Why the study?
Intensity-dependent amplitude changes have been linked to psychiatric disorders, but the application of functional near-infrared spectroscopy in these paradigms and its relationship to event-related potentials required exploration.
Does auditory intensity affect ERP components and fNIRS hemodynamic activity in human subjects?
Does auditory intensity affect ERP components and fNIRS hemodynamic activity in human subjects?
The study demonstrates a brain response to auditory intensity changes detectable by both EEG and fNIRS, supporting the neurovascular coupling process.
May guide multimodal auditory neuroimaging protocols; leaves open clinical translation and validation.
Intensity Dependent Amplitude Changes (IDAP) have been extensively studied using Event-Related Potentials (ERPs) and have been linked to several psychiatric disorders. This study aimed to explore the application of functional near-infrared spectroscopy (fNIRS) in IDAP paradigms and to relate it to ERPs. Thirty-three and thirty-one subjects participated in two experiments, respectively. The first experiment consisted of the presentation of three-tone intensities (77.9dB, 84.5dB, and 89.5dB) lasting 500 ms, each type randomly presented 54 times, while the second experiment consisted of the presentation of five-tone intensities (70.9dB, 77.9dB, 84.5dB, 89.5dB, and 95.5dB) in blocks composed of eight tones of the same intensity lasting 70 ms each one, in total 20 blocks were presented. EEG was used to measure ERP components: N1, P2, and N1-P2 peak-to-peak amplitude. fNIRS allowed the analysis of the hemodynamic activity in the auditory and prefrontal cortices. The results showed an increase in N1, P2, and N1-P2 peak-to-peak amplitude with auditory intensity. Similarly, oxyhemoglobin and deoxyhemoglobin concentrations showed amplitude increases and decreases, respectively, with auditory intensity in the auditory and prefrontal cortices. Spearman correlation analysis showed a relationship between the left auditory cortex and N1 and the right dorsolateral cortex and P2 amplitude. These results suggest that there is a brain response to auditory intensity changes that can be obtained by EEG and fNIRS, supporting the neurovascular coupling process. Overall, this study contributes to the understanding and application of fNIRS in auditory paradigms and highlights its potential to be used in a complementary manner to ERPs.
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Muñoz et al. (2023) studied this question.
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