Simulating Partial Conduction Delays in VEPs Via Asynchronous and Contrast-Modulated Stimulation.

IF 2.7 3区 医学 Q2 OPHTHALMOLOGY
Leon A Pfeiffer, Julia Haldina, Sven P Heinrich
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引用次数: 0

Abstract

Purpose: To investigate the origin of P100 double peaks occasionally observed in patients with optic neuritis by experimentally inducing timing asynchronies between visual field locations and modulating stimulus strength via contrast reduction in transient and steady-state VEPs (trVEP and ssVEP).

Methods: The trVEPs and ssVEPs were recorded using a checkerboard stimulus vertically split into nasal and temporal half-fields. Timing asynchrony was induced by delaying the temporal half-field by 24, 35, or 47 ms; stimulus strength was modulated by reducing the temporal half-field contrast to 20% or 8%. Full-field and half-field responses were quantitatively analyzed and qualitatively compared to characterize the superposition effects induced by these stimulus changes.

Results: In trVEPs, contrast reduction produced smaller, broader P100 responses with modest peak-time delays and only sporadic double-peak formation. Conversely, induced temporal half-field delays robustly generated P100 double peaks (incidence: 50% at 24 ms, 85% at 35 ms, and 100% at 47 ms). Quantitative and qualitative analyses demonstrated that the P100 peaks of the half-field responses aligned temporally with the two peaks of the full-field double peak. In ssVEPs, increasing delays reduced the absolute harmonic magnitude and altered the second-to-first harmonic ratio (decreased at 24 and 35 ms; increased at 47 ms).

Conclusions: Spatially localized timing asynchronies reliably reproduce double-peaked P100 morphologies, supporting differential conduction speeds within the optic nerve as a plausible mechanism in patients with optic neuritis.

Translational relevance: Linking experimentally induced conduction-delay effects to VEP morphology enhances the clinical interpretation of atypical VEP waveforms in suspected optic neuritis.

通过异步和对比调制刺激模拟vep的部分传导延迟。
目的:通过实验诱导瞬态和稳态vep (trVEP和ssVEP)之间的时间不同步,并通过降低对比度调节刺激强度,探讨视神经炎患者偶尔观察到的P100双峰的来源。方法:采用棋盘状刺激,将其垂直分为鼻半场和颞半场,记录trvep和ssvep。延时24、35、47 ms诱发时间异步;刺激强度通过将颞叶半场对比度降低到20%或8%来调节。对全场和半场反应进行了定量分析和定性比较,以表征这些刺激变化引起的叠加效应。结果:在trVEPs中,对比度降低产生更小、更广泛的P100反应,伴有适度的峰时延迟,只有偶发的双峰形成。相反,诱导的时间半场延迟强烈地产生P100双峰(发生率:24 ms时50%,35 ms时85%,47 ms时100%)。定量和定性分析表明,半场响应的P100峰与全场双峰的两个峰在时间上排列一致。在ssvep中,延迟的增加降低了绝对谐波幅度,改变了第二次与第一次谐波比(在24和35 ms时下降;在47 ms时增加)。结论:空间定位的时间不同步可靠地再现了双峰P100形态,支持视神经内传导速度的差异是视神经炎患者的合理机制。翻译相关性:将实验诱导的传导延迟效应与VEP形态学联系起来,增强了疑似视神经炎的非典型VEP波形的临床解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Translational Vision Science & Technology
Translational Vision Science & Technology Engineering-Biomedical Engineering
CiteScore
5.70
自引率
3.30%
发文量
346
审稿时长
25 weeks
期刊介绍: Translational Vision Science & Technology (TVST), an official journal of the Association for Research in Vision and Ophthalmology (ARVO), an international organization whose purpose is to advance research worldwide into understanding the visual system and preventing, treating and curing its disorders, is an online, open access, peer-reviewed journal emphasizing multidisciplinary research that bridges the gap between basic research and clinical care. A highly qualified and diverse group of Associate Editors and Editorial Board Members is led by Editor-in-Chief Marco Zarbin, MD, PhD, FARVO. The journal covers a broad spectrum of work, including but not limited to: Applications of stem cell technology for regenerative medicine, Development of new animal models of human diseases, Tissue bioengineering, Chemical engineering to improve virus-based gene delivery, Nanotechnology for drug delivery, Design and synthesis of artificial extracellular matrices, Development of a true microsurgical operating environment, Refining data analysis algorithms to improve in vivo imaging technology, Results of Phase 1 clinical trials, Reverse translational ("bedside to bench") research. TVST seeks manuscripts from scientists and clinicians with diverse backgrounds ranging from basic chemistry to ophthalmic surgery that will advance or change the way we understand and/or treat vision-threatening diseases. TVST encourages the use of color, multimedia, hyperlinks, program code and other digital enhancements.
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