Groenewald Karolien, Warwick James, Dupont Patrick, Ackerman Jan-Hendrik, Amsterdam Olivia, Carr Jonathan
Department of Neurology and Nuclear Medicine, University of Stellenbosch, Cape Town, South Africa.
Mov Disord Clin Pract. 2025 Apr;12(4):437-445. doi: 10.1002/mdc3.14307. Epub 2024 Dec 13.
Rapid eye movement sleep behavior disorder (RBD) is an established prodrome and symptom of synucleinopathies. The pathophysiology of this disorder has been well studied but there is a lack of functional imaging data to illustrate the dysfunction in vivo.
We aimed to investigate the functional changes of RBD, by performing ictal REM sleep SPECT, comparing subjects with Parkinson's Disease (PD) and evidence of RBD to subjects with PD and no RBD.
Participants underwent a targeted clinical assessment, followed by video polysomnography (vPSG). Ictal Tc-HMPAO SPECT was performed by injecting the tracer during vPSG confirmed REM sleep in seven cases (PD with RBD) and five controls (PD without RBD). Voxel-wise, whole brain regional relative perfusion changes between both groups were assessed using statistical parametric mapping.
No difference in relative regional brain perfusion was demonstrated at a family wise error corrected p-value of 0.05 between the case and control groups. At an uncorrected P-value of <0.01, combined with a cluster extent threshold of 300 voxels, four clusters of increased perfusion were identified in the case group compared to the control group. The clusters were seen in the motor, somatosensory association, and prefrontal cortices. The reverse contrast did not show any significant clusters.
Increased perfusion of the motor cortex is in keeping with previous publications and motor phenomena seen in RBD. However, clusters included additional cortical regions. These findings demonstrate RBD as a wider sleep network dysfunction, rather than a manifestation of simple pontomedullary interruption.
快速眼动睡眠行为障碍(RBD)是突触核蛋白病已确定的前驱症状。该障碍的病理生理学已得到充分研究,但缺乏功能成像数据来说明体内功能障碍。
我们旨在通过进行发作期快速眼动睡眠单光子发射计算机断层扫描(SPECT),比较患有帕金森病(PD)且有RBD证据的受试者与患有PD但无RBD的受试者,来研究RBD的功能变化。
参与者接受了针对性的临床评估,随后进行了视频多导睡眠图(vPSG)检查。在7例(PD伴RBD)和5例对照(PD无RBD)的vPSG确认的快速眼动睡眠期间注射示踪剂,进行发作期锝-六甲基丙烯胺肟SPECT检查。使用统计参数映射评估两组之间体素级全脑区域相对灌注变化。
在病例组和对照组之间进行家族性错误校正p值为0.05时,未显示相对区域脑灌注存在差异。在未校正的P值<0.01且聚类范围阈值为300体素的情况下,与对照组相比,病例组中发现了四个灌注增加的聚类。这些聚类出现在运动、体感联合和前额叶皮质。反向对比未显示任何显著聚类。
运动皮质灌注增加与先前关于RBD的出版物以及RBD中观察到的运动现象一致。然而,聚类包括其他皮质区域。这些发现表明RBD是更广泛的睡眠网络功能障碍,而不是单纯脑桥延髓中断的表现。