The neurophysiological brain-fingerprint of Parkinson's disease.

Jason da Silva Castanheira, Alex I Wiesman, Justine Y Hansen, Bratislav Misic, Sylvain Baillet
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Abstract

In this study, we investigate the clinical potential of brain-fingerprints derived from electrophysiological brain activity for diagnostics and progression monitoring of Parkinson's disease (PD). We obtained brain-fingerprints from PD patients and age-matched healthy controls using short, task-free magnetoencephalographic recordings. The rhythmic components of the individual brain-fingerprint distinguished between patients and healthy participants with approximately 90% accuracy. The most prominent cortical features of the Parkinson's brain-fingerprint mapped to polyrhythmic activity in unimodal sensorimotor regions. Leveraging these features, we also show that Parkinson's disease stages can be decoded directly from cortical neurophysiological activity. Additionally, our study reveals that the cortical topography of the Parkinson's brain-fingerprint aligns with that of neurotransmitter systems affected by the disease's pathophysiology. We further demonstrate that the arrhythmic components of cortical activity are more variable over short periods of time in patients with Parkinson's disease than in healthy controls, making individual differentiation between patients based on these features more challenging and explaining previous negative published results. Overall, we outline patient-specific rhythmic brain signaling features that provide insights into both the neurophysiological signature and clinical staging of Parkinson's disease. For this reason, the proposed definition of a rhythmic brain-fingerprint of Parkinson's disease may contribute to novel, refined approaches to patient stratification and to the improved identification and testing of therapeutic neurostimulation targets.

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帕金森病患者运动和认知能力下降的神经生理学大脑指纹。
大脑指纹是一种神经成像方法,它正在扩展神经科学对健康和疾病个体间多样性的看法。在本研究中,我们使用大脑指纹来推进帕金森病(PD)的神经生理学特征。我们根据短暂和无任务脑磁图记录的节律和心律失常频谱特征,得出了PD患者和年龄匹配的健康对照组的脑指纹。使用这种方法,患者与健康对照组的个体分化准确率为81%,患者的分化程度随其认知和运动症状的严重程度而定。我们发现,与健康对照组(90%)相比,患者之间的分化更具挑战性(77%的准确率),因为PD患者的神经生理学频谱特征随着时间的推移不太稳定。区分健康对照组的最显著特征映射到大脑功能层次中的高阶区域。相反,患者分化的最明显特征是体感运动皮层。我们还报告了患者的大脑指纹与帕金森病中受影响的神经递质系统的皮层地形图一致。我们得出结论,与年龄匹配的健康对照组相比,帕金森病会影响患者的大脑光谱指纹,个体之间存在显著的异质性,并且在短时间内变异性增加。我们的研究证明了神经生理学指纹与临床神经科学的相关性,并强调了其在患者分层、疾病建模以及个性化干预措施的开发和评估方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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