Jancic Jasna, Zarkovic Nikola, Nikolic Blazo, Ivancevic Nikola, Rovcanin Branislav, Nesic Dejan
Clinic of Neurology and Psychiatry for Children and Youth, Belgrade, Serbia.
Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Front Neurol. 2024 Jul 22;15:1410101. doi: 10.3389/fneur.2024.1410101. eCollection 2024.
Neurofibromatosis type 1 (NF type 1) is an autosomal dominant disease with typical clinical manifestations, such as skin lesions, Lisch nodules, optic pathway gliomas, and neurofibromas, caused by the mutation of the NF1 gene. Visual evoked potentials (VEP) present a measure of the electrophysiological response of visual cortex to a visual stimulus. The role of VEP in the pathophysiology of NF type 1 is very complex and requires additional research.
We examined the differences between NF type 1 patients with normal and altered VEP and analyzed the correlation between the prolongation of P100 latency and disease severity.
Two groups were formed: a control group and a study group with NF type 1 patients. Based on the control group analysis, a threshold value for a normal VEP finding of 116 ms was obtained, and it was used to divide the study group into subgroups with normal and altered VEP. We proceeded with examining the differences in clinical manifestations of the disease between the subgroups, after which we checked if there is a correlation between the prolongation of the P100 latency and the severity of the clinical picture according to the Riccardi scale. Statistical analysis was performed using the Pearson chi-square test and the Spearman correlation test in the program SPSS 28.0, with levels of statistical significance = 0.05 and = 0.001.
In the group with the abnormal VEP we found a statistically significant more frequent occurrence of optic tract glioma ( = 0.008), tumors ( = 0.032), epilepsy ( = 0.043), and cognitive disorders ( = 0.028), while the other clinical signs had an equal prevalence in both groups. A moderately strong correlation ( = 0.665) was observed between the prolongation of P100 latency and the severity of the clinical picture.
Our results showed the important role of VEP in the description of clinical phenotypes of NF type 1. The authors of the study propose VEP to be included in the diagnostic algorithms designed for patients with NF type 1.
1型神经纤维瘤病(NF1型)是一种常染色体显性疾病,由NF1基因突变引起,具有典型的临床表现,如皮肤病变、Lisch结节、视路胶质瘤和神经纤维瘤。视觉诱发电位(VEP)是衡量视觉皮层对视觉刺激的电生理反应的指标。VEP在NF1型病理生理学中的作用非常复杂,需要进一步研究。
我们研究了VEP正常和异常的NF1型患者之间的差异,并分析了P100潜伏期延长与疾病严重程度之间的相关性。
分为两组:对照组和NF1型患者研究组。根据对照组分析,得出VEP正常结果的阈值为116毫秒,并用它将研究组分为VEP正常和异常的亚组。我们接着检查亚组之间疾病临床表现的差异,之后根据Riccardi量表检查P100潜伏期延长与临床症状严重程度之间是否存在相关性。使用SPSS 28.0程序中的Pearson卡方检验和Spearman相关性检验进行统计分析,统计显著性水平为=0.05和=0.001。
在VEP异常的组中,我们发现视束胶质瘤(=0.008)、肿瘤(=0.032)、癫痫(=0.043)和认知障碍(=0.028)的发生率在统计学上显著更高,而其他临床体征在两组中的患病率相等。观察到P100潜伏期延长与临床症状严重程度之间存在中度强相关性(=0.665)。
我们的结果表明VEP在描述NF1型临床表型方面具有重要作用。该研究的作者建议将VEP纳入为NF1型患者设计的诊断算法中。