| Literature DB >> 28840162 |
Antonio M Chiarelli1, Filippo Zappasodi2,3, Francesco Di Pompeo2,3, Arcangelo Merla2,3.
Abstract
Multimodal monitoring has become particularly common in the study of human brain function. In this context, combined, synchronous measurements of functional near-infrared spectroscopy (fNIRS) and electroencephalography (EEG) are getting increased interest. Because of the absence of electro-optical interference, it is quite simple to integrate these two noninvasive recording procedures of brain activity. fNIRS and EEG are both scalp-located procedures. fNIRS estimates brain hemodynamic fluctuations relying on spectroscopic measurements, whereas EEG captures the macroscopic temporal dynamics of brain electrical activity through passive voltages evaluations. The "orthogonal" neurophysiological information provided by the two technologies and the increasing interest in the neurovascular coupling phenomenon further encourage their integration. This review provides, together with an introduction regarding the principles and future directions of the two technologies, an evaluation of major clinical and nonclinical applications of this flexible, low-cost combination of neuroimaging modalities. fNIRS-EEG systems exploit the ability of the two technologies to be conducted in an environment or experimental setting and/or on subjects that are generally not suited for other neuroimaging modalities, such as functional magnetic resonance imaging, positron emission tomography, and magnetoencephalography. fNIRS-EEG brain monitoring settles itself as a useful multimodal tool for brain electrical and hemodynamic activity investigation.Entities:
Keywords: electroencephalography; flexible brain imaging; functional near-infrared spectroscopy; multimodal monitoring; neurovascular coupling; noninvasive brain imaging
Year: 2017 PMID: 28840162 PMCID: PMC5566595 DOI: 10.1117/1.NPh.4.4.041411
Source DB: PubMed Journal: Neurophotonics ISSN: 2329-423X Impact factor: 3.593
Fig. 1(a) Example of a typical “BOLD” response recorded by fNIRS in a task-activated brain region. Average changes in HHb and concentrations are reported together with their variability (standard error) for each time point. The BOLD response in active brain areas is characterized by an overcompensatory supply of with a concurrent wash-out of HHb, typically with a ratio () of and consisting of few changes. (b) Coronal head slice of a typical continuous wave light-sensitivity pattern (logarithmic scale) for a source–detector couple positioned on the scalp (fNIRS channel), overlaid on a structural MRI. The light-sensitivity pattern was computed using a finite element method approach. (c) Example of a possible optical array and channels’ average light sensitivity pattern (logarithmic scale, averaged across multiple channels), employed to the imaging of motor and sensorimotor cortices, overlaid on a subject structural MRI and extracted gray matter. Multiple sources and detectors are required to increase the “field of view” of the fNIRS technology.
Fig. 2(a) Schematic representation of the EEG signal generation. The synchronous activity of a large number of neurons generates electric fields that, if synchronous, can add up to produce a signal intense enough to be detectable by electrodes placed on the scalp. The primary currents are mainly the result of the synaptic potentials in correspondence of the dendritic trees, which follow a preferential direction, as in the case of the pyramidal neurons. The neurons are surrounded by the cerebral tissues, i.e., a conductive medium. The primary current provokes extracellular currents flowing thorough this medium, as well as through the cerebrospinal fluid, the skull, and the scalp. These currents, named secondary or volume currents, reach the scalp and generate voltage differences, detectable by a pair of EEG electrodes. (b) Example of time-frequency representation of EEG signal at C3 (located over the left motor cortex) during a visually guided finger tapping task, executed with the right hand. For each frequency, the power is expressed as percentage variation of the corresponding value in the premovement period, evidencing a reduction in the alpha and beta rhythms during the movement (ERD) and an increase of theta rhythm within the first 500 ms from the movement onset (ERS). (c) Example of VEP obtained by a pattern-reversal stimulation. The EEG activity was recorded by a 128-channel system (EGI). Top: average response locked to the stimulus for the electrode Oz (referred to Cz), placed on the occipital lobe in correspondence to the visual cortex. The VEP consists of a sequence of negative-positive-negative peaks at specific latencies. The parameters that are considered to describe these waves are the latency and the amplitude of such peaks, which are referred to as N (negative) or P (positive) depending on the polarity with respect to a specific montage. In the case of the VEP, N75-, P100-, and N135-components can be seen. Bottom: on the left the topographical map shows the interpolation above the scalp surface of the values of all EEG sensors at the p100 latency. On the right, the P100 cerebral source is obtained by voltage scalp distribution and superimposed to the realistic volume conductor cortex model reconstructed from the individual anatomical magnetic resonance images. Localization was performed by means of the Curry 6.0 (Neuroscan) analysis software. For an overview on the localization procedures see Darvas et al.
Fig. 3(a) Numbers of scientific papers published from 1990 to 2016 grouped at a 5-year pace. The papers are reported divided by macroapplication (nonclinical and clinical) and as a total. The dashed lines represent the expected publication at the end of 2019, since the last group of papers was produced in only 2 years (2015 to 2016). (b) Pie chart separating the papers by macroarea. (c) Pie chart separating nonclinical papers by area of interest. (d) Pie chart separating clinical papers by area of interest.