Evidence map›Paper›PMID 37525241›Full record

ArticleBiomedical engineering online2023

Gait asymmetry in children with Duchenne muscular dystrophy: evaluated through kinematic synergies and muscle synergies of lower limbs.

Qiliang Xiong, Yuan Liu, Jieyi Mo, Yuxia Chen, Lianghong Zhang, Zhongyan Xia, Chen Yi, Shaofeng Jiang, Nong Xiao

Abstract read
In one paragraph

Article in Biomedical engineering online, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. The use of digital tools in rare neurological diseases towards a new care model: a narrative review.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Qiliang Xiong *Department of Biomedical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, China.
Yuan Liu *Department of Rehabilitation, Children's Hospital of Chongqing Medical University, Chongqing, China.
Jieyi MoDepartment of Biomedical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, China.
Yuxia ChenDepartment of Rehabilitation, Children's Hospital of Chongqing Medical University, Chongqing, China.
Lianghong ZhangDepartment of Biomedical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, China.
Zhongyan XiaDepartment of Biomedical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, China.
Chen YiDepartment of Biomedical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, China.
Shaofeng JiangDepartment of Biomedical Engineering, Nanchang Hangkong University, Nanchang, Jiangxi, China.
Nong XiaoDepartment of Rehabilitation, Children's Hospital of Chongqing Medical University, Chongqing, China. xiaonongwl@163.com.

Funding

National Natural Science Foundation of China 32000979
6 · The paper itself

Abstract

backgroundGait is a complex, whole-body movement that requires the coordinated action of multiple joints and muscles of our musculoskeletal system. In the context of Duchenne muscular dystrophy (DMD), a disease characterized by progressive muscle weakness and joint contractures, previous studies have generally assumed symmetrical behavior of the lower limbs during gait. However, such a symmetric gait pattern of DMD was controversial. One aspect of this is criticized, because most of these studies have primarily focused on univariate variables, rather than on the coordination of multiple body segments and even less investigate gait symmetry under a motor synergy of view.

methodsWe investigated the gait pattern of 20 patients with DMD, compared to 18 typical developing children (TD) through 3D Gait Analysis. Kinematic and muscle synergies were extracted with principal component analysis (PCA) and non-negative matrix factorization (NNMF), respectively. The synergies extracted from the left and right sides were compared with each other to obtain a symmetry value. In addition, bilateral spatiotemporal variables of gait, such as stride length, percentage of stance and swing phase, step length, and percentage of double support phase, were used for calculating the symmetry index (SI) to evaluate gait symmetry as well.

resultsCompared with the TD group, the DMD group walked with decreased gait velocity (both p < 0.01), stride length (both p < 0.01), and step length (both p < 0.001). No significant difference was found between groups in SI of all spatiotemporal parameters extracted between the left and right lower limbs. In addition, the DMD group exhibited lower kinematic synergy symmetry values compared to the TD group (p < 0.001), while no such significant group difference was observed in symmetry values of muscle synergy.

conclusionsThe findings of this study suggest that DMD influences, to some extent, the symmetry of synergistic movement of multiple segments of lower limbs, and thus kinematic synergy appears capable of discriminating gait asymmetry in children with DMD when conventional spatiotemporal parameters are unchanged.

Indexed as

Muscular Dystrophy, DuchenneBiomechanical PhenomenaChildGaitHumansLower ExtremityMuscle, Skeletal

Identifiers

PMID37525241
PMCPMC10388506

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.