Cerebellum and basal ganglia connectivity in isolated REM sleep behaviour disorder and Parkinson's disease: an exploratory study.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Michael J Firbank, Jacopo Pasquini, Laura Best, Victoria Foster, Hilmar P Sigurdsson, Kirstie N Anderson, George Petrides, David J Brooks, Nicola Pavese
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Abstract

REM sleep behaviour disorder (RBD) is a parasomnia characterised by dream-enacting behaviour with loss of muscle atonia during REM sleep and is a prodromal feature of α-synucleinopathies like Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy. Although cortical-to-subcortical connectivity is well-studied in RBD, cerebellar and subcortical nuclei reciprocal connectivity is less established. Nonetheless, it could be relevant since RBD pathology involves brainstem structures with an ascending gradient. In this study, we utilised resting-state functional MRI to investigate 13 people with isolated RBD (iRBD), 17 with Parkinson's disease and 16 healthy controls. We investigated the connectivity between the basal ganglia, thalamus and regions of the cerebellum. The cerebellum was segmented using a functional atlas, defined by a resting-state network-based parcellation, rather than an anatomical one. Controlling for age, we found a significant group difference (F4,82 = 5.47, pFDR = 0.017) in cerebellar-thalamic connectivity, with iRBD significantly lower compared to both control and Parkinson's disease. Specifically, cerebellar areas involved in this connectivity reduction were related to the default mode, language and fronto-parietal resting-state networks. Our findings show functional connectivity abnormalities in subcortical structures that are specific to iRBD and may be relevant from a pathophysiological standpoint. Further studies are needed to investigate how connectivity changes progress over time and whether specific changes predict disease course or phenoconversion.

孤立快速眼动睡眠行为障碍和帕金森病的小脑和基底神经节连通性:一项探索性研究。
快速眼动睡眠行为障碍(RBD)是一种寄生性失眠症,其特征是快速眼动睡眠期间肌肉失张力的做梦行为,是帕金森病、路易体痴呆和多系统萎缩等α-突触核蛋白病的前兆特征。虽然皮层与皮层下之间的连接在 RBD 中得到了深入研究,但小脑与皮层下核之间的相互连接却不那么成熟。然而,由于RBD的病理变化涉及具有上升梯度的脑干结构,因此这可能是相关的。在这项研究中,我们利用静息态功能磁共振成像研究了13名孤立RBD(iRBD)患者、17名帕金森病患者和16名健康对照者。我们研究了基底节、丘脑和小脑区域之间的连接性。我们使用功能图谱而不是解剖图谱对小脑进行了分割,功能图谱是由基于静息态网络的解析图谱定义的。在控制年龄的前提下,我们发现小脑-丘脑连通性存在显著的组间差异(F4,82 = 5.47, pFDR = 0.017),iRBD明显低于对照组和帕金森病组。具体来说,这种连接性降低所涉及的小脑区域与默认模式、语言和前顶叶静息态网络有关。我们的研究结果表明,皮层下结构的功能连接异常是iRBD所特有的,可能与病理生理学的观点有关。我们还需要进一步研究连通性的变化是如何随时间推移而发展的,以及特定的变化是否能预测疾病的进程或表型转换。
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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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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