Department of Medical Physics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Brain Behav. 2024 Mar;14(3):e3460. doi: 10.1002/brb3.3460.
Rapid eye movement behavior disorder (RBD) is a parasomnia characterized by the loss of skeletal muscle atonia during the rapid eye movement (REM) sleep phase. On the other hand, idiopathic RDB (iRBD) is considered the prelude of the various α-synucleinopathies, including Parkinson's disease (PD), dementia with Lewy bodies and multiple system atrophy. Consequently, over 40% of patients eventually develop PD. Recent neuroimaging studies utilizing structural magnetic resonance imaging (s-MRI), diffusion-weighted imaging (DWI), and functional magnetic resonance imaging (fMRI) with graph theoretical analysis have demonstrated that patients with iRBD and Parkinson's disease have extensive brain abnormalities. Thus, it is crucial to identify new biomarkers that aid in determining the underlying physiopathology of iRBD group. This review was conducted systematically on the included full-text articles of s-MRI, DWI, and fMRI studies using graph theoretical analysis on patients with iRBD, per the procedures recommended by Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). The literature search was conducted through the PubMed and Google scholar databases concentrating on studies from September to January 2022. Based on the three perspectives of integration, segregation, and centrality, the reviewed articles demonstrated that iRBD is associated with segregation disorders in frontal and limbic brain regions. Moreover, this study highlighted the need for additional longitudinal and multicenter studies to better understand the potential of graph metrics as brain biomarkers for identifying the underlying physiopathology of iRBD group.
快速眼动行为障碍(RBD)是一种睡眠障碍,其特征是在快速眼动(REM)睡眠阶段骨骼肌失去紧张。另一方面,特发性 RBD(iRBD)被认为是各种α-突触核蛋白病的前奏,包括帕金森病(PD)、路易体痴呆和多系统萎缩。因此,超过 40%的患者最终会发展为 PD。最近利用结构磁共振成像(s-MRI)、弥散加权成像(DWI)和功能磁共振成像(fMRI)以及图论分析的神经影像学研究表明,iRBD 和帕金森病患者的大脑存在广泛的异常。因此,识别有助于确定 iRBD 组潜在病理生理学的新生物标志物至关重要。本综述系统地回顾了使用图论分析对 iRBD 患者进行 s-MRI、DWI 和 fMRI 研究的全文文章,这些文章符合系统评价和荟萃分析的首选报告项目(PRISMA)的程序。文献检索通过 PubMed 和 Google Scholar 数据库进行,重点是 2022 年 9 月至 1 月的研究。基于整合、分离和中心性三个视角,综述文章表明 iRBD 与额部和边缘脑区的分离障碍有关。此外,本研究强调需要进行更多的纵向和多中心研究,以更好地理解图度量作为识别 iRBD 组潜在病理生理学的脑生物标志物的潜力。