Abstract

.Functional near-infrared spectroscopy (fNIRS) signals are prone to problems caused by motion artifacts and physiological noises. These noises unfortunately reduce the fNIRS sensitivity in detecting the evoked brain activation while increasing the risk of statistical error. In fNIRS measurements, the repetitive resting-stimulus cycle (so-called block-design analysis) is commonly adapted to increase the sample number. However, these blocks are often affected by noises. Therefore, we developed an adaptive algorithm to identify, reject, and select the noise-free and/or least noisy blocks in accordance with the preset acceptance rate. The main features of this algorithm are personalized evaluation for individual data and controlled rejection to maintain the sample number. Three typical noise criteria (sudden amplitude change, shifted baseline, and minimum intertrial correlation) were adopted. Depending on the quality of the dataset used, the algorithm may require some or all noise criteria with distinct parameters. Aiming for real applications in a pediatric study, we applied this algorithm to fNIRS datasets obtained from attention deficit/hyperactivity disorder (ADHD) children as had been studied previously. These datasets were divided for training and validation purposes. A validation process was done to examine the feasibility of the algorithm regardless of the types of datasets, including those obtained under sample population (ADHD or typical developing children), intervention (nonmedication and drug/placebo administration), and measurement (task paradigm) conditions. The algorithm was optimized so as to enhance reproducibility of previous inferences. The optimum algorithm design involved all criteria ordered sequentially (0.047 mM mm of amplitude change, of baseline slope, and range of outlier threshold for each criterion, respectively) and presented complete reproducibility in both training and validation datasets. Compared to the visual-based rejection as done in the previous studies, the algorithm achieved 71.8% rejection accuracy. This suggests that the algorithm has robustness and potential to substitute for visual artifact-detection.

Highlights

  • We introduced the concepts of acceptance rate and quantitative data ranking depending on noise level to determine rejections and maintain the statistical sample number

  • Even for the same noise criteria, we found that complete reproducibility was obtained from different acceptance rates: the GNG dataset required an acceptance rate (i.e., ≥three epochs) lower than that of the OB dataset (i.e., ≥four epochs)

  • We have proposed an approach to manage motion artifacts in Functional near-infrared spectroscopy (fNIRS) data sets using an adaptive algorithm for guaranteeing an acceptance rate (e.g., ≥three epochs)

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Summary

Introduction

Functional near-infrared spectroscopy (fNIRS) noninvasively measures the product of concentration changes of cerebral hemoglobin (oxygenated∕O2Hb and deoxygenated/HHb) and optical length using two or more near-infrared spectra (650 to 950 nm).[1,2,3,4] It measures blood-related signals that indirectly correspond to brain activation (i.e., neurovascular coupling theorem).[5,6] After >20 years of development,[7] fNIRS has gained much attention in broad applications including studies of neuropsychiatry and cognition in infants and children.[8,9,10] Compared to other functional imaging techniques, it shows significant advantages in terms of system flexibility (without confinement or head restrainers) and motion tolerability since probes areThe issue of detecting and removing motion artifacts has been extensively studied; there is no golden approach to detect and remove them. Functional near-infrared spectroscopy (fNIRS) noninvasively measures the product of concentration changes of cerebral hemoglobin (oxygenated∕O2Hb and deoxygenated/HHb) and optical length using two or more near-infrared spectra (650 to 950 nm).[1,2,3,4] It measures blood-related signals that indirectly correspond to brain activation (i.e., neurovascular coupling theorem).[5,6] After >20 years of development,[7] fNIRS has gained much attention in broad applications including studies of neuropsychiatry and cognition in infants and children.[8,9,10] Compared to other functional imaging techniques, it shows significant advantages in terms of system flexibility (without confinement or head restrainers) and motion tolerability since probes are. Direct and complete data rejection might be infeasible due to limited and insufficient sample number,[14] motion correction techniques with supplementary measurements or corrective algorithms pose technical limitations in measurement and insufficient practicability in analysis.[15,16,17,18] Implementing an additional system or devices to detect motions (e.g., an accelerometer) on infants or children can complicate the measurement system and induce inconvenience for subjects, which can result in higher probability that

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