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CLINICAL TRIAL article

Front. Neurol., 06 June 2023
Sec. Neurorehabilitation
This article is part of the Research Topic Individual’s Mechanics, Movement and Kinematics Post-Stroke View all 10 articles

Gait characteristics related to fall risk in patients with cerebral small vessel disease

\r\nYajing Wang,&#x;Yajing Wang1,2Yanna Li,&#x;Yanna Li1,2Shoufeng Liu,Shoufeng Liu1,2Peipei Liu,Peipei Liu1,2Zhizhong Zhu,Zhizhong Zhu1,3Jialing Wu,
Jialing Wu1,2*
  • 1Clinical College of Neurology, Neurosurgery and Neurorehabilitation, Tianjin Medical University, Tianjin, China
  • 2Department of Neurology, Tianjin Huanhu Hospital, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Diseases, Tianjin Neurosurgical Institute, Tianjin, China
  • 3Department of Rehabilitation, Tianjin Huanhu Hospital, Tianjin, China

Background: Falls and gait disturbance are significant clinical manifestations of cerebral small vessel disease (CSVD). However, few relevant studies are reported at present. We aimed to investigate gait characteristics and fall risk in patients with CSVD.

Methods: A total of 119 patients with CSVD admitted to the Department of Neurology at Tianjin Huanhu Hospital between 17 August 2018 and 7 November 2018 were enrolled in this study. All patients underwent cerebral magnetic resonance imaging scanning and a 2-min walking test using an OPAL wearable sensor and Mobility Lab software. Relevant data were collected using the gait analyzer test system to further analyze the time-space and kinematic parameters of gait. All patients were followed up, and univariate and multivariate logistic regression analyses were conducted to analyze the gait characteristics and relevant risk factors in patients with CSVD at an increased risk of falling.

Results: All patients were grouped according to the presence or absence of falling and fear of falling and were divided into a high-fall risk group (n = 35) and a low-fall risk group (n = 72). Logistic multivariate regression analysis showed that the toe-off angle [odds ratio (OR) = 0.742, 95% confidence interval (CI) 0.584–0.942, p < 0.05], toe-off angle coefficient of variation (CV) (OR = 0.717, 95% CI: 0.535–0.962, p < 0.05), stride length CV (OR = 1.256, 95% CI: 1.017–1.552, p < 0.05), and terminal double support CV (OR = 1.735, 95% CI: 1.271–2.369, p < 0.05) were statistically significant (p < 0.05) and were independent risk factors for high-fall risk in patients with CSVD.

Conclusion: CSVD patients with seemingly normal gait and ambulation independently still have a high risk of falling, and gait spatiotemporal-kinematic parameters, gait symmetry, and gait variability are important indicators to assess the high-fall risk. The decrease in toe-off angle, in particular, and an increase in related parameters of CV, can increase the fall risk of CSVD patients.

1. Introduction

Cerebral small vascular disease (CSVD) refers to a series of imaging and clinical manifestations that characterize a syndrome caused by any functional or structural pathological damage to small cerebral vessels, such as terminal arterioles, venules, and capillaries. Gait disorder is one of the main symptoms of CSVD patients (1, 2). Studies have shown that most falls of stroke patients after discharge occurs during walking, and gait disorder is an independent predictor of patients' fall risk. However, most studies are described by scale, observation, and other methods, with low accuracy, strong subjectivity, and limited dimensions (3). With the development of ergonomics, a large number of gait parameters can be obtained using wearable sensor devices, and gait symmetry and gait variability can be calculated (4). Both reflect the ability to maintain a stable and consistent walking rhythm in the motor control system. However, we found that there were few studies on gait symmetry and variability in patients with CSVD (5, 6). Therefore, we used wearable devices to measure the parameters related to the gait of patients with CSVD. Furthermore, we calculated gait symmetry and variability. We investigated the gait parameters that contributed to the high risk of falls among follow-up patients with a high risk of falling. Through our study, we can provide early rehabilitation treatment for patients with CSVD and reduce the occurrence of falls.

2. Materials and methods

2.1. Patients

In this study, 119 patients with CSVD were hospitalized at the Department of Neurology of Tianjin Huanhu Hospital, Tianjin, China between 17 August 2018 and 7 November 2018. The study was registered with the Chinese Clinical Trial Registry (Clinical Trial Registration No. ChiCTR2100042031) and was approved by the Ethics Committee of Tianjin Huanhu Hospital. All patients underwent head magnetic resonance imaging, including T2, fluid-attenuated inversion recovery, diffusion-weighted imaging, apparent diffusion coefficient, and gradient echo sequences. All patients were able to walk and complete the evaluation independently. All the clinical data were complete.

The inclusion criteria were as follows: (1) age ≥18 years; (2) met the diagnostic criteria for mild stroke [National Institutes of Health Stroke Scale (NIHSS) score ≤3]; (3) according to the pathogenesis, the selection (Trial of Org 10172 in Acute Stroke Treatment) type was small-artery occlusion; (4) all participants could walk independently and safely for 2 min without help from others or assistive devices; and (5) all participants were fully informed of the research process and signed the informed consent form.

The exclusion criteria were as follows: clinical diagnosis of dementia, mental disorders, severe cerebral hemorrhage, and other systemic diseases affecting gait, such as joint injury, arthritis, cervical spine disease, and lumbar spine disease.

Participants were selected according to inclusion criteria and exclusion criteria (Figure 1).

FIGURE 1
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Figure 1. Flow chart of the inclusion and exclusion process of included patients.

2.2. Study design

2.2.1. General assessment

General clinical data of all patients, including age, sex, height, weight, and medical history, were collected and analyzed.

2.2.2. Assessment of gait function

All enrolled patients underwent a 2-min walk test under the guidance of a physician, which was conducted in an empty room dedicated to the evaluation. The patients walked freely along a straight line which could be turned back for 2 min. Patients were simulated in advance to ensure that they were familiar with the test. At the start of the experiment, the OPAL wearable sensor (APDM) and Mobility Lab software (https://apdm.com/wearable-sensors/) were used for the 2-min walking test. The instrument had a total of six sensors, which were placed on the patient's body by professionals according to the following positions. The first sensor was worn at the uppermost sternal handle of the sternum, the second sensor was worn at the lowermost fifth lumbar vertebra at the lumbosacral junction, and the third and fourth sensors were worn on the dorsal side of the bilateral wrist joint. The fifth and sixth sensors were worn on the dorsum of both feet.

2.2.3. Assessment of gait parameters

Gait parameter data were collected through the gait analysis and test system and transmitted to a computer terminal. Then, the time-space and kinematic gait parameters were analyzed. Gait symmetry was assessed using the Asymmetry Index (AI). The AI was calculated as follows:

AI=|XL-XR|/max(XL,XR)× 100,

with L and R representing the left and right sides of the patient, respectively (5). X represents the corresponding gait parameter used in the analysis. This study mainly included stride length, single-limb support, terminal double support, swing, foot strike angle, and toe-off angle. Gait variability was assessed using the coefficient of variation. First, the coefficient of variation (CV) was calculated using the formula “standard deviation/mean,” which represents the gait variability (CVL represents the left variability and CVR represents the right variability). The next step was to integrate the variability of the left and right gait parameters using the formula (7, 8):

(CVL+CVR)/2×100.

The parameters included were stride length, single limb support, terminal double support, swing, toe-off angle, and foot strike angle.

2.2.4. Main outcomes

All patients were followed up for the presence of falls and the presence of fear of falling (FOF). The assessment of FOF was as follows: According to the FOF scale developed by American scholar Tinetti in 1993 (9), patients were asked, “Are you afraid or worried about falling?” The presence of FOF was determined by answering “not afraid,” “slightly afraid,”' “somewhat afraid,” and “very afraid.” Those who answered “not afraid” were defined as having no FOF, and those who answered with any other option were defined as having a FOF. Based on the presence of FOF or falling, the patients were divided into a high-fall risk (HFR) group and a low-fall risk (LFR) group. If the patient had no history of falls and answered as “not afraid,” they were assigned to the LFR group, and patients who had a history of falls or answered “slightly afraid,” “somewhat afraid,” or “very afraid,” were assigned to the HFR group.

2.3. Statistical analysis

Data processing was performed using SPSS 24.0 software (SPSS Inc., Chicago, IL, USA). Normally distributed numerical data were presented as the mean ± standard deviation (x ± s), and the independent sample t-test was used for comparison between the groups. Numerical data that showed a skewed distribution were presented as the median (the first quartile, third quartile) [M (Q1, Q3)], and the Mann–Whitney U-test was used for comparison between groups. Count data were expressed in the form of cases (percentage) [n (%)], and an X2 test was used for comparison between groups. Data from both groups were analyzed using multivariate logistic regression, and a p-value of <0.05 was considered statistically significant. In this study, logistic regression was used for the multivariate analysis of the two groups of data.

3. Results

3.1. Baseline clinical characteristics

The demographic characteristics of the LFR and HFR groups are summarized in Table 1. A total of 119 patients were included in this study, and the mean (SD) age was 59.55 (9.89) years. In total, 94 cases were male patients, 25 cases were female patients, and 12 cases were lost to follow-up, including the LFR (72 cases) and HFR group (35 cases). Age, sex, height, weight, diabetes mellitus, cardiac disease, and smoking did not differ significantly between the groups; however, the presence of hypertension was higher in the HFR group compared with the LFR group (p < 0.05) (Table 1).

TABLE 1
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Table 1. Demographic characteristics of participants.

3.2. Gait analysis in the LFR group and HFR group

Compared to patients in the LFR group, patients in the HFR group had lower stride frequency, slower stride speed, shorter stride length, and longer gait cycle time (p < 0.05). Simultaneously, the proportion of double limb support and terminal double support increased during each gait cycle, while the proportion of single limb support and swing decreased (p < 0.05). As shown in Table 2, the patients in the HFR group had smaller foot strike and toe-off angles (p < 0.05) (Table 2).

TABLE 2
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Table 2. Comparison of time-space and kinematic parameters between the two groups (x ± s).

3.3. Comparison of gait symmetry between the two groups

This study compared gait symmetry between the two groups and found that the foot strike angle AI increased in patients in the HFR group (p < 0.05), whereas the stride length AI, toe-off angle AI, single-limb support AI, terminal double support AI, and swing AI showed no significant differences between the groups (p > 0.05) (Table 3).

TABLE 3
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Table 3. Comparison of gait symmetry between the two groups [%, M (Q1, Q3)].

3.4. Comparison of gait variability between the two groups

After analyzing gait variability in both groups, we found that the stride length CV, single limb support CV, terminal double support CV, swing CV, foot strike angle CV, and toe-off angle CV were significantly higher in the HFR vs. LFR group (p < 0.05) (Table 4).

TABLE 4
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Table 4. Comparison of gait variability between the two groups [%, M (Q1, Q3)].

3.5. The regression analysis of influencing factors

All statistically significant gait indicators were included in the logistic multivariate regression analysis. The parameters of the toe-off angle, toe-off angle CV, stride length CV, and terminal double support CV were statistically significant (p < 0.05). These were identified as independent risk factors for falling in patients with CSVD. However, the remaining time-space and kinematic parameters of gait, gait symmetry parameters, and gait variability parameters were not statistically significant (p > 0.05) (Table 5).

TABLE 5
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Table 5. Results of the multivariate logistic regression analysis.

4. Discussion

4.1. Fall and fear of falling in patients with CSVD

Falls caused by gait disorders in patients with CSVD seriously affect their quality of life and are closely related to a poor prognosis (1, 2). FOF is a precursor to falling in patients with CSVD. FOF refers to the reduction of confidence or fall efficacy to avoid falling while participating in certain activities that the patients are capable of (9). Some studies (10) have shown that FOF not only exists in elderly people who have a history of falling but also in elderly people who have never experienced a fall. FOF reduces the patients' confidence in activities, which is not conducive to the rehabilitation of motor function in patients with stroke and affects the recovery of their neurological function. One study has shown that the incidence of FOF in patients with stroke during hospitalization was 54%, and the incidence of FOF in stroke patients after discharge was 32–66% (11). Our study found that the incidence of FOF in patients with CSVD who could walk independently was 32.71%. The possible reasons are related to the included population in this study and the time from onset to follow-up. The mean age of CSVD patients included in this study was 59.55 ± 9.89 years, NIHSS score ≤3 points, and the time from onset to follow-up was 4 years. Therefore, younger patients, mild stroke, and short follow-up time may lead to a lower risk of falls.

4.2. Time-space parameters and kinematic parameters of gait in patients with CSVD

Spatio-temporal parameters and kinematic parameters are important indicators of gait. Abnormal spatio-temporal and kinematic parameters often lead to gait instability, and patients are more likely to fall (12). In our study, we found that patients with CSVD in the HFR group had a shortened stride length, reduced stride frequency, and decreased stride speed. A reduction in stride length usually means a reduction in forward propulsion force and impairment of balance (13). Stride speed reflects the movement ability of an individual, and a decrease of 0.1 m/s has a significant clinical significance (14). The decline in walking speed reflects a decrease in the propulsion of the gait and is a sign of gait damage, and patients are more likely to fall when they want to increase their walking speed or are not prepared. In our study, the average stride speed in the HFR group decreased by 0.13 m/s compared to the LFR group, i.e., fall risk increased. We found that not only was the gait cycle of patients in the HFR group extended but also the proportion of double limb support and terminal double support in the gait cycle was extended, and the proportion of single limb support was reduced. This was to prevent falls and maintain body balance, which further absorbed shocks and maintained load-bearing stability by extending the time both feet contact the ground during double limb support and shortening the instability of single limb support (15). Stride frequency is negatively correlated with the gait cycle (16). When the gait cycle is prolonged, the gait frequency decreases, which is a compensatory manifestation of gait. Once entering the decompensation stage, the probability of patients falling increases sharply. Swing mainly reflects an individual's floor-clearance ability (17). The proportion of swing-phase patients in the HFR group was significantly shortened, resulting in a reduction in their floor clearance ability.

We included the important parameters of gait kinematics: the foot strike angle and toe-off angle. The foot strike angle reflects shock absorption and maintains forward stability (18), while the toe-off angle reflects the forward gait force, which is an important reflection of the ground clearance ability of the foot (19). In our study, we found that the foot strike and toe-off angles in patients with high-fall risk decreased during walking, indicating that CSVD not only affects the stability of the body moving forward but also affects the driving force for forward movement, resulting in patients with decreased ground clearance ability of the foot, increased instability, and increased fall risk.

4.3. Symmetry and variability of gait in patients with CSVD

In our study, not only the conventional gait parameters were analyzed, but the symmetry and variability of gait were quantified using formulas. The AI of the foot strike angle in the HFR group was significantly higher compared to the LFR group. In related studies (20), human gait symmetry is typically assumed to be consistent with left and right gait functions. The gait symmetry of healthy humans can effectively reduce the energy consumption of walking, reduce the risk of falling, and provide a stable and comfortable walking mode (21). The higher the AI, the greater the asymmetry deviation of the bilateral limbs during walking, and the higher the influence on the stability of walking (22). Therefore, the results of our study indicated that the lower extremities of patients in the HFR group had greater differences in shock absorption and maintenance of progressive stability while walking stability was poor. Compared with the LFR group, the AI of each gait parameter in the HFR group was higher, indicating that the gait asymmetry of the left and right limbs was more prominent in the HFR group during walking. Some studies have found that the increase of gait parameter asymmetry in stroke patients during walking is related to the decrease in progressive stability, impaired balance function, and increased risk of falls. Our further analysis found that there was a significant difference in the AI elevation of the foot strike angle between the two groups, and the foot strike angle reflected the foot clearance ability, so our study showed that the foot clearance ability of patients in the HFR group increased asymmetrically and increased the risk of fall.

Gait variability refers to the stability of gait during walking, which reflects the ability of the motion control system to maintain a stable and consistent walking rhythm (23). However, some studies have shown that the heterogeneity of gait time-space parameters is large, and gait variability is more effective in evaluating fall risk (24). In our study, we found that the stride length CV, single-limb support CV, terminal double support CV, swing CV, foot strike angle CV, and toe-off angle CV of patients with CSVD in the HFR group were significantly higher than those in the LFR group, suggesting that patients in the HFR group had decreased gait stability during walking. In addition, increased gait variability leads to increased energy expenditure, resulting in difficulty in maintaining postural balance and a higher risk of falls (25). We further included the indicators with statistical differences between the two groups for logistic regression analysis and found that toe-off angle, toe-off angle CV, stride length CV, and terminal double support CV were independent risk factors for falls in patients with CSVD. Terminal double support, which accounts for 10% of the gait cycle, is mainly responsible for weight release and weight transfer during walking (26). Its increased variability indicates that as the inconsistency of weight release and transfer of the lower limbs increases, the ability of the body to maintain stability decreases, and the risk of falling increases.

5. Conclusion

The high risk of falls in patients with CSVD is closely related to the time-space and kinematic parameters of gait, as well as the symmetry and variability of gait. In particular, toe-off angle, toe-off angle CV, stride length CV, and terminal double support CV were independent risk factors for falling in patients with CSVD. Our study could promote a better understanding of the risk factors for falling caused by gait disturbance in patients with CSVD. Our findings provide evidence for clinical work, which is helpful in administering targeted drugs or early rehabilitation intervention. However, this study has some room for improvement. First, some kinematic parameters, such as knee joint and hip joint, could be included while selecting some kinematic parameters which have the greatest impact on gait. In this way, it would be more sufficient in reflecting the comprehensive effect of cerebral microvascular disease on gait. Second, we could conduct a multicenter study and carry out rehabilitation interventions on gait disorders in patients so as to provide a more effective basis for guiding clinical treatment.

Data availability statement

The datasets presented in this study can be found in online repositories. The name of the repository and accession number can be found below: Figshare, https://figshare.com/, doi: 10.6084/m9.figshare.22096259.

Ethics statement

The studies involving human participants were reviewed and approved by Ethics Committee member: Xinping Wang, Yanming Zhang, Jinling Zhang, Tong Han, Yi Li, Yangui Xu, and Mingyu Li. Chairman: Xinping Wang. The patients/participants provided their written informed consent to participate in this study.

Author contributions

YW conceived the study and was responsible for all research aspects. YL collected the data. SL and PL completed all statistical analyses and wrote the manuscript. ZZ assessed the gait function of patients. JW reviewed and commented on the data analysis and drafts. All the authors critically reviewed and approved the final version of the manuscript.

Funding

This study was funded by the Tianjin Key Medical Discipline (Specialty) Construction Project (No. TJYXZDXK-052B) and Tianjin Health Research Project (No. TJWJ2022MS031 and No. TJWJ2022MS030).

Acknowledgments

We are grateful to the patients and their families. We would also like to thank our colleagues for their assistance. Finally, we wish to thank Editage (www.editage.cn) for English language editing.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. van der Holst HM, van Uden IW, Tuladhar AM, de Laat KF, van Norden AG, Norris DG, et al. Factors associated with 8-year mortality in older patients with cerebral small vessel disease: the Radboud University Nijmegen diffusion tensor and magnetic resonance cohort (RUN DMC) study. JAMA Neurol. (2016) 73:402–9. doi: 10.1001/jamaneurol.2015.4560

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Bower K, Thilarajah S, Pua YH, Williams G, Tan D, Mentiplay B, et al. Dynamic balance and instrumented gait variables are independent predictors of falls following stroke. J Neuroeng Rehabil. (2019) 16:3. doi: 10.1186/s12984-018-0478-4

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Kim YJ, Kwon HK, Lee JM, Cho H, Kim HJ, Park HK, et al. Gray and white matter changes linking cerebral small vessel disease to gait disturbances. Neurology. (2016) 86:1199–207. doi: 10.1212/WNL.0000000000002516

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Ichihashi N, Ikezoe T, Sato S, Ibuki S. Gait asymmetry assessment for older adults by measuring circular gait speed. Geriatr Gerontol Int. (2019) 19:736–9. doi: 10.1111/ggi.13691

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Galna B, Lord S, Rochester L. Is gait variability reliable in older adults and Parkinson's disease? Towards an optimal testing protocol. Gait Posture. (2013) 37:580–5. doi: 10.1016/j.gaitpost.2012.09.025

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Son M, Han SH, Lyoo CH, Lim JA, Jeon J, Hong KB, et al. The effect of levodopa on bilateral coordination and gait asymmetry in Parkinson's disease using inertial sensor. npj Parkinsons Dis. (2021) 7:42. doi: 10.1038/s41531-021-00186-7

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Zhang M, Artan NS, Gu H, Dong Z, Burina Ganatra L, Shermon S, et al. Gait study of Parkinson's disease subjects using haptic cues with A motorized walker. Sensors.(2018) 18:3549. doi: 10.20944/preprints201809.0211.v1

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Serrao M, Chini G, Caramanico G, Bartolo M, Castiglia SF, Ranavolo A, et al. Prediction of responsiveness of gait variables to rehabilitation training in Parkinson's disease. Front Neurol. (2019) 10:826. doi: 10.3389/fneur.2019.00826

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Tinetti ME, Powell L. Fear of falling and low self-efficacy: a case of dependence in elderly persons. J Gerontol. (1993) 48:35–8. doi: 10.1093/geronj/48.Special_Issue.35

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Friedman SM, Munoz B, West SK, Rubin GS, Fried LP. Falls and fear of falling: which comes first? A longitudinal prediction model suggests strategies for primary and secondary prevention. J Am Geriatr Soc. (2002) 50:1329–35. doi: 10.1046/j.1532-5415.2002.50352.x

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Liu TW, Ng GYF, Ng SSM. Effectiveness of a combination of cognitive behavioral therapy and task-oriented balance training in reducing the fear of falling in patients with chronic stroke: study protocol for a randomized controlled trial. Trials. (2018) 19:168. doi: 10.1186/s13063-018-2549-z

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Li P, Wang Y, Jiang Y, Zhang K, Yang Q, Yuan Z, et al. Cerebral small vessel disease is associated with gait disturbance among community-dwelling elderly individuals: the Taizhou imaging study. Aging. (2020) 12:2814–24. doi: 10.18632/aging.102779

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Studenski S, Perera S, Patel K, Rosano C, Faulkner K, Inzitari M, et al. Gait speed and survival in older adults. JAMA. (2011) 305:50–8. doi: 10.1001/jama.2010.1923

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Cha HG, Kim TH, Kim MK. Therapeutic efficacy of walking backward and forward on a slope in normal adults. J Phys Ther Sci. (2016) 28:1901–3. doi: 10.1589/jpts.28.1901

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Prateek GV, Mazzoni P, Earhart GM, Nehorai A. Gait cycle validation and segmentation using inertial sensors. IEEE Trans Bio Med Eng. (2020) 67:2132–44. doi: 10.1109/TBME.2019.2955423

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Lindemann U. Spatiotemporal gait analysis of older persons in clinical practice and research: which parameters are relevant? Z Gerontol Geriatr. (2020) 53:171–8. doi: 10.1007/s00391-019-01520-8

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Sakuma K, Tateuchi H, Nishishita S, Okita Y, Kitatani R, Koyama Y, et al. Immediate effects of stance and swing phase training on gait in patients with stroke. Int J Rehabil Res. (2021) 44:152–8. doi: 10.1097/MRR.0000000000000464

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Moore SR, Martinez A, Kröll J, Strutzenberger G, Schwameder H. Simple foot strike angle calculation from three-dimensional kinematics: a methodological comparison. J Sports Sci. (2022) 40:1343–50. doi: 10.1080/02640414.2022.2080162

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Anderson FC, Goldberg SR, Pandy MG, Delp SL. Contributions of muscle forces and toe-off kinematics to peak knee flexion during the swing phase of normal gait: an induced position analysis. J Biomech. (2004) 37:731–7. doi: 10.1016/j.jbiomech.2003.09.018

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Auvinet E, Multon F, Manning V, Meunier J, Cobb JP. Validity and sensitivity of the longitudinal asymmetry index to detect gait asymmetry using Microsoft Kinect data. Gait Posture. (2017) 51:162–8. doi: 10.1016/j.gaitpost.2016.08.022

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Cabral S, Fernandes R, Selbie WS, Moniz-Pereira V, Veloso AP. Inter-session agreement and reliability of the Global Gait Asymmetry index in healthy adults. Gait Posture. (2017) 51:20–4. doi: 10.1016/j.gaitpost.2016.09.014

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Cabral S, Resende RA, Clansey AC, Deluzio KJ, Selbie WS, Veloso AP. A global gait asymmetry index. J Appl Biomech. (2016) 32:171–7. doi: 10.1123/jab.2015-0114

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Jabbar KA, Tan DGH, Seah WT, Lau LK, Pang BW, Ng DH, et al. Enhanced gait variability index and cognitive performance in Asian adults: results from the Yishun Study. Gait Posture. (2022) 97:216–21. doi: 10.1016/j.gaitpost.2022.07.156

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Nohelova D, Bizovska L, Vuillerme N, Svoboda Z. Gait variability and complexity during single and dual-task walking on different surfaces in outdoor environment. Sensors. (2021) 21. doi: 10.3390/s21144792

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Schlachetzki JCM, Barth J, Marxreiter F, Gossler J, Kohl Z, Reinfelder S, et al. Wearable sensors objectively measure gait parameters in Parkinson's disease. PLoS ONE. (2017) 12:e0183989. doi: 10.1371/journal.pone.0183989

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Michnik R, Nowakowska K, Jurkojć J, Jochymczyk-Wozniak K, Kopyta I. Motor functions assessment method based on energy changes in gait cycle. Acta Bioeng Biomech. (2017) 19:63–75. doi: 10.1007/978-3-319-39904-1_7

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: cerebral small vessel disease, walking, fall, gait analysis, gait parameters

Citation: Wang Y, Li Y, Liu S, Liu P, Zhu Z and Wu J (2023) Gait characteristics related to fall risk in patients with cerebral small vessel disease. Front. Neurol. 14:1166151. doi: 10.3389/fneur.2023.1166151

Received: 14 February 2023; Accepted: 15 May 2023;
Published: 06 June 2023.

Edited by:

Yih-Kuen Jan, University of Illinois at Urbana-Champaign, United States

Reviewed by:

Chi-Wen Lung, Asia University, Taiwan
Qinyin Qiu, Rutgers University, Newark, United States

Copyright © 2023 Wang, Li, Liu, Liu, Zhu and Wu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jialing Wu, wywjl2009@hotmail.com

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.