Kudo Shoma, Fujimoto Masahiro, Nagano Akinori
Health and Medical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Kagawa, Japan.
College of Sport and Health Science, Ritsumeikan University, Shiga, Japan.
Front Bioeng Biotechnol. 2025 Jan 13;12:1524751. doi: 10.3389/fbioe.2024.1524751. eCollection 2024.
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.
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.
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.
骨骼肌生理特性中与衰老相关的缺陷限制了步行过程中动态稳定性的控制。然而,这些因素之间的具体因果关系仍不清楚。本研究评估了肌肉特性中与衰老相关的缺陷对步行过程中动态稳定性的影响。
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。为了评估肌肉功能中与衰老相关的缺陷对步行过程中动态稳定性的影响,创建了五个具有不同肌肉特性的模型,即青年成人(YA)模型和老年成人(OA)模型、最大等长肌力降低的模型、最大肌肉收缩速度降低的模型以及肌肉失活时间延长的模型(分别为∆F、∆V和∆T模型)。稳定性裕度(MoS)用作步行过程中动态稳定性的度量。
OA模型的MoS值大于YA模型,且∆F模型产生的MoS值大于∆V和∆T模型。因此,与YA模型相比,OA模型实现了更动态稳定的状态,并且与∆V和∆T模型相比,∆F模型需要更稳定的状态来维持持续步行。这些发现表明,肌肉功能中与衰老相关的缺陷限制了步行过程中动态稳定性的控制,其中最大等长肌力的退化是最有影响的因素。这些发现有助于制定一项干预计划,以有效降低老年人跌倒的风险。