Jacqueline Romkes , Katrin Bracht-Schweizer , Michèle Widmer , Morgan Sangeux , Elke Viehweger
{"title":"杜氏肌营养不良症患儿上半身步态偏差。","authors":"Jacqueline Romkes , Katrin Bracht-Schweizer , Michèle Widmer , Morgan Sangeux , Elke Viehweger","doi":"10.1016/j.clinbiomech.2024.106402","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Duchenne muscular dystrophy is primarily a disease of progressive muscle degeneration affecting the whole body. It is important to preserve the patients' walking ability as long as possible. Inconclusive information on Duchenne muscular dystrophy gait pattern is available for the lower body and missing for the upper body. This study aimed to objectively investigate upper body gait deviations in a group of patients with Duchenne muscular dystrophy compared to typically developing peers.</div></div><div><h3>Methods</h3><div>Kinematic data of twelve boys with Duchenne muscular dystrophy that underwent three-dimensional full-body gait analysis were investigated retrospectively. Data were compared to sixteen healthy children of same age at similar walking speed. Statistical tests included the student independent <em>t</em>-test (with Holm-Bonferroni correction), Hedges'g for effect size, and statistical non-parametric mapping two-sample t-test (with Bonferroni correction).</div></div><div><h3>Findings</h3><div>Duchenne muscular dystrophy compared to the healthy group: In the sagittal plane, the thorax segment was more posteriorly tilted. In addition, the relative angle between pelvis and thorax segment showed more backwards lean with increased shoulder extension. In the frontal plane, the patients walked with increased shoulder abduction and took wider strides. In the transverse plane, thorax rotation was not different between groups. Thorax range of motion was increased in all three planes.</div></div><div><h3>Interpretation</h3><div>Including the upper body gait kinematics, especially of the trunk, adds valuable objective information on the understanding of the Duchenne muscular dystrophy gait pattern. Our findings contribute to improved understanding of full-body gait compensations in this patient group.</div></div>","PeriodicalId":50992,"journal":{"name":"Clinical Biomechanics","volume":"122 ","pages":"Article 106402"},"PeriodicalIF":1.4000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Upper body gait deviations in children with Duchenne muscular dystrophy\",\"authors\":\"Jacqueline Romkes , Katrin Bracht-Schweizer , Michèle Widmer , Morgan Sangeux , Elke Viehweger\",\"doi\":\"10.1016/j.clinbiomech.2024.106402\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Duchenne muscular dystrophy is primarily a disease of progressive muscle degeneration affecting the whole body. It is important to preserve the patients' walking ability as long as possible. Inconclusive information on Duchenne muscular dystrophy gait pattern is available for the lower body and missing for the upper body. This study aimed to objectively investigate upper body gait deviations in a group of patients with Duchenne muscular dystrophy compared to typically developing peers.</div></div><div><h3>Methods</h3><div>Kinematic data of twelve boys with Duchenne muscular dystrophy that underwent three-dimensional full-body gait analysis were investigated retrospectively. Data were compared to sixteen healthy children of same age at similar walking speed. Statistical tests included the student independent <em>t</em>-test (with Holm-Bonferroni correction), Hedges'g for effect size, and statistical non-parametric mapping two-sample t-test (with Bonferroni correction).</div></div><div><h3>Findings</h3><div>Duchenne muscular dystrophy compared to the healthy group: In the sagittal plane, the thorax segment was more posteriorly tilted. In addition, the relative angle between pelvis and thorax segment showed more backwards lean with increased shoulder extension. In the frontal plane, the patients walked with increased shoulder abduction and took wider strides. In the transverse plane, thorax rotation was not different between groups. Thorax range of motion was increased in all three planes.</div></div><div><h3>Interpretation</h3><div>Including the upper body gait kinematics, especially of the trunk, adds valuable objective information on the understanding of the Duchenne muscular dystrophy gait pattern. Our findings contribute to improved understanding of full-body gait compensations in this patient group.</div></div>\",\"PeriodicalId\":50992,\"journal\":{\"name\":\"Clinical Biomechanics\",\"volume\":\"122 \",\"pages\":\"Article 106402\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Biomechanics\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0268003324002341\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"ENGINEERING, BIOMEDICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Biomechanics","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0268003324002341","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
Upper body gait deviations in children with Duchenne muscular dystrophy
Background
Duchenne muscular dystrophy is primarily a disease of progressive muscle degeneration affecting the whole body. It is important to preserve the patients' walking ability as long as possible. Inconclusive information on Duchenne muscular dystrophy gait pattern is available for the lower body and missing for the upper body. This study aimed to objectively investigate upper body gait deviations in a group of patients with Duchenne muscular dystrophy compared to typically developing peers.
Methods
Kinematic data of twelve boys with Duchenne muscular dystrophy that underwent three-dimensional full-body gait analysis were investigated retrospectively. Data were compared to sixteen healthy children of same age at similar walking speed. Statistical tests included the student independent t-test (with Holm-Bonferroni correction), Hedges'g for effect size, and statistical non-parametric mapping two-sample t-test (with Bonferroni correction).
Findings
Duchenne muscular dystrophy compared to the healthy group: In the sagittal plane, the thorax segment was more posteriorly tilted. In addition, the relative angle between pelvis and thorax segment showed more backwards lean with increased shoulder extension. In the frontal plane, the patients walked with increased shoulder abduction and took wider strides. In the transverse plane, thorax rotation was not different between groups. Thorax range of motion was increased in all three planes.
Interpretation
Including the upper body gait kinematics, especially of the trunk, adds valuable objective information on the understanding of the Duchenne muscular dystrophy gait pattern. Our findings contribute to improved understanding of full-body gait compensations in this patient group.
期刊介绍:
Clinical Biomechanics is an international multidisciplinary journal of biomechanics with a focus on medical and clinical applications of new knowledge in the field.
The science of biomechanics helps explain the causes of cell, tissue, organ and body system disorders, and supports clinicians in the diagnosis, prognosis and evaluation of treatment methods and technologies. Clinical Biomechanics aims to strengthen the links between laboratory and clinic by publishing cutting-edge biomechanics research which helps to explain the causes of injury and disease, and which provides evidence contributing to improved clinical management.
A rigorous peer review system is employed and every attempt is made to process and publish top-quality papers promptly.
Clinical Biomechanics explores all facets of body system, organ, tissue and cell biomechanics, with an emphasis on medical and clinical applications of the basic science aspects. The role of basic science is therefore recognized in a medical or clinical context. The readership of the journal closely reflects its multi-disciplinary contents, being a balance of scientists, engineers and clinicians.
The contents are in the form of research papers, brief reports, review papers and correspondence, whilst special interest issues and supplements are published from time to time.
Disciplines covered include biomechanics and mechanobiology at all scales, bioengineering and use of tissue engineering and biomaterials for clinical applications, biophysics, as well as biomechanical aspects of medical robotics, ergonomics, physical and occupational therapeutics and rehabilitation.