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帕金森病中精细调整的γ轨迹药物治疗周期:一项动态脑感知研究

Finely Tuned γ Tracks Medication Cycles in Parkinson's Disease: An Ambulatory Brain-Sense Study.

作者信息

Colombo Aaron, Bernasconi Elena, Alva Laura, Sousa Mario, Debove Ines, Nowacki Andreas, Serquet Camille, Petermann Katrin, Nguyen T A Khoa, Magalhães Andreia D, Lachenmayer Lenard, Waskönig Julia, Nef Tobias, Schuepbach Michael, Pollo Claudio, Krack Paul, Averna Alberto, Tinkhauser Gerd

机构信息

Department of Neurology, Bern University Hospital and University of Bern, Bern, Switzerland.

ARTORG Center for Biomedical Engineering Research, University of Bern, Bern, Switzerland.

出版信息

Mov Disord. 2025 May;40(5):881-895. doi: 10.1002/mds.30160. Epub 2025 Mar 13.

Abstract

BACKGROUND

Novel commercial brain-sense neurostimulators enable us to contextualize brain activity with symptom and medication states in real-life ambulatory settings in Parkinson's disease (PD). Although various candidate biomarkers have been proposed for adaptive deep brain stimulation (DBS), a comprehensive comparison of their ambulatory profiles is lacking.

OBJECTIVES

To systematically compare the ambulatory neurophysiological dynamics and clinical properties of three candidate biomarkers-low-frequency, beta (β), and finely tuned γ (FTG) activity.

METHODS

We investigated 14 PD patients implanted with the Medtronic Percept PC, who underwent up to two 4-week ambulatory multimodal recording periods on their regular medication and stimulation. Subthalamic nucleus local field potentials (LFPs) of low-frequency, β, and FTG activity were recorded. Additionally, objective motor symptom states, physical activity and heart rate using wearables, as well as medication-intake times, sleep-awake times, and subjective symptom states using diaries were co-registered. LFP dynamics were also compared to high-resolution in-hospital recordings under off/on dopaminergic medication and stimulation conditions.

RESULTS

FTG reliably indexed off to on medication states in the ambulatory setting at the group and individual levels, and these spectral dynamics could be anticipated by high-resolution in-hospital recordings. Both FTG and low-frequency correlated with wearable-based dyskinesia scores, whereas diary-based dyskinesia events were only linked to FTG. Importantly, FTG indicated on-medication states regardless of the presence of dyskinesia and despite potential motion and heart rate artifacts. The 24-hour profile revealed large circadian power shifts that may overdrive medication-intake dynamics.

CONCLUSION

Despite the limitations of low-temporal resolution recordings, this work provides valuable insights into the real-life dynamics of biomarkers. Specifically, it highlights the utility of FTG as a primary and reliable indicator of medication states for adaptive DBS. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

摘要

背景

新型商用脑感知神经刺激器使我们能够在帕金森病(PD)的现实生活动态环境中,将脑活动与症状及药物状态相关联。尽管已经提出了各种候选生物标志物用于适应性深部脑刺激(DBS),但缺乏对其动态特征的全面比较。

目的

系统比较三种候选生物标志物——低频、β和精细调谐γ(FTG)活动的动态神经生理特性和临床特征。

方法

我们研究了14名植入美敦力Percept PC的PD患者,他们在常规药物治疗和刺激下,进行了长达两个为期4周的动态多模态记录期。记录了丘脑底核低频、β和FTG活动的局部场电位(LFP)。此外,还同步记录了使用可穿戴设备测量的客观运动症状状态、身体活动和心率,以及使用日记记录的药物服用时间、睡眠-觉醒时间和主观症状状态。还将LFP动态与在多巴胺能药物开/关和刺激条件下的高分辨率院内记录进行了比较。

结果

在动态环境中,FTG在组和个体水平上都能可靠地指示药物从停药到服药的状态,并且这些频谱动态可以通过高分辨率院内记录预测。FTG和低频都与基于可穿戴设备的异动症评分相关,而基于日记的异动症事件仅与FTG相关。重要的是,无论是否存在异动症,且尽管存在潜在的运动和心率伪迹,FTG都能指示服药状态。24小时动态显示出较大的昼夜节律功率变化,这可能会过度驱动药物服用动态。

结论

尽管记录的时间分辨率较低存在局限性,但这项工作为生物标志物的现实生活动态提供了有价值的见解。具体而言,它突出了FTG作为适应性DBS药物状态的主要且可靠指标的效用。© 2025作者。《运动障碍》由Wiley Periodicals LLC代表国际帕金森和运动障碍协会出版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1860/12089918/e68ca8b8ac77/MDS-40-881-g002.jpg

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