尾状核多巴胺能末梢的相对稀缺是帕金森病静止性震颤的一个特征

IF 6.7 1区 医学 Q1 NEUROSCIENCES NPJ Parkinson's Disease Pub Date : 2024-11-18 DOI:10.1038/s41531-024-00818-8
Marcelo D. Mendonça, Pedro C. Ferreira, Francisco Oliveira, Raquel Barbosa, Bruna Meira, Durval C. Costa, Albino J. Oliveira-Maia, Joaquim Alves da Silva
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引用次数: 0

摘要

静止性震颤(RT)是帕金森病(PD)的一种症状,与多巴胺能系统的关系尚不明确。我们分析了帕金森病进展标志物倡议的 432 名受试者、57 名其他帕金森病患者和对照组以及 86 名转诊的多巴胺转运体单光子发射计算机断层扫描(DaT-SPECT)受试者的数据。RT患者的尾状体结合率(CBR)较高,但推拿门结合率并不高。此外,较高的基线CBR与RT的发展有关。在较小的队列中,来自惯性传感器的基于4-6赫兹振荡的指标与RT振幅相关,可将对照组与DaT结合率降低的患者区分开来,并与后者的CBR相关。硅学建模发现,RT 患者较高的 CBR 可以解释多个数据集中发现的 RT 与 DaT-SPECT 之间的相关性,支持 CBR 与 RT 之间同侧相关性的虚假来源。这些结果表明,尾状体多巴胺能终端的完整性是RT的一个特征,具有潜在的病理生理学意义。
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Relative sparing of dopaminergic terminals in the caudate nucleus is a feature of rest tremor in Parkinson’s disease

Resting tremor (RT) is a Parkinson’s disease (PD) symptom with an unclear relationship to the dopaminergic system. We analysed data from 432 subjects from the Parkinson’s Progression Markers Initiative, 57 additional PD patients and controls and 86 subjects referred for dopamine transporter single-photon emission computed tomography (DaT-SPECT). Caudate binding ratio (CBR), but not putamen binding ratio, was higher in RT patients. Furthermore, higher baseline CBR was linked to RT development. In the smaller cohorts, a 4–6 Hz oscillation-based metric from inertial sensors correlated with RT amplitude, distinguished controls from patients with reduced DaT binding and correlated with CBR in the latter group. In silico modelling uncovered that higher CBR in RT patients explained correlations between RT and DaT-SPECT found in several datasets, supporting a spurious origin for ipsilateral correlations between CBR and RT. These results suggest that caudate dopaminergic terminals integrity is a feature of RT with potential pathophysiological implications.

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来源期刊
NPJ Parkinson's Disease
NPJ Parkinson's Disease Medicine-Neurology (clinical)
CiteScore
9.80
自引率
5.70%
发文量
156
审稿时长
11 weeks
期刊介绍: npj Parkinson's Disease is a comprehensive open access journal that covers a wide range of research areas related to Parkinson's disease. It publishes original studies in basic science, translational research, and clinical investigations. The journal is dedicated to advancing our understanding of Parkinson's disease by exploring various aspects such as anatomy, etiology, genetics, cellular and molecular physiology, neurophysiology, epidemiology, and therapeutic development. By providing free and immediate access to the scientific and Parkinson's disease community, npj Parkinson's Disease promotes collaboration and knowledge sharing among researchers and healthcare professionals.
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