Complexity synchronization analysis of neurophysiological data: Theory and methods

神经生理数据的复杂性同步分析:理论与方法

阅读:1

Abstract

INTRODUCTION: We present a theoretical foundation based on the spontaneous self-organized temporal criticality (SOTC) and multifractal dimensionality μ to model complex neurophysiological and behavioral systems to infer the optimal empirical transfer of information among them. We hypothesize that heterogeneous time series characterizing the brain, heart, and lung organ-networks (ONs) are necessarily multifractal, whose level of complexity and, therefore, their information content is measured by their multifractal dimensions. METHODS: We apply modified diffusion entropy analysis (MDEA) to assess multifractal dimensions of ON time series (ONTS), and complexity synchronization (CS) analysis to infer information transfer among ONs that are part of a network-of-organ-networks (NoONs). An automated parameter selection process is proposed that relies on the Kolmogorov-Smirnov statistic to properly choose stripe sizes which are crucial in the MDEA analysis using synthetic duration times derived from the Mittag-Leffler map, shows the strength of KS-based stripe size selection to track changes in the IPL parameter μ . The purpose of this paper is to advance the validation, standardization, and reconstruct-ability of MDEA and CS analysis of heterogeneous neurophysiological time series data. RESULTS: Results from processing these datasets show that the complexity of brain, heart, and lung ONTS co-vary over time during cognitive task performance in 44% of subjects, while complexity of brain-heart interactions significantly co-vary in 85% of subjects. DISCUSSION: We conclude that certain principles, guidelines, and strategies for the application of MDEA analysis need further consideration. We conclude with a summary of the MDEA's limitations and future research directions.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。