Centre for Systems Neuroscience, University of Leicester, United Kingdom.
Leibniz Institute for Neurobiology, Magdeburg, Germany; Experimental Neurology, University of Magdeburg, Germany; Kliniken Schmieder Heidelberg, Heidelberg, Germany.
J Neurosci Methods. 2021 Aug 1;360:109230. doi: 10.1016/j.jneumeth.2021.109230. Epub 2021 May 27.
There is an active debate about the mechanism underlying the generation of event-related potentials, and, particularly, whether these are generated by additive components, independent of the background EEG, or the phase-resetting of ongoing oscillations.
We present a new metric to evaluate trial-by-trial covariations of successive ERP components. Our main assumption is that if two successive ERP components are generated by phase-resetting of a unitary oscillation, they should be time-locked to each other and their single-trial latencies should covary. In contrast, if the components are generated by independent additive components, single-trial latency covariations should not be observed. To quantify the covariance between the single-trial latencies, we define a metric based on latency-corrected averages, which we applied to both simulated and real ERPs.
For the simulated data, there was a clear distinction in latency covariation between the ERPs generated with unitary phase-resetting versus additive models. For real visual and auditory ERPs, we observed a lack of latency covariation of successive components.
The new metric is complementary to other approaches to study the mechanisms underlying ERP generation, and does not suffer from potential caveats due to filtering artifacts. Moreover, the method proved to be more sensitive than another estimation of single-trial latency covariations using the cross-correlation function.
The observed lack of latency covariation shows the presence of parallel, independent processing within each cortical sensory pathway.
关于事件相关电位的产生机制存在激烈的争论,特别是这些电位是由独立于背景 EEG 的附加成分产生的,还是由正在进行的振荡的相位重置产生的。
我们提出了一种新的度量标准来评估连续 ERP 成分的逐次试验变异性。我们的主要假设是,如果两个连续的 ERP 成分是通过单一振荡的相位重置产生的,它们应该彼此锁定,并且它们的单次潜伏期应该相关。相比之下,如果这些成分是由独立的附加成分产生的,则不应观察到单个试验潜伏期的变异性。为了量化单个试验潜伏期之间的协方差,我们定义了一个基于潜伏期校正平均值的度量标准,并将其应用于模拟和真实 ERP。
对于模拟数据,在具有单一相位重置与附加模型生成的 ERP 之间,潜伏期变异性有明显的区别。对于真实的视觉和听觉 ERP,我们观察到连续成分的潜伏期没有相关性。
新的度量标准与研究 ERP 产生机制的其他方法相辅相成,并且不会受到滤波伪影等潜在缺陷的影响。此外,该方法比使用互相关函数估计单个试验潜伏期变异性的另一种方法更敏感。
观察到的潜伏期变异性缺乏表明每个皮质感觉通路中存在并行的、独立的处理。