Berger Alisa, Steinberg Fabian, Thomas Fabian, Doppelmayr Michael
Department of Sport Psychology, Institute of Sport Science, Johannes Gutenberg-University Mainz, Mainz, Germany.
School of Kinesiology, Louisiana State University, Baton Rouge, LA, United States.
Front Aging Neurosci. 2020 Dec 10;12:594810. doi: 10.3389/fnagi.2020.594810. eCollection 2020.
Motor control is associated with suppression of oscillatory activity in alpha (8-12 Hz) and beta (12-30 Hz) ranges and elevation of oxygenated hemoglobin levels in motor-cortical areas. Aging leads to changes in oscillatory and hemodynamic brain activity and impairments in motor control. However, the relationship between age-related changes in motor control and brain activity is not yet fully understood. Therefore, this study aimed to investigate age-related and task-complexity-related changes in grip force control and the underlying oscillatory and hemodynamic activity. Sixteen younger [age (mean ± SD) = 25.4 ± 1.9, 20-30 years] and 16 older (age = 56.7 ± 4.7, 50-70 years) healthy men were asked to use a power grip to perform six trials each of easy and complex force tracking tasks (FTTs) with their right dominant hand in a randomized within-subject design. Grip force control was assessed using a sensor-based device. Brain activity in premotor and primary motor areas of both hemispheres was assessed by electroencephalography (EEG) and functional near-infrared spectroscopy (fNIRS). Older adults showed significantly higher inaccuracies and higher hemodynamic activity in both FTTs than did young adults. Correlations between grip force control owing to task complexity and beta activity were different in the contralateral premotor cortex (PMC) between younger and older adults. Collectively, these findings suggest that aging leads to impairment of grip force control and an increase in hemodynamic activity independent of task complexity. EEG beta oscillations may represent a task-specific neurophysiological marker for age-related decline in complex grip force control and its underlying compensation strategies. Further EEG-fNIRS studies are necessary to determine neurophysiological markers of dysfunctions underlying age-related motor disabilities for the improvement of individual diagnosis and therapeutic approaches.
运动控制与抑制α(8 - 12赫兹)和β(12 - 30赫兹)频段的振荡活动以及运动皮层区域氧合血红蛋白水平的升高有关。衰老会导致大脑振荡和血液动力学活动的变化以及运动控制的受损。然而,与年龄相关的运动控制变化和大脑活动之间的关系尚未完全明确。因此,本研究旨在调查与年龄和任务复杂性相关的握力控制变化以及潜在的振荡和血液动力学活动。16名年轻健康男性[年龄(均值±标准差)= 25.4 ± 1.9,20 - 30岁]和16名年长健康男性(年龄 = 56.7 ± 4.7,50 - 70岁)被要求采用强力握法,以随机的被试内设计,用其优势右手对简单和复杂的力跟踪任务(FTT)各进行6次试验。使用基于传感器的设备评估握力控制。通过脑电图(EEG)和功能近红外光谱(fNIRS)评估双侧半球运动前区和初级运动区的大脑活动。与年轻成年人相比,年长成年人在两项FTT中均表现出明显更高的误差和更高的血液动力学活动。年轻和年长成年人在对侧运动前皮层(PMC)中,由于任务复杂性导致的握力控制与β活动之间的相关性有所不同。总体而言,这些发现表明衰老导致握力控制受损以及血液动力学活动增加,且与任务复杂性无关。EEGβ振荡可能代表了与年龄相关的复杂握力控制下降及其潜在补偿策略的特定任务神经生理标志物。有必要进行进一步的EEG - fNIRS研究,以确定与年龄相关的运动障碍潜在功能障碍的神经生理标志物,从而改善个体诊断和治疗方法。