Faes L, Marinazzo D, Jurysta F, Nollo G
BIOtech, Department of Industrial Engineering, University of Trento, and IRCS PAT-FBK. Trento, Italy.
Physiol Meas. 2015 Apr;36(4):683-98. doi: 10.1088/0967-3334/36/4/683. Epub 2015 Mar 23.
In this study, the physiological networks underlying the joint modulation of the parasympathetic component of heart rate variability (HRV) and of the different electroencephalographic (EEG) rhythms during sleep were assessed using two popular measures of directed interaction in multivariate time series, namely Granger causality (GC) and transfer entropy (TE). Time series representative of cardiac and brain activities were obtained in 10 young healthy subjects as the normalized high frequency (HF) component of HRV and EEG power in the δ, θ, α, σ, and β bands, measured during the whole duration of sleep. The magnitude and statistical significance of GC and TE were evaluated between each pair of series, conditional on the remaining series, using respectively a linear model-based approach exploiting regression models, and a nonlinear model-free approach combining nearest-neighbor entropy estimation with a procedure for dimensionality reduction. The contribution of nonlinear dynamics to the TE was also assessed using surrogate data. GC and TE consistently detected structured networks of physiological interactions, with links directed predominantly from HRV to the EEG waves in the brain-heart network, and from the σ and β EEG waves to the δ, θ, and α waves in the brain-brain network. While these common patterns supported the suitability of a linear model-based analysis, we also found a significant contribution of nonlinear dynamics, particularly involving the information transferred out of the δ node in the two networks. This suggested the importance of nonparametric TE estimation for evidencing the fine structure of the physiological networks underlying the autonomic regulation of cardiac and brain functions during sleep.
在本研究中,使用多变量时间序列中两种常用的定向相互作用测量方法,即格兰杰因果关系(GC)和转移熵(TE),评估了睡眠期间心率变异性(HRV)的副交感神经成分与不同脑电图(EEG)节律联合调制的生理网络。在10名年轻健康受试者中获取了代表心脏和大脑活动的时间序列,作为睡眠全过程中测量的HRV归一化高频(HF)成分以及δ、θ、α、σ和β频段的EEG功率。分别使用基于线性模型的利用回归模型的方法以及结合最近邻熵估计与降维程序的无非线性模型方法,在每对序列之间评估GC和TE的大小及统计显著性,并以其余序列为条件。还使用替代数据评估了非线性动力学对TE的贡献。GC和TE一致地检测到生理相互作用的结构化网络,在心脏 - 大脑网络中,连接主要从HRV指向脑电波,在大脑 - 大脑网络中,从σ和β脑电波指向δ、θ和α波。虽然这些常见模式支持基于线性模型分析的适用性,但我们也发现了非线性动力学的显著贡献,特别是涉及从两个网络中的δ节点传出的信息。这表明非参数TE估计对于揭示睡眠期间心脏和大脑功能自主调节背后生理网络的精细结构很重要。