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Ghouse, A.

Publications and source records attributed to Ghouse, A..

2 recordsLinked to original sources

Directed Functional Connectivity by Variational Cross-mapping of Psychophysiological Variables

Understanding the functional connectivity between different brain regions is vital for improving our comprehension of neural processing and cognition. While directed functional connectivity methods can provide us with statistical estimates of information exchange between regions, classic exploratory methods may not capture the nonlinear temporal effects that are observed in fMRI-BOLD data during task-evoked neural activity. To address this limitation, we propose a novel methodology that leverages variational cross-mapping analysis, inspired by psychophysiological interactions, to identify directional influence between connected regions of interest. Our approach can help uncover previously unknown patterns of information exchange and account for nonlinear effects, making it a valuable addition to the toolkit of researchers studying brain function. We demonstrate the effectiveness of our method using simulated neurovascular signals and publicly available fMRI data from 680 human participants performing an emotional face processing task. Our results suggest information flows from the occipital face area to the superior temporal sulcus and the fusiform face area, and additionally from the superior temporal sulcus to the fusiform gyrus. These findings are consistent with previously documented effective connectivity findings in face processing and provide new insights into the exploratory analyses of non-linear directed connectivity for task-evoked data. Overall, our findings contribute to advancing our understanding of directed functional connectivity in the brain and demonstrate the potential of our method to uncover previously unknown patterns of information exchange. Author summaryThe advent of large datasets has made it possible for many research groups to explore functional connectivity between different brain regions. The ability to assess directed connectivity between multiple regions from task-evoked neural responses could potentially uncover connections that were not previously hypothesized based on available data. However, classic methods for exploring task-evoked effects often rely on specific assumptions that are frequently violated by the data, such as nonlinearity, stationarity, and separability of cause from effect. Recent studies have attempted to address these issues using sliding window approaches or parameterized forward causal models, but these methods have limitations such as fixed contextual effect windows or restricted search space for forward models. To overcome these challenges, we propose a Bayesian non-parametric cross-mapping method that can address non-linearity and separability while using specially designed covariance functions to address non-stationarity. We demonstrate through simulations that our proposed method can detect pair-wise interacting neural populations with high sensitivity and specificity, and accurately infer changes in connections between tasks in both acyclical and cyclical neural networks. We also show that our method can replicate known connectivity findings about emotional face processing in a publicly available dataset. Thus, our method represents a promising exploratory connectivity tool for cognitive and behavioral neurosciences.

neuroscience↗

Nonlinear Neural Patterns Are Revealed In High Frequency fNIRS Analysis

Vasomotor tone has a direct implication in oxygen transport to neural tissue, and its dynamics are known to be under constant control from feedback loops with visceral signals, such as sympathovagal interactions. Functional Near Infrared Spectroscopy (fNIRS) offers a nuanced measure of hemoglobin concentration that also comprises high frequencies, though most fNIRS literature studies traditional frequency ranges of hemodynamics (< 0.2 Hz). Linear theory of the hemodynamic response function supports this low frequency band, but we hypothesize that nonlinear effects elicited from the complex system sustaining vasomotor tone presents itself in higher frequencies. To characterize these effects, we investigate how plausible modulation of autoregulatory effects impact aforementioned high frequency components of fNIRS through simulations of mechanistic hemodynamic models. Then, we compare representational similarities between fast (0.2 Hz to 0.6 Hz) and slow (< 0.2 Hz) wave fNIRS to demonstrate that representations acquired through nonlinear analysis are distinct between the frequency bands, whereas when using linear time-domain analysis they are not. Furthermore, by comparing topoplots of significant detectors using nonlinear random vector correlation methods (distance correlation), we demonstrate through a 2nd level group analysis that the median concentrations acquired by fNIRS are independent when analyzing the nonlinearity of their dynamics in their fast and slow component, while they are dependent when utilizing linear time-domain analysis. This study not only provides motivation for researchers to also include higher frequency components in their analysis, but also provides motivation to explore nonlinear effects, e.g. topological entropy. The results of this study motivate future research to explore the nonlinear autoregulatory impacts of regional blood flow and hemoglobin concentrations. Author summaryConventionally, hemodynamic response from induced neural metabolic demand is studied as a slow signal, i.e < 0.2 Hz. Though this may be justified in linear analysis of hemodynamics, vascular mechanics nonlinearly transform the neural metabolic demand to hemodynamic response, where a nonlinear spectral profile may show higher frequency responses. Higher frequency ranges may give insight into local vascular dynamics, particularly their reflection of autoregulatory phenomena, hypothesized to be controlled by sympathovagal feedback loops, thus opening a new avenue for studying brain-body interactions. Functional near infrared spectroscopy (fNIRS) offers a method with high temporal resolution (10 Hz) for observing these effects in hemoglobin concentrations. In this study, we utilize stochastic dynamical simulations of plausible autoregulatory phenomena and an open fNIRS dataset to study differences of fast and slow wave neurovascular representations. We demonstrate that, while linear time-domain analysis provides similar representations of fast and slow wave activity, representations derived from nonlinear methods are not. Furthermore, we show how stress tasks, which may elicit autonomic activity, further desynchronizes nonlinear activity between fast and slow wave signals compared to a non-stress inducing task, demonstrating unique high frequency neurovascular phenomena that is mediated by stress processing.

neuroscience↗