Department of Cardiovascular, Neural and Metabolic Sciences Istituto Auxologico Italiano, IRCCS, Milan, Italy.
Department of Medicine and Surgery, University of Milano-Bicocca, Milan, Italy.
Philos Trans A Math Phys Eng Sci. 2021 Dec 13;379(2212):20200254. doi: 10.1098/rsta.2020.0254. Epub 2021 Oct 25.
Recent advancements in detrended fluctuation analysis (DFA) allow evaluating multifractal coefficients scale-by-scale, a promising approach for assessing the complexity of biomedical signals. The multifractality degree is typically quantified by the singularity spectrum width (), a method that is critically unstable in multiscale applications. Thus, we aim to propose a robust multiscale index of multifractality, compare it with and illustrate its performance on real biosignals. The proposed index is the cumulative function of squared increments between consecutive DFA coefficients at each scale : (). We compared it with calculated scale-by-scale considering monofractal/monoscale, monofractal/multiscale, multifractal/monoscale and multifractal/multiscale random processes. The two indices provided qualitatively similar descriptions of multifractality, but () differentiated better the multifractal components from artefacts due to crossovers or detrending overfitting. Applied on 24 h heart rate recordings of 14 participants, the singularity spectrum failed to always satisfy the concavity requirement for providing meaningful , while () demonstrated a statistically significant heart rate multifractality at night in the scale ranges 16-100 and 256-680 s. Furthermore, () did not reject the hypothesis of monofractality at daytime, coherently with previous reports of lower nonlinearity and monoscale multifractality during the day. Thus, () appears a robust index of multiscale multifractality that is useful for quantifying complexity alterations of physiological series. This article is part of the theme issue 'Advanced computation in cardiovascular physiology: new challenges and opportunities'.
最近,去趋势波动分析(DFA)的进展使得能够按比例评估多重分形系数,这是评估生物医学信号复杂性的一种很有前途的方法。多重分形程度通常通过奇异谱宽度()来量化,这是一种在多尺度应用中极不稳定的方法。因此,我们旨在提出一种稳健的多尺度多重分形指数,并将其与进行比较,并说明其在真实生物信号上的性能。所提出的指数是在每个尺度上连续 DFA 系数之间平方增量的累积函数:()。我们将其与在单分形/单尺度、单分形/多尺度、多分形/单尺度和多分形/多尺度随机过程中按比例计算的进行了比较。这两个指数对多重分形性提供了定性相似的描述,但()由于交叉或去趋势过度拟合,更好地区分了多重分形成分和伪影。应用于 14 名参与者的 24 小时心率记录,奇异谱未能始终满足提供有意义的的凹度要求,而()在 16-100 和 256-680 s 的尺度范围内显示出夜间心率的多重分形性具有统计学意义。此外,()在白天没有拒绝单分形性的假设,与白天非线性和单尺度多重分形性较低的先前报道一致。因此,()似乎是一种稳健的多尺度多重分形指数,可用于量化生理序列复杂性的变化。本文是“心血管生理学中的高级计算:新的挑战和机遇”主题问题的一部分。