Martín-Fuentes Isabel, Solis-Urra Patricio, Ruiz-Malagón Emilio J, Coca-Pulido Andrea, Toval Angel, Fernandez-Gamez Beatriz, Olvera-Rojas Marcos, Bellón Darío, Sclafani Alessandro, Mora-Gonzalez Jose, Sánchez-Aranda Lucía, Sanchez-Martinez Javier, Martínez-Barbero José Pablo, Gómez-Río Manuel, Liu-Ambrose Teresa, Erickson Kirk I, Ortega Francisco B, Esteban-Cornejo Irene
Faculty of Sport Sciences, Department of Physical Education and Sports, Sport and Health University Research Institute (iMUDS), University of Granada, Granada, Spain.
AdventHealth Research Institute, Neuroscience, Orlando, Florida, USA.
Innov Aging. 2025 May 6;9(6):igaf045. doi: 10.1093/geroni/igaf045. eCollection 2025.
Aging is associated with both gait impairments and cognitive decline; however, the relationship between specific gait variability parameters, gray matter volume (GMV), and cognitive function remains poorly understood. This study aims to examine the associations between gait variability parameters (derived from stride length, step length, step time, and gait velocity) and GMV and its associations with cognitive function in cognitively normal older adults.
Eighty-seven older adults (48 female) aged 65-80 from the AGUEDA trial participated in this cross-sectional analysis. The Optogait system was used to record gait parameters. T1-weighted brain images were acquired magnetic resonance imaging scanner, and GMV was calculated by whole-brain voxel-based morphometric analysis using SPM12. Cognitive function was calculated from different cognitive tests.
Greater stride length variability was associated with lower GMV ( < .001) in clusters located in the supramarginal gyrus ( = 4.014, = 179, β = -0.494) and hippocampus ( = 3.670, = 334, β = -0.394), whereas greater step length variability was linked to lower GMV in the parahippocampal gyrus ( = 3.624, = 76, β = -0.410). However, greater step time variability was associated with greater GMV in the supplementary motor area ( = 4.117, = 274, β = 0.449). Gait velocity variability did not show any association with GMV. Furthermore, greater GMV in the supramarginal gyrus was associated with better working memory (β = 0.252, = .008); greater GMV in the hippocampus was associated with better attentional/inhibitory control (β = 0.275, = .010); and greater GMV in the parahippocampal gyrus was associated with better EF (β = 0.212, = .035), attentional/inhibitory control (β = 0.241, = .019), and working memory (β = 0.233, = .027).
These results suggest that gait variability could be an indicator of neurocognitive decline in older adults. Understanding these associations is essential for early dementia detection and sheds light on the complex interplay between physical function, brain health, and cognitive function during aging.
衰老与步态障碍和认知衰退均相关;然而,特定步态变异性参数、灰质体积(GMV)和认知功能之间的关系仍知之甚少。本研究旨在探讨步态变异性参数(源自步幅长度、步长、步时和步态速度)与GMV之间的关联及其与认知功能正常的老年人认知功能的关联。
来自AGUEDA试验的87名65 - 80岁的老年人(48名女性)参与了这项横断面分析。使用Optogait系统记录步态参数。通过磁共振成像扫描仪采集T1加权脑图像,并使用SPM12通过基于全脑体素的形态计量分析计算GMV。从不同的认知测试中计算认知功能。
更大的步幅长度变异性与位于缘上回(t = 4.014,df = 179,β = -0.494)和海马体(t = 3.670,df = 334,β = -0.394)区域的较低GMV相关,而更大的步长变异性与海马旁回较低的GMV相关(t = 3.624,df = 76,β = -0.410)。然而,更大的步时变异性与辅助运动区更大的GMV相关(t = 4.117,df = 274,β = 0.449)。步态速度变异性与GMV未显示出任何关联。此外,缘上回更大的GMV与更好的工作记忆相关(β = 0.252,p = .008);海马体更大的GMV与更好的注意力/抑制控制相关(β = 0.275,p = .010);海马旁回更大的GMV与更好的执行功能(β = 0.212,p = .035)、注意力/抑制控制(β = 0.241,p = .019)和工作记忆(β = 0.233,p = .027)相关。
这些结果表明步态变异性可能是老年人神经认知衰退的一个指标。理解这些关联对于早期痴呆检测至关重要,并有助于揭示衰老过程中身体功能、脑健康和认知功能之间复杂的相互作用。