Evidence map›Paper›PMID 35324896›Full record

ArticlePLoS computational biology2022

Oscillator decomposition of infant fNIRS data.

Takeru Matsuda, Fumitaka Homae, Hama Watanabe, Gentaro Taga, Fumiyasu Komaki

Abstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Takeru MatsudaRIKEN Center for Brain Science, RIKEN, Wako, Japan.ORCID 0000-0002-1572-5085
Fumitaka HomaeDepartment of Language Sciences, Tokyo Metropolitan University, Tokyo, Japan.
Hama WatanabeGraduate School of Education, The University of Tokyo, Tokyo, Japan.
Gentaro TagaGraduate School of Education, The University of Tokyo, Tokyo, Japan.
Fumiyasu KomakiRIKEN Center for Brain Science, RIKEN, Wako, Japan.ORCID 0000-0001-8371-5092

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The functional near-infrared spectroscopy (fNIRS) can detect hemodynamic responses in the brain and the data consist of bivariate time series of oxygenated hemoglobin (oxy-Hb) and deoxygenated hemoglobin (deoxy-Hb) on each channel. In this study, we investigate oscillatory changes in infant fNIRS signals by using the oscillator decompisition method (OSC-DECOMP), which is a statistical method for extracting oscillators from time series data based on Gaussian linear state space models. OSC-DECOMP provides a natural decomposition of fNIRS data into oscillation components in a data-driven manner and does not require the arbitrary selection of band-pass filters. We analyzed 18-ch fNIRS data (3 minutes) acquired from 21 sleeping 3-month-old infants. Five to seven oscillators were extracted on most channels, and their frequency distribution had three peaks in the vicinity of 0.01-0.1 Hz, 1.6-2.4 Hz and 3.6-4.4 Hz. The first peak was considered to reflect hemodynamic changes in response to the brain activity, and the phase difference between oxy-Hb and deoxy-Hb for the associated oscillators was at approximately 230 degrees. The second peak was attributed to cardiac pulse waves and mirroring noise. Although these oscillators have close frequencies, OSC-DECOMP can separate them through estimating their different projection patterns on oxy-Hb and deoxy-Hb. The third peak was regarded as the harmonic of the second peak. By comparing the Akaike Information Criterion (AIC) of two state space models, we determined that the time series of oxy-Hb and deoxy-Hb on each channel originate from common oscillatory activity. We also utilized the result of OSC-DECOMP to investigate the frequency-specific functional connectivity. Whereas the brain oscillator exhibited functional connectivity, the pulse waves and mirroring noise oscillators showed spatially homogeneous and independent changes. OSC-DECOMP is a promising tool for data-driven extraction of oscillation components from biological time series data.

Indexed as

HemoglobinsSpectroscopy, Near-InfraredBrainBrain MappingHumansInfantOxyhemoglobinsHemoglobinsOxyhemoglobins

Identifiers

PMID35324896
PMCPMC8982875

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.