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Non-invasive Optical Low-frequency Oscillation Study of the Prefrontal Cortex Based on fNIRS

6 août 2026 mis à jour par: Ting Li, Peking Union Medical College
The investigators aimed to investigate the effects of different cognitive load tasks (1-back, 2-back, 3-back) on low-frequency oscillations (LFOs) in the prefrontal cortex of healthy young individuals, analyze the relationship between LFO parameters (power, peak amplitude, peak frequency) and behavioral performance (reaction time, accuracy), and validate the feasibility of using LFOs as a quantitative measure of brain resting-state activity and a sensitive indicator of cognitive load.Low-frequency oscillations (LFO, 0.05-0.15 Hz) are a core feature of cerebral hemodynamics and are closely related to neural activity, blood pressure regulation, and metabolic function. Existing studies suggest that LFO may be influenced by cognitive load during mental tasks, but the underlying mechanisms remain unclear. Functional near-infrared spectroscopy (fNIRS), with its advantages of non-invasiveness, portability, and high temporal resolution, enables precise monitoring of hemodynamic parameters in the prefrontal cortex, including changes in oxygenated and deoxygenated hemoglobin concentrations (Δ[oxy-Hb], Δ[deoxy-Hb]). This study combines the N-back working memory task to investigate how cognitive load modulates LFO, offering a novel approach for assessing brain function.In this study, the investigators used a portable 16-channel continuous-wave functional near-infrared spectroscopy (fNIRS) system to measure dynamic changes in prefrontal cortex (PFC) hemodynamic parameters-Δ[oxy-Hb], Δ[deoxy-Hb], and Δ[tot-Hb]-in 48 healthy participants under varying task loads. The investigators then analyzed low-frequency oscillations (LFOs) based on the detected hemodynamic parameter fluctuations, following established methodologies from prior research. Using Welch's method, LFOs were extracted from power spectral density (PSD) of different hemodynamic parameters across three task conditions (1-back, 2-back, and 3-back). The principle of fNIRS relies on near-infrared light penetrating the skull and brain, being absorbed by chromophores [HbO₂] and [Hb] with distinct absorption spectra. Assuming constant scattering and applying the modified Beer-Lambert law during calculations, sensitive light intensity detectors can detect concentration changes of these chromophores within the subject's brain tissue. The experimental setup consisted of a 4.4 cm × 15 cm sensor array distributed across the forehead, a dedicated data acquisition control box with a sampling rate of 3.3 Hz, and a computer for data storage and analysis software. The current flexible sensor comprises four light sources and ten detectors. The light sources include three built-in LEDs with peak wavelengths at 735 nm, 805 nm, and 850 nm, while the detectors are designed to image the sub-frontal cortical regions (dorsolateral and ventromedial prefrontal cortices). The distance between each source and its surrounding detectors is 2.89 cm, enabling hemodynamic measurements at depths of 2-3 cm beneath the scalp, focusing primarily on the cerebral cortex. Each light source is arranged in an X-shape with four adjacent detectors, where the source is centered and detectors positioned at the corners, forming channels connecting each source to individual detectors. The prefrontal cortex is a region strongly associated with cognitive processing and plays a critical role in working memory tasks. Task load was implemented through working memory tasks-a mechanism by which the brain temporarily processes and stores information crucial for handling complex cognitive demands. Understanding how the amplitude of hemodynamic oscillations is modulated by different cognitive loads is significant, as microvascular blood flow is regulated by myogenic mechanisms. These foundational insights will help improve the analysis and interpretation of hemodynamic neuroimaging data. This study employs fNIRS, a non-invasive neuroimaging technique highly sensitive to microvascular activity, to investigate the interactive effects of cognitive load on brain hemodynamic LFOs.

Aperçu de l'étude

Type d'étude

Observationnel

Inscription (Réel)

47

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Tianjin Municipality
      • Tianjin, Tianjin Municipality, Chine, 300192
        • 16 channel fNIRS

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

47 right-handed volunteers (23 males and 24 females) were recruited. Their ages ranged from 18 to 23 years, with an average age of 22.1 years for males and 21.5 years for females. The participants were young adults, as the study aimed to investigate the effects of LFO on cognitive activation, which involved a relatively challenging 3-back working memory task. All participants had normal or corrected-to-normal vision. Female participants were excluded if they were within their menstrual cycle, as hormonal fluctuations during this period may affect certain prefrontal cortical functions. None of the participants had a history of neurological or psychiatric disorders, nor were they taking any psychotropic medications. Participants abstained from alcohol, caffeine, and nicotine for at least 24 hours prior to the experiment.

La description

Inclusion Criteria:

  • Aged 18 to 23 years
  • Right-hand
  • Normal or corrected-to-normal vision
  • Willing to abstain from alcohol, caffeine, and nicotine for at least 24 hours prior to the experiment
  • Able to understand the study procedures and provide written informed consent

Exclusion Criteria:

  • History of neurological or psychiatric disorders (e.g., epilepsy, severe insomnia, or anxiety)
  • History of arrhythmia or other severe cardiovascular conditions
  • Current or long-term use of psychotropic medications or other medications affecting the nervous system
  • Contraindications for wearing skin-mounted optical devices
  • Female participants currently in their menstrual cycle (due to potential hormonal effects on prefrontal cortical functions)
  • Inability to follow experimental instructions or complete the testing tasks

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
Intervention / Traitement
No category
The investigators employed the N-back visual working memory task, a continuous letter task with varying working memory load demands. The task consisted of four fixation blocks and three task blocks, lasting a total of 377 seconds. Each fixation block lasted 20 seconds, during which participants were instructed to fixate their gaze on a central point. The working memory load gradually increased from 1-back to 3-back across the task blocks. Participants were required to determine whether the current letter matched the previous letter (1-back), the letter two positions back (2-back), or the letter three positions back (3-back) in terms of features, responding with one button for "yes" and another for "no."

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Peak Amplitude of Low-Frequency Oscillations (LFO) Measured by functional Near-Infrared Spectroscopy (fNIRS)
Délai: Day1, The assessment time point was after the n-back task, with spectral analysis performed on low-frequency oscillation data collected during the 377-second n-back experiment.
  1. The peak amplitude of LFO (0.05-0.15 Hz) will be extracted from the power spectral density (PSD) of the relative changes in oxygenated and deoxygenated hemoglobin concentrations in the prefrontal cortex. This is measured using a 16-channel portable continuous-wave fNIRS system during different cognitive load tasks (1-back, 2-back, and 3-back).
  2. Measurement Tool: 16-channel continuous-wave fNIRS system.
  3. Unit of Measure: Perived from relative hemoglobin concentration changes and after log-transformed-power spectral density (PSD) in certain frequency :lg(μM^2/Hz).
Day1, The assessment time point was after the n-back task, with spectral analysis performed on low-frequency oscillation data collected during the 377-second n-back experiment.
Peak frequency of Low-Frequency Oscillations (LFO) Measured by fNIRS
Délai: Day1, The assessment time point was after the n-back task, with spectral analysis performed on low-frequency oscillation data collected during the 377-second n-back experiment.
  1. The frequency at which the maximum power occurs within the low-frequency band (0.05-0.15 Hz) derived from the PSD of prefrontal cortex hemoglobin concentration changes. This assesses the shift in vascular oscillation frequency under varying cognitive loads (1-back, 2-back, 3-back).
  2. Measurement Tool: 16-channel continuous-wave fNIRS system.
  3. Unit of Measure: Hertz (Hz).
Day1, The assessment time point was after the n-back task, with spectral analysis performed on low-frequency oscillation data collected during the 377-second n-back experiment.
Power of Low-Frequency Oscillations (LFO) Measured by fNIRS
Délai: Day1, The assessment time point was after the n-back task, with spectral analysis performed on low-frequency oscillation data collected during the 377-second n-back experiment.
  1. The total signal power within the low-frequency band (0.05-0.15 Hz) calculated from the PSD of hemoglobin concentration changes during the working memory tasks. The power spectral data undergoes a logarithmic transformation prior to statistical analysis to ensure normal distribution.
  2. Measurement Tool: 16-channel continuous-wave fNIRS system.
  3. Unit of Measure: derived from relative hemoglobin concentration changes after log-transformed: lg(μM^2)
Day1, The assessment time point was after the n-back task, with spectral analysis performed on low-frequency oscillation data collected during the 377-second n-back experiment.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Reaction Time Assessed by N-back Behavioral Task System
Délai: Day1, The assessment time point was after the n-back task, analyzing behavioral reaction times during the 377-second n-back experiment.
  1. The average time participants take to make a judgment (via button press) on whether the currently displayed letter matches the target letter during the 1-back, 2-back, and 3-back working memory task blocks.
  2. Measurement Tool: Computerized N-back visual working memory task software.
Day1, The assessment time point was after the n-back task, analyzing behavioral reaction times during the 377-second n-back experiment.
Accuracy Rate Assessed by N-back Behavioral Task System
Délai: Day 1, the assessment time point was after the n-back task, analyzing behavioral accuracy rate during the 377-second n-back experiment.
  1. The percentage of correct button press responses made by the participant across the 30 randomly presented letters within each N-back task block (1-back, 2-back, 3-back).
  2. Measurement Tool: Computerized N-back visual working memory task software.
  3. Unit of Measure: Percentage (%).
Day 1, the assessment time point was after the n-back task, analyzing behavioral accuracy rate during the 377-second n-back experiment.
Correlation Between LFO Parameters and Task Behavioral Performance
Délai: Day 1, the assessment time point was after the n-back task, analyzing behavioral correlation between low frequency oscillation parameters and task behavioral performance during the 377-second n-back experiment.
  1. The statistical correlation evaluating the relationship between the fNIRS-derived LFO parameters (peak amplitude, peak frequency, log-transformed power) and the behavioral performance metrics (reaction time and accuracy) across different cognitive loads. This directly evaluates the feasibility of using LFO as a quantitative indicator of cognitive load.
  2. Measurement Tool: Statistical correlation analysis (e.g., Pearson or Spearman correlation coefficient).
  3. Unit of Measure: Correlation coefficient (r-value)
Day 1, the assessment time point was after the n-back task, analyzing behavioral correlation between low frequency oscillation parameters and task behavioral performance during the 377-second n-back experiment.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

  • [1] Biswal B, Zerrin Yetkin F, Haughton V M, et al. Functional connectivity in the motor cortex of resting human brain using echo-planar MRI[J]. Magnetic resonance in medicine, 1995, 34(4): 537-541. [2] Tong Y, Hocke L M, Licata S C, et al. Low-frequency oscillations measured in the periphery with near-infrared spectroscopy are strongly correlated with blood oxygen level-dependent functional magnetic resonance imaging signals[J]. Journal of biomedical optics, 2012, 17(10): 106004-106004. [3] Auer D P. Spontaneous low-frequency blood oxygenation level-dependent fluctuations and functional connectivity analysis of the 'resting'brain[J]. Magnetic resonance imaging, 2008, 26(7): 1055-1064. [4] Morita Y, Hardebo J E, Bouskela E. Influence of cerebrovascular sympathetic, parasympathetic, and sensory nerves on autoregulation and spontaneous vasomotion[J]. Acta physiologica scandinavica, 1995, 154(2): 121-130 [5] Vern B A, Schuette W H, Leheta B, et al. Low-frequency oscillations of cortical oxidative metabolism in waking and sleep[J]. Journal of Cerebral Blood Flow & Metabolism, 1988, 8(2): 215-226. [6] Lin PY, Roche-Labarbe N, Dehaes M, Carp S, Fenoglio A, Barbieri B, Hagan K, Grant PE, Franceschini MA. Non-invasive optical measurement of cerebral metabolism and hemodynamics in infants. J Vis Exp. 2013 Mar 14;(73):e4379. [7] Diehl R R, Linden D, Lücke D, et al. Spontaneous blood pressure oscillations and cerebral autoregulation[J]. Clinical Autonomic Research, 1998, 8(1): 7-12. [8] Katura T, Tanaka N, Obata A, et al. Quantitative evaluation of interrelations between spontaneous low-frequency oscillations in cerebral hemodynamics and systemic cardiovascular dynamics[J]. Neuroimage, 2006, 31(4): 1592-1600. [9] Cui X, Bray S, Bryant DM, Glover GH, Reiss AL. A quantitative comparison of NIRS and fMRI across multiple cognitive tasks. Neuroimage. 2011 Feb 14;54(4):2808-21. [10] Biswal B B, Kylen J V, Hyde J S. Simultaneous assessment of flow and BOLD signals in resting-state fu

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 juin 2025

Achèvement primaire (Réel)

1 juillet 2025

Achèvement de l'étude (Réel)

1 octobre 2025

Dates d'inscription aux études

Première soumission

24 juin 2026

Première soumission répondant aux critères de contrôle qualité

6 août 2026

Première publication (Réel)

12 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

12 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

6 août 2026

Dernière vérification

1 août 2026

Plus d'information

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