Next Article in Journal
Effects of Repetitive Transcranial Magnetic Stimulation at the Cerebellum on Working Memory
Previous Article in Journal
A Fast and Effective Spike Sorting Method Based on Multi-Frequency Composite Waveform Shapes
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

A Study of Brain Function Characteristics of Service Members at High Risk for Accidents in the Military

Department of Protection and Safety Engineering, Seoul National University of Science and Technology, Seoul 01811, Republic of Korea
*
Author to whom correspondence should be addressed.
Brain Sci. 2023, 13(8), 1157; https://doi.org/10.3390/brainsci13081157
Submission received: 3 June 2023 / Revised: 23 July 2023 / Accepted: 29 July 2023 / Published: 2 August 2023
(This article belongs to the Section Neuropsychology)

Abstract

:
Military accidents are often associated with stress and depressive psychological conditions among soldiers, and they often fail to adapt to military life. Therefore, this study analyzes whether there are differences in EEG and pulse wave indices between general soldiers and three groups of soldiers who have not adapted to military life and are at risk of accidents. Data collection was carried out using a questionnaire and a device that can measure EEG and pulse waves, and data analysis was performed using SPSS. The results showed that the concentration level and brain activity indices were higher in the general soldiers and the soldiers in the first stage of accident risk. The body stress index was higher for each stage of accident risk, and the physical vitality index was higher for general soldiers. Therefore, it can be seen that soldiers who have not adapted to military life and are at risk of accidents have somewhat lower concentration and brain activity than general soldiers, and have symptoms of stress and lethargy. The results of this study will contribute to reducing human accidents through EEG and pulse wave measurements not only in the military but also in occupations with a high risk of accidents such as construction.

1. Introduction

1.1. Background and Purpose of the Study

Casualties in the military are not only demoralizing but also undermine public confidence in the military. However, the South Korean military is currently a conscription system, meaning that all young men with certain qualifications are enlisted regardless of their will. Therefore, the military has implemented various efforts to prevent casualties, such as operating counselors, developing suicide prevention education programs, and establishing safety systems for each discharge, but they have not led to a decrease in casualties [1,2,3].
According to a 2022 military release [4], there are more than 80 casualties per year, increasing public anxiety and reducing the military’s combat capabilities, and there is an urgent need to prevent military casualties.
The military has analyzed casualty incidents and assessed that although there are various causes, severe stress, anxiety, lethargy, and depression among soldiers contribute to human errors and suicides [5,6,7,8,9,10,11]. Among individual characteristics, research on stress has shown that stress is an important catalyst for psychiatric disorders such as depression and anxiety [12,13,14,15,16]. Stress-induced negative emotions lead to unclear decision-making, poor attention, and accidents [17], and there has been a 60–80% correlation between stress and accident rates [18,19,20,21,22].
While there have been many studies using EEG and pulse waves to measure stress and depression in the general population [23,24,25,26], there is a lack of research on the relationship between EEG and pulse waves and the psychological state of military personnel [27,28,29,30,31].
Therefore, the purpose of this study is to analyze and present the differences in brain function and autonomic nervous system between general soldiers who are well-adjusted to military life and soldiers who are not well-adjusted to military life and are at risk of accidents. Therefore, EEG and pulse waves were measured and analyzed to determine the differences in terms of four EEG indices and five pulse wave indices.

1.2. Brain Function and Autonomic Nervous System Characteristics

Brain waves are electrical signals composed of multiple oscillatory components that result from the complex interaction of excitatory and inhibitory neurons and can be categorized by frequency band [32,33]. Brain waves are categorized into five types in order of decreasing frequency: delta (δ) waves from 1 to 4 Hz, theta (θ) waves from 4 to 8 Hz, alpha (α) waves from 8 to 13 Hz, beta (β) waves from 13 to 30 Hz, and gamma (γ) waves from 30 to 50 Hz [34,35,36].
In a resting EEG with eyes closed, natural oscillations reflecting an idle cortical state become dominant, with the dominant peak frequency typically located in the 4–13 Hz band. Previous reports have observed that the dominant oscillation frequency, which typically appears in the alpha band during normal aging, is lower in patients with cognitive impairment [37,38,39,40].
Pulse waves are the waves formed by the pulse as it travels to the peripheral nerves, and are the wavelengths at which blood propagates in waves from the heart [41,42]. Pulse wave measurements can be used to test the function of the autonomic nerves that directly control the heartbeat. The autonomic nervous system is composed of sympathetic and parasympathetic nerves, which act antagonistically to each other [43,44,45]. In stressful situations, the sympathetic nerves, which are responsible for attack/defense mechanisms, are relatively more active than the parasympathetic nerves, which are responsible for restoration/relaxation mechanisms [46]. In 1981, power spectral analysis was introduced as a way to quantitatively assess parasympathetic and sympathetic control of the heart and to quantify the balance of the autonomic nervous system, allowing for more detailed functional testing [41].
The five pulse wave indices that can be measured through pulse waves are mainly used to measure and analyze physical stress and autonomic nerve health through PPG (Photoplethysmography).

1.3. Stress, Depression, and Their Relationship to Brain Function and the Autonomic Nervous System

Preclinical and clinical studies have demonstrated that stress or depression can lead to atrophy and cell loss in limbic brain structures that are critically involved in depression [47,48,49,50,51,52,53]. Convergent evidence over the past 20 years indicates that prolonged stress leads to overall neuronal atrophy and synaptic depression in the PFC and hippocampus [54,55,56,57], while regions such as the amygdala and NAc exhibit changes consistent with neuronal hypertrophy and synaptic potentiation [54,58,59]. The hippocampus provides inputs to other brain regions, including the prefrontal cortex, cingulate cortex, and amygdala, which contributes heavily to altered mood and emotion in depression [47,60,61,62,63]. Many studies report reduced hippocampal and prefrontal cortex volumes in depressed patients [47,64,65,66,67,68,69].
Previous studies have shown that 20–40% of patients with depression have abnormal EEG findings [70,71,72], with asymmetries in EEG activity in frontal regions [73,74,75,76]. The prefrontal cortex is affected by depression, anxiety, and stress, and alpha waves in the prefrontal cortex tend to be less active in depressed patients than in normal people [77,78,79]. Researchers have also found an average decrease in alpha and theta waves and an increase in beta waves in the EEG of depressed patients [80,81]. Neurotransmitters such as serotonin and dopamine play a role in regulating mood and cognitive function. Stress also causes changes in beta waves, which are associated with attention and persistence among EEG indices [12,82,83,84,85]. Reduced noradrenaline (NE) release to target areas such as the prefrontal cortex and amygdala limits anxious behavior [86,87].
There is a causative relationship between human mood and physical diseases such as HT. Patients with CVD commonly have anxiety and depression [88,89]. A previous study in a heterogeneous population of all ages showed that anxiety, depression, and HT are clearly related [88,90,91]. Inflammatory cytokines are increased in depression, which may explain the serotonergic, noradrenergic, and dopaminergic dysfunction of depression [92,93,94,95].
Humans experience pulse wave changes when subjected to external stressful stimuli [96], mental stress has been proven to lead to changes in the autonomic nervous system and further affect cardiac activity [97,98,99,100,101], and many studies on stress and depression have used heart rate variability (HRV) analysis to detect mental state [102,103,104,105,106]. Furthermore, Kang et al. [107] have categorized several combinations of EEG waves into formulas that best represent stress states, using the ratio of theta and M-beta waves.

2. Previous Research

2.1. Characteristics of Military Organizations

Kwon In-hyuk (2004) [108] found that the military is internally conflicted due to the uniformity and closure of the military culture and its conflict with the democratic and open culture of the new generation of soldiers. It was found that the embedded conflict structure relaxes the military organization and disrupts the military discipline, leading to a weakening of combat power and causing accidents. In addition, undemocratic practices directly increase soldier stress and contribute to accidents.

2.2. Relationship between Stress, Depression, and Traumatic Events

The compensatory imbalance of job stress is the greatest risk factor for problems with psychiatric disorders, and while stress is not a direct cause of errors, it does lead to inappropriate strategies for dealing with stressful situations [109,110,111,112]. Stress, anxiety, and depression are important markers that can affect the brain, behavior, and cognition, and stress and depression have been linked to the occurrence of accidents [17,113,114]. Worker stress levels have been shown to have a negative impact on safety behavior [115,116,117], and it has been argued that reductions in occupational stress can improve safety compliance. Alonso et al. [117] reported a high prevalence of job stress and emotional exhaustion symptoms. Kaushik, P. [75] stated in a study that depression causes sadness and anhedonia, which leads to decreased work performance and productivity, and in extreme cases can even lead to suicide, which is the fourth leading cause of death among 15–29-year-olds.

3. Research Methods

3.1. Choosing Who to Study

The South Korean military categorizes health status through enlistment physicals and personality tests, and sends personnel in generally good health to the Forward Corps. Personnel who are at risk of accidents due to their inability to adapt to military life after enlistment are managed by risk level. Stage 1 risk soldiers with mild maladjustment are managed separately by their units, while stage 2 risk soldiers with severe maladjustment are convened by forward corps to receive two weeks of service adjustment training by experts, including character education and counseling. Tier 3 at-risk Soldiers who have determined that further military life is limited and are in the process of being discharged are convened by their forward corps and managed until discharge.
The study population was divided into two groups: one group of normal soldiers who were well-adjusted to military life and three groups of soldiers who were at risk of accidents. The personnel were selected from eight units of the Forward Corps (Gyeonggi-do and Gangwon-do, South Korea), including 136 general soldiers, 42 soldiers with a risk of an accident, 47 soldiers with a very high risk of an accident, and 26 soldiers with the highest risk of an accident. To minimize the effect of enlistment, we excluded individuals who were taking medication for illness before enlistment. Regular soldiers and Phase 1 soldiers were selected from the infantry, artillery, engineer, and information technology units under the Forward Corps. For the second and third-tier soldiers, we excluded two soldiers who were not willing to participate in the study from the accident risk group, which is convened and managed by the Forward Corps.

3.2. Scope and Procedure of the Study

The scope of this study was to determine the differences in brain function and autonomic nervous system between soldiers who are well-adjusted to military life and those who are not and are at risk of accidents through EEG and pulse wave measurements and questionnaires. The procedure of the study was as follows.
First, we measured the EEG and pulse waves of one group of normal soldiers and three groups of soldiers at risk for accidents.
Second, a survey was conducted among those whose EEG and pulse waves were measured.
Third, we conducted a statistical analysis using the collected data.

3.3. Measurement Equipment

For EEG and pulse wave measurements, we used the EEG 2-channel dry and non-invasive measurement device shown in Figure 1, developed by Laxa and OmniCNC. This equipment is a medical device that connects via Bluetooth communication and transmits measurement data to a tablet. This product was tested on 300 healthy adult volunteers aged 19 to 69 years old from December 2007 to March 2008 at the Clinical Research Center of Asan Medical Center in Seoul.

3.4. Data Collection and Analysis

3.4.1. Brain Waves

Electroencephalography is a method of recording the electrical activity of cortical pyramidal neurons in the brain; therefore, when a large number of neurons are activated simultaneously, enough postsynaptic potentials can be generated to be detected from the scalp of the brain [118,119,120]. By comparing and analyzing EEG waves at different wavelengths, it is possible to determine the level of concentration level, psychological stress, imbalance of left and right brain activity, and brain activity. Scalp EEG methods are non-invasive, relatively safe and fast, inexpensive and widely available, and allow for numerous repeat measurements [120,121,122,123].
This study analyzed MDF, PF, and ATR from EEG data measured while sitting comfortably and with eyes closed [124].
The MDF measured the median frequency and was calculated in two steps.
  • All spectral power values in the 4–13 Hz frequency domain were summed and divided by 2.
  • The frequency where the cumulative power in the 4–13 Hz frequency domain first exceeded the value calculated in step 1 was selected.
PF was determined as the frequency at which the EEG spectrum has the most power in the 4–13 Hz frequency range.
ATR measures the ratio of power in the alpha rhythm (8–12.99 Hz) to the theta rhythm (4–7.99 Hz).

3.4.2. Pulse Wave

Heart rate variability (HRV) has been used in clinical practice to assess overall autonomic function and can be used to assess autonomic cardiovascular function and health, as well as monitor stress and fatigue [125,126,127]. HRV can be investigated non-invasively using photoplethysmography (PPG), which can detect changes in blood volume in microvascular beds, and the HRV index is known to be an important indicator of cardiorespiratory performance. The greater the HRV index, the lower and wider the distribution pattern, the healthier the person [128,129,130]. PPG pulses are used to measure pulse variability and assess the sympathetic and autonomic nervous systems, and waveform analysis can determine the values of various indicators related to the cardiovascular system. However, due to the difficulty of recognizing inflection points in the pulse, the second derivative of the PPG pulse (SDPPG) and TDPPG are used for detailed and objective evaluation [131,132,133].
In this study, the PPG device was used to measure heart rate pulses while sitting comfortably and with eyes closed. The PPG sensor system used visible light with a wavelength of 640 nm and a relative sensitivity of 60%. The sensor circuit unit converts current to voltage, amplifies and filters the signal, and provides the final output signal. The frequency response of the receiver (photodiode) is 0.3–5 Hz in the −3 dB band of the characteristic curve (gain with frequency). This frequency response of the filter removes unwanted noise. The PPG data were measured at a 250 Hz sampling frequency. To remove trends and drifts, the initial preprocessing step prioritized trend removal. Low- and high-frequency noise, such as traveling noise and breathing noise, was removed from the DC component using a fourth-order bandpass zero-phase Butterworth filter with a cutoff frequency of 0.4 to 9 Hz, accounting for phase delay and distortion [134,135,136]. For the morphologically volumetric pulse trajectory, the point where the notch is minimized after passing through the mid-vein notch was set as the end of the pulse. Immediately after is the start of the pulse and is defined by the pulse-to-pulse interval [137,138,139]. Representative single-pulse values were obtained from the values of the pulse-to-pulse interval by calculating the average of each time point relative to the pulse onset. The second and third derivatives were used to obtain SDPPG and TDPPG from the single-pulse PPG signal of each subject [133,140,141].

4. Group Design and Participants

Looking at the demographic characteristics of the study subjects, 94 (39.2%) were 20 years old, with one each of 18 and 32 years old. In terms of education, 171 (71.2%) were enrolled in college, and 58 (24.2%) had a high school diploma or less, including one middle school graduate. Other general characteristics of the study subjects, such as rank and physical fitness, are shown in Figure 2.

5. Data Collection and Analysis Approaches

All data collected in this study were processed using the statistical program SPSS 27.0, and the significance level of the statistics was set at 95% (p < 0.05). A one-way analysis of variance (ANOVA) was performed to calculate the mean, and standard deviation, and test for significant differences between groups. Then, a post hoc test was used to test whether there was a difference between the groups.
We also correlated the EEG and pulse wave measurements of 251 participants with the survey results of 240 participants, excluding 11 who refused to complete the survey. The analysis utilized Pearson correlation analysis (significance level < 0.05), a method used to determine the degree of linear relationship between variables measured on a quantitative scale (equal/ratio scale).

6. EEG, Pulse Waves, and Survey Results

6.1. Analyze the EEG Index of Four Populations

The EEG analysis analyzed “Concentration level”, which evaluates the interest in the surroundings and the ability to immerse oneself in a particular object; “Brain activity”, which evaluates the activation of brain cognitive activity at the level of mental workload; “Psychological stress”, which evaluates the level of brain tension and anxiety; and “Imbalance of left and right brain activity”, which checks the neurological balance of left and right brain waves.
First, we compared the means between the groups for each EEG index to check for differences, and used a one-way analysis of variance (ANOVA) to determine the probability of significance between the groups to determine if there was a significant difference. Then, post hoc tests (multiple comparisons) were performed on the EEG indices that showed significant differences between groups.

6.1.1. Compare between-Group Means by EEG Index

As shown in Table 1, The “Concentration level” index, which assesses the ability to concentrate, was highest for general soldiers and lower for each accident risk level. This suggests that acclimatization to military life and concentration are correlated, and that poor acclimatization can lead to weaker concentration due to anxiety symptoms. “Brain activity”, which assesses the activation of brain cognitive activity, was higher for soldiers in accident risk 1 and the general population than for soldiers in accident risk 2 and 3. This suggests that soldiers who have a normal routine in their units have more active brain activity than soldiers who spend their days sitting still and attending training sessions in the forward corps. “Psychological stress”, which assesses the level of tension and anxiety in the brain, was highest for regular soldiers, followed by accident risk levels 2, 1, and 3. In general, you would expect to see a higher percentage of people who have not adjusted to military life, but due to the nature of the military organization, there is a higher percentage of soldiers who are responsible and follow a normal routine. “Imbalance of left and right brain activity”, a measure of the balance between left and right brain waves, was highest for soldiers in accident risk 1, followed by general soldiers, accident risk 2, and accident risk 3.

6.1.2. Compare Groups by EEG Index

We tested the homogeneity of variance for each EEG index, and as shown in Table 2, the significance level is greater than 0.05 for three indices except for concentration, so the groups have the same variance. We then tested whether there were differences in the four EEG indices between the groups using an analysis of variance.
As shown in Table 3, The Concentration level index showed that the probability of significance (p = 0.001) of the test statistic (F = 6.093) was less than the significance level (α = 0.05), and the brain activity index showed that the probability of significance (p = 0.001) of the test statistic (F = 5.495) was less than the significance level (α = 0.05). However, the Psychological stress index showed that the probability of significance (p = 0.168) of the test statistic (F = 1.698) was greater than the significance level (α = 0.05), and the Imbalance of left and right brain activity index showed that the probability of significance (p = 0.469) of the test statistic (F = 0.848) was greater than the significance level (α = 0.05).
Therefore, the EEG showed that the Concentration level index was different between groups with unequal variance, while the brain activity index was different between groups with the same variance.

6.1.3. Brain Wave Post-Test

Post hoc tests (multiple comparisons) were performed on the Concentration level and brain activity indices that differed between the four groups, including the concentration index, which had unequal variances in the homogeneity of variance test, to determine which groups differed.
As shown in Table 4, Concentration level indices with unequal variances were subjected to multiple comparisons using Dunnett T3. The results showed that the significance probabilities of normal soldiers, accident risk stage 2 soldiers, and accident risk stage 3 soldiers were 0.014 and 0.000, respectively, which were less than the significance level (α = 0.05), and the significance probability of accident risk stage 1 soldiers and accident risk stage 3 soldiers was 0.003, which showed a significant difference.
The Brain activity indices with the same variance were subjected to Scheffe’s multiple comparison. As a result, there was no significant difference between normal soldiers and accident risk 1 soldiers with a significance level of 0.981, but there was a significant difference between normal soldiers, accident risk 2 soldiers, and accident risk 3 soldiers with a significance level of 0.039 and 0.040, respectively.
Thus, of the four EEG indices, we can see that the Concentration level indices and Brain activity indices are significantly different between the groups.

6.2. Analyze Pulse Wave Indices for Four Populations

Pulse wave measurements were used to analyze heart health, body stress and cumulative fatigue, physical vitality, and autonomic nerve system health. “Heart health” is determined by analyzing heart rate variability (HRV). “Body stress” is the immediate body response to current stress. “Cumulative fatigue” analyzes weakened autonomic nerve function and decreased heart rate variability to determine the body’s fatigue due to repetitive stress. “Physical vitality” analyzes the ratio of sympathetic and parasympathetic nerves to determine your current level of vitality or lethargy. “Autonomic nervous system health” is the health of the autonomic nervous system, which is responsible for metabolism.
The test procedure was to compare the means of the groups by pulse wave index to check for differences, and to determine whether there was a significant difference between the groups using a one-way analysis of variance (ANOVA). Post hoc tests (multiple comparisons) were performed on the pulse wave indices that showed significant differences between groups.

6.2.1. Compare Group Means by Pulse Wave Index

As shown in Table 5, The “Heart health” index, as measured by heart rate variability (HRV) analysis, was highest for regular soldiers. The results also showed similarities between normal soldiers living a normal life in the unit and those in the first stage of accident risk, and differences between those in the third and second stages of accident risk, which are managed separately by the corps. The “Body stress” index, which measures the immediate physical response to stress, showed the following results: accident risk 3, 2, 1, and normal soldier. This suggests that the psychological state of being under stress due to not adapting to military life is a physical reaction, as previous studies have shown. The “Cumulative fatigue” index, which checks the body’s fatigue due to repetitive stress, was higher for general soldiers living a normal life in the unit and for soldiers in the first stage of accident risk than for soldiers in the second and third stages of accident risk, who are separately convened and receive character education and counseling. The “Cumulative fatigue” index analyzes the weakening of autonomic nerve function and decreased heart rate variability, a phenomenon that occurs because normal military life is accompanied by constant physical fatigue and mental stress such as responsibility. The “Physical vitality” index, which determines how energized or helpless you feel at any given moment, was as follows: general soldier, accident risk 2, 1, and 3. This reflects the feelings of helplessness and depression that often accompany soldiers who are unable to adjust to military life. The “Autonomic nervous system health” index, which measures the health of the autonomic nervous system, showed the following results: general soldiers, accident risk 1, 3, and 2. We know that stress, depression, and anxiety affect the autonomic nervous system in soldiers at high risk for accidents.

6.2.2. Compare Groups by Pulse Wave Index

We tested the homogeneity of variance of each pulse wave index, and as shown in Table 6, except for “Cumulative fatigue” and “Physical vitality”, the significance probability is greater than 0.05 for three indices, so the groups of three indices have the same variance. Then, the analysis of variance was used to test whether there is a difference in the five indices of pulse wave between the groups.
As shown in Table 7, The p-value for the “Heart health” index (F = 1.873), the p-value for the “Cumulative fatigue” index (F = 1.467), and the p-value for the “Autonomic nervous system health” index (F = 2.594) are all greater than the significance level (α = 0.05), indicating that there is no difference between the groups.
However, there was a statistically significant difference between the groups, as the test statistic for the “Body stress” index (F = 4.977) (p = 0.002) and the test statistic for the “Physical vitality” index (F = 3.289) (p = 0.021) were smaller than the significance level (α = 0.05) (p < 0.05).
Therefore, the “Physical vitality” index in the pulse wave was analyzed as having a difference between groups with unequal variance, while the “Body stress” index was analyzed as having a difference between groups with equal variance.

6.2.3. Pulse Wave Post-Test

Post hoc tests (multiple comparisons) were performed on the “Body stress” and “Physical vitality” indices that showed differences between the four groups, including the “Physical vitality” index, which did not have equal variances in the homogeneity of variance test, to determine which groups differed.
As shown in Table 8, The “Body stress” index with the same variance was subjected to a Scheffe multiple comparison. As a result, there was no significant difference between general soldiers and soldiers in the first stage of accident risk with a significance rate of 0.953, but there was a significant difference between normal soldiers, accident risk tier 2 soldiers, and accident risk tier 3 soldiers with a significance level of 0.027 and 0.042, respectively. The “Physical vitality” indices with unequal variances were subjected to multiple comparisons using Dunnett’s t test. The result shows that there is a significant difference between general soldiers and accident risk stage 3 soldiers with a significance probability of 0.007.
Therefore, among the five indices of pulse wave, we can see that the “Body stress” and “Physical vitality” indices are significantly different between the groups.

6.3. Correlate EEG, Pulse Waves, and Survey Results

Of the 251 people whose EEG and pulse waves were measured, 240 were surveyed, excluding 11 who refused to participate. The questionnaire was fully explained beforehand so that the participants could fill out the questionnaire as honestly as possible about their psychological state. The questionnaire utilized a 24-item scale for categorizing types of maladjustment used by Liu (2014) [142]. Each item was scored on a 5-point scale ranging from “very much so” to “not at all”, with higher scores indicating closer to the corresponding scale.
Correlations were analyzed between EEG, pulse wave, maladjustment, and suicidal ideation. The analysis utilized Pearson’s correlation analysis (significance level < 0.05), a method used to determine the degree of linear relationship between variables measured on a quantitative scale (equivalence/ratio scale).
The means of the EEG, pulse wave, maladjustment, and suicidal ideation indices are shown in Table 9, with standard deviations ranging from 0.4 to 7.8.

6.3.1. Analyzing the Correlation between EEG and Pulse Wave Indices

As shown in Table 10, The brain activity index, psychological stress index, and imbalance of left and right brain activity index in the EEG were not correlated with any of the five indices in the pulse wave at a significance level of 0.085 or higher. However, the concentration level index was correlated with the autonomic health index in the pulse wave at a significance level of 0.034.

6.3.2. Correlating Brainwave Indices with Survey Results

As shown in Table 11, Among the EEG indices, the concentration level index correlates with the maladjustment scale and the suicidal ideation scale at 0.002 and 0.001, respectively. The brain activity index is also correlated with the maladjustment scale at 0.002 and with the suicidal ideation scale at 0.000.

6.3.3. Correlate Pulse Wave Indices with Survey Results

As shown in Table 12, Among the indices measured by pulse wave, the physical stress index correlates with the maladjustment scale and the suicidal ideation scale at 0.002 and 0.000, respectively. In addition, the physical vitality index correlated with the maladjustment scale at 0.005 and the suicidal ideation scale at 0.043.

7. Conclusions

Neurotransmitters and specific synaptic receptor activation influence stress-related behavioral and physiological responses [143,144,145,146,147]. In addition, many studies have shown that psychological conditions such as stress, depression, and anxiety are linked to physical health, including cardiovascular disease [89,148,149,150,151]. Advances in neuroimaging and NIBS techniques have enabled researchers to explore the underlying mechanisms of disorders such as depression, SCZ, anxiety, and post-traumatic stress disorders [152,153,154,155]. Identifying the neural circuits and networks involved in these disorders can lead to targeted interventions that aim to modulate brain activity and restore normal function [152,156]. Therefore, if it is possible to check the psychological state using brain waves and pulse waves, it will contribute to preventing suicide accidents and safety accidents caused by human error.
The results of the study showed differences in brain function and autonomic nervous system between normal soldiers and soldiers maladjusted to military life. and that EEG and pulse waves are correlated and reliable when compared to survey results. These results do not take into account all the different conditions, such as the health of the individual and the environment. Furthermore, there are many contradictions when it comes to psychological health based on just a few indices of EEG and pulse waves. However, it is significant that the military maladjusted soldiers generally showed lower levels of concentration and brain activity in the EEG and higher levels of physical stress, and lower levels of physical vitality in the pulse wave.
The study focused solely on determining whether there were differences in EEG and pulse waves between soldiers who were well-adjusted to military life and those who were not and were at risk of accidents. In the future, further research is needed on the correlation between EEG and pulse wave indices and the correlation of EEG and pulse wave measurements with the military’s current character and relationship type tests. Further research is needed on how to manage identified accident-risk soldiers by applying neurofeedback training.
There have been countless studies of EEG and pulse waves in civilian populations. However, there have been very few studies on military personnel. This is due to the nature of the military, which makes it difficult to get permission to study soldiers, and even when permission is granted, it is difficult to study soldiers who are spread out across the country. The significance of this study is that it was conducted among soldiers across the country, and in order to be more precise, it was divided into three groups of soldiers who were unable to adjust to military life based on their psychological state. In addition, the data analysis is presented in an average-oriented manner to make it easier for anyone to understand, even those who do not have expertise in EEG and pulse waves.
We believe that in the future, more military personnel and academics will be interested in neuroscience and contribute to its research.

Author Contributions

Validation, J.-G.C.; Formal analysis, J.-G.C.; Investigation, S.-O.C.; Writing—original draft, S.-O.C.; Writing—review & editing, J.-Y.Y. and S.-O.C.; Supervision, J.-Y.Y. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare that the literature review research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

  1. Yoon, M.J. The study of soldier’s human right and the program for preventing suicide incidentin Korean Military. Democr. Hum. Rights 2008, 8, 79–109. [Google Scholar]
  2. Yang, M.; Song, M.; Shin, H. The Military Peer Counselling Training Program. Youth Couns. Res. 2009, 17, 19–31. [Google Scholar]
  3. Lee, J.-H.; Cho, J.-Y. Anxiety, Depression and Impulsiveness according to Military Service Duration in Army-Enlisted Males. J. Korean Neuropsychiatr. Assoc. 1999, 966–972. Available online: https://pesquisa.bvsalud.org/portal/resource/pt/wpr-49526 (accessed on 1 March 2022).
  4. Military Culture Innovation Team, Ministry of National Defense Personnel Welfare Center. Status of Military Deaths; e-Country Indicators; Military Culture Innovation Team, Ministry of National Defense Personnel Welfare Center: Seoul, Republic of Korea, 2022. [Google Scholar]
  5. Sampson, L.; Gradus, J.L.; Cabral, H.J.; Rosellini, A.J.; Fink, D.S.; Cohen, G.H.; Liberzon, I.; Galea, S. Stressful life events and incident depression among U.S. military personnel. Soc. Psychiatry Psychiatr. Epidemiol. 2023, 58, 1009–1018. [Google Scholar] [CrossRef]
  6. Yoon, M.J. The Sociological Analysis of Military Culture and Suicide Accidents in Korea. Korean Soc. Soc. Hist. 2008, 201, 165–193. [Google Scholar]
  7. Lewandowski-Romps, L.; Peterson, C.; Berglund, P.A.; Collins, S.; Cox, K.; Hauret, K.; Jones, B.; Kessler, R.C.; Mitchell, C.; Park, N.; et al. Risk Factors for Accident Death in the U.S. Army, 2004−2009. Am. J. Prev. Med. 2014, 47, 745–753. [Google Scholar] [CrossRef] [Green Version]
  8. Greden, J.F.; Valenstein, M.; Spinner, J.; Blow, A.; Gorman, L.A.; Dalack, G.W.; Marcus, S.; Kees, M. Buddy-to-Buddy, a citizen soldier peer support program to counteract stigma, PTSD, depression, and suicide. Ann. N. Y. Acad. Sci. 2010, 1208, 90–97. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Scofield, D.E.; Proctor, S.P.; Kardouni, J.R.; Hill, O.T.; McKinnon, C.J. Risk Factors for Mild Traumatic Brain Injury and Subsequent Post-Traumatic Stress Disorder and Mental Health Disorders among United States Army Soldiers. J. Neurotrauma 2017, 34, 3249–3255. [Google Scholar] [CrossRef]
  10. Ge, Q.-Q.; Zhou, X.-N.; Liu, Y.-Z.; Su, W.-J.; Wang, W. Role of neuroticism in depressive symptoms among officers and soldiers: Mediating effects of negative automatic thoughts and response psychological stress. Acad. J. Nav. Med. Univ. 2022, 43, 821–826. [Google Scholar]
  11. Bandoli, G.; Campbell-Sills, L.; Kessler, R.C.; Heeringa, S.G.; Nock, M.K.; Rosellini, A.J.; Sampson, N.A.; Schoenbaum, M.; Ursano, R.J.; Stein, M.B. Childhood adversity, adult stress, and the risk of major depression or generalized anxiety disorder in US soldiers: A test of the stress sensitization hypothesis. Psychol. Med. 2017, 47, 2379–2392. [Google Scholar] [CrossRef]
  12. Vanhollebeke, G.; De Smet, S.; De Raedt, R.; Baeken, C.; van Mierlo, P.; Vanderhasselt, M.-A. The neural correlates of psychosocial stress: A systematic review and meta-analysis of spectral analysis EEG studies. Neurobiol. Stress 2022, 18, 100452. [Google Scholar] [CrossRef] [PubMed]
  13. Daviu, N.; Bruchas, M.R.; Moghaddam, B.; Sandi, C.; Beyeler, A. Neurobiological links between stress and anxiety. Neurobiol. Stress 2019, 11, 100191. [Google Scholar] [CrossRef]
  14. Mazure, C.M. Life stressors as risk factors in depression. Clin. Psychol. Sci. Pract. 1998, 5, 291–313. [Google Scholar] [CrossRef]
  15. Lazarus, R.S. Stress, Appraisal, and Coping; Springer Publishing Company: Berlin/Heidelberg, Germany, 1984; ISBN 0-8261-4191-9. [Google Scholar]
  16. Folkman, S. Stress: Appraisal and Coping. In Encyclopedia of Behavioral Medicine; Springer International Publishing: Cham, Switzerland, 2020; pp. 2177–2179. [Google Scholar]
  17. Demichelis, O.P.; Grainger, S.A.; Hubbard, R.E.; Henry, J.D. Emotion regulation mediates the relationship between social frailty and stress, anxiety, and depression. Sci. Rep. 2023, 13, 6430. [Google Scholar] [CrossRef] [PubMed]
  18. Steffy, B.D.; Jones, J.W.; Murphy, L.R.; Kunz, L. A demonstration of the impact of stress abatement program on reducing employee’s accidents and their costs. Am. J. Health Promot. 1986, 1, 25–32. [Google Scholar] [CrossRef]
  19. Sutherland, V.J.; Cooper, C.L. Stress and Accidents in the Offshore Oil and Gas Industry; Gulf Publishing Company: Houston, TX, USA, 1991; p. 227. [Google Scholar]
  20. Bakhtiari, A.; Basirat, Z.; Nasiri-Amiri, F. Sexual dysfunction in women undergoing fertility treatment in Iran: Prevalence and associated risk factors. J. Reprod. Infertil. 2016, 17, 26–33. [Google Scholar]
  21. Ramya, S.; Poornima, P.; Jananisri, A.; Geofferina, I.P.; Bavyataa, V.; Divya, M.; Priyanga, P.; Vadivukarasi, J.; Sujitha, S.; Elamathi, S.; et al. Role of Hormones and the Potential Impact of Multiple Stresses on Infertility. J. Stress. 2023, 3, 454–474. [Google Scholar] [CrossRef]
  22. Ghahvehchi-Hosseini, F.; Manshadi, E.; Mohammadi, A.; Jahromi, G.P.; Hatef, B. Evaluation of the persistence effect acute social stress test on the alpha band power. J. Mil. Med. 2018, 20, 509–518. [Google Scholar]
  23. Mane, S.A.M.; Shinde, A. StressNet: Hybrid model of LSTM and CNN for stress detection from electroencephalogram signal (EEG). Results Control Optim. 2023, 11, 100231. [Google Scholar] [CrossRef]
  24. Morris, A.T.; Temereanca, S.; Zandvakili, A.; Thorpe, R.; Sliva, D.D.; Greenberg, B.D.; Carpenter, L.L.; Philip, N.S.; Jones, S.R. Fronto-central resting-state 15–29 Hz transient beta events change with therapeutic transcranial magnetic stimulation for posttraumatic stress disorder and major depressive disorder. Sci. Rep. 2023, 13, 6366. [Google Scholar] [CrossRef]
  25. Anijärv, T.E.; Can, A.T.; Gallay, C.C.; Forsyth, G.A.; Dutton, M.; Mitchell, J.S.; Hermens, D.F.; Lagopoulos, J. Spectral Changes of EEG Following a 6-Week Low-Dose Oral Ketamine Treatment in Adults With Major Depressive Disorder and Chronic Suicidality. Int. J. Neuropsychopharmacol. 2023, 26, 259–267. [Google Scholar] [CrossRef] [PubMed]
  26. Lytaev, S. Psychological and Neurophysiological Screening Investigation of the Collective and Personal Stress Resilience. Behav. Sci. 2023, 13, 258. [Google Scholar] [CrossRef] [PubMed]
  27. Loganovsky, K.N.; Zdanevich, N.A.; Gresko, M.V.; Marazziti, D.; Loganovskaja, T.K. Neuropsychiatric characteristics of antiterrorist operation combatants in the Donbass (Ukraine). CNS Spectr. 2018, 23, 178–184. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Bedford, C.E.; Nakamura, Y.; Marchand, W.R.; Garland, E.L. Heightened autonomic reactivity to negative affective stimuli among activeduty soldiers with PTSD and opioid-treated chronic pain. Psychiatry Res. 2022, 309, 114394. [Google Scholar] [CrossRef] [PubMed]
  29. Stojar, R.; Fučík, J.; Frank, L. Wars without Soldiers and Casualties or Victories in Hearts and Minds? In Proceedings of the Modelling and Simulation for Autonomous Systems: 6th International Conference, MESAS 2019, Palermo, Italy, 29–31 October 2019; Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics); Springer International Publishing: Berlin/Heidelberg, Germany, 2020; pp. 372–378. [Google Scholar]
  30. Britton, J.W.; Frey, L.C.; Hopp, J.L.; Korb, P.; Koubeissi, M.Z.; Lievens, W.E.; Pestana-Knight, E.M.; Louis, E.K.S. Electroencephalography (EEG): An Introductory Text and Atlas of Normal and Abnormal Findings in Adults, Children, and Infants; Louis, E.K.S., Frey, L.C., Eds.; American Epilepsy Society: Chicago, IL, USA, 2016. [Google Scholar]
  31. Soininen, H.; Reinikainen, K.; Partanen, J.; Mervaala, E.; Paljarvi, L.; Helkala, E. Slowing of the dominant occipital rhythm in electroencephalogram is associated with low concentration of noradrenaline in the thalamus in patients with Alzheimer’s disease. Neurosci. Lett. 1992, 137, 5–8. [Google Scholar] [CrossRef]
  32. Lee, G.; Shin, J. Effects of the barefoot walking experience program on EEG and brain utilization ability of elementary school students. J. Korean Assoc. Learn.-Centered Curric. Instr. 2019, 19, 219–238. [Google Scholar] [CrossRef]
  33. Park, Y.-J.; Lim, U.-N.; Park, S.; Shin, J.-H. Effect of Brain and Pulse Waves on Safety Consciousness and Safety Commitment of Workers at Construction Sites. Sensors 2021, 21, 2753. [Google Scholar] [CrossRef] [PubMed]
  34. Lian, J.; Xu, L.; Song, T.; Peng, Z.; Zhang, Z.; An, X.; Chen, S.; Zhong, X.; Shao, Y. Reduced Resting-State EEG Power Spectra and Functional Connectivity after 24 and 36 Hours of Sleep Deprivation. Brain Sci. 2023, 13, 949. [Google Scholar] [CrossRef]
  35. Koudelková, Z.; Strmiska, M.; Jašek, R. Analysis of brain waves according to their frequency. Int. J. Biol. Biomed. Eng. 2018, 12, 202–207. [Google Scholar]
  36. Mody, C.; McIntyre, H.; Miller, B.; Altman, K.; Read, S. Computerized EEG frequency analysis and topographic brain mapping in Alzheimer’s disease. Ann. N. Y. Acad. Sci. 1991, 620, 45–56. [Google Scholar] [CrossRef]
  37. Du, J.; Chen, X.; Xi, L.; Jiang, B.; Ma, J.; Yuan, G.; Hassan, A.; Fu, E.; Huang, Y. Electroencephalography-Based Neuroemotional Responses in Cognitively Normal and Cognitively Impaired Elderly by Watching the Ardisia mamillata Hance with Fruits and without Fruits. Int. J. Environ. Res. Public Health 2022, 19, 10020. [Google Scholar] [CrossRef] [PubMed]
  38. Jelic, V.; Kowalski, J. Evidence-based evaluation of diagnostic accuracy of resting EEG in dementia and mild cognitive impairment. Clin. EEG Neurosci. 2009, 40, 129–142. [Google Scholar] [CrossRef] [PubMed]
  39. Du, J.; Yin, J.; Chen, X.; Hassan, A.; Fu, E.; Li, X. Electroencephalography (EEG)-Based Neural Emotional Response to Flower Arrangements (FAs) on Normal Elderly (NE) and Cognitively Impaired Elderly (CIE). Int. J. Environ. Res. Public Health 2022, 19, 3971. [Google Scholar] [CrossRef] [PubMed]
  40. Murty, D.V.P.S.; Manikandan, K.; Kumar, W.S.; Ramesh, R.G.; Purokayastha, S.; Nagendra, B.; Abhishek, M.L.; Balakrishnan, A.; Javali, M.; Rao, N.P.; et al. Stimulus-induced gamma rhythms are weaker in human elderly with mild cognitive impairment and Alzheimer’s disease. eLife 2021, 10, e61666. [Google Scholar] [CrossRef]
  41. Kelly, R.; Hayward, C.; Avolio, A.; O’Rourke, M. Noninvasive determination of age-related changes in the human arterial pulse. Circulation 1989, 80, 1652–1659. [Google Scholar] [CrossRef] [Green Version]
  42. Takazawa, K.; Tanaka, N.; Takeda, K.; Kurosu, F.; Ibukiyama, C. Underestimation of vasodilator effects of nitroglycerin by upper limb blood pressure. Hypertension 1995, 26, 520–523. [Google Scholar] [CrossRef]
  43. Task Force of the European Society of Cardiology; The North American Society of Pacing and Electrophysiology. Heart rate variability: Standards of measurement, physiological interpretation, and clinical use. Eur. Heart J. 1996, 17, 354–381. [Google Scholar] [CrossRef] [Green Version]
  44. Casolo, G.C.; Stroder, P.; Signorini, C.; Calzolari, F.; Zucchini, M.; Balli, E.; Sulla, A.; Lazzerini, S. Heart rate variability during the acute phase of myocardial infarction. Circulation 1992, 85, 2073–2079. [Google Scholar] [CrossRef] [Green Version]
  45. Stein, K.M.; Borer, J.S.; Hochreiter, C.; Okin, P.M.; Herrold, E.M.; Devereux, R.B.; Kligfield, P. Prognostic value and physiological correlates of heart rate variability in chronic severe mitral regurgitation. Circulation 1993, 88, 127–135. [Google Scholar] [CrossRef] [Green Version]
  46. Smeets, T.; Cornelisse, S.; Quaedflieg, C.; Meyer, T.; Jelicic, M.; Merckelbach, H. Introducing the maastricht acute stress test (MAST): A quick and non-invasive approach to elicit robust autonomic and glucocorticoid stress responses. Psychoneuroendocrinology 2012, 37, 1998–2008. [Google Scholar] [CrossRef]
  47. Duman, R.S. Depression: A case of neuronal life and death? Biol. Psychiatry 2004, 56, 140–145. [Google Scholar] [CrossRef]
  48. Duman, R.S.; Malberg, J.; Nakagawa, S. Regulation of adult neurogenesis by psychotropic drugs and stress. J. Pharmacol. Exp. Ther. 2001, 299, 401–407. [Google Scholar]
  49. Posener, J.A.; Wang, L.; Price, J.L.; Gado, M.H.; Province, M.A.; Miller, M.I.; Babb, C.M.; Csernansky, J.G. High-dimensional mapping of the hippocampus in depression. Am. J. Psychiatry 2003, 160, 83–89. [Google Scholar] [CrossRef] [PubMed]
  50. Gage, F.H. Mammalian neural stem cells. Science 2000, 287, 1433–1438. [Google Scholar] [CrossRef] [PubMed]
  51. Sapolsky, R.M. Chickens, eggs and hippocampal atrophy. Nat. Neurosci. 2002, 5, 1111–1113. [Google Scholar] [CrossRef]
  52. Kempermann, G.; Gage, F.H. Genetic determinants of adult hippocampal neurogenesis correlate with acquisition, but not probe trial performance, in the water maze task. Eur. J. Neurosci. 2002, 16, 129–136. [Google Scholar] [CrossRef]
  53. McEwen, B.S. Stress and hippocampal plasticity. Annu. Rev. Neurosci. 1999, 22, 105–122. [Google Scholar] [CrossRef] [Green Version]
  54. Abdallah, C.G.; Sanacora, G.; Duman, R.S.; Krystal, J.H. Ketamine and rapid-acting antidepressants: A window into a new neurobiology for mood disorder therapeutics. Annu. Rev. Med. 2015, 66, 509–523. [Google Scholar] [CrossRef] [Green Version]
  55. Bessa, J.M.; Ferreira, D.; Melo, I.; Marques, F.; Cerqueira, J.J.; Palha, J.A.; Almeida, O.F.X.; Sousa, N. The mood-improving actions of antidepressants do not depend on neurogenesis but are associated with neuronal remodeling. Mol. Psychiatry 2009, 14, 764–773. [Google Scholar] [CrossRef] [Green Version]
  56. Yuen, E.Y.; Wei, J.; Liu, W.; Zhong, P.; Li, X.; Yan, Z. Repeated Stress Causes Cognitive Impairment by Suppressing Glutamate Receptor Expression and Function in Prefrontal Cortex. Neuron 2012, 73, 962–977. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Kang, H.J.; Voleti, B.; Hajszan, T.; Rajkowska, G.; Stockmeier, C.A.; Licznerski, P.; Lepack, A.; Majik, M.S.; Jeong, L.S.; Banasr, M.; et al. Decreased expression of synapse-related genes and loss of synapses in major depressive disorder. Nat. Med. 2012, 18, 1413–1417. [Google Scholar] [CrossRef] [PubMed]
  58. Vyas, A.; Pillai, A.G.; Chattarji, S. Recovery after chronic stress fails to reverse amygdaloid neuronal hypertrophy and enhanced anxiety-like behavior. Neuroscience 2004, 128, 667–673. [Google Scholar] [CrossRef]
  59. Bessa, J.M.; Morais, M.; Marques, F.; Pinto, L.; Palha, J.A.; Almeida, O.F.X.; Sousa, N. Stress-induced anhedonia is associated with hypertrophy of medium spiny neurons of the nucleus accumbens. Transl. Psychiatry 2013, 3, e266. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  60. Drevets, W.C. Neuroimaging and neuropathological studies of depression: Implications for the cognitive-emotional features of mood disorders. Curr. Opin. Neurobiol. 2001, 11, 240–249. [Google Scholar] [CrossRef] [PubMed]
  61. Santarelli, L.; Saxe, M.; Gross, C.; Surget, A.; Battaglia, F.; Dulawa, S.; Weisstaub, N.; Lee, J.; Duman, R.; Arancio, O.; et al. Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants. Science 2003, 301, 805–809. [Google Scholar] [CrossRef] [Green Version]
  62. Czéh, B.; Michaelis, T.; Watanabe, T.; Frahm, J.; De Biurrun, G.; Van Kampen, M.; Bartolomucci, A.; Fuchs, E. Stress-induced changes in cerebral metabolites, hippocampal volume, and cell proliferation are prevented by antidepressant treatment with tianeptine. Proc. Natl. Acad. Sci. USA 2001, 98, 12796–12801. [Google Scholar] [CrossRef]
  63. Manji, H.K.; Drevets, W.C.; Charney, D.S. The cellular neurobiology of depression. Nat. Med. 2001, 7, 541–547. [Google Scholar] [CrossRef]
  64. Bremner, J.D.; Narayan, M.; Anderson, E.R.; Staib, L.H.; Miller, H.L.; Charney, D.S. Hippocampal volume reduction in major depression. Am. J. Psychiatry 2000, 157, 115–117. [Google Scholar] [CrossRef]
  65. Drevets, W.C.; Price, J.L.; Simpson, J.R., Jr.; Todd, R.D.; Reich, T.; Vannier, M.; Raichle, M.E. Subgenual prefrontal cortex abnormalities in mood disorders. Nature 1997, 386, 824–827. [Google Scholar] [CrossRef]
  66. Nasca, C.; Bigio, B.; Zelli, D.; Nicoletti, F.; McEwen, B.S. Mind the gap: Glucocorticoids modulate hippocampal glutamate tone underlying individual differences in stress susceptibility. Mol. Psychiatry 2015, 20, 755–763. [Google Scholar] [CrossRef] [Green Version]
  67. Shah, P.J.; Ebmeier, K.P.; Glabus, M.F.; Goodwin, G.M. Cortical grey matter reductions associated with treatment-resistant chronic unipolar depression: Controlled magnetic resonance imaging study. Br. J. Psychiatry 1998, 172, 527–532. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  68. Steffens, D.C.; Byrum, C.E.; McQuoid, D.R.; Greenberg, D.L.; Payne, M.E.; Blitchington, T.F.; MacFall, J.R.; Krishnan, K.R.R. Hippocampal volume in geriatric depression. Biol. Psychiatry 2000, 48, 301–309. [Google Scholar] [CrossRef] [PubMed]
  69. MacQueen, G.M.; Campbell, S.; McEwen, B.S.; Macdonald, K.; Amano, S.; Joffe, R.T.; Nahmias, C.; Trevor Young, L. Course of illness, hippocampal function, and hippocampal volume in major depression. Proc. Natl. Acad. Sci. USA 2003, 100, 1387–1392. [Google Scholar] [CrossRef] [PubMed]
  70. Kan, D.P.X.; Lee, P.F. Decrease alpha waves in depression: An electroencephalogram(EEG) study. In Proceedings of the International Conference on BioSignal Analysis, Processing and Systems, Kuala Lumpur, Malaysia, 26–28 May 2015; ICBAPS 7292237. pp. 156–161. [Google Scholar]
  71. Galderisi, S.; Mucci, A.; Bucci, P.; Romano, G.; Maj, M. Quantitative EEG test dose procedure in the prediction of response to treatment with antipsychotic drugs. Psychiatry Res. Neuroimaging 1997, 68, 162–163. [Google Scholar] [CrossRef]
  72. Hughes, J.R.; John, E.R. Conventional and quantitative elecroencephalography in psychiatry. J. Neuropsychiatry Clin. Neurosci. 1999, 11, 190–208. [Google Scholar] [CrossRef] [Green Version]
  73. Allen, B.; Urry, H.L.; Hitt, S.K.; Coan, J.A. The stability of resting frontal electroencephalographic asymmetry in depression. Psychophysiology 2004, 41, 269–280. [Google Scholar] [CrossRef]
  74. Debener, S.; Beauducel, A.; Nessler, D.; Brocke, B.; Heilemann, H.; Kayser, J. Is resting anterior EEG alpha asymmetry a trait marker for depression? Findings for healthy adults and clinically depressed patients. Neuropsychobiology 2000, 41, 31–37. [Google Scholar] [CrossRef] [Green Version]
  75. Kaushik, P.; Yang, H.; Roy, P.P.; van Vugt, M. Comparing resting state and task-based EEG using machine learning to predict vulnerability to depression in a non-clinical population. Sci. Rep. 2023, 13, 7467. [Google Scholar] [CrossRef]
  76. Chaudhury, D.; Liu, H.; Han, M.-H. Neuronal correlates of depression. Cell. Mol. Life Sci. 2015, 72, 4825–4848. [Google Scholar] [CrossRef] [Green Version]
  77. Hammond, D.C. Neurofeedback treatment of depression and anxiety. J. Adult Dev. 2005, 12, 131–137. [Google Scholar] [CrossRef]
  78. Hosseinifard, B.; Hassan, M.; Rostami, R. Classifying depression patients and normal subjects using machine learning techniques and nonlinear features from EEG signal. Comput. Methods Program. Biomed. 2012, 109, 339–345. [Google Scholar] [CrossRef]
  79. Gotlib, I.H.; Rosenfeld, C.J.P. Frontal EEG Alpha Asymmetry Depression and Cognitive Functioning. Cogn. Emot. 1998, 12, 449–478. [Google Scholar] [CrossRef]
  80. Mohammadzadeh, B.; Sattari, K.; Lotfizadeh, M. Determining the relationship between depression and brain waves in depressed subjects using Pearson correlation and regression. Int. J. Epidemiol. Res. 2016, 3, 375–384. [Google Scholar]
  81. Smit, D.J.; Posthuma, D.; Boomsma, D.I.; De Geus, E.J. The relation between frontal EEG asymmetry and the risk for anxiety and depression. Biol. Psychol. 2007, 74, 26–33. [Google Scholar] [CrossRef] [Green Version]
  82. Canli, T.; Qiu, M.; Omura, K.; Lesch, K.P. Neural correlates of epigenesis. Biol. Sci. 2006, 103, 16033–16038. [Google Scholar] [CrossRef]
  83. Allen, J.J.B.; Coan, J.A.; Nazarian, M. Issues and assumptions on the road from raw signals to metrics of frontal EEG asymmetry in emotion. Biol. Psychol. 2004, 67, 183–218. [Google Scholar] [CrossRef]
  84. Engel, A.K.; Fries, P. Beta-band oscillations—Signalling the status quo? Curr. Opin. Neurobiol. 2010, 20, 156–165. [Google Scholar] [CrossRef]
  85. Andrzej, W. Beta activity: A carrier for visual attention. Acta Neurobiol. Exp. 2000, 60, 247–260. [Google Scholar]
  86. Lin, T.-W.; Kuo, Y.-M. Exercise Benefits Brain Function: The Monoamine Connection. Brain Sci. 2013, 3, 39–53. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  87. Sciolino, N.R.; Holmes, P.V. Exercise offers anxiolytic potential: A role for stress and brain noradrenergic-galaninergic mechanisms. Neurosci. Biobehav. Rev. 2012, 36, 1965–1984. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  88. Duman, H.; Duman, H.; Puşuroğlu, M.; Yılmaz, A.S. Anxiety disorders and depression are associated with resistant hypertension. Adv. Clin. Exp. Med. 2023; ahead of print. [Google Scholar] [CrossRef]
  89. Cohen, B.E.; Edmondson, D.; Kronish, I.M. State of the art review: Depression, stress, anxiety, and cardiovascular disease. Am. J. Hypertens. 2015, 28, 1295–1302. [Google Scholar] [CrossRef] [Green Version]
  90. Johnson, H.M. Anxiety and Hypertension: Is There a Link? A Literature Review of the Comorbidity Relationship between Anxiety and Hypertension. Curr. Hypertens. Rep. 2019, 21, 66. [Google Scholar] [CrossRef] [PubMed]
  91. Polishchuk, O.Y.; Tashchuk, V.K.; Barchuk, N.I.; Amelina, T.M.; Hrechko, S.I.; Trefanenko, I.V. Anxiety and Depressive Disorders in Patients with Arterial Hypertension. Wiad. Lek. 2021, 74, 455–459. [Google Scholar] [CrossRef]
  92. Török, N.; Maszlag-Török, R.; Molnár, K.; Szolnoki, Z.; Somogyvári, F.; Boda, K.; Tanaka, M.; Klivényi, P.; Vécsei, L. Single Nucleotide Polymorphisms of Indoleamine 2,3-Dioxygenase 1 Influenced the Age Onset of Parkinson’s Disease. Front. Biosci.—Landmark 2022, 27, 265. [Google Scholar] [CrossRef] [PubMed]
  93. Lee, E.C.; Hong, D.-Y.; Lee, D.-H.; Park, S.-W.; Lee, J.Y.; Jeong, J.H.; Kim, E.-Y.; Chung, H.-M.; Hong, K.-S.; Park, S.-P.; et al. Inflammation and Rho-Associated Protein Kinase-Induced Brain Changes in Vascular Dementia. Biomedicines 2022, 10, 446. [Google Scholar] [CrossRef] [PubMed]
  94. Agita, A.; Alsagaff, M.T. Inflammation, Immunity, and Hypertension. Acta Medica Indones. 2017, 49, 158–165. [Google Scholar]
  95. Sfera, A.; Hazan, S.; Kozlakidis, Z.; Klein, C. Microbiota-derived psychedelics: Lessons from COVID-19. Adv. Clin. Exp. Med. 2023, 32, 395–399. [Google Scholar] [CrossRef]
  96. Asano, M.; Kajiwara, Y.; Shimakawa, H. Estimating Working Stressor Based on Pulse Wave. In Proceedings of the 9th International Conference on Machine Learning and Computing, Singapore, 24–26 February 2017; pp. 23–27. [Google Scholar]
  97. Sriramprakash, S.; Prasanna, V.D.; Murthy, O.V.R. Stress Detection in Working People. Procedia Comput. Sci. 2017, 115, 359–366. [Google Scholar] [CrossRef]
  98. Jiao, Y.; Wang, X.; Liu, C.; Du, G.; Zhao, L.; Dong, H.; Zhao, S.; Liu, Y. Feasibility study for detection of mental stress and depression using pulse rate variability metrics via various durations. Biomed. Signal Process. Control 2023, 79, 104145. [Google Scholar] [CrossRef]
  99. Watkins, L.L.; Grossman, P.; Krishnan, R.; Blumenthal, J.A. Anxiety reduces baroreflex cardiac control in older adults with major depression. Psychosom. Med. 1999, 61, 334–340. [Google Scholar] [CrossRef]
  100. Seldenrijk, A.; van Hout, H.P.J.; van Marwijk, H.W.J. Depression, Anxiety, and Arterial Stiffness. Biol. Psychiatry 2011, 69, 795–803. [Google Scholar] [CrossRef] [PubMed]
  101. Yeragani, V.K.; Tancer, M.; Seema, K.P.; Josyula, K.; Desai, N. Increased pulse-wave velocity in patients with anxiety: Implications for autonomic dysfunction. J. Psychosom. Res. 2006, 61, 25–31. [Google Scholar] [CrossRef] [PubMed]
  102. Hernando, A.; Lazaro, J.; Gil, E.; Arza, A.; Garzon, J.M.; Lopez-Anton, R.; de la Camara, C.; Laguna, P.; Aguilo, J.; Bailon, R. Inclusion of respiratory frequency information in heart rate variability analysis for stress assessment. IEEE J. Biomed. Health Inform. 2016, 20, 1016–1025. [Google Scholar] [CrossRef] [PubMed]
  103. Chen, L.L.; Zhao, Y.; Ye, P.F.; Zhang, J.; Zou, J.Z. Detecting driving stress in physiological signals based on multimodal feature analysis and kernel classifiers. Expert Syst. Appl. 2017, 85, 279–291. [Google Scholar] [CrossRef]
  104. Byun, S.; Kim, A.Y.; Jang, E.H.; Kim, S.; Choi, K.W.; Yu, H.Y.; Jeon, H.J. Detection of major depressive disorder from linear and nonlinear heart rate variability features during mental task protocol. Comput. Biol. Med. 2019, 112, 103381. [Google Scholar] [CrossRef]
  105. Healey, J.A.; Picard, R.W. Detecting stress during real-world driving tasks using physiological sensors. IEEE Trans. Intell. Transp. Syst. 2005, 6, 156–166. [Google Scholar] [CrossRef] [Green Version]
  106. Betti, S.; Lova, R.M.; Rovini, E.; Acerbi, G.; Santarelli, L.; Cabiati, M.; Del Ry, S.; Cavallo, F. Evaluation of an integrated system of wearable physiological sensors for stress monitoring in working environments by using biological markers. IEEE Trans. Biomed. Eng. 2018, 65, 1748–1758. [Google Scholar]
  107. Kang, J.S.; Jang, G.J.; Lee, M.H. Stress status classification based on EEG signals. J. Inst. Internet Broadcast. Commun. 2016, 16, 103–108. [Google Scholar] [CrossRef]
  108. Kwon, I. A Study on the Consciousness Tendency and the Military Stress and Adjustment of New-Generation Soldiers; Hannam University: Daejeon, Republic of Korea, 2004. [Google Scholar]
  109. Stansfeld, S.; Candy, B. Psychosocial work environment and mental health-a meta-analytic review. Scand. J. Work Environ. Health 2006, 32, 443–462. [Google Scholar] [CrossRef]
  110. Reason, J. Managing the Risks of Organizational Accidents; Routledge: London, UK, 2016; pp. 1–252. [Google Scholar]
  111. Mazure, C.M.; Bruce, M.L.; Maciejewski, P.K.; Jacobs, S.C. Adverse life events and cognitive-personality characteristics in the prediction of major depression and antidepressant response. Am. J. Psychiatry 2000, 157, 896–903. [Google Scholar] [CrossRef] [PubMed]
  112. Hammen, C.L.; Mayol, A. Depression and cognitive characteristics of stressful life-event types. J. Abnorm. Psychol. 1982, 91, 165–174. [Google Scholar] [CrossRef] [PubMed]
  113. Beckes, L.; Coan, J.A. Social Baseline Teory and the Social Regulation of Emotion. Sci. Couple 2013, 12, 93–106. [Google Scholar]
  114. Beckes, L.; Sbarra, D.A. Social baseline theory: State of the science and new directions. Curr. Opin. Psychol. 2022, 43, 36–41. [Google Scholar] [CrossRef] [PubMed]
  115. Adhikari, B.; Poudel, L.; Bhandari, N.; Adhikari, N.; Shrestha, B.; Poudel, B.; Bishwokarma, A.; Kuikel, B.S.; Timalsena, D.; Paneru, B.; et al. Prevalence and factors associated with depression, anxiety and stress symptoms among construction workers in Nepal. PLoS ONE 2023, 18, e0284696. [Google Scholar] [CrossRef] [PubMed]
  116. Alsulami, H.; Serbaya, S.H.; Rizwan, A.; Saleem, M.; Maleh, Y.; Alamgir, Z. Impact of emotional intelligence on the stress and safety of construction workers’ in Saudi Arabia. Eng. Constr. Archit. Manag. 2023, 30, 1365–1378. [Google Scholar] [CrossRef]
  117. Alonso, F.; Esteban, C.; Gonzalez-Marin, A.; Alfaro, E.; Useche, S.A. Job stress and emotional exhaustion at work in Spanish workers: Does unhealthy work affect the decision to drive? PLoS ONE 2020, 15, e0227328. [Google Scholar] [CrossRef] [Green Version]
  118. Monllor, P.; Cervera-Ferri, A.; Lloret, M.-A.; Esteve, D.; Lopez, B.; Leon, J.-L.; Lloret, A. Electroencephalography as a non-invasive biomarker of Alzheimer’s disease: A forgotten candidate to substitute CSF molecules? Int. J. Mol. Sci. 2021, 22, 10889. [Google Scholar] [CrossRef]
  119. Müller-Putz, G.R. Chapter 18—Electroencephalography. In Handbook of Clinical Neurology; Elsevier: Amsterdam, The Netherlands, 2020; Volume 168, pp. 249–262. [Google Scholar]
  120. Malver, L.P.; Brokjær, A.; Staahl, C.; Graversen, C.; Andresen, T. Electroencephalography and analgesics. Br. J. Clin. Pharmacol. 2013, 77, 72–95. [Google Scholar] [CrossRef] [Green Version]
  121. Tsolaki, A.; Kazis, D.; Kompatsiaris, I.; Kosmidou, V.; Tsolaki, M. Electroencephalogram and Alzheimer’s disease: Clinical and research approaches. Int. J. Alzheimers Dis. 2014, 2014, 349249. [Google Scholar] [CrossRef] [Green Version]
  122. de Aguiar Neto, F.S.; Rosa, J.L.G. Depression biomarkers using non-invasive EEG: A review. Neurosci. Biobehav. Rev. 2019, 105, 83–93. [Google Scholar] [CrossRef]
  123. Mantri, S.; Patil, D.; Agrawal, P.; Wadhai, V. Noninvasive EEG signal processing framework for real time depression analysis. In Proceedings of the 2015 SAI Intelligent Systems Conference (IntelliSys), London, UK, 10–11 November 2015. [Google Scholar] [CrossRef]
  124. Adamis, D.; Sahu, S.; Treloar, A. The utility of EEG in dementia: A clinical perspective. Int. J. Geriatr. Psychiatry 2005, 20, 1038–1045. [Google Scholar] [CrossRef] [PubMed]
  125. Kleiger, R.E.; Stein, P.K.; Bigger, J.T. Heart rate variability: Measurement and clinical utility. Ann. Noninvasive Electrocardiol. 2005, 10, 88–101. [Google Scholar] [CrossRef] [PubMed]
  126. Segerstrom, S.C.; Nes, L.S. Heart rate variability reflects self-regulatory strength, effort, and fatigue. Psychol. Sci. 2007, 18, 275–281. [Google Scholar] [CrossRef] [PubMed]
  127. Tran, Y.; Wijesuriya, N.; Tarvainen, M.; Karjalainen, P.; Craig, A. The relationship between spectral changes in heart rate variability and fatigue. J. Psychophysiol. 2009, 23, 143–151. [Google Scholar] [CrossRef]
  128. Malik, M.; Xia, R.; Odemuyiwa, O.; Staunton, A.; Poloniecki, J.; Camm, A. Influence of the recognition artefact in automatic analysis of longterm electrocardiograms on time-domain measurement of heart rate variability. Med. Biol. Eng. Comput. 1993, 31, 539–544. [Google Scholar] [CrossRef]
  129. Mongin, D.; Chabert, C.; Extremera, M.G.; Hue, O.; Courvoisier, D.S.; Carpena, P.; Bernaola Galvan, P.A. Decrease of heart rate variability during exercise: An index of cardiorespiratory fitness. PLoS ONE 2022, 17, e0273981. [Google Scholar] [CrossRef]
  130. Voss, A.; Schroeder, R.; Heitmann, A.; Peters, A.; Perz, S. Short-term heart rate variability—Influence of gender and age in healthy subjects. PLoS ONE 2015, 10, e0118308. [Google Scholar] [CrossRef] [Green Version]
  131. Inoue, N.; Kawakami, H.; Yamamoto, H.; Ito, C.; Fujiwara, S.; Sasaki, H.; Kihara, Y. Second derivative of the finger photoplethysmogram and cardiovascular mortality in middle-aged and elderly Japanese women. Hypertens. Res. 2017, 40, 207–211. [Google Scholar] [CrossRef]
  132. Asyrafi, H.; Sunarno, F.; Waruwu, M.M.; Wijaya, R. Photoplethysmography (PPG) Signal-Based Chronological Age Estimation Algorithm. In Proceedings of the 2022 International Conference of Science and Information Technology in Smart Administration, Denpasar, Indonesia, 10–12 November 2022; ICSINTESA 2022. pp. 128–132. [Google Scholar]
  133. Tsai, P.-Y.; Huang, C.-H.; Guo, J.-W.; Li, Y.-C.; Wu, A.-Y.A.; Lin, H.-J.; Wang, T.-D. Coherence between decomposed components of wrist and finger ppg signals by imputing missing features and resolving ambiguous features. Sensors 2021, 21, 4315. [Google Scholar] [CrossRef]
  134. Rinkevĭcius, M.; Kontaxis, S.; Gil, E.; Bailón, R.; Lázaro, J.; Laguna, P.; Marozas, V. Photoplethysmogram Signal Morphology-Based Stress Assessment. In Proceedings of the 2019 Computing in Cardiology (CinC), Singapore, 8–11 September 2019. [Google Scholar]
  135. Santos, S.A.; Venema, B.; Leonhardt, S. Accelerometer-assisted PPG measurement during physical exercise using the LAVIMO sensor system. Acta Polytech. 2012, 52, 80–85. [Google Scholar] [CrossRef]
  136. Georgieva-Tsaneva, G.; Gospodinova, E.; Gospodinov, M.; Cheshmedzhiev, K. Portable sensor system for registration, processing and mathematical analysis of PPG signals. Appl. Sci. 2020, 10, 1051. [Google Scholar] [CrossRef] [Green Version]
  137. Elgendi, M. On the analysis of fingertip photoplethysmogram signals. Curr. Cardiol. Rev. 2012, 8, 14–25. [Google Scholar] [CrossRef] [PubMed]
  138. Pfefferbaum, A.; Chanraud, S.; Pitel, A.-L.; Shankaranarayanan, A.; Alsop, D.C.; Rohlfing, T.; Sullivan, E.V. Volumetric cerebral perfusion imaging in healthy adults: Regional distribution, laterality, and repeatability of pulsed continuous arterial spin labeling (PCASL). Psychiatry Res.—Neuroimaging 2010, 182, 266–273. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  139. Zhu, Q.; Tian, X.; Wong, C.-W.; Wu, M. Learning Your Heart Actions from Pulse: ECG Waveform Reconstruction from PPG. IEEE Internet Things J. 2021, 8, 16734–16748. [Google Scholar] [CrossRef]
  140. Huotari, M.; Maatta, K.; Kostamovaara, J. A pulse waveform data decomposition based on multi component curve fit compared with second derivative photoplethysmography and phase plane plot. In Proceedings of the BIOSIGNALS 2011—International Conference on Bio-Inspired Systems and Signal Processing, Rome, Italy, 26–29 January 2011; pp. 477–480. [Google Scholar]
  141. Reddy, G.N.K.; Manikandan, M.S.; Murty, N.V.L.N. Evaluation of Objective Distortion Measures for Automatic Quality Assessment of Processed PPG Signals for Real-Time Health Monitoring Devices. IEEE Access 2022, 10, 15707–15745. [Google Scholar] [CrossRef]
  142. Ryu, M.-O.; Lee, S.; Baek, K.-K. A study on the Brain function specialty based on the Maladaptive Soldier by Brain waves analysis. J. Korean Soc. Ind. Eng. Technol. 2014, 15, 1916–1922. [Google Scholar]
  143. Moghaddam, B. Stress activation of glutamate neurotransmission in the prefrontal cortex: Implications for dopamine-associated psychiatric disorders. Biol. Psychiatry 2002, 51, 775–787. [Google Scholar] [CrossRef]
  144. Popoli, M.; Yan, Z.; McEwen, B.S.; Sanacora, G. The stressed synapse: The impact of stress and glucocorticoids on glutamate transmission. Nat. Rev. Neurosci. 2012, 13, 22–37. [Google Scholar] [CrossRef] [Green Version]
  145. Swanson, C.J.; Bures, M.; Johnson, M.P.; Linden, A.-M.; Monn, J.A.; Schoepp, D.D. Metabotropic glutamate receptors as novel targets for anxiety and stress disorders. Nat. Rev. Drug Discov. 2005, 4, 131–144. [Google Scholar] [CrossRef]
  146. Hennebelle, M.; Champeil-Potokar, G.; Lavialle, M.; Vancassel, S.; Denis, I. Omega-3 polyunsaturated fatty acids and chronic stress-induced modulations of glutamatergic neurotransmission in the hippocampus. Nutr. Rev. 2014, 72, 99–112. [Google Scholar] [CrossRef]
  147. Berridge, C.W.; Waterhouse, B.D. The locus coeruleus-noradrenergic system: Modulation of behavioral state and state-dependent cognitive processes. Brain Res. Rev. 2003, 42, 33–84. [Google Scholar] [CrossRef] [PubMed]
  148. Sanchez-Gonzalez, M.A.; May, R.W.; Koutnik, A.P.; Kabbaj, M.; Fincham, F.D. Sympathetic vasomotor tone is associated with depressive symptoms in young females: A potential link between depression and cardiovascular disease. Am. J. Hypertens. 2013, 26, 1389–1397. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  149. Kubzansky, L.D.; Koenen, K.C.; Spiro, A., III; Vokonas, P.S.; Sparrow, D. Prospective study of posttraumatic stress disorder symptoms and coronary heart disease in the normative aging study. Arch. Gen. Psychiatry 2007, 64, 109–116. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  150. Scherrer, J.F.; Chrusciel, T.; Zeringue, A.; Garfield, L.D.; Hauptman, P.J.; Lustman, P.J.; Freedland, K.E.; Carney, R.M.; Bucholz, K.K.; Owen, R.; et al. Anxiety disorders increase risk for incident myocardial infarction in depressed and nondepressed Veterans Administration patients. Am. Heart J. 2010, 159, 772–779. [Google Scholar] [CrossRef]
  151. Boscarino, J.A. A prospective study of PTSD and early-age heart disease mortality among vietnam veterans: Implications for surveillance and prevention. Psychosom. Med. 2008, 70, 668–676. [Google Scholar] [CrossRef] [Green Version]
  152. Tanaka, M.; Diano, M.; Battaglia, S. Editorial: Insights into structural and functional organization of the brain: Evidence from neuroimaging and non-invasive brain stimulation techniques. Front. Psychiatry 2023, 14, 1225755. [Google Scholar] [CrossRef]
  153. Borgomaneri, S.; Battaglia, S.; Sciamanna, G.; Tortora, F.; Laricchiuta, D. Memories are not written in stone: Re-writing fear memories by means of non-invasive brain stimulation and optogenetic manipulations. Neurosci. Biobehav. Rev. 2021, 127, 334–352. [Google Scholar] [CrossRef]
  154. Battaglia, S.; Harrison, B.J.; Fullana, M.A. Does the human ventromedial prefrontal cortex support fear learning, fear extinction or both? A commentary on subregional contributions. Mol. Psychiatry 2022, 27, 784–786. [Google Scholar] [CrossRef]
  155. Battaglia, S.; Garofalo, S.; di Pellegrino, G.; Starita, F. Revaluing the role of vmPFC in the acquisition of pavlovian threat conditioning in humans. J. Neurosci. 2020, 40, 8491–8500. [Google Scholar] [CrossRef]
  156. Liu, M.; Xie, X.; Xie, J.; Tian, S.; Du, X.; Feng, H.; Zhang, H. Early-onset Alzheimer’s disease with depression as the first symptom: A case report with literature review. Front. Psychiatry 2023, 14, 1192562. [Google Scholar] [CrossRef]
Figure 1. Omnifit headset.
Figure 1. Omnifit headset.
Brainsci 13 01157 g001
Figure 2. General characteristics of research subjects.
Figure 2. General characteristics of research subjects.
Brainsci 13 01157 g002
Table 1. Technical Statistics.
Table 1. Technical Statistics.
NAverageStandard DeviationStandard Error95% for the Mean
Confidence Interval
MinimumMaximum
Lower LimitUpper Limit
Concentration LevelGeneral
soldiers
1366.5552.00310.17186.2156.8952.010.0
Accident risk level 1 soldier426.5172.02040.31185.8877.1463.29.9
Accident risk level 2 soldier475.6491.59980.23345.1796.1192.69.8
Accident risk level 3 soldier265.1690.97680.19164.7755.5643.57.2
Subtotal2516.2351.91160.12075.9986.4732.010.0
Brain
activity
General
soldiers
13677.437.8830.67676.1078.774393
Accident risk level 1 soldier4278.008.1751.26175.4580.556195
Accident risk level 2 soldier4773.686.7630.98771.7075.675287
Accident risk level 3 soldier2672.696.6381.30270.0175.375781
Subtotal25176.337.8210.49475.3677.314395
Psychological stressGeneral
soldiers
1366.0961.28350.11015.8786.3133.710.0
Accident risk level 1 soldier425.7071.00860.15565.3936.0214.28.2
Accident risk level 2 soldier475.8701.23600.18035.5076.2333.88.9
Accident risk level 3 soldier265.6881.02030.20015.2766.1014.08.5
Subtotal2515.9461.21300.07665.7956.0973.710.0
Imbalance of left and right brain activityGeneral
soldiers
1365.0070.60240.05174.9055.1103.07.0
Accident risk level 1 soldier425.1670.48970.07565.0145.3195.07.0
Accident risk level 2 soldier475.0850.45820.06684.9515.2204.07.0
Accident risk level 3 soldier265.0380.82370.16154.7065.3713.07.0
Subtotal2515.0520.58760.03714.9795.1253.07.0
Table 2. Test for homogeneity of variance.
Table 2. Test for homogeneity of variance.
Levene Statisticsdf1df2CTT Significance
Concentration Level 6.73432470.000
Brain activity0.75632470.520
Psychological stress1.57732470.195
Imbalance of left and right brain activity0.45332470.715
Table 3. Analysis of variance (ANOVA) results for EEG.
Table 3. Analysis of variance (ANOVA) results for EEG.
The Sum of SquaresThe Degree of FreedomMean SquareFSignificance Probability
Concentration Level Between groups62.947320.9826.0930.001
Within the group850.6282473.444
The entire913.574250
Brain
activity
Between groups956.7333318.9115.4950.001
Within the group14,335.15624758.037
The entire15,291.888250
Psychological stressBetween groups7.43432.4781.6980.168
Within the group360.4102471.459
The entire367.844250
Imbalance of left and right brain activityBetween groups0.88030.2930.8480.469
Within the group85.4472470.346
The entire86.327250
Table 4. EEG Multicomparison Results.
Table 4. EEG Multicomparison Results.
Dependent VariableGroup (I)Group (J)Average Difference
(I–J)
Standardization
Error
Probability of
Significance
95% Confidence Interval
for the Average
Lower LimitUpper Limit
Dunnett T3Concentration
level
General
soldiers
Accident risk level 2 soldier0.9062 * 0.28980.0140.1291.683
Accident risk level 3 soldier1.3859 *0.25730.0000.6912.081
Accident risk level 1 soldierAccident risk level 3 soldier1.3474 *0.36590.0030.3552.340
ScheffeBrain activityGeneral soldiers
General
soldiers
Accident risk level 1 soldier−0.5661.3450.981−4.353.22
Accident risk level 2 soldier3.753 *1.2890.0390.127.38
Accident risk level 3 soldier4.742 *1.6310.0400.159.33
* Mean differences are significant at the 0.05 level.
Table 5. Technical Statistics.
Table 5. Technical Statistics.
NAverageStandard DeviationStandard Error95% for the Mean
Confidence Interval
MinimumMaximum
Lower LimitUpper Limit
Heart healthGeneral
soldiers
13613.77653.570910.3062013.170914.38202.0024.50
Accident risk level 1 soldier4213.72713.739570.5770312.561814.89256.3023.50
Accident risk level 2 soldier4712.36703.256480.4750111.410913.32326.6825.00
Accident risk level 3 soldier2613.38854.110290.8060911.728315.04865.8524.00
Subtotal25113.46413.620980.2285513.014013.91422.0025.00
Body stressGeneral
soldiers
13643.6844.91660.421642.85044.51830.062.0
Accident risk level 1 soldier4244.2145.69350.878542.44045.98933.066.0
Accident risk level 2 soldier4746.3624.91420.716844.91947.80534.058.0
Accident risk level 3 soldier2646.8856.15351.206844.39949.37035.069.0
Subtotal25144.6065.31110.335243.94545.26630.069.0
Cumulative fatigueGeneral
soldiers
1364.8090.44750.03844.7334.8852.05.0
Accident risk level 1 soldier424.8570.35420.05464.7474.9684.05.0
Accident risk level 2 soldier474.6810.47120.06874.5434.8194.05.0
Accident risk level 3 soldier264.7310.53350.10464.5154.9463.05.0
Subtotal2514.7850.44890.02834.7294.8412.05.0
Physical
Vitality
General
soldiers
1364.9340.30310.02604.8824.9853.05.0
Accident risk level 1 soldier424.8330.53720.08294.6665.0013.05.0
Accident risk level 2 soldier474.8510.41590.06074.7294.9733.05.0
Accident risk level 3 soldier264.6540.74520.14624.3534.9553.05.0
Subtotal2514.8730.43780.02764.8184.9273.05.0
Autonomic nervous system healthGeneral
soldiers
1367.67460.759250.065107.54587.80335.689.17
Accident risk level 1 soldier427.66670.815870.125897.41247.92095.469.78
Accident risk level 2 soldier477.32090.837910.122227.07487.56695.638.79
Accident risk level 3 soldier267.51120.760820.149217.20397.81855.548.73
Subtotal2517.59010.791620.049977.49177.68855.469.78
Table 6. Test for homogeneity of variance.
Table 6. Test for homogeneity of variance.
Levene Statisticsdf1df2CTT Significance
Heart health0.92432470.430
Body Stress0.10032470.960
Cumulative fatigue4.18632470.006
Physical Vitality13.00832470.000
Autonomic nervous system health0.20532470.893
Table 7. Analysis of variance (ANOVA) results for Pulse Wave.
Table 7. Analysis of variance (ANOVA) results for Pulse Wave.
The Sum of SquaresThe Degree of FreedomMean SquareFSignificance Probability
heart healthBetween groups72.893324.2981.8730.135
Within the group3204.97624712.976
The entire3277.869250
Body StressBetween groups401.9713133.9904.9770.002
Within the group6649.98124726.923
The entire7051.952250
Cumulative
fatigue
Between groups0.88230.2941.4670.224
Within the group49.5002470.200
The entire50.382250
Physical vitalityBetween groups1.84130.6143.2890.021
Within the group46.0802470.187
The entire47.921250
Autonomic
nervous system health
Between groups4.78631.5952.5940.053
Within the group151.8802470.615
The entire156.666250
Table 8. Pulse Wave Multicomparison Results.
Table 8. Pulse Wave Multicomparison Results.
Dependent
Variable
Group (I)Group (J)Average Difference
(I–J)
Standardization
Error
Probability
of
Significance
95% Confidence
Interval for the
Average
Lower LimitUpper Limit
ScheffeBody
stress
General
soldiers
Accident risk level 1 soldier−0.53050.91600.953−3.1092.048
Accident risk level 2 soldier−2.6779 *0.87790.027−5.149−0.207
Accident risk level 3 soldier−3.2008 *1.11060.042−6.327−0.075
Dunnett t Physical vitalityGeneral
soldiers
Accident risk level 3 soldier0.2008 *0.09520.007−0.0660.494
Accident risk level 1 soldierAccident risk level 3 soldier0.17950.10780.200−0.0700.429
Accident risk level 2 soldierAccident risk level 3 soldier0.1970 *0.10560.1350.0470.441
* Mean differences are significant at the 0.05 level.
Table 9. EEG, pulse wave, maladjustment, and suicidal ideation index averages.
Table 9. EEG, pulse wave, maladjustment, and suicidal ideation index averages.
AverageStandard
Deviation
N
Concentration Level6.2351.9116251
Brain activity76.337.821251
Psychological stress5.9461.2130251
Imbalance of left and right brain activity5.0520.5876251
Body Stress44.6065.3111251
Cumulative fatigue4.7850.4489251
heart health13.46413.62098251
Physical vitality4.8730.4378251
Autonomic nervous
system health
7.59010.79162251
Maladjustment2.20831.11388240
Suicidal concerns1.92691.13635240
Table 10. Correlation between EEG and pulse wave indices.
Table 10. Correlation between EEG and pulse wave indices.
Body StressCumulated
Fatigue
Heart HealthPhysical
Vitality
Autonomic
Neuronal
System Activity
Concentration LevelPearson
correlation
−0.1020.0510.0620.0660.134 *
Probability of
significance
(both sides)
0.1090.4180.3270.3000.034
N251251251251251
Brain activityPearson
correlation
−0.036−0.0390.038−0.0950.034
Probability of
significance
(both sides)
0.5690.5420.5450.1340.588
N251251251251251
Psychological stressPearson
correlation
−0.0770.0620.0040.1090.050
Probability of
significance
(both sides)
0.2210.3310.9510.0850.432
N251251251251251
Imbalance of left and right brain activityPearson
correlation
−0.0420.073−0.048−0.0210.034
Probability of
significance
(both sides)
0.5060.2510.4490.7420.596
N251251251251251
* Correlation is significant at 0.05 level (both sides).
Table 11. Correlating brain wave indices with survey results.
Table 11. Correlating brain wave indices with survey results.
Concentration LevelBrain ActivityPsychological StressImbalance of Left and Right Brain Activity
MaladjustmentPearson
correlation
−0.203 **−0.198 **−0.101−0.004
Probability of
significance
(both sides)
0.0020.0020.1170.951
N240240240240
Suicidal
concerns
Pearson
correlation
−0.216 **−0.229 **−0.073−0.004
Probability of
significance
(both sides)
0.0010.0000.2590.946
N240240240240
** Correlation is significant at 0.01 level (both sides).
Table 12. Correlate pulse wave index with survey results.
Table 12. Correlate pulse wave index with survey results.
Body StressCumulative FatigueHeart HealthPhysical
Vitality
Autonomic Nervous System Health
MaladjustmentPearson
correlation
0.201 **−0.088−0.068−0.182 **−0.114
Probability of
significance
(both sides)
0.0020.1720.2960.0050.078
N240240240240240
Suicidal
concerns
Pearson
correlation
0.231**−0.108−0.086−0.131 *−0.123
Probability of
significance
(both sides)
0.0000.0950.1840.0430.057
N240240240240240
* Correlation is significant at 0.05 level (both sides). ** Correlation is significant at 0.01 level (both sides).
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Choi, S.-O.; Choi, J.-G.; Yun, J.-Y. A Study of Brain Function Characteristics of Service Members at High Risk for Accidents in the Military. Brain Sci. 2023, 13, 1157. https://doi.org/10.3390/brainsci13081157

AMA Style

Choi S-O, Choi J-G, Yun J-Y. A Study of Brain Function Characteristics of Service Members at High Risk for Accidents in the Military. Brain Sciences. 2023; 13(8):1157. https://doi.org/10.3390/brainsci13081157

Chicago/Turabian Style

Choi, Sung-Oh, Jong-Geun Choi, and Jong-Yong Yun. 2023. "A Study of Brain Function Characteristics of Service Members at High Risk for Accidents in the Military" Brain Sciences 13, no. 8: 1157. https://doi.org/10.3390/brainsci13081157

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop