Department of Industrial Engineering and BIOtech, University of Trento, Trento, Italy.
Physiol Meas. 2018 Jan 30;39(1):014002. doi: 10.1088/1361-6579/aa9a91.
A defining feature of physiological systems under the neuroautonomic regulation is their dynamical complexity. The most common approach to assess physiological complexity from short-term recordings, i.e. to compute the rate of entropy generation of an individual system by means of measures of conditional entropy (CE), does not consider that complexity may change when the investigated system is part of a network of physiological interactions. This study aims at extending the concept of short-term complexity towards the perspective of network physiology, defining multivariate CE measures whereby multiple physiological processes are accounted for in the computation of entropy rates.
Univariate and multivariate CE measures are computed using state-of-the-art methods for entropy estimation and applied to time series of heart period (H), systolic (S) and diastolic (D) arterial pressure, and respiration (R) variability measured in healthy subjects monitored in a resting state and during conditions of postural and mental stress.
Compared with the traditional univariate metric of short-term complexity, multivariate measures provide additional information with plausible physiological interpretation, such as (i) the dampening of respiratory sinus arrhythmia and activation of the baroreflex control during postural stress; (ii) the increased complexity of heart period and blood pressure variability during mental stress, reflecting the effect of respiratory influences and upper cortical centers; (iii) the strong influence of D on S, mediated by left ventricular ejection fraction and vascular properties; (iv) the role of H in reducing the complexity of D, related to cardiac run-off effects; and (v) the unidirectional role of R in influencing cardiovascular variability.
Our results document the importance of employing a network perspective in the evaluation of the short-term complexity of cardiovascular and respiratory dynamics across different physiological states.
受神经自主调节的生理系统的一个显著特征是其动力复杂性。最常见的评估短期记录下生理复杂性的方法是通过条件熵(CE)度量来计算单个系统熵产生的速率,但是这种方法没有考虑到当被研究的系统成为生理相互作用网络的一部分时,复杂性可能会发生变化。本研究旨在将短期复杂性的概念扩展到网络生理学的角度,定义多元 CE 度量,在计算熵率时考虑多个生理过程。
使用熵估计的最新方法计算单变量和多变量 CE 度量,并将其应用于健康受试者在休息状态和姿势及心理应激条件下测量的心率(H)、收缩压(S)、舒张压(D)和呼吸(R)变异性的时间序列。
与传统的短期复杂性单变量度量相比,多变量度量提供了具有合理生理解释的附加信息,例如:(i)姿势应激时呼吸窦性心律失常的衰减和压力反射控制的激活;(ii)心理应激时心率和血压变异性的复杂性增加,反映了呼吸影响和皮质中枢的作用;(iii)D 对 S 的强烈影响,由左心室射血分数和血管特性介导;(iv)H 在降低 D 的复杂性中的作用,与心脏流出效应有关;(v)R 对心血管变异性的单向影响。
我们的研究结果证明了在不同生理状态下评估心血管和呼吸动力学的短期复杂性时采用网络视角的重要性。