Functional near-infrared spectroscopy (fNIRS) is a noninvasive neuroimaging technique that uses low levels of red to near-infrared light to measure changes in cerebral blood oxygenation. Spontaneous (resting state) functional connectivity (sFC) has become a critical tool for cognitive neuroscience for understanding task-independent neural networks, revealing pertinent details differentiating healthy from disordered brain function, and discovering fluctuations in the synchronization of interacting individuals during hyperscanning paradigms. Two of the main challenges to sFC-NIRS analysis are (i) the slow temporal structure of both systemic physiology and the response of blood vessels, which introduces false spurious correlations, and (ii) motion-related artifacts that result from movement of the fNIRS sensors on the participants’ head and can introduce non-normal and heavy-tailed noise structures. In this work, we systematically examine the false-discovery rates of several time- and frequency-domain metrics of functional connectivity for characterizing sFC-NIRS. Specifically, we detail the modifications to the statistical models of these methods needed to avoid high levels of false-discovery related to these two sources of noise in fNIRS. We compare these analysis procedures using both simulated and experimental resting-state fNIRS data. Our proposed robust correlation method has better performance in terms of being more reliable to the noise outliers due to the motion artifacts.
Functional near-infrared spectroscopy (fNIRS) is a noninvasive neuroimaging technique used to measure changes in oxygenated hemoglobin (oxy-Hb) and deoxygenated hemoglobin (deoxy-Hb) in the brain. In this study, we present a decomposition approach based on single-channel independent component analysis (scICA) to investigate the contribution of physiological noise to fNIRS signals during rest. Single-channel ICA is an underdetermined decomposition method, which separates a single time series into components containing nonredundant spectral information. Using scICA, fNIRS signals from a total of 17 subjects were decomposed into the constituent physiological components. The percentage contribution of the classes of physiology to the fNIRS signals including low-frequency (LF) fluctuations, respiration, and cardiac oscillations was estimated using spectral domain classification methods. Our results show that LF oscillations accounted for 40% to 55% of total power of both the oxy-Hb and deoxy-Hb signals. Respiration and its harmonics accounted for 10% to 30% of the power, and cardiac pulsations and cardio-respiratory components accounted for 10% to 30%. We describe this scICA method for decomposing fNIRS signals, which unlike other approaches to spatial covariance reduction is applicable to both single- or multiple-channel fNIRS signals and discuss how this approach allows functionally distinct sources of noise with disjoint spectral support to be separated from obscuring systemic physiology.
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