Reflections on the topics: EEG frequency bands and regulation of vigilance.

S Kubicki, W M Herrmann, K Fichte, G Freund
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引用次数: 3

Abstract

A critical analysis of quantitative pharmaco-electroencephalography begins with parametrization into variables. The determination of frequency bands according to clinical criteria should be reconsidered. Alternatives may be the determination of factor scores or the definition of frequency bands based on factor analysis. If the latter procedure is used, the clinical alpha-band is subdivided into a lower (alpha 1F = 8,5-10.5 HZ) and an upper (alpha 2F = 10.5-12.5 HZ) part. Furthermore parts of the clinical theta-band (and the delta-band are combined into the delta F-band (1.5-6.0 HZ), for awake healthy volunteers with an occipital alpha-rhythm. Existing concepts of vigilance for the awake stages are not contradictory to the following observations: the factor structure of EEG relative power spectrum variables shows a negative correlation of slow alpha-frequencies with those in the delta F- and beta 3F-band. There is also a negative correlation between slow and fast alpha-wave relative power values.

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主题思考:脑电图频带和警觉性调节。
定量药物脑电图的关键分析开始于参数化为变量。应重新考虑根据临床标准确定频带。替代方案可能是确定因子得分或基于因子分析定义频带。如果采用后一种方法,临床α波段被细分为较低(α 1F = 8,5-10.5 HZ)和较高(α 2F = 10.5-12.5 HZ)部分。此外,临床上的部分θ波段(和δ波段)被合并为δ f波段(1.5-6.0 HZ),用于清醒的健康志愿者的枕部α节律。现有的清醒阶段警觉性概念与以下观察结果并不矛盾:脑电图相对功率谱变量的因子结构显示慢α -频率与δ F-和β 3f -频带的因子结构呈负相关。慢波和快波的相对功率值之间也存在负相关。
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