Jonak Kamil
Department of Clinical Neuropsychiatry, Medical University of Lublin, 20-439 Lublin, Poland.
Brain Sci. 2020 Sep 8;10(9):622. doi: 10.3390/brainsci10090622.
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.
Leber遗传性视神经病变(LHON)是一种罕见的母系遗传的线粒体DNA突变所致的遗传性疾病。经典描述强调了患者视束各部位的结构异常;然而,目前的研究已证明,这些变化还会影响许多皮质和皮质下结构,而不仅仅是属于视觉系统的结构。本研究旨在增进我们对LHON神经生理损伤的理解。首先,我们想了解在全脑源脑电图(EEG)分析中,健康对照者与LHON受试者之间是否存在差异。其次,我们想研究观察结果与Leber病临床表现的某些选定方面之间的关联。为实现这些目标,对20例LHON患者和20例年龄匹配的健康对照(HC)受试者进行了检查。为了研究HC组和LHON组之间的电生理差异,对全脑电流源密度进行了定量分析。信号分析方法基于头皮EEG数据和一种称为低分辨率脑电磁断层成像(eLORETA)的逆解方法。与健康受试者相比,LHON参与者在α和γ频段的神经元活动显著降低;更具体地说,在α频段,活动降低主要见于枕叶和二级视皮层,而在γ频段,活动降低发生在多个皮质区域。此外,在LHON参与者中,右侧二级视皮层的α频段活动与右侧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与广泛的皮质失活有关,而不仅仅是构成视觉系统的结构异常。