Difficulties of motion-onset VEP interpretation in school-age children

被引:7
|
作者
Kubova, Zuzana [1 ]
Kuba, Miroslav [1 ]
Kremlacek, Jan [1 ]
Langrova, Jana [1 ]
Szanyi, Jana [1 ]
Vit, Frantisek [1 ]
Chutna, Marie [1 ]
机构
[1] Charles Univ Prague, Fac Med Hradec Kralove, Dept Pathophysiol, Hradec Kralove 50038, Czech Republic
关键词
Motion-onset visual evoked potentials; VEPs; M-VEPs; Children; VISUAL-EVOKED-POTENTIALS; PATTERN; SYSTEM; NEUROBORRELIOSIS; ADAPTATION; RESPONSES; GLAUCOMA; DYSLEXIA; DEFICIT;
D O I
10.1007/s10633-014-9429-y
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background In adults, motion-onset visual evoked potentials (M-VEPs) with a dominant N2 peak represent a useful diagnostic tool. However, it is difficult to use this type of VEP in children because of the long maturation (up to 18 years) of M-VEPs, which is characterised by a gradual decrease in N2 peak latency and shape development. Moreover, in some children, M-VEPs are difficult to identify with standard stimuli. Methods We tested features of M-VEPs in 30 children (7-12 years) with the following set of standard stimuli used in our lab for examining adults (https://web.lfhk.cuni.cz/elf): low-contrast translation motion (TM) and expansion/contraction motion (ExCoM) in full field and in periphery (with central 20 degrees masked). In 16 children, a high-contrast TM was also tested. Results With standard (low-contrast) stimuli, a common M-VEP to TM and to ExCoM was detected in 77 and 83 % of children, respectively. The M-VEPs to ExCoM in the periphery were detected in only 43 % of children. An abnormal dominant P1 peak was found in 9 % of VEPs to TM, 12 % of VEPs to full-field ExCoM and 14 % of VEPs to peripheral ExCoM. The M-VEPs to all low-contrast stimuli displayed large inter-individual latency variability (N2 peak latency differed for more than 100 ms). High contrast (more suitable for the non-mature magnocellular pathway) shortened M-VEP latencies and improved amplitudes. Conclusions Our findings show that the maturation of motion perception in children is inter-individually variable, which limits the diagnostic use of M-VEPs.
引用
收藏
页码:121 / 129
页数:9
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