School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
J Gerontol A Biol Sci Med Sci. 2024 May 1;79(5). doi: 10.1093/gerona/glae043.
Gait impairment leads to increased mobility decline and may have neurological contributions. This study explores how neurological biomarkers are related to gait in older adults.
We studied participants in the Cardiovascular Health Study, a population-based cohort of older Americans, who underwent a serum biomarker assessment from samples collected in 1996-1997 for neurofilament light chain (NfL), glial fibrillary acidic protein, ubiquitin carboxy-terminal hydrolase L1, and total tau (n = 1 959, mean age = 78.0 years, 60.8% female). In a subsample (n = 380), cross-sectional associations with quantitative gait measures were explored. This subsample was assessed on a mat for gait speed, step length, double support time, step time, step length variability, and step time variability. Gait speed was also measured over a 15-ft walkway annually from 1996-1997 to 1998-1999 for longitudinal analyses. Linear regression models assessed cross-sectional associations of biomarkers with gait measures, whereas mixed effects models assessed longitudinal gait speed change from baseline to 1998-1999.
Neurofilament light chain was significantly associated with annual gait speed decline (standardized β = -0.64 m/s, 95% CI: [-1.23, -0.06]) after adjustment for demographic and health factors. Among gait mat-assessed phenotypes, NfL was also cross-sectionally associated with gait speed (β = 0.001 m/s [0.0003, 0.002]) but not with other gait measures. None of the remaining biomarkers were significantly related to gait in either longitudinal or cross-sectional analyses.
Higher NfL levels were related to greater annual gait speed decline. Gait speed decline may be related to axonal degeneration. The clinical utility of NfL should be explored.
步态障碍会导致活动能力下降,并且可能与神经学因素有关。本研究旨在探讨神经生物标志物与老年人步态之间的关系。
我们对心血管健康研究中的参与者进行了研究,这是一项基于人群的美国老年人队列研究,他们在 1996-1997 年接受了神经丝轻链(NfL)、胶质纤维酸性蛋白、泛素羧基末端水解酶 L1 和总 tau 的血清生物标志物评估(n=1959,平均年龄 78.0 岁,60.8%为女性)。在一个子样本(n=380)中,我们探讨了与定量步态测量的横断面关联。该子样本在垫子上进行步态速度、步长、双支撑时间、步时、步长变异性和步时变异性的评估。从 1996-1997 年到 1998-1999 年,每年还使用 15 英尺过道测量步态速度进行纵向分析。线性回归模型评估了生物标志物与步态测量的横断面关联,而混合效应模型评估了从基线到 1998-1999 年的纵向步态速度变化。
在调整了人口统计学和健康因素后,NfL 与每年的步态速度下降显著相关(标准化β=-0.64 m/s,95%CI:[-1.23,-0.06])。在步态垫评估的表型中,NfL 也与步态速度呈横断面相关(β=0.001 m/s [0.0003,0.002]),但与其他步态测量无关。其余生物标志物在纵向或横断面分析中均与步态无显著关系。
较高的 NfL 水平与更大的年度步态速度下降相关。步态速度下降可能与轴突退化有关。应该探索 NfL 的临床应用价值。