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Widespread Reductions of Spontaneous Neurophysiological Activity in Leber’s Disease—An Application of EEG Source Current Density Reconstruction

机译:Leber疾病中自发性神经生理活性的广泛降低 - eEG源电流密度重构的应用

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摘要

Leber’s hereditary optic neuropathy (LHON) is a rare, maternally inherited genetic disease caused by a mutation of mitochondrial DNA. Classical descriptions have highlighted structural abnormalities in various parts of patients’ optic tracts; however, current studies have proved that changes also affect many cortical and subcortical structures, not only these belonging to the visual system. This study aimed at improving our understanding of neurophysiological impairments in LHON. First of all, we wanted to know if there were any differences between the health control and LHON subjects in the whole-brain source electroencephalography (EEG) analysis. Second, we wanted to investigate the associations between the observed results and some selected aspects of Leber’s disease’s clinical picture. To meet these goals, 20 LHON patients and 20 age-matched healthy control (HC) subjects were examined. To investigate the electrophysiological differences between the HC and LHON groups, a quantitative analysis of the whole-brain current source density was performed. The signal analysis method was based on scalp EEG data and an inverse solution method called low-resolution brain electromagnetic tomography (eLORETA). In comparison with the healthy subjects, LHON participants showed significantly decreased neuronal activity in the alpha and gamma bands; more specifically, in the alpha band, the decrease was mainly found in the occipital lobes and secondary visual cortex, whereas, in the gamma band, the reduced activity occurred in multiple cortical areas. Additionally, a correlation was found between the alpha band activity of the right secondary visual cortex and the averaged thickness of the right retinal nerve fiber layer in the LHON participants. Our study suggests that LHON is associated with widespread cortical de-activation, rather than simply abnormalities of structures constituting the visual system.
机译:莱伯的遗传视神经病变(LHON)是一种罕见的母遗传遗传遗传疾病,由线粒体DNA突变引起。经典描述突出了患者视神经中各部分的结构异常;然而,已经证明了当前的研究表明,变化也会影响许多皮质和皮质标结构,而不仅仅是这些属于视觉系统。本研究旨在改善我们对吕氏神经生理障碍的理解。首先,我们想知道全脑源脑电图(EEG)分析中的健康控制和LHON受试者是否存在任何差异。其次,我们希望调查观察结果与Leber病的临床图的一些选定方面之间的关联。为了满足这些目标,研究了20名LHON患者和20名匹配的健康对照(HC)受试者。为了研究HC和LHON组之间的电生理学差异,进行了对全脑电流源密度的定量分析。信号分析方法基于头皮EEG数据和称为低分辨率脑电磁性断层扫描(ELORETA)的反溶液方法。与健康受试者相比,LHON参与者在α和γ带中显示出显着降低的神经元活性;更具体地,在α带中,在枕叶和次要视觉皮层中主要发现的减少,而在伽马带中,在多种皮质区域发生降低的活性。另外,在LHON参与者中右二级视觉皮层的α带活动和右视网膜神经纤维层的平均厚度之间存在相关性。我们的研究表明,LHON与广泛的皮质解除激活相关,而不是基于构成视觉系统的结构的异常。

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