Department of Neurology, Oregon Health & Science University, Portland, OR, United States.
Department of Neurology, Oregon Health & Science University, Portland, OR, United States; Department of Sport, Exercise and Rehabilitation, Northumbria University, Newcastle Upon Tyne, UK.
Parkinsonism Relat Disord. 2021 May;86:10-14. doi: 10.1016/j.parkreldis.2021.03.014. Epub 2021 Mar 27.
Cholinergic dysfunction contributes to mobility deficits in Parkinson's disease (PD). People with PD rely on limited prefrontal executive-attentional resources for the control of locomotion, including turning. Cortical and behavioral responses to cholinergic augmentation during turning remains unclear. We examined prefrontal cortex (PFC) activity while turning-in-place and spatiotemporal measures of turns in response to usual dopaminergic medication and adjunct cholinergic augmentation.
This study consisted of a single-site, randomized, double-blind crossover trial. Twenty PD participants were assessed in the levodopa-off state and then randomized to either levodopa + donepezil (5 mg) or levodopa + placebo treatments for two weeks followed by a 2-week washout before crossover. The primary outcome was change from off state in PFC activity while turning-in-place (assessed with functional near-infrared spectroscopy). Secondary outcomes were changes in spatiotemporal turning measures (assessed with body-worn inertial measurement units) and accuracy in the secondary task.
Nineteen participants completed the trial. While levodopa + placebo had no effect on PFC activity when turning-in-place with a dual-task, levodopa + donepezil led to a large reduction in PFC activity (effect size, -0.82). Spatiotemporal measures of turning improved with both treatments, with slightly greater effect sizes observed for levodopa + donepezil. Additionally, the accuracy in the concurrent cognitive task improved only with levodopa + donepezil (effect size, 0.63).
The addition of cholinergic therapy with donepezil (5 mg/day for 2 weeks) to standard dopaminergic therapy reduced the burden on prefrontal executive-attentional resources while turning with a dual-task and improved secondary task accuracy and turning.
胆碱能功能障碍导致帕金森病(PD)的运动障碍。PD 患者依赖有限的前额叶执行注意资源来控制运动,包括转弯。在转弯过程中,皮层和行为对胆碱能增强的反应仍不清楚。我们研究了前额叶皮层(PFC)在原地转弯时的活动,以及在接受常规多巴胺能药物治疗和辅助胆碱能增强治疗时转弯的时空测量。
本研究包括一项单中心、随机、双盲交叉试验。20 名 PD 参与者在左旋多巴停药状态下接受评估,然后随机分为左旋多巴+多奈哌齐(5mg)或左旋多巴+安慰剂治疗两周,然后在交叉前进行两周洗脱期。主要结局是从原地转弯时 PFC 活动的关闭状态改变(用功能近红外光谱评估)。次要结局是转弯时空测量(用身体佩戴惯性测量单元评估)和次要任务准确性的变化。
19 名参与者完成了试验。当在双重任务中原地转弯时,左旋多巴+安慰剂对 PFC 活动没有影响,但左旋多巴+多奈哌齐导致 PFC 活动大幅减少(效应大小为-0.82)。转弯的时空测量指标在两种治疗方法下都有所改善,左旋多巴+多奈哌齐的效果略大。此外,只有在使用左旋多巴+多奈哌齐时,同时进行的认知任务的准确性才会提高(效应大小为 0.63)。
在标准多巴胺能治疗的基础上,添加多奈哌齐(每天 5mg,持续 2 周)的胆碱能治疗可减轻双重任务转弯时前额叶执行注意资源的负担,并提高次要任务准确性和转弯。