RESUMO
Significance: Signal contamination is a major hurdle in functional near-infrared spectroscopy (fNIRS) of the human head as the NIR signal is contaminated with the changes corresponding to superficial tissue, therefore occluding the functional information originating from the cerebral region. For continuous wave, this is generally handled through linear regression of the shortest source-detector (SD) distance intensity measurement from all of the signals. Although phase measurements utilizing frequency domain (FD) provide deeper tissue sampling, the use of the shortest SD distance phase measurement for regression of superficial signal contamination can lead to misleading results, therefore suppressing cortical signals. Aim: An approach for FD fNIRS that utilizes a short-separation intensity signal directly to regress both intensity and phase measurements, providing a better regression of superficial signal contamination from both data-types, is proposed. Approach: Simulated data from realistic models of the human head are used, and signal regression using both intensity and phase-based components of the FD fNIRS is evaluated. Results: Intensity-based phase regression achieves a suppression of superficial signal contamination by 68% whereas phase-based phase regression is only by 13%. Phase-based phase regression is also shown to generate false-positive signals from the cortex, which are not desirable. Conclusions: Intensity-based phase regression provides a better methodology for minimizing superficial signal contamination in FD fNIRS.
RESUMO
Functional Near-Infrared Spectroscopy (fNIRS) aims to recover changes in tissue optical parameters relating to tissue hemodynamics, to infer functional information in biological tissue. A widely-used application of fNIRS relies on continuous wave (CW) methodology that utilizes multiple distance measurements on human head for study of brain health. The typical method used is spatially resolved spectroscopy (SRS), which is shown to recover tissue oxygenation index (TOI) based on gradient of light intensity measured between two detectors. However, this methodology does not account for tissue scattering which is often assumed. A new parameter recovery algorithm is developed, which directly recovers both the scattering parameter and scaled chromophore concentrations and hence TOI from the measured gradient of light-attenuation at multiple wavelengths. It is shown through simulations that in comparison to conventional SRS which estimates cerebral TOI values with an error of ±12.3%, the proposed method provides more accurate estimate of TOI exhibiting an error of ±5.7% without any prior assumptions of tissue scatter, and can be easily implemented within CW fNIRS systems. Using an arm-cuff experiment, the obtained TOI using the proposed method is shown to provide a higher and more realistic value as compared to utilizing any prior assumptions of tissue scatter.