{"title":"与衰老相关的肌肉退化对行走时动态稳定性的影响:一项肌肉骨骼计算机模拟研究。","authors":"Shoma Kudo, Masahiro Fujimoto, Akinori Nagano","doi":"10.3389/fbioe.2024.1524751","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Aging-related deficits in the physiological properties of skeletal muscles limit the control of dynamic stability during walking. However, the specific causal relationships between these factors remain unclear. This study evaluated the effects of aging-related deficits in muscle properties on dynamic stability during walking.</p><p><strong>Methods: </strong>Walking movements were simulated using two-dimensional musculoskeletal models consisting of 18 Hill-type muscles. To assess the effects of aging-related deficits in muscle function on dynamic stability during walking, five models with different muscle properties were created, namely young adult (YA) and older adult (OA) models, models with reduced maximum isometric muscle force, reduced maximum muscle contraction velocity, and prolonged muscle deactivation time (∆F, ∆V, and ∆T models, respectively). The margin of stability (MoS) was used as a measure of dynamic stability during walking.</p><p><strong>Results and discussion: </strong>The MoS value of the OA model was greater than that of the YA model, and the ∆F model yielded a larger MoS value than those of the ∆V and ∆T models. Therefore, the OA model achieved a more dynamically stable state than the YA model and the ∆F model required a more stable state to sustain continuous walking compared to the ∆V and ∆T models. These findings indicate that aging-related deficits in muscle function limit the control of dynamic stability during walking with the degeneration of maximum isometric muscle force being the most influential factor. These findings could aid in the development of an intervention program to reduce the risk of falls in older adults effectively.</p>","PeriodicalId":12444,"journal":{"name":"Frontiers in Bioengineering and Biotechnology","volume":"12 ","pages":"1524751"},"PeriodicalIF":4.3000,"publicationDate":"2025-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11769994/pdf/","citationCount":"0","resultStr":"{\"title\":\"Effects of aging-related muscle degeneration on dynamic stability during walking: a musculoskeletal computer simulation study.\",\"authors\":\"Shoma Kudo, Masahiro Fujimoto, Akinori Nagano\",\"doi\":\"10.3389/fbioe.2024.1524751\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Aging-related deficits in the physiological properties of skeletal muscles limit the control of dynamic stability during walking. 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The margin of stability (MoS) was used as a measure of dynamic stability during walking.</p><p><strong>Results and discussion: </strong>The MoS value of the OA model was greater than that of the YA model, and the ∆F model yielded a larger MoS value than those of the ∆V and ∆T models. Therefore, the OA model achieved a more dynamically stable state than the YA model and the ∆F model required a more stable state to sustain continuous walking compared to the ∆V and ∆T models. These findings indicate that aging-related deficits in muscle function limit the control of dynamic stability during walking with the degeneration of maximum isometric muscle force being the most influential factor. 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引用次数: 0
摘要
简介骨骼肌生理特性中与衰老有关的缺陷限制了行走过程中对动态稳定性的控制。然而,这些因素之间的具体因果关系仍不清楚。本研究评估了与衰老相关的肌肉特性缺陷对步行过程中动态稳定性的影响:方法:使用由 18 块希尔型肌肉组成的二维肌肉骨骼模型模拟步行运动。为了评估与衰老相关的肌肉功能缺陷对步行过程中动态稳定性的影响,我们创建了五个具有不同肌肉特性的模型,即青年(YA)和老年(OA)模型,以及最大等长肌力降低、最大肌肉收缩速度降低和肌肉失活时间延长的模型(分别为∆F、∆V和∆T模型)。结果和讨论:OA 模型的 MoS 值大于 YA 模型,而 ∆F 模型的 MoS 值大于 ∆V 和 ∆T 模型。因此,与 ∆V 和 ∆T 模型相比,OA 模型比 YA 模型达到了更高的动态稳定状态,而 ∆F 模型则需要更稳定的状态来维持连续行走。这些研究结果表明,与衰老相关的肌肉功能缺陷限制了行走过程中对动态稳定性的控制,而最大等长肌力的退化是影响最大的因素。这些发现有助于制定干预计划,有效降低老年人跌倒的风险。
Effects of aging-related muscle degeneration on dynamic stability during walking: a musculoskeletal computer simulation study.
Introduction: Aging-related deficits in the physiological properties of skeletal muscles limit the control of dynamic stability during walking. However, the specific causal relationships between these factors remain unclear. This study evaluated the effects of aging-related deficits in muscle properties on dynamic stability during walking.
Methods: Walking movements were simulated using two-dimensional musculoskeletal models consisting of 18 Hill-type muscles. To assess the effects of aging-related deficits in muscle function on dynamic stability during walking, five models with different muscle properties were created, namely young adult (YA) and older adult (OA) models, models with reduced maximum isometric muscle force, reduced maximum muscle contraction velocity, and prolonged muscle deactivation time (∆F, ∆V, and ∆T models, respectively). The margin of stability (MoS) was used as a measure of dynamic stability during walking.
Results and discussion: The MoS value of the OA model was greater than that of the YA model, and the ∆F model yielded a larger MoS value than those of the ∆V and ∆T models. Therefore, the OA model achieved a more dynamically stable state than the YA model and the ∆F model required a more stable state to sustain continuous walking compared to the ∆V and ∆T models. These findings indicate that aging-related deficits in muscle function limit the control of dynamic stability during walking with the degeneration of maximum isometric muscle force being the most influential factor. These findings could aid in the development of an intervention program to reduce the risk of falls in older adults effectively.
期刊介绍:
The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs.
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