视觉扫描神经疾病的潜在来源

J. Rolfs
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引用次数: 0

摘要

目的。光线会在视网膜感光器中引发化学反应。电信号通过视觉通路的所有神经元传递到视觉皮层。由此产生的电位波动可以导出为视觉诱发电位(VEP),并分析其潜伏期和振幅,以获得视觉通路内病理变化的指示。方法。本文将解释导致视觉皮层出现电位的过程,哪些方法和技术是可用的,以及哪些神经系统疾病具有临床诊断的附加价值。结果。在VEP中,所有神经元的响应都是由中央视野分量产生的。为了能够表征仅影响部分视野区域的病变,发明了多焦诱发电位(mfVEP)测量技术,利用该技术可以将电位分配到视网膜的某些区域。在神经病学中,VEP主要用于检测视神经炎,主要是在多发性硬化症(MS)和视神经脊髓炎视谱障碍(NMOSD)的情况下。在多发性硬化症中,急性期典型的潜伏期延迟和幅度降低,消退后仅典型的潜伏期延迟。在NMOSD中,振幅的强烈减小是一个典型的信号。MfVEP证实了VEP的病理改变,但在MS中也表现为中心振幅降低,而在NMOSD中中心电位几乎消失。在其他神经系统疾病中,VEP可能发生变化,但不是特异性的,因此它们不会给诊断带来任何额外的临床益处。结论。在神经系统疾病中,VEP可以显示特定的变化,特别是视神经突,因此可以为诊断带来临床附加价值。关键词VEP,多发性硬化症,帕金森病,阿尔茨海默病,偏头痛
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Visuell evozierte Potenziale bei neurologischen Erkrankungen
Purpose. Light triggers a chemical reaction in the retinal photoreceptors. Electrical signals are transmitted through all neurons of the visual pathway into the visual cortex. Resulting potential fluctuations can be derived as visually evoked po- tentials (VEP) and analyzed regarding latency and amplitude in order to get an indication of pathological changes within the visual pathway. Method. This article shall explain the processes leading to the emergence of potentials in the visual cortex, which methods and techniques of VEP are available and in which neurological diseases a clinical added value for finding a diagnosis is given. Results. In VEP, a response of all neurons is represented, which is mainly generated by central visual field components. In order to be able to represent pathologies, that affect only partial areas of the visual field, the measurement technique of multifocal evoked potentials (mfVEP) was invented, with which potentials can be assigned to certain retinal areas. In neurology, VEP are mostly used for testing for optic neuritis,mainly in the context of multiple sclerosis (MS) and neuro- myelitis optica spectrum disorders (NMOSD). In MS, latency delay and amplitude reduction are typical in the acute stage, after subsiding only latency delays are typical. In NMOSD, a very strong reduction of the amplitude is a typical sign. MfVEP confirm pathological changes of VEP, but also show a central amplitude reduction in MS, while in NMOSD the central potentials are almost extinguished. In other neurolog- ical diseases, changes in VEP may occur, but are not specific, therefore they do not bring any additional clinical benefit to the diagnosis. Conclusion. In neurological diseases, VEP can show specific changes, especially in optic neurites, and can therefore bring clinical added value in finding a diagnosis. Keywords VEP, Multiple Sclerosis, Parkinson’s, Alzheimer’s, Migraine
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