Lirani-Silva Ellen, Silva Layla C S, Orcioli-Silva Diego, Beretta Victor S, França Lucas G S, Coelho Daniel B, Vitorio Rodrigo
Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
Department of Sport, Exercise and Rehabilitation, Northumbria University, Newcastle upon Tyne, UK.
Neurorehabil Neural Repair. 2025 Sep;39(9):742-751. doi: 10.1177/15459683251347631. Epub 2025 Jun 24.
BackgroundThe extent to which the cholinergic system contributes to gait impairments in Parkinson's disease (PD) remains unclear. Electroencephalography (EEG) alpha reactivity, which refers to change in alpha power over occipital electrodes upon opening the eyes, has been suggested as a marker of cholinergic function. We compared alpha reactivity between people with PD and healthy individuals and explored its potential association with gait measures.MethodsEyes-closed and eyes-open resting-state EEG data were recorded from 20 people with idiopathic PD and 19 healthy individuals with a 64-channel EEG system. Alpha reactivity was calculated as the relative change in alpha power (8-13 Hz) over occipital electrodes from eyes-closed to eyes-open. Gait spatiotemporal measures were obtained with an electronic walkway.ResultsAlpha reactivity was reduced in people with PD compared to healthy individuals ( = 105, = .017); the rank-biserial correlation of .447 indicated a moderate effect size. When controlling for global cognition (Mini Mental State Examination), the group difference in alpha reactivity was no longer significant. Alpha reactivity associated with measures of gait variability only (ρ = -.437 to -.532).ConclusionsResting-state alpha reactivity is reduced in PD, suggesting impaired cholinergic function. Reduced alpha reactivity was associated with greater gait variability, indicating a role of the cholinergic system in the mechanisms underlying gait variability. Therefore, the cholinergic system may represent a target for treatments aiming to reduce gait variability and alpha reactivity should be further explored as an endpoint for clinical trials.
背景
胆碱能系统在帕金森病(PD)步态障碍中所起的作用程度尚不清楚。脑电图(EEG)α反应性,即睁眼时枕叶电极上α波功率的变化,已被认为是胆碱能功能的一个标志物。我们比较了PD患者与健康个体之间的α反应性,并探讨了其与步态指标的潜在关联。
方法
使用64导EEG系统记录了20例特发性PD患者和19例健康个体闭眼和睁眼静息状态下的EEG数据。α反应性计算为枕叶电极从闭眼到睁眼时α波功率(8 - 13Hz)的相对变化。使用电子步道获得步态时空指标。
结果
与健康个体相比,PD患者的α反应性降低(= 105,= 0.017);等级二列相关系数为0.447,表明效应量中等。在控制整体认知(简易精神状态检查表)后,α反应性的组间差异不再显著。α反应性仅与步态变异性指标相关(ρ = -0.437至-0.532)。
结论
PD患者静息状态下的α反应性降低,提示胆碱能功能受损。α反应性降低与更大的步态变异性相关,表明胆碱能系统在步态变异性潜在机制中起作用。因此,胆碱能系统可能是旨在降低步态变异性的治疗靶点,α反应性应作为临床试验的终点进一步探索。