A method to assess Granger causality, isolation and autonomy in the time and frequency domains: theory and application to cerebrovascular variability

TL;DR

This paper introduces spectral measures of Granger causality, isolation, and autonomy to analyze coupled physiological processes, providing new insights into cerebrovascular dynamics during postural stress.

Contribution

It develops spectral measures for Granger isolation and autonomy within the linear parametric framework, extending causality analysis to the frequency domain with practical applications.

Findings

Spectral GA reflects internal dynamics regularity.

Spectral GC and GI detect altered cerebrovascular responses.

New measures complement existing causality tools.

Abstract

Concepts of Granger causality (GC) and Granger autonomy (GA) are central to assess the dynamics of coupled physiologic processes. While causality measures have been already proposed and applied in time and frequency domains, measures quantifying self-dependencies are still limited to the time-domain formulation and lack of a clear spectral representation. We embed into the classical linear parametric framework for computing GC from a driver random process X to a target process Y a measure of Granger Isolation (GI) quantifying the part of the dynamics of Y not originating from X, and a new spectral measure of GA assessing frequency-specific patterns of self-dependencies in Y. The measures are illustrated in theoretical simulations and applied to time series of mean arterial pressure and cerebral blood flow velocity obtained in subjects prone to develop postural syncope and healthy controls. Simulations show that GI is complementary to GC but not trivially related to it, while GA reflects the regularity of the internal dynamics of the analyzed target process. In the application to cerebrovascular interactions, spectral GA quantified the physiological response to postural stress of slow cerebral blood flow oscillations, while spectral GC and GI detected an altered response to postural stress in subjects prone to syncope, likely related to impaired cerebral autoregulation. The new spectral measures of GI and GA are useful complements to GC for the analysis of interacting oscillatory processes, and detect physiological and pathological responses to postural stress which cannot be traced in the time domain. The assessment of causality, isolation and autonomy opens new perspectives for the analysis of coupled biological processes in both physiological and clinical investigations.