 Explain test and write consent
3 Health survey
4 Inbody test and equip IMU wearable devices 5
5 Gait analysis 1: 6 m-gait analysis 10 step-gait 3
6 Tinetti test 15
7 Timed Up and Go test 2
8 Exit (rest and check data collection) 5
Total time 40

IMU, inertial measurement unit.

Table 5.

Baseline characteristics of the subjects

Variable Total CKD group Normal group p-value
No. of subjects 493 276 217
Age (yr) 52.90 ± 19.06 64.78 ± 13.35 37.79 ± 13.82 <0.001
Male sex 244 (49.5) 157 (64.3) 87 (35.7) <0.001
CKD stage
 1 36 NA
 2 43 NA
 3 62 NA
 4 23 NA
 5 47 NA
 5D 65 NA
Body mass index (kg/m2) 24.39 ± 3.97 24.98 ± 4.20 23.63 ± 3.51 <0.001
ASMI (kg/m2) 7.03 ± 1.30 7.06 ± 1.26 6.99 ± 1.38 0.63
Sarcopenia 104 (21.1) 73 (26.4) 31 (14.3) 0.001
TUG results (sec) 11.51 ± 4.22 12.47 ± 5.24 10.31 ± 1.78 <0.001
TUG outcome, slow 333 (67.5) 204 (73.9) 129 (59.4) <0.001
Grip strength 28.25 ± 13.67 25.97 ± 11.78 31.15 ± 15.29 <0.001
Weak grip strength 130 (26.4) 98 (35.5) 32 (14.7) <0.001
Tinetti test results 25.89 ± 3.79 24.89 ± 4.73 27.17 ± 1.14 <0.001
Tinetti test outcome (n = 483)
 Low 426 (88.2) 216 (79.7) 210 (99.1) <0.001
 Moderate 32 (6.6) 31 (11.4) 1 (0.5)
 High 25 (5.2) 24 (8.9) 1 (0.5)

Data are expressed as mean ± standard deviation or number (%).

ASMI, appendicular skeletal muscle index; BMI, body mass index, CKD, chronic kidney disease; NA, not available; TUG, Timed Up and Go test.