Laboratory of Early Markers of Neurodegeneration, Neurological Institute, Tel Aviv Sourasky Medical Center, Tel Aviv 6423906, Israel.
School of Medicine, Tel Aviv University, Tel Aviv 6997801, Israel.
Sensors (Basel). 2023 Oct 6;23(19):8266. doi: 10.3390/s23198266.
The G2019S- gene mutation is a common cause of hereditary Parkinson's disease (PD), associated with a higher frequency of the postural instability gait difficulty (PIGD) motor phenotype yet with preserved cognition. This study investigated neurophysiological changes during motor and cognitive tasks in PD patients with and without the mutation.
33 iPD patients and 22 patients performed the visual Go/NoGo task (VGNG) during sitting (single-task) and walking (dual-task) while wearing a 64-channel EEG cap. Event-related potentials (ERP) from Fz and Pz, specifically N200 and P300, were extracted and analyzed to quantify brain activity patterns.
The group performed better in the VGNG than the iPD group (grouptask; = 0.05). During Go, the iPD group showed reduced N2 amplitude and prolonged N2 latency during walking, whereas the group showed only shorter latency (grouptask = 0.027). During NoGo, opposite patterns emerged; the iPD group showed reduced N2 and increased P3 amplitudes during walking while the group demonstrated increased N2 and reduced P3 (N2: grouptask, = 0.010, P3: grouptask, = 0.012).
The group showed efficient early cognitive processes, reflected by N2, resulting in greater neural synchronization and prominent ERPs. These processes are possibly the underlying mechanisms for the observed better cognitive performance as compared to the iPD group. As such, future applications of intelligent medical sensing should be capable of capturing these electrophysiological patterns in order to enhance motor-cognitive functions.
G2019S 基因突变是遗传性帕金森病(PD)的常见病因,与姿势不稳步态困难(PIGD)运动表型的更高频率相关,但认知功能保留。本研究调查了携带和不携带突变的 PD 患者在进行运动和认知任务时的神经生理变化。
33 名 iPD 患者和 22 名健康对照者在佩戴 64 通道 EEG 帽的情况下,分别在坐立位(单任务)和行走位(双任务)下进行视觉 Go/NoGo 任务(VGNG)。提取和分析 Fz 和 Pz 的事件相关电位(ERP),即 N200 和 P300,以量化大脑活动模式。
携带突变的患者在 VGNG 中的表现优于 iPD 患者(组间任务,P=0.05)。在 Go 阶段,iPD 组在行走时表现出 N2 振幅降低和 N2 潜伏期延长,而突变组仅表现出潜伏期缩短(组间任务,P=0.027)。在 NoGo 阶段,出现相反的模式;iPD 组在行走时表现出 N2 降低和 P3 增加,而突变组表现出 N2 增加和 P3 降低(N2:组间任务,P=0.010,P3:组间任务,P=0.012)。
携带突变的患者表现出高效的早期认知过程,这反映在 N2 上,导致更大的神经同步和明显的 ERP。这些过程可能是观察到的与 iPD 患者相比更好的认知表现的潜在机制。因此,未来智能医疗传感的应用应该能够捕捉这些电生理模式,以增强运动认知功能。