Stuart Samuel, Belluscio Valeria, Quinn Joseph F, Mancini Martina
Department of Neurology, Oregon Health and Science University, Portland, OR, United States.
Department of Movement, Human and Health Sciences, Università degli Studi di Roma Foro Italico, Rome, Italy.
Front Neurol. 2019 May 22;10:536. doi: 10.3389/fneur.2019.00536. eCollection 2019.
Mobility declines with age and further with neurodegenerative disorders, such as Parkinson's disease (PD). Walking and turning ability, in particular, are vital aspects of mobility that deteriorate with age and are further impaired in PD. Such deficits have been linked with reduction in automatic control of movement and the need for compensatory cognitive cortical control via the pre-frontal cortex (PFC), however the underlying neural mechanisms remain unclear. Establishing and using a robust methodology to examine PFC activity during continuous walking and turning via mobile functional near infra-red spectroscopy (fNIRS) may aid in the understanding of mobility deficits and help with development of appropriate therapeutics. This study aimed to: (1) examine test re-test reliability of PFC activity during continuous turning and walking via fNIRS measurement; and (2) compare PFC activity during continuous turning and walking in young, old and Parkinson's subjects. Twenty-five young (32.3 ± 7.5 years), nineteen older (65.4 ± 7.0 years), and twenty-four PD (69.3 ± 4.1 years) participants performed continuous walking and 360° turning-in-place tasks, each lasting 2 min. Young participants repeated the tasks a second time to allow fNIRS measurement reliability assessment. The primary outcome was PFC activity, assessed via measuring changes in oxygenated hemoglobin (HbO) concentrations. PFC activity during continuous walking and turning was moderately reproducible (Intra-class correlation coefficient = 0.67). The PD group had higher PFC activation than young and older adults during walking and turning, with significant group differences for bilateral PFC activation ( = 0.025), left PFC activation ( = 0.012), and the early period (first 40 s) of walking ( = 0.007), with greater activation required in PD. Interestingly, older adults had similar PFC activation to young adults across conditions, however older adults required greater activation than young adults during continuous turning, specifically the early period of the turning task (Cohens = 0.86). PFC activity can be measured during continuous walking and turning tasks with acceptable reliability, and can differentiate young, older and PD groups. PFC activation was significantly greater in PD compared to young and older adults during walking, particularly when beginning to walk.
随着年龄增长,身体活动能力会下降,而患有神经退行性疾病(如帕金森病(PD))时这种下降会更明显。行走和转身能力,尤其是身体活动能力的重要方面,会随着年龄增长而恶化,在帕金森病患者中会进一步受损。这些缺陷与运动自动控制能力的下降以及通过前额叶皮质(PFC)进行代偿性认知皮质控制的需求有关,然而其潜在的神经机制仍不清楚。建立并使用一种强大的方法,通过移动功能近红外光谱(fNIRS)来检测连续行走和转身过程中的前额叶皮质活动,可能有助于理解身体活动能力缺陷,并有助于开发合适的治疗方法。本研究旨在:(1)通过fNIRS测量来检测连续转身和行走过程中前额叶皮质活动的重测信度;(2)比较年轻人、老年人和帕金森病患者在连续转身和行走过程中的前额叶皮质活动。25名年轻人(32.3±7.5岁)、19名老年人(65.4±7.0岁)和24名帕金森病患者(69.3±4.1岁)进行了连续行走和原地360°转身任务,每项任务持续2分钟。年轻参与者重复进行这些任务,以便进行fNIRS测量的可靠性评估。主要结果是前额叶皮质活动,通过测量氧合血红蛋白(HbO)浓度的变化来评估。连续行走和转身过程中的前额叶皮质活动具有中等程度的可重复性(组内相关系数=0.67)。帕金森病组在行走和转身过程中的前额叶皮质激活程度高于年轻人和老年人,双侧前额叶皮质激活(=0.025)、左侧前额叶皮质激活(=0.012)以及行走早期(前40秒)(=0.007)存在显著的组间差异,帕金森病患者需要更大的激活。有趣的是,在各种情况下老年人的前额叶皮质激活与年轻人相似,然而在连续转身过程中,尤其是转身任务的早期,老年人比年轻人需要更大的激活(科恩斯=0.86)。在连续行走和转身任务中可以以可接受的可靠性测量前额叶皮质活动,并且可以区分年轻人、老年人和帕金森病组。与年轻人和老年人相比,帕金森病患者在行走过程中,尤其是开始行走时,前额叶皮质激活明显更大。