SignificanceNear-infrared spectroscopy (NIRS) is a non-invasive optical method that measures changes in hemoglobin concentration and oxygenation. The measured light intensity is susceptible to reduced signal quality due to the presence of melanin.AimWe quantify the influence of melanin concentration on NIRS measurements taken with a frequency-domain near-infrared spectroscopy system using 690 and 830 nm.ApproachUsing a forehead NIRS probe, we measured 35 healthy participants and investigated the correlation between melanin concentration indices, which were determined using a colorimeter, and several key metrics from the NIRS signal. These metrics include signal-to-noise ratio (SNR), two measurements of oxygen saturation (arterial oxygen saturation, SpO2, and tissue oxygen saturation, StO2), and optical properties represented by the absorption coefficient (μa) and the reduced scattering coefficient (μs′).ResultsWe found a significant negative correlation between the melanin index and the SNR estimated in oxy-hemoglobin signals (rs=−0.489, p=0.006) and SpO2 levels (rs=−0.413, p=0.023). However, no significant changes were observed in the optical properties and StO2 (rs=−0.146, p=0.44).ConclusionsWe found that estimated SNR and SpO2 values show a significant decline and dependence on the melanin index, whereas StO2 and optical properties do not show any correlation with the melanin index.
SignificanceUsing functional near-infrared spectroscopy (fNIRS) in bottlenose dolphins (Tursiops truncatus) could help to understand how echolocating animals perceive their environment and how they focus on specific auditory objects, such as fish, in noisy marine settings.AimTo test the feasibility of near-infrared spectroscopy (NIRS) in medium-sized marine mammals, such as dolphins, we modeled the light propagation with computational tools to determine the wavelengths, optode locations, and separation distances that maximize sensitivity to brain tissue.ApproachUsing frequency-domain NIRS, we measured the absorption and reduced scattering coefficient of dolphin sculp. We assigned muscle, bone, and brain optical properties from the literature and modeled light propagation in a spatially accurate and biologically relevant model of a dolphin head, using finite-element modeling. We assessed tissue sensitivities for a range of wavelengths (600 to 1700 nm), source–detector distances (50 to 120 mm), and animal sizes (juvenile model 25% smaller than adult).ResultsWe found that the wavelengths most suitable for imaging the brain fell into two ranges: 700 to 900 nm and 1100 to 1150 nm. The optimal location for brain sensing positioned the center point between source and detector 30 to 50 mm caudal of the blowhole and at an angle 45 deg to 90 deg lateral off the midsagittal plane. Brain tissue sensitivity comparable to human measurements appears achievable only for smaller animals, such as juvenile bottlenose dolphins or smaller species of cetaceans, such as porpoises, or with source–detector separations ≫100 mm in adult dolphins.ConclusionsBrain measurements in juvenile or subadult dolphins, or smaller dolphin species, may be possible using specialized fNIRS devices that support optode separations of >100 mm. We speculate that many measurement repetitions will be required to overcome hemodynamic signals originating predominantly from the muscle layer above the skull. NIRS measurements of muscle tissue are feasible today with source–detector separations of 50 mm, or even less.
Diffuse optical tomography (DOT) is a widely used optical method for functional neuroimaging. When a dense grid of optodes is used, DOT can produce functional brain imaging maps that are comparable with fMRI in terms of spatial resolution. However, when the available number of sources and detectors are limited, it is important to understand where to place them to image a region of interest (ROI) with optimal coverage and sensitivity to the brain. Conventionally, the optode configuration is heuristically determined by the experimenter. Recently, a total sensitivity maximizing algorithm was proposed to answer the question as an optimization problem. However, in larger ROIs and complex geometries, optodes tend to crowd over only a small portion of the ROI and have therefore unsatisfactory coverage of the ROI. ArrayDesigner was proposed as an attempt to address these limitations by adding a coverage term, so that the algorithm can balance between sensitivity and coverage of the ROI. In this work, we demonstrate that such modification still may not suffice in certain geometries, and the inherent nature of sensitivity maximization can limit the uniformity of imaging. We propose a resolution- based optimization algorithm Grid Resolution with Optimized Uniformity Placement (GROUP)" that aims to provide high-resolution, uniform DOT imaging. We show simulated data using a realistic head model that GROUP can provide better uniformity of resolution and has the flexibility to tune the focus to voxels of different depths.
Significance: Electroencephalography (EEG) and functional near-infrared spectroscopy (fNIRS) are both commonly used methodologies for neuronal source reconstruction. While EEG has high temporal resolution (millisecond-scale), its spatial resolution is on the order of centimeters. On the other hand, in comparison to EEG, fNIRS, or diffuse optical tomography (DOT), when used for source reconstruction, can achieve relatively high spatial resolution (millimeter-scale), but its temporal resolution is poor because the hemodynamics that it measures evolve on the order of several seconds. This has important neuroscientific implications: e.g., if two spatially close neuronal sources are activated sequentially with only a small temporal separation, single-modal measurements using either EEG or DOT alone would fail to resolve them correctly.
Aim: We attempt to address this issue by performing joint EEG and DOT neuronal source reconstruction.
Approach: We propose an algorithm that utilizes DOT reconstruction as the spatial prior of EEG reconstruction, and demonstrate the improvements using simulations based on the ICBM152 brain atlas.
Results: We show that neuronal sources can be reconstructed with higher spatiotemporal resolution using our algorithm than using either modality individually. Further, we study how the performance of the proposed algorithm can be affected by the locations of the neuronal sources, and how the performance can be enhanced by improving the placement of EEG electrodes and DOT optodes.
Conclusions: We demonstrate using simulations that two sources separated by 2.3-3.3 cm and 50 ms can be recovered accurately using the proposed algorithm by suitably combining EEG and DOT, but not by either in isolation. We also show that the performance can be enhanced by optimizing the electrode and optode placement according to the locations of the neuronal sources.
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