Open access peer-reviewed chapter

EEG Measurement as a Tool for Rehabilitation Assessment and Treatment

By Hideki Nakano

Submitted: July 23rd 2020Reviewed: November 2nd 2020Published: November 23rd 2020

DOI: 10.5772/intechopen.94875

Downloaded: 416

Abstract

In recent years, neuroscience-based rehabilitation, also known as neurorehabilitation, has been attracting increasing attention worldwide. Electroencephalography (EEG) has been widely used in clinical practice as a tool for the evaluation and treatment of rehabilitation because of its noninvasive and simple measurement of human brain activity. EEG-electromyography coherence is a method to analyze the synchronization between the motor cortex and muscle activity during movement and to quantitatively assess how the motor cortex controls muscle activity. In addition, recent advances in analysis and measurement techniques have made it possible to estimate the source of EEG signals, thus serving as a method to evaluate rehabilitation. The brain-machine interface, which integrates medicine and engineering, has been widely applied in the treatment of rehabilitation and for improving the quality of life. This chapter provides an overview of EEG, and its uses as a tool for rehabilitation assessment and treatment.

Keywords

  • EEG
  • non-invasive brain function measurement
  • rehabilitation
  • EEG–EMG coherence
  • EEG mapping
  • EEG source imaging
  • brain-machine interface

1. Introduction

Ever since the first human electroencephalography (EEG) [1] and electromyography (EMG) [2] recordings were performed in the 1920s, the theoretical aspects, test techniques, and clinical applications of each have rapidly advanced [3]. Methods for imaging brain function have appeared one after another over the past century beginning with evoked potentials [4] in the 1940s, event-related potential [5, 6] and magnetoencephalography (MEG) [7] in the 1960s, positron emission tomography (PET) [8, 9] in the 1970s, and functional magnetic resonance imaging (fMRI) [10, 11] in the 1990s. Currently, the noninvasive methods available for measuring brain function are broadly divided into two categories: electrophysiological examinations and imaging techniques based on hemodynamic principles. The former includes EEG, MEG, and transcranial magnetic stimulation (TMS), while the latter includes fMRI, PET, single photon emission computed tomography (SPECT), and near-infrared spectroscopy (NIRS) [12].

EEG is widely used in rehabilitation as it is well suited to the field’s demands for measurement, which includes simple, safe, and portable equipment. In the past, EEG has primarily been an analysis method used to capture brain activity accompanying a given phenomenon or during a given task as an electric field and subsequently estimates the source of that activity based on the distribution on the scalp. In contrast, recent advancements have led to the development of a method capable of capturing fluctuations in the power of rhythms in a certain frequency band. When this power decreases accompanying a given phenomenon or task, it is called event-related desynchronization (ERD). Conversely, when this power increases accompanying a given phenomenon or task, it is called event-related synchronization (ERS) [13, 14, 15]. Thus, electric field analysis is an analysis of the temporal domain, while the second method is an analysis of the frequency domain. In frequency analysis, ERD is thought to reflect a state of increased cortical activity in the region, while ERS is thought to reflect a state of decreased activity or return to a low level. This chapter will outline the clinical applications for treatment and evaluation of rehabilitation using these features of EEG focusing specifically on EEG–EMG coherence, scalp mapping, and brain-machine interface.

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2. EEG-EMG coherence

Like brain waves, it has long been known that myoelectric activity—the final output of the motor system—is rhythmic. Since a correlation between EEG and EMG rhythms was first reported, the concept of EEG–EMG coherence has become a field of study attracting much attention [16, 17, 18]. As EMG measures the collective firing of a motor unit, if rectified such that the positivity or negativity of individual spikes is irrelevant, EMG signals are thought to correspond to action potentials of spinal motor neurons [19]. At the same time, EEG activity reflects the collective activity of neurons, particularly their postsynaptic potential. Therefore, EEG–EMG coherence is considered capable of measuring the control of spinal motor neurons by the cerebral cortex.

In healthy individuals, EEG–EMG coherence shows a distribution following the somatotopy of the primary sensorimotor cortex contralateral to the muscle for which myoelectric activity was recorded. Research using MEG has found that the source of coherent rhythmic activity can be found in the primary motor cortex [20, 21]. Further, peak coherence has been reported to roughly correspond to hot spots during TMS [17]. Significant coherence is primarily seen in the β frequency band (13–30 Hz) but has also been observed in the lower frequency α band and the γ band near 40 Hz. Thus, coherence in these various frequency bands may be derived from different mechanisms [22].

Research measuring the time lag between EEG and EMG has found that EEG invariably precedes EMG for the β band, yet there is almost no lag for the α band [18]. This suggests that the mechanisms of coherence in the α and β bands differ. One theory to explain this is that a muscle’s peripheral centrifugal sensory input is involved in α band coherence. However, a previous study found that coherence in this band was not affected when peripheral sensory input was modified using vibration stimulation [18]. Thus, it appears that the reason there is no time lag between cortical activity and myoelectric activity is that subcortical rhythmic activity contributes to both brain wave rhythms and myoelectric activity. Further, studies have found that intensifying muscle contraction changes the coherence peak frequency from the β band to the γ band [23, 24]. This γ band coherence is thought to contribute to the control of myoelectric activity (piper rhythm) at approximately 40 Hz, as is seen during strong muscle contraction. Interestingly, the coherence peak does not transition smoothly from the β band to the γ band as myoelectric activity changes from weak contraction to strong contraction; rather, it shifts in a step-like manner. This suggests that the mechanism involved in coherence in the γ band differs from that of the β band. However, there is no difference between the two frequency bands when measuring the time lag between brain activity and myoelectric activity; brain activity precedes myoelectric activity for both. Accordingly, coherence in both of these frequency bands is thought to be involved in centrifugal output from the cerebral cortex to spinal motor neurons. This type of coherence is localized to the primary sensorimotor cortex contralateral to the muscle. However, subdural recordings of patients with intractable epilepsy requiring surgical intervention have shown EEG–EMG coherence in other brain areas, such as the premotor cortex and supplementary motor cortex [25]. Anatomically, its well known that there are direct projections from the premotor cortex and supplementary motor cortex to spinal motor neurons [26, 27], suggesting that these brain areas are involved in the control of myoelectric activity.

Due to its ability to non-invasively measure frequency-specific coupling of the cerebral cortex (specifically the primary motor cortex) and spinal motor neurons, clinical applications of EEG–EMG coherence are ongoing and include illuminating the pathophysiology and evaluation of diseases featuring motor impairment or involuntary movement. A relatively slow resting tremor of 3–6 Hz is one of the core symptoms of Parkinson’s disease. While the rhythm of these tremors is thought to originate in the basal ganglia-thalamo-cortical loop, the mechanism of onset remains unknown. One study exploring the EEG–EMG coherence of these resting tremors found that primary sensorimotor cortex activity corresponds to the tremors [28]. As Parkinson’s disease patients exhibit EEG–EMG coherence at their tremors’ peak frequency or double harmonic frequency, stronger coherence is observed between 5 and 12 Hz, a range that displays low coherence in healthy individuals. At the same time, such patients show reduced coherence in other frequency bands (15–60 Hz) [29]. This abnormal coherence pattern has been found to approach that of healthy individuals (strong coherence for 15–60 Hz) with the use of deep brain stimulation or pharmacotherapy using drugs such as levodopa [30, 31]. Thus, the dopaminergic system may influence the occurrence of this coherence. Studies also report EEG–EMG coherence features resembling those of resting tremors in relation to freezing of gait, a typical gait disorder seen in patients with Parkinson’s disease [32, 33]. Accordingly, EEG–EMG coherence is considered widely applicable as a tool for evaluating the effects of rehabilitation interventions and elucidating the pathology of movement disorders in patients with Parkinson’s disease.

Reduced EEG–EMG coherence has been reported not only in patients with Parkinson’s disease, but also in stroke patients and older adults. One study examining the EEG–EMG coherence of the hemiplegic and non-hemiplegic sides of subcortical infarction patients found that although the EEG and EMG power showed similar patterns for both the hemiplegic and non-hemiplegic sides, the coherence was significantly lower on the hemiplegic side [34]. This reduced EEG–EMG coherence on the hemiplegic side has been shown to improve as the patient’s motor function recovers [35], suggesting that this may be a useful biomarker reflecting motor function recovery in stroke patients. Meanwhile, EEG–EMG coherence in older adults is significantly lower than that in younger individuals and has been shown to have a significant correlation with muscle strength [36]. This suggests that lower EEG–EMG coherence in older adults may be one factor in the decline in strength, motor skills, and coordination that accompanies aging.

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3. EEG mapping and source imaging

Interpreting an EEG visually requires experience, but a two-dimensional representation of brain electrical activity (topography) is a way to display brain waves more objectively as a planar map of electrical activity on the scalp’s surface. Techniques are also being developed to estimate areas of activity within the brain from multichannel EEG data obtained from the scalp, thereby increasing the precision of brain function analysis using EEG.

EEG scalp mapping analyses include spatial analysis (two-dimensional and three-dimensional), coherence, and complexity (Ω). As brain waves consist of multiple frequencies with different physiological significances, it is vital to perform frequency analysis based on a fast Fourier transform (FFT) to consider each frequency independently. It is also integral to select the appropriate analysis and interpretation with consideration to the items to be evaluated and features of each disease using these analysis techniques [37].

A previous study reported the spatial distribution of EEG topography independent of electrode placement by epoch and found that the standard topographies of various intervals were separated by instantaneous transitions [38]. In other words, it was unusual for one shape to slowly change into the next. Different topographies are thought to reflect different regions of neural activity and represent different stages of information processing. In light of this, dividing brain waves according to the temporal similarity of their spatial distribution on the scalp is considered a potentially useful method for studying information processing within the brain as it changes moment to moment. EEG microstate modeling and analysis was developed as a method of microstate segmentation using cluster analysis to determine the optimal topography and number of segments from a sequence of brain electrical activity corresponding to the characteristics of a mental activity [39]. This method is used to efficiently extract data based on the temporal and spatial structure of background EEG activity and explore the pathophysiology of brain function in a number of diseases [40, 41].

Importantly, a three-dimensional approach is necessary when considering actual brain pathology. Estimating the source of brain waves has recently been gaining attention as one approach to three-dimensional EEG analysis. This approach can be broadly divided into equivalent dipole estimation methods [42, 43, 44] and low-resolution brain electromagnetic tomography (LORETA) [45, 46, 47], a standard method of current density distribution estimation. While there are advantages and disadvantages to each, one challenge faced by the former, for which it is essential to stipulate the number of sources of activity in advance, is the difficulty of selecting which combination of dipoles is valid because different combinations of dipoles result in similar scalp distributions (inverse problem). The latter depicts the spread of neural activity within the brain in three-dimensional tomography using EEG data collected from the scalp based on the hypothesis that adjacent groups of neurons have roughly the same activity. Excluding special cases such as epileptic seizures, actual brain activity is not limited to one specific area, making this method useful in understanding complex brain activity such as higher brain function. More specifically, LORETA excels in primary processing, analyzing raw data to display an image, and secondary processing, carrying out statistical analyses to extract maps and find differences in current density distributions, and is therefore a form of EEG mapping used in diverse branches of neuroscience. As discussed above, LORETA estimates a three-dimensional distribution of brain tissue activity from EEG data measured on the scalp based on the hypothesis that adjacent neuron groups carry out similar activity. In other words, assuming a number of cubic lattices within the cerebral parenchyma, this method generates a three-dimensional blurred image of the current source by selecting the smoothest option from among combinations of three-dimensional current density distributions based on the Laplacian operation. Unlike other programs, the initial location value or number of dipoles is not set in advance. The operation is relatively simple, and while the resolution is low, the result is not a primitive spherical model, but instead a tomographic image superimposed onto Talairach atlas, which can be shown in color and three dimensions (Figure 1) [48, 49, 50]. LORETA is being improved, and it has recently become possible to evaluate functional lagged connectivity and the directionality of that connectivity (isolated effective coherence; iCoh) between different areas of the brain.

Figure 1.

Statistical non-parametric maps of LORETA of the alpha band comparing pre-rest and post-rest of hand massage (A) and foot massage (B) [48]. White blobs indicate increased activity at post-rest for each massage.

As demonstrated above, delving deeper into background EEG activity by first exploring the time domain using methods such as microstate segmentation, then investigating the frequency domain using FFT, and the spatial domain both two-dimensionally (topography) and three-dimensionally (equivalent dipole estimation, FFT-dipole-approximation, LORETA) has a wide range of clinical applications, including elucidating pathological mechanisms and evaluating rehabilitation.

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4. Brain-machine interface (BMI)

BMI techniques are methods of connecting the exchange of information between the external world and the brain using artificial electric circuits to restore and supplement its function. In the field of rehabilitation, output-type BMI applications, which read motor intention from brain activity and use this information to operate various devices and computers, are commonly used. Output-type BMI, which interprets motor intention from brain activity to operate external equipment, is classified into invasive and noninvasive types based on the method by which brain activity is measured. The former uses intracranial or epidural electrodes; the latter uses scalp EEG or functional brain imaging techniques. In addition to the conventional methods of restoring function using BMI, such as directly operating a robot arm or environmental control apparatus using brain activity, research geared toward therapeutic BMI applications, which utilize BMI for rehabilitation or reconstruction of functional neural networks, is also underway.

Neurofeedback is a method of learning to voluntarily control one’s own brain activity through the presentation of said activity as real-time sensory information (visual, auditory, etc.) (Figure 2) [51]. Neurofeedback requires technology that measures brain activity and analyzes the measured data in real time. The technologies involved in brain signal processing and interpretation are shared with those of BMI and, in a broad sense, neurofeedback can be considered a therapeutic form of BMI. In fact, EEG-based neurofeedback is widely used as a tool for improving motor, cognitive, and psychological functions not only in individuals with diseases, but also in healthy individuals ranging from childhood to old age. The delta (<4 Hz), theta (4–8 Hz), alpha (8–13 Hz), beta (14–30 Hz), and gamma (>40 Hz) frequency bands are most commonly used in evaluation and training [52]. As the functional characteristics of each frequency band differ, it is essential to select the appropriate frequency band for neurofeedback depending on the pathology of the case or the type of function one wishes to improve (Table 1) [53].

Figure 2.

Motor imagery training using neurofeedback, a therapeutic BMI [51]. EEG activity feedback during motor imagery (μband EEG activity in the sensorimotor area) is given using sensory modalities such as vision or hearing and the participant is trained to control their own EEG activity.

ProtocolPurpose
↓ thetaCognitive training after stroke;
Cognitive training of healthy adults with a risk for neurodegenerative disorder.
↑ thetaAiming to increase capabilities of executive functions on healthy students;
Memory consolidation training.
↑ theta, ↓ alphaRelaxation training;
Training to improve creative performance (playing music, dancing), effects on mood.
↓ alphaAttentional training;
Frontal alpha-asymmetry self-regulation training to influence mood;
Training for increased motor performance.
↑ alpha;Training to reduce anxiety;
Training to improve cognitive performance;
Relaxation training for stress reduction.
↑ high alphaTraining to improve cognitive performance.
↑ SMR (12-15 Hz)Training to decrease epileptic seizures;
Training to improve declarative learning and sleeping pattern;
Training to improve cognition and memory in stroke patients;
Training to enhance golf putting.
↑ SMR, ↓ thetaTraining to optimize microsurgical skills;
Training to minimize ADHD symptoms on a healthy population.
↑ SMR, ↓ theta, ↓ high betaTraining to improve cognitive performance;
Training to improve Asperger’s syndrome and autistic spectrum disorder symptoms.
↑ low betaTraining to improve cognitive performance;
Training to modulate sleep spindle activity and overnight memory consolidation.
↑ beta, ↓ thetaTypical training for improvement of ADHD symptoms.
↑ beta, ↓ theta, ↓ low alphaTraining of attention.
↑ gammaTraining of cognitive control;
Training of memory and intelligence.

Table 1.

An overview of already used protocols of frequency EEG-neurofeedback training with the references to exemplary studies and their main therapeutic purpose [53].

Neurofeedback is also gaining popularity as a technique for neuromodulation, that is, the regulation of local brain activity. Neurofeedback is considered very safe compared to methods such as repetitive transcranial magnetic stimulation (rTMS) or transcranial direct current stimulation (tDCS), as it does not use external stimulation and therefore avoids the risk of side effects such as seizure or burns that occur with rTMS and tDCS. At the same time, output-type BMI has been gaining interest in recent years as a tool for supporting the daily activities of persons who have difficulty with independent living or spontaneous expression due to disease, disability, or aging. Specifically, it will soon become possible to operate a variety of assistive devices, including wheel chairs, exoskeletons, drones, and communication robots using the operator’s EEG signals (Figure 3) [54]. Researchers are also developing and exploring the effectiveness of smart homes that incorporate these BMI technologies [55]. Smart homes are equipped with technology that interprets the user’s motion intention or emotional state using methods such as EEG, which can easily measure brain activity with no special training or burden on the user. Specifically, smart homes assist with daily life by measuring the brain activity that occurs when the user naturally moves their body accompanying a motion intention, for example, to operate the television or air conditioner, recognizing what kind of motion intention is occurring, and manipulating the environment in accordance with the user’s intention. They may also detect when the user is feeling discomfort and modify the environment accordingly using technology that captures an emotional state (discomfort) by measuring and analyzing the user’s brain activity. This information can further be communicated to family members or caregivers to allow them to provide assistance based on the user’s emotional state. In addition to the above, it is also possible to assist a user’s own actions in a standard living environment using BMI actuation technology that moves an exoskeleton-type robot actuator linked to brain activity [54, 55]. It is hoped that such BMI technologies will increase communication in a variety of settings and create an environment where people can continue to live independent fulfilled lives.

Figure 3.

EEG-based BMI for assisting with daily activities and improving quality of life [54].

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5. Conclusion

The development of brain function imaging techniques has led to a new understanding of previously unexplained brain functions as well as the creation of clinical applications, scientific techniques, and assistive devices based on these findings. Elucidation of brain function fully utilizing the advantages of EEG is expected to continue as high definition EEG and accompanying analysis methods become more advanced. EEG is also advantageous in that it is relatively easy to record simultaneously with other methods of brain function measurement. Therefore, it is imperative that we do not simply interpret pathology and brain function using EEG results alone but gain a comprehensive picture of the brain’s physiological function and dysfunction through the simultaneous use of multiple methods of brain function measurement and by capturing various clinical parameters in a multidimensional manner.

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Acknowledgments

This research was funded by the Japanese Physical Therapy Association.

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Conflict of interest

The authors declare no conflict of interest.

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Appendices

EEG

electroencephalography

EMG

electromyography

MEG

magnetoencephalography

PET

positron emission tomography

fMRI

functional magnetic resonance imaging

TMS

transcranial magnetic stimulation

SPECT

single photon emission computed tomography

NIRS

near-infrared spectroscopy

ERD

event-related desynchronization

ERS

event-related synchronization

FFT

fast Fourier transform

LORETA

low-resolution brain electromagnetic tomography

BMI

brain-machine interface

rTMS

repetitive transcranial magnetic stimulation

tDCS

transcranial direct current stimulation

SMR

sensorimotor rhythm

ADHD

attention-deficit hyperactivity disorder

© 2020 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Hideki Nakano (November 23rd 2020). EEG Measurement as a Tool for Rehabilitation Assessment and Treatment, Electroencephalography - From Basic Research to Clinical Applications, Hideki Nakano, IntechOpen, DOI: 10.5772/intechopen.94875. Available from:

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