帕金森病患者对躯体运动刺激的脑血管反应:一项多变量分析

Sam C Barnes, R. Panerai, L. Beishon, M. Hanby, T. Robinson, V. Haunton
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引用次数: 3

摘要

帕金森病(PD)是一种常见的神经退行性疾病,但对该患者群体的脑血流动力学知之甚少。先前评估动态大脑自动调节(dCA)、神经血管耦合(NVC)和血管运动反应(VMR)的研究得出了相互矛盾的结果。通过使用多变量模型,我们旨在确定PD患者的脑血流量(CBF)调节是否受损。健康对照(HC) 55例,PD患者49例。PD受试者在一段时间停止服用抗帕金森药物后进行了第二次记录。连续双侧经颅多普勒测量大脑中动脉,每搏平均动脉血压(MAP;Finapres),心率(HR;潮末CO2 (EtCO2;摄摄)。5分钟基线期后,进行被动运动模式,包括60秒的肘关节屈曲。多元模型量化了MAP、ETCO2和神经刺激对脑血流速度(CBFV)变化的贡献。量化dCA、VMR和NVC以评估CBF调节的完整性。神经刺激是主要的输入。PD组dCA、NVC、VMR均较HC组受损(p < 0.01, p = 0.04, p < 0.01)。我们的数据表明PD可能与CBF调节下降有关。这需要使用不同的神经刺激进一步评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebrovascular responses to somatomotor stimulation in Parkinson’s disease: A multivariate analysis
Parkinson’s disease (PD) is a common neurodegenerative disorder, yet little is known about cerebral haemodynamics in this patient population. Previous studies assessing dynamic cerebral autoregulation (dCA), neurovascular coupling (NVC) and vasomotor reactivity (VMR) have yielded conflicting findings. By using multi-variate modelling, we aimed to determine whether cerebral blood flow (CBF) regulation is impaired in PD patients. 55 healthy controls (HC) and 49 PD patients were recruited. PD subjects underwent a second recording following a period of abstinence from their anti-Parkinsonian medication. Continuous bilateral transcranial Doppler in the middle cerebral arteries, beat-to-beat mean arterial blood pressure (MAP; Finapres), heart rate (HR; electrocardiogram), and end-tidal CO2 (EtCO2; capnography) were measured. After a 5-min baseline period, a passive motor paradigm comprising 60 s of elbow flexion was performed. Multi-variate modelling quantified the contributions of MAP, ETCO2 and neural stimulation to changes in CBF velocity (CBFV). dCA, VMR and NVC were quantified to assess the integrity of CBF regulation. Neural stimulation was the dominant input. dCA, NVC and VMR were all found to be impaired in the PD population relative to HC (p < 0.01, p = 0.04, p < 0.01, respectively). Our data suggest PD may be associated with depressed CBF regulation. This warrants further assessment using different neural stimuli.
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