Nagy Zoltan, Mukli Peter, Herman Peter, Eke Andras
Institute of Clinical Experimental Research, Semmelweis UniversityBudapest, Hungary.
Department of Physiology, Semmelweis UniversityBudapest, Hungary.
Front Physiol. 2017 Jul 26;8:533. doi: 10.3389/fphys.2017.00533. eCollection 2017.
Physiological processes-such as, the brain's resting-state electrical activity or hemodynamic fluctuations-exhibit scale-free temporal structuring. However, impacts common in biological systems such as, noise, multiple signal generators, or filtering by transport function, result in multimodal scaling that cannot be reliably assessed by standard analytical tools that assume unimodal scaling. Here, we present two methods to identify breakpoints or crossovers in multimodal multifractal scaling functions. These methods incorporate the robust iterative fitting approach of the focus-based multifractal formalism (FMF). The first approach (moment-wise scaling range adaptivity) allows for a breakpoint-based adaptive treatment that analyzes segregated scale-invariant ranges. The second method (scaling function decomposition method, SFD) is a crossover-based design aimed at decomposing signal constituents from multimodal scaling functions resulting from signal addition or co-sampling, such as, contamination by uncorrelated fractals. We demonstrated that these methods could handle multimodal, mono- or multifractal, and exact or empirical signals alike. Their precision was numerically characterized on ideal signals, and a robust performance was demonstrated on exemplary empirical signals capturing resting-state brain dynamics by near infrared spectroscopy (NIRS), electroencephalography (EEG), and blood oxygen level-dependent functional magnetic resonance imaging (fMRI-BOLD). The NIRS and fMRI-BOLD low-frequency fluctuations were dominated by a multifractal component over an underlying biologically relevant random noise, thus forming a bimodal signal. The crossover between the EEG signal components was found at the boundary between the δ and θ bands, suggesting an independent generator for the multifractal δ rhythm. The robust implementation of the SFD method should be regarded as essential in the seamless processing of large volumes of bimodal fMRI-BOLD imaging data for the topology of multifractal metrics free of the masking effect of the underlying random noise.
生理过程,如大脑的静息态电活动或血液动力学波动,呈现出无标度时间结构。然而,生物系统中常见的影响因素,如噪声、多个信号发生器或传输函数滤波,会导致多峰标度,而标准分析工具假设单峰标度,无法可靠地评估这种多峰标度。在此,我们提出两种方法来识别多峰多重分形标度函数中的断点或交叉点。这些方法纳入了基于焦点的多重分形形式主义(FMF)的稳健迭代拟合方法。第一种方法(矩尺度范围适应性)允许基于断点的自适应处理,该处理分析分离的尺度不变范围。第二种方法(标度函数分解方法,SFD)是一种基于交叉点的设计,旨在从信号相加或共采样产生的多峰标度函数中分解信号成分,例如不相关分形的污染。我们证明,这些方法可以同样地处理多峰、单分形或多重分形以及精确或经验信号。它们的精度在理想信号上进行了数值表征,并在通过近红外光谱(NIRS)、脑电图(EEG)和血氧水平依赖性功能磁共振成像(fMRI-BOLD)捕获静息态脑动力学的示例性经验信号上展示了稳健性能。NIRS和fMRI-BOLD低频波动在潜在生物相关随机噪声之上由多重分形成分主导,从而形成双峰信号。在EEG信号成分之间发现交叉点位于δ和θ频段之间的边界处,这表明多重分形δ节律有一个独立的发生器。对于无潜在随机噪声掩盖效应的多重分形度量拓扑结构的大量双峰fMRI-BOLD成像数据的无缝处理,SFD方法的稳健实现应被视为至关重要。