Document Type : Original Research

Authors

1 Department of Biomedical Engineering, Kermanshah University of Medical Sciences, Kermanshah, Iran

2 Department of Radiology, Firoozgar Hospital, Iran University of Medical Sciences, Tehran, Iran

3 Department of Radiology, School of Paramedicine, Iran University of Medical Sciences, Tehran, Iran

4 Department of Psychology, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran

5 Department of Radiology and Nuclear Medicine, Faculty of Paramedical, Kermanshah University of Medical Sciences (KUMS), Kermanshah, Iran

10.31661/jbpe.v0i0.2408-1813

Abstract

Background: Selective attention is the ability to concentrate on specific sensory inputs while ignoring other stimuli and sensory inputs, and it is related to job performance, especially in military personnel.
Objective: This study aimed to evaluate selective attention in military personnel rather than normal individuals.
Material and Methods: In this cross-sectional study, 40 individuals were divided into two groups: military personnel and normal individuals. Participants were shown a modified flanker task in a military environment, and functional magnetic resonance imaging (fMRI) was used to assess brain activation and functional connectivity through an attention task.
Results: Military personnel demonstrated quicker response times than civilians in both high- and low-threat environments, particularly in incongruent trials. In high-threat scenarios, the left Medial Frontal Gyrus (MFG) showed increased voxel counts, while the right MFG was more active in low-threat trials. Additionally, military personnel exhibited stronger functional connectivity in attention regions compared to civilians. 
Conclusion: Functional connectivity analysis reveals that military personnel show increased connectivity in attention regions during high-threat situations, indicating adaptive neural strategies for managing danger. The study also finds that congruent stimuli demand less neural coordination than incongruent ones, resulting in the understanding improvement of threat perception and attentional processes in military contexts, with significant implications for training and performance.

Highlights

Hamid Sharini (Google Scholar)

Maziar Jalalvandi (Google Scholar)

Keywords

Introduction

The brain is a complex network with specific functions like attention, information processing, and executive function. Selective attention improves the processing of stimuli by directing the mind toward a particular aspect, thereby diminishing the influence of extraneous information and directing human cognition and behavior toward objectives. Early cognitive science theories likened selective attention to a mental filter, sifting through incoming information and prioritizing what matters most [ 1 ]. Thus, selective attention as a subset of the cognitive control ability of the brain plays a decisive role in recognizing useful information and ignoring unnecessary information in humans and also allows individuals to focus on aspects of a situation that align with their goals while disregarding irrelevant information [ 2 ].

Cognitive control is necessary for the filtration of irrelevant information and the selection of optimal responses. It encompasses mental focus and attention directed towards specific tasks and is widely acknowledged to comprise three fundamental components: inhibition (including behavioral control), Working Memory (WM), and cognitive flexibility (also referred to as mental flexibility) [ 3 , 4 ]. Inhibitory attention control means selectively choosing and focusing on specific information and suppressing attention to another stimulus in space [ 5 ]. This mechanism requires coordination between different cognitive abilities, including short-term memory, decision-making, task-keeping, response selection, and suppression. The flanker task, as a cognitive test that examines selective attention and executive control, requires a prompt and correct response to the target stimuli. This task typically includes congruent and incongruent trials. In congruent trials, matching stimulus and target leads to quicker responses. In incongruent trials, different stimuli cause interference, slowing down responses [ 6 ]. The difference in Response Time (RTs) between incongruent and congruent conditions measures the ability to overcome cognitive conflicts.

The flanker task assesses attention by measuring focus, accuracy, and selective attention efficiently. Several studies explore brain regions in conflict processing at different levels: detection, assessment, and action consequence evaluation. In particular, the dorsolateral prefrontal cortex (DLPFC) and anterior cingulate cortex (ACC) are involved in conflict detection and resolution. In different studies, it is assumed that the ACC recognizes the interference between the input information flow to the brain and increases attention to the relevant stimuli by sending a signal to the frontal cortex while reducing interference. The medial frontal cortex (MFC) is involved in performance monitoring, and response conflict left inferior frontal gyrus suppresses irrelevant information in terms of meaning [ 7 - 9 ].

In recent decades, neuroimaging research has revealed insights into brain functions and structures. Advancements in functional neuroimaging now offer improved methods to assess brain region connections. Functional connectivity is specified as the temporal dependences of neuron activation patterns of structurally separate brain areas. Furthermore, different research has shown the ability to recognize functional connections between brain areas during different tasks. Various task-oriented functional magnetic resonance imaging (fMRI) investigations have significantly enhanced our understanding of the brain areas engaged in performing specific tasks [ 10 ]. On the other hand, attention is crucial for job performance, particularly in roles requiring precision and speed, like military personnel. Emotional control, accuracy, focus, and selective attention are critical topics in military, psychological, and neurocognitive studies. One of the main parts of military training is mental preparation exercises. Mental preparation involves utilizing thoughts, emotions, behaviors, and activities to exhibit purposeful behavior in high-pressure situations. The effectiveness of mental training programs for enhancing the psychological readiness of military personnel lacks accurate data, particularly regarding their attention. An important question in human psychology, especially in very stressful jobs, such as soldiers and pilots, is whether brain imaging features can train and increase the soldier’s attention in different situations (danger and safe conditions). Therefore, this study evaluated the brain by focusing on areas of related attention in different war environment conditions. Consequently, the current study aimed to explore one or more clearly defined, lightly replicable, and highly dependable brain functional networks, which are believed to coincide with patterns of activation or deactivation while performing attentional tasks like the flanker test.

Scope of the present study

This study examined brain activity related to cognitive control in military personnel compared to normal individuals to identify differences. Military personnel’s quick decision-making and emotional regulation were crucial for their job performance. The study hypothesized that military personnel would exhibit higher mental fitness due to their occupational demands. The flanker task was conducted in high- and low-threat zones to mimic military work environments and assess brain responses. fMRI was used to compare brain activity and stimulus responses between military and non-military individuals, with a focus on attention and cognitive processing regions.

Material and Methods

Participants

In this cross-sectional study, 40 healthy men participated in this study. Two groups of volunteers with an equal number of participants were selected for the study: military personnel (mean age 27.3±2.38 years) and normal individuals (mean age 28.4±3.46 years). The individuals who took part in the study were all right-handed, which was a specific criterion for inclusion. Furthermore, they were thoroughly screened to confirm that none of them had any psychiatric or neurological disorders that could potentially interfere with the research outcomes. Additionally, it was ensured that none of the participants suffered from claustrophobia, which could affect their comfort during the study. Additionally, none of the participants possessed any metal fragments in their bodies, such as pacemakers, which could pose risks during the procedures involved. Each participant was also a native speaker of Persian, ensuring that language barriers did not impact the study’s effectiveness or the data collection process. Figure 1 shows the flowchart of the current study.

Figure 1. The flowchart illustrates the steps involved in functional magnetic resonance imaging (fMRI) data analysis, from subject selection and task design to group-level statistical analysis.

Flanker Task

The flanker cognitive task assesses inhibitory response by measuring the ability to ignore irrelevant stimuli amidst related ones. We created a modified version featuring varying levels of conflict. In the traditional patterns of the Eriksen–Flanker task, congruent trials consist of >>>>>, and incongruent trials consist of >><>>. Congruent trials are those, where the target and distractors are all oriented in the same direction (e.g., all arrows pointing right). Incongruent trials are those where the distractors are oriented in a different direction than the target (e.g., target pointing right, distractors pointing left).

The flanker task was modified for a simulated military environment, requiring participants to focus more than in traditional settings. The proposed design considered individuals’ job and operational conditions to better reflect military work scenarios.

Participants completed a modified flanker task in high- and low-threat zones. In low-threat zones, peaceful backgrounds were used, while war and military operation images were shown in high-threat zones. Subjects were instructed to select the correct answer in both incongruent and congruent conditions. We used four blocks of modified flanker tasks; each block included 24 task trials (including 2 congruent and 12 incongruent trials); a total of 96 trials (48 trials in low-threat zones and 48 trials in high-threat zones) randomly were shown to each participant. The interval time (Inter-Trial Interval (ITI)) between each block was 12 seconds. The interval between stimuli was 1.5-3 seconds; each trial was shown for 2 s. These trials are shown to participants in two-dimensional frames at specific times. The subject must press certain buttons at a maximum speed of 2000 ms based on the direction of the arrow and select the appropriate answer. Results are displayed regarding the number and percentage of correct responses for congruent and incongruent stimuli in each block and the average reaction time in milliseconds for congruent and incongruent stimuli in each block. Figure 2 delineates the various trial types in the flanker task.

Figure 2. The figure illustrates the different trial types used in the flanker task, showcasing congruent and incongruent stimuli in both low-threat and high-threat zones.

Image Acquisition

The fMRI images were acquired using a 3 Tesla Magnetic Resonance Imaging (MRI) System with a standard twenty-channel head coil. A high-resolution T1-weighted brain image was obtained for each participant, comprising 176 continuous slices captured using a magnetization-prepared rapid gradient echo (MPRAGE[P2]) sequence (Repetition Time (TR)=2500 ms, Echo Time (TE)=3.93 ms, TI=900 ms, Field of View (FOV)=256[P3]×256 mm2, acquisition matrix=256×256, voxel size=1 mm3). Whole-brain functional volumes were acquired through Echo Planar Imaging (EPI) with a TE of 30 ms and a TR of 2000 ms, utilizing an 80° flip angle. A total of 40 continuous slices (3mm×3mm×4mm) were gathered. Additionally, the PsychoToolbox-3 software was employed to present tasks to participants.

Behavioral Analysis

Response Times (RT) for accurate answers were calculated in congruent and incongruent trials. Reaction times (RTs) were calculated as the time elapsed between trial onset and key press (in milliseconds). Only correct responses were included in the ANOVA analysis, conducted at the 5% significance level.

fMRI Data Analysis

The fMRI data were analyzed using the SPM12 toolbox (http://www.fil.ion.ucl.ac.uk/spm/software/spm12), running on MATLAB 2016a. The data pre-processing phases contained the following: field map correction, co-registration of functional and anatomical scans, realignment, segmentation, normalization, and smoothing. Brain activation analysis involved first-level and second-level analyses. First-level maps were created for participants using a linear regression model with two event-related regressors (congruent and incongruent trials). Second-level analysis calculated similarities and differences in data, with activation maps derived from a fixed-effect general linear model [ 11 ]. The General Linear Model (GLM) serves as a robust technique for analyzing fMRI data, utilized to assess the variability of activity across various conditions. The GLM can accommodate both qualitative and quantitative independent variables and is represented through an equation that includes: predictors, parameters, and errors. We set P-value=0.05 and a minimum of 20 voxels to identify activated brain areas, reducing false positives.

Functional Connectivity

Functional connectivity modeling determines activated brain regions and mostly depends on interregional communication. It can also assess the relationships between regions and particular pathways in the cerebral cortex, as well as the temporal dependence of activation (causality) within brain regions [ 12 ]. In the current research, functional connectivity modeling was used to detect the connectivity patterns in the brain attention network while executing the attentional flanker task. Graph theory posits the brain as a sophisticated neuronal network made up of various nodes and edges, facilitating the examination of the topological arrangement of brain correlation networks. Th the overall and specific attributes of brain regions can be assessed based on the graph theory [ 13 , 14 ]. At this stage, fMRI functional analysis was performed to extract the brain attention network using the ROI-to-ROI (region of interest) function in the CONN toolbox. For two-way ROI-to-ROI analysis, False Discovery Rate (FDR) analysis was considered for different brain parts that are involved in attention processing, such as frontal eye field (FEF), Lateral Prefrontal Cortex (LPFC), Insular Cortex (IC), Superior Parietal Lobule (SPL), Anterior Cingulate Cortex (ACC), precuneus, and thalamus regions. General and regional brain characteristics for different ROIs were obtained using graph theory analysis and calculating the correlation coefficients and their FDR-corrected values with a significant P-value≤0.05.

Results

a) Behavioral Results

Mean response times were calculated for incongruent and congruent trials in military personnel and normal individuals. In high-threat zones, incongruent RT was 731.2±161.2 ms for the military and 801±99.2 ms for normal individuals; congruent RT was 627.6±146.5 ms for the military and 682.4±102.3 ms for normal individuals. In low-threat zones, incongruent RT was 711.9±253.8 ms for the military and 752±105.9 ms for normal individuals; congruent RT was 590.5±181.1 ms for the military and 644.3±109.1 ms for normal individuals. Figure 3 shows response time in behavioral assessments during the flanker conflict task.

Figure 3. Behavioral response time during the conflict flanker task.

The average errors in the incongruent conditions of the high- and low-threat zones, as well as in the simple mode of the flanker task were 96.32±6.43 and 97.01±5.02 for military personnel and 94.63±7.89 and 95.74±6.12 for normal individuals, respectively. In congruent trials, the average errors in the military group were 97.28±5.36 and 97.86±4.57, and 95.77±6.21 and 96.39±4.68 in normal individuals, respectively. Table 1 illustrates the findings of the flanker task related to behavior.

Task Trials Military Personnel (mean±sd) Normal Individuals (mean±sd) P_value
Incongruent Conditions High_threat zones 96.32±6.43 94.63±7.89 0.048
Low_threat zones 97.01±5.02 95.74±6.12 0.037
Congruent Conditions High_threat zones 97.28±5.36 95.77±6.21 0.042
Low_threat zones 97.86±4.57 96.39±4.68 0.136
Table 1. Behavioral results of flanker task. There were differences between conditions for accuracy (P<0.05).

b) fMRI Data Analysis Result

The group analysis showed that in military personnel, the left Medial prefrontal cortex (NVox=301) is one of the brain areas with the highest activation during the incongruent trials in high-threat zones. Analysis of brain activation maps revealed that military personnel exhibited peak activity in the right medial frontal gyrus during low-threat zones (NVox=216). In contrast, normal individuals showed maximum activation in the left medial prefrontal cortex (NVox=238) and inferior frontal gyrus (NVox=208) during incongruent trials of the flanker task across varying threat levels. Table 2 shows cortical activations in the brain concerning the attention network under incongruent conditions across various trials of the flanker task, compared between the two participant groups.

Military Personnel Normal Individuals
Contrast Map and Brain Region Cluster Size Analysis (z) Contrast Map and Brain Region Cluster Size Analysis (z)
High_threat zones L Medial PFC 301 5.2645 L Medial PFC 238 4.3093
Cingulate Gyrus 83 3.4467 Cingulate Gyrus 64 3.9213
Thalamus 54 3.4097 Thalamus 61 3.4787
R Insular cortex 97 4.5653 R Insular cortex 89 4.2548
L Insular cortex 71 5.1186 L Insular cortex 47 4.2605
Parietal cortex 128 4.6234 Parietal cortex 119 3.7055
L Superior frontal gyrus 251 4.1311 L Superior frontal gyrus 202 3.9551
R Superior frontal gyrus 108 3.8324 R Superior frontal gyrus 126 3.9118
L Middle Frontal Gyrus 167 4.8581 L Middle Frontal Gyrus 79 2.6816
R Middle Frontal Gyrus 84 4.2567 R Middle Frontal Gyrus 33 3.8985
L Superior Temporal Gyrus 45 -3.6236 L Superior Temporal Gyrus ------- -------
R Superior Temporal Gyrus 31 4.0256 R Superior Temporal Gyrus ------- -------
R Inferior Temporal Gyrus ------- ------- R Inferior Temporal Gyrus 42 -2.7536
Low_threat zones R Medial PFC 216 5.0205 R Medial PFC 176 4.949
Cingulate Gyrus 51 4.6693 Cingulate Gyrus ------- --------
Thalamus 40 -2.4592 Thalamus 52 3.9215
R Insular cortex 73 2.5131 R Insular cortex 60 -3.6361
Parietal cortex 93 3.5743 Parietal cortex 81 3.875
L Superior frontal gyrus 206 3.9558 L Superior frontal gyrus 208 3.8128
R Superior frontal gyrus 121 3.4658 R Superior frontal gyrus 132 3.1342
R Middle Frontal Gyrus 62 5.7288 R Middle Frontal Gyrus 41 3.4426
R Middle Temporal Gyrus 33 2.3245 R Middle Temporal Gyrus 29 2.1425
R Inferior Temporal Gyrus 37 -2.2175 R Inferior Temporal Gyrus 49 2.4865
PFC: Prefrontal Cortex
Table 2. Brain cortical activations relative to attention network in incongruent condition during different trials of flanker task between the two groups of participants.

Activation maps obtained from congruent trials showed that military personnel exhibited maximum activity in different brain regions under varying threat conditions. In high-threat zones, the left medial prefrontal cortex (NVox=227) displayed maximum activity, while in low-threat zones, the left superior frontal cortex (NVox=175) showed the highest activation. Figure 4 demonstrates maps of brain activation for the flanker task involving conflict. In normal individuals, brain activation patterns differed based on the perceived threat level during task performance. During high-threat zone tasks, the left superior frontal gyrus (NVox=191) showed the highest activation. Conversely, in low-threat zone tasks, the left medial prefrontal cortex (NVox=146) displayed maximum activity. Table 3 shows cortical activations linked to the attention network in the congruent condition during flanker task trials for both participant groups.

Figure 4. Brain activation maps for conflict flanker task. a) High-threat zones, b) low-threat zones. Brain activation maps displaying voxels with different blood oxygenation level dependent (BOLD) responses to cue incongruent trials (incongruent vs. congruent trials) in distinct regions of brain (Red indicates the brain activity of military personnel and blue indicates the brain activity of normal individuals).

Military Personnel Normal People
Contrast Map and Brain Region Cluster Size Analysis (z) Contrast Map and Brain Region Cluster Size Analysis (z)
High_threat zones L Medial PFC 227 4.9816 L Medial PFC 173 4.3215
Cingulate Gyrus 60 3.9213 Cingulate Gyrus 54 2.8493
Thalamus 41 3.0312 Thalamus 48 -2.5924
L Insular cortex 58 3.6118 L Insular cortex 39 2.3499
Parietal cortex 107 3.3055 Parietal cortex 97 3.3364
L Superior frontal gyrus 198 3.9551 L Superior frontal gyrus 191 4.0221
R Superior frontal gyrus 116 3.2605 R Superior frontal gyrus 106 3.5653
L Middle Frontal Gyrus 97 4.8985 L Middle Frontal Gyrus 51 2.6327
R Middle Frontal Gyrus 65 -2.8931 R Middle Frontal Gyrus 36 -2.3965
R Middle Temporal Gyrus 24 -2.5912 R Middle Temporal Gyrus ------- -------
L Precentral Gyrus 37 2.7634 L Precentral Gyrus ------- -------
Low_threat zones L Medial PFC 152 4.1838 L Medial PFC 146 3.9196
Cingulate Gyrus 43 2.9156 Cingulate Gyrus 48 -2.6909
Thalamus 38 -2.519 Thalamus 31 2.4618
L Insular cortex 44 3.0494 L Insular cortex 29 -2.3547
Parietal cortex 89 3.2707 Parietal cortex 65 3.1157
L Superior frontal gyrus 175 3.7765 L Superior frontal gyrus 127 3.4236
R Superior frontal gyrus 91 3.4722 R Superior frontal gyrus 72 3.0494
L Middle Frontal Gyrus 61 3.1139 L Middle Frontal Gyrus 42 2.8623
R Middle Temporal Gyrus 72 3.2018 R Middle Temporal Gyrus 80 3.1057
R Superior Temporal Gyrus 38 2.6257 R Superior Temporal Gyrus ------- -------
PFC: Prefrontal Cortex
Table 3. Brain cortical activations relative to attention network in congruent condition during different trials of flanker task between the two groups of participants.

Functional Connectivity Analysis

In the military group, during incongruent mode in the high-threat zone part, the IC l region had a powerful functional connection to the IC r region and the IC l region to the thalamus left and right regions. In the normal group, the IC l region was functionally connected to IC r and the right thalamus. In the low- threat zone, in military personnel, the IC r was connected to the IC l, and in normal individuals, the SPL r had a more powerful functional connection to the SPL l. Figure 5 shows functional connectivity under incongruent conditions.

Figure 5. Functional connectivity in incongruent condition. a) High-threat zone, b) low-threat zone. There were more and powerful connections in military personnel than normal individuals.

In military personnel and under incongruent conditions, connections between SPL l to AC and IC r to SPL r are shown to have the lowest connection power in high-threat zones tasks, as well as in normal individuals; they are shown to have the lowest connection power between Thalamus l to Precuneous and SPL r to IC r. In low-threat zones, military personnel and normal individuals have lesser connection power than in other regions, respectively in FEF l to LPFC l and thalamus l to AC. Functional analysis showed that military personnel during incongruent conditions have more functional brain connections between attention regions than normal individuals. Table 4 presents graph theory analysis of functional connectivity values for military and civilian individuals during incongruent flanker tasks in high and low threat zones).

Military Personnel Normal People
Functional connectivity T p.FDR Functional connectivity T p.FDR
High_threat zones IC r - IC l 13.90 0.0004 IC l-IC r 18.40 0.0000
IC l -IC r 13.90 0.0004 IC r-IC l 18.40 0.0000
IC l- Thalamus l 8.83 0.0017 Thalamus r-Thalamus l 13.77 0.0000
Thalamus l- IC l 8.83 0.0034 Thalamus l-Thalamus r 13.77 0.0000
Thalamus l-Thalamus r 7.97 0.0055 SPL r-SPL l 10.38 0.0000
Thalamus r-Thalamus l 7.97 0.0055 SPL l-SPL r 10.38 0.0000
IC r- AC 6.41 0.0075 LPFC l-LPFC r 6.37 0.0014
SPL l-SPL r 7.40 0.0078 LPFC r-LPFC l 6.37 0.0014
SPL r-SPL l 7.40 0.0078 Thalamus l-AC 5.43 0.0023
AC- IC r 6.41 0.0079 Thalamus r-IC l 5.02 0.0029
AC-IC r -5.88 0.0079 Thalamus r-IC r 4.96 0.0029
IC l -AC 5.79 0.0079 IC l-Thalamus r 5.02 0.0033
AC- IC l 5.79 0.0079 IC l-AC 4.85 0.0033
IC l- SPL r 4.56 0.0123 IC r-Thalamus r 4.96 0.0043
IC l- SPL l 4.46 0.0123 AC-Thalamus l 5.43 0.0046
IC l-IC r -4.45 0.0123 AC-IC l 4.85 0.0050
IC r-AC -5.88 0.0134 IC l-SPL l 4.36 0.0050
IC r-IC l 5.64 0.0134 AC-IC r 4.35 0.0068
IC r-SPL l 4.78 0.0183 IC r-AC 4.35 0.0068
IC l-Precuneous 3.63 0.0237 AC-Thalamus r 3.98 0.0088
IC r-IC l -4.45 0.0239 Thalamus r-AC 3.98 0.0088
IC r-Precuneous -3.82 0.0239 SPL l-IC l 4.36 0.0100
IC l-Thalamus l -3.79 0.0239 AC-FEF l 3.44 0.0162
SPL l-IC r 4.78 0.0243 IC l-Thalamus l 3.37 0.0182
SPL l-IC l 4.46 0.0243 IC r-SPL r 3.31 0.0248
SPL l-Precuneous 3.96 0.0266 IC l-SPL r 3.01 0.0270
SPL l-Thalamus l 3.84 0.0266 Thalamus l-IC l 3.37 0.0303
Precuneous-SPL l 3.96 0.0332 Thalamus l-Precuneous 2.91 0.0477
Precuneous-IC r -3.82 0.0332 SPL r-IC r 3.31 0.0496
Precuneous-IC l 3.63 0.0332 ………. ……. …….
SPL r-IC l 4.56 0.0333 ………. ……. …….
IC r-Thalamus l 3.25 0.0416 ………. ……. …….
SPL r-Precuneous 3.65 0.0430 ………. ……. …….
SPL l-AC 3.20 0.0439 ………. ……. …….
IC r-SPL r 3.01 0.0466 ………. ……. …….
Low_threat zones IC r-IC l 9.34 0.0001 SPL r-SPL l 9.67 0.0001
IC l-IC r 9.34 0.0001 SPL l-SPL r 9.67 0.0001
LPFC l-LPFC r 8.30 0.0002 Thalamus r-Thalamus l 8.97 0.0001
LPFC r-LPFC l 8.30 0.0002 Thalamus l-Thalamus r 8.97 0.0001
SPL r-SPL l 6.30 0.0015 IC l-IC r 8.31 0.0002
SPL l-SPL r 6.30 0.0015 IC r-IC l 8.31 0.0002
IC l-Thalamus r 5.70 0.0016 SPL r-FEF r 6.75 0.0005
IC l-Thalamus l 5.26 0.0019 FEF r-SPL r 6.75 0.0009
Thalamus r-IC l 5.70 0.0019 SPL l-FEF l 4.44 0.0090
Thalamus r-Thalamus l 5.56 0.0019 AC-Precuneous 4.58 0.0134
Thalamus l-Thalamus r 5.56 0.0029 IC r-AC 4.17 0.0134
Thalamus l-IC l 5.26 0.0029 AC-IC r 4.17 0.0134
IC l-AC 4.74 0.0029 Precuneous-AC 4.58 0.0145
Thalamus l-LPFC l 4.76 0.0038 LPFC l-LPFC r 4.57 0.0149
Thalamus l-IC r 4.26 0.0050 LPFC r-LPFC l 4.57 0.0149
Thalamus l-LPFC r 4.21 0.0050 FEF l-SPL l 4.44 0.0180
LPFC l-Thalamus l 4.76 0.0057 AC-Thalamus r 3.50 0.0190
Thalamus r-AC 4.35 0.0068 AC-LPFC l -3.48 0.0190
Thalamus r-IC r 4.06 0.0078 AC-Thalamus l 3.33 0.0193
AC-IC l 4.74 0.0101 AC-IC l 3.21 0.0196
AC-Thalamus r 4.35 0.0101 Thalamus r-AC 3.50 0.0369
IC r-Thalamus l 4.26 0.0104 LPFC l-AC -3.48 0.0379
IC r-Thalamus r 4.06 0.0104 LPFC l-FEF r -3.09 0.0478
LPFC r-Thalamus l 4.21 0.0125 Thalamus l-AC 3.33 0.0482
AC-Precuneous 3.84 0.0145 ………. ……. …….
AC-IC r 3.65 0.0147 ………. ……. …….
IC r-AC 3.65 0.0147 ………. ……. …….
IC l-FEF l 3.30 0.0203 ………. ……. …….
Thalamus r-Precuneous 3.22 0.0230 ………. ……. …….
Thalamus l-FEF l 2.97 0.0269 ………. ……. …….
Thalamus l-AC 2.92 0.0269 ………. ……. …….
IC r-FEF l 3.05 0.0302 ………. ……. …….
AC-Thalamus l 2.92 0.0377 ………. ……. …….
FEF l-IC l 3.30 0.0430 ………. ……. …….
FEF l-LPFC l -3.13 0.0430 ………. ……. …….
FDR: False Discovery Rate, IC: Insular Cortex, AC: Anterior Cingulate, SPL: Superior Parietal Lobule, LPFC: Lateral Prefrontal Cortex, FEF: Frontal Eye Field
Table 4. Functional connectivity values calculated using graph theory analysis for military personnel and normal people during incongruent condition in high and low threat zones Flanker task.

In the congruent condition, both military personnel showed less number of connections between different brain regions than in the incongruent. In the high-threat zone, military personnel show the highest and lowest power of connections in IC l to IC r and SPL r to FEF l, and normal individuals show IC r to IC l and LPFC l to LPFC r, respectively. Figure 6 shows functional connectivity under congruent conditions. In the low-threat zone, military personnel and normal individuals show the highest connection power in IC r to IC l and lowest in AC to IC l (Table 5) illustrates Graph theory analysis of functional connectivity in military personnel and civilians during congruent flanker tasks in high- and low-threat zones).

Figure 6. Functional connectivity analysis in congruent condition. a) High-threat zone, b) low-threat zone. There were more and powerful connections in military personnel than normal individuals.

Military Personnel Normal People
Functional connectivity T p.FDR Functional connectivity T p.FDR
High_threat zones IC l-IC r 10.08 0.0000 IC r-IC l 10.89 0.0001
IC r-IC l 10.08 0.0000 IC l-IC r 10.89 0.0001
Thalamus l-Thalamus r 7.41 0.0002 SPL r-SPL l 8.87 0.0033
Thalamus l-AC 7.41 0.0002 SPL l-SPL r 8.87 0.0033
SPL l-SPL r 7.77 0.0003 SPL r-LPFC l -6.44 0.0074
SPL r-SPL l 7.77 0.0003 LPFC l-SPL r -6.44 0.0148
Thalamus r-Thalamus l 7.41 0.0004 Thalamus r-Thalamus l 6.06 0.0195
AC-Thalamus l 7.41 0.0004 Thalamus l-Thalamus r 6.06 0.0195
LPFC l-LPFC r 7.07 0.0006 IC r-AC 4.04 0.0373
LPFC r-LPFC l 7.07 0.0006 IC r-FEF r 4.01 0.0373
SPL l-FEF r 4.98 0.0042 AC-Precuneous 4.44 0.0408
FEF r-SPL l 4.98 0.0071 AC-IC r 4.04 0.0408
FEF r-SPL r 4.60 0.0071 AC-Thalamus r 3.92 0.0408
SPL r-FEF r 4.60 0.0071 AC-IC l 3.61 0.0408
Thalamus r-IC r 4.36 0.0100 Thalamus r-AC 3.92 0.0412
IC r-Thalamus r 4.36 0.0100 LPFC l-LPFC r 3.88 0.0412
Thalamus r-IC l 3.81 0.0153 ………. ……. …….
Thalamus r-AC 3.61 0.0154 ………. ……. …….
IC l-Thalamus r 3.81 0.0229 ………. ……. …….
AC-Thalamus r 3.61 0.0309 ………. ……. …….
SPL r-FEF l 3.25 0.0369 ………. ……. …….
Low_threat zones IC r-IC l 11.90 0.0001 IC r-IC l 9.78 0.0004
IC l-IC r 11.90 0.0001 IC l-IC r 9.78 0.0004
SPL r-SPL l 8.87 0.0033 IC l-FEF l 8.83 0.0017
SPL l-SPL r 8.87 0.0033 FEF l-IC l 8.83 0.0034
SPL r-IC r -6.44 0.0074 Thalamus l-Thalamus r 7.97 0.0055
IC r-SPL r -6.44 0.0148 Thalamus r-Thalamus l 7.97 0.0055
Thalamus r-Thalamus l 6.06 0.0195 IC r-AC 6.41 0.0075
Thalamus l-Thalamus r 6.06 0.0195 SPL l-SPL r 7.40 0.0078
IC r-AC 4.04 0.0373 SPL r -SPL l 7.40 0.0078
IC-Precuneous 4.01 0.0373 AC-IC r 6.41 0.0079
AC-Precuneous 4.44 0.0408 AC-LPFC l -5.88 0.0079
AC-IC r 4.04 0.0408 IC l-AC 5.79 0.0079
AC-Thalamus r 3.92 0.0408 AC-IC l 5.79 0.0079
AC-IC l 3.61 0.0422 ………. ……. …….
FDR: False Discovery Rate, IC: Insular Cortex, AC: Anterior Cingulate, SPL: Superior Parietal Lobule, LPFC: Lateral Prefrontal Cortex, FEF: Frontal Eye Field
Table 5. Functional connectivity values calculated using graph theory analysis for military personnel and normal people during congruent condition in high and low threat zones Flanker task.

Discussion

This study utilized a modified flanker fMRI task to identify brain regions linked to stimulus incongruency. A modified flanker task assessed brain activation related to motivation and stress. GLM analysis showed activation changes during the conflict task, while functional connectivity analyses revealed complex networks post-attention. The research aimed to evaluate functional brain process changes between military and civilian individuals during congruent and incongruent effects.

The flanker task serves as an effective tool for evaluating selective attention, as it measures the ability to concentrate, accuracy, and attentional response to stimuli within a short time [ 15 ]. Selective attention and attention maintenance in particular situations, particularly in military employees, and those who need a high rate of attention to execute their tasks are essential topics in military and psychological research [ 16 , 17 ]. The results of the present study showed that the response time and error rate in all three conditions (congruent and incongruent task) in the military is less than in normal individuals. A similar study by Robert et al. on fighter pilots and normal individuals found similar results. Accordingly, although there were differences in response speed between the two groups in all conditions except during incongruent tasks in low-threat zone conditions, like the current study, Robert showed that pilots were more accurate and more responsive [ 18 ]. In this study, the error rate was lower in military personnel, indicating a higher inhibitory response rate. This means that it could be used to measure the ability to inhibit attention to related stimuli while ignoring irrelevant stimuli. Significant effects of stress were found on behavioral measures during the modified flanker task.

Also, results showed that the reaction time to incongruent conditions in both groups is higher than the congruent conditions, and this time is less in military personnel than in the control group. The diversity in RTs between incongruent and congruent trials is a measure of the ability to overcome cognitive conflicts. Incongruent and incongruent conditions, the medial prefrontal cortex, superior frontal gyrus, and middle frontal gyrus were mostly activated in military personnel in high- and low-threat zonesconditions. In normal individuals in high- and low-threat zones task, the medial PFC, insular cortex, and cingulate gyrus were the most activated, and our results are very similar to those of previous studies [ 19 , 20 ]. Military personnel exhibit significantly higher levels of selective attention in data analysis compared to civilians due to their precise and disciplined approach to tasks [ 21 ]. The findings of this study indicate that order and discipline in the military environment can improve selective attention. The results of the present study were in line with and confirmed previous studies. The results of a study on athletes from interceptive and strategic sports indicated the main role of PFC and Inferior Frontal Gyrus (IFG) in selective attention processing [ 22 ].

The brain’s medial and lateral frontal cortices play a crucial role in generating appropriate responses amidst conflicting options. Functional imaging research of the brain has consistently shown an increase in activity in the frontal areas during the performance of so-called “response conflict tasks” [ 23 ], but recent research suggests that different parts of the parietal lobule may be equally important [ 24 ].

Findings from earlier research and our investigation consistently indicate that the prefrontal cortex plays a crucial role in cognitive control, and it may also participate in conflict-related processes within the brain [ 20 , 25 - 28 ]. Investigating the connection changes between activated brain regions based on functional connectivity analysis in the military group during incongruent part has shown the most potent connection between the right IC and the left IC in high-threat and low-threat zones. In these areas, a stronger positive correlation with the default mode component was linked to increased overall activity induced by tasks. On the other hand, normal individuals were shown the strongest connection between the right IC and the left IC in the high-threat zone and between the right SPL and the left SPL in low-threat zones. Notably, the frontal and parietal areas, encompassing regions, such as the SPL, the FEF, and the IC, have shown consistent activation across different tasks that require spatially focused attention [ 20 , 24 , 29 ]. Various research indicates a frontoparietal network engaged in the processing of attention. Regions in the frontal and parietal lobes play a role in attentional regulation and processing during activities, implying that the mechanisms involved activate comparable neural systems.

The functional connectivity analysis revealed that military personnel exhibited more connections between brain regions involved in attention processing during most conditions of the modified flanker task compared to normal individuals. These connections suggest that military personnel engage more brain regions in attention processing, possibly due to stress effects, which may reflect the body’s defense mechanisms. In high-threat zone trials, the number of connections was more significant than in low-threat zones, and in high-threat zones, the power of those connections was more significant than in low-threat zones in most conditions. They believed those brain networks are involved in achieving and maintaining the alert state [ 30 ]. Neuroimaging reveals overlapping neural networks for attention in adults, involving frontal and parietal areas [ 14 ].

In this study, we could distinguish between selective attention in military personnel and normal individuals using the flanker task model. The results showed that the response to the stimulus in military personnel was shorter than in normal individuals. On the other hand, brain areas were activated with a greater number and extent in military personnel than in normal individuals, showing that military personnel have higher mental readiness in response to attention stimuli than ordinary individuals.

Despite the endeavors, the current study had some limitations, as follows: 1) while the study provides valuable insights into attentional control during modified visual flanker stimuli, the relatively small sample size of 40 healthy men limits the generalizability of the findings to the broader population and 2) the exclusive use of military personnel may introduce biases due to their unique characteristics and experiences. Future studies with larger and more diverse samples could help to address these limitations and enhance the robustness of the conclusions. It is recommended that a broader age range and a larger sample size be employed to improve future studies. The study’s findings may apply to other high-stress professions, such as firefighters and nurses. Future research could compare these groups to better understand the effects of stress across different occupations. Also, a longitudinal study in the future could offer additional insights into the long-term implications of this training.

Conclusion

Military environments affect personnel’s physical and cognitive performance, increasing human error due to stress. Research utilizing GLM and functional connectivity analyzed brain networks during the flanker task, revealing distinct neural connectivity patterns in attention processing. Increased activity in the frontal cortex and parietal lobule was observed, with different brain activation maps for congruent and incongruent trials. This study demonstrates the potential of fMRI as a tool to assess military readiness and recommends further research on cognitive tasks, especially those involving female participants, to deepen our understanding of selective attention in military personnel.

Acknowledgment

The authors wish to thank the AJA University of Medical Sciences for the financial and instrumental support of this research.

Authors’ Contribution

M. Jalalvandi conceived the idea. Introduction of the paper was written by H. Sharini, E. Rajeyan, and M. Jalalvandi. Sh. Faraji and E. Rajeyan gathered the images and the related literature. The method implementation was carried out by H. Sharini, A. Faramarzi, M. Ahmadi, and M. Jalalvandi. Results and Analysis was carried out by Sh. Faraji and M. Jalalvandi. The manuscript was revised by M. Jalalvandi, H. Sharini, and M. Ahmadi. All the authors read, modified, and approved the final version of the manuscript.

Ethical Approval

The protocol of the human study was approved by the Local Ethics Committee of AJA University of Medical Sciences (approval number: IR.AJAUMS.REC.1398.258).

Informed Consent

All experimental methods were performed in accordance with the Declaration of Helsinki; participants provided written informed consent.

Funding

This project was supported by AJA University of Medical Sciences Grant No. 1398.258.

Conflict of Interest

None

Data Availability Statement

The datasets generated during the current study are available from the corresponding author on reasonable request.

References

  1. Desimone R, Duncan J. Neural mechanisms of selective visual attention. Annu Rev Neurosci. 1995; 18:193-222.
  2. Tillman CM, Wiens S. Behavioral and ERP indices of response conflict in Stroop and flanker tasks. Psychophysiology. 2011; 48(10):1405-11. DOI | PubMed
  3. Lehto JE, Juujärvi P, Kooistra L, Pulkkinen L. Dimensions of executive functioning: Evidence from children. Br J Dev Psychol. 2003; 21(1):59-80. DOI
  4. Miyake A, Friedman NP, Emerson MJ, Witzki AH, Howerter A, Wager TD. The unity and diversity of executive functions and their contributions to complex “Frontal Lobe” tasks: a latent variable analysis. Cogn Psychol. 2000; 41(1):49-100. DOI | PubMed
  5. Posner MI, DiGirolamo GJ. Executive Attention: Conflict, Target Detection, and Cognitive Control. In: R. Parasuraman(Ed.), The attentive brain. Cambridge, MA, US: The MIT Press; 1998.
  6. Fassbender C, Foxe JJ, Garavan H. Mapping the functional anatomy of task preparation: priming task-appropriate brain networks. Hum Brain Mapp. 2006; 27(10):819-27. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  7. Carter CS, van Veen V. Anterior cingulate cortex and conflict detection: an update of theory and data. Cogn Affect Behav Neurosci. 2007; 7(4):367-79. DOI | PubMed
  8. Ye Z, Zhou X. Conflict control during sentence comprehension: fMRI evidence. Neuroimage. 2009; 48(1):280-90. DOI | PubMed
  9. Novick JM, Kan IP, Trueswell JC, Thompson-Schill SL. A case for conflict across multiple domains: memory and language impairments following damage to ventrolateral prefrontal cortex. Cogn Neuropsychol. 2009; 26(6):527-67. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  10. Sharini H, Zolghadriha S, Riyahi Alam N, Jalalvandi M, Khabiri H, Arabalibeik H, Nadimi M. Assessment of Motor Cortex in Active, Passive and Imagery Wrist Movement Using Functional MRI. J Biomed Phys Eng. 2021; 11(4):515-26. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  11. Jalalvandi M, Riahi Alam N, Sharini H. Optical Imaging of Brain Motor Cortex Activation During Wrist Movement Using Functional Near-Infrared Spectroscopy (fNIRS). Arch Neurosci. 2019; 6(Brain Mapping):e90089. DOI
  12. Sharini H, Fooladi M, Masjoodi S, Jalalvandi M, Yousef Pour M. Identification of the pain process by cold stimulation: Using dynamic causal modeling of effective connectivity in functional near-infrared spectroscopy (fNIRS). IRBM. 2019; 40(2):86-94. DOI
  13. Cai X, Li X, Razmjooy N, Ghadimi N. Breast Cancer Diagnosis by Convolutional Neural Network and Advanced Thermal Exchange Optimization Algorithm. Comput Math Methods Med. 2021; 2021:5595180. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  14. Dedovic K, D’Aguiar C, Pruessner JC. What stress does to your brain: a review of neuroimaging studies. Can J Psychiatry. 2009; 54(1):6-15. DOI | PubMed
  15. Harrivel AR, Weissman DH, Noll DC, Peltier SJ. Monitoring attentional state with fNIRS. Front Hum Neurosci. 2013; 7:861. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  16. Braun DA, Nagengast AJ, Wolpert DM. Risk-sensitivity in sensorimotor control. Front Hum Neurosci. 2011; 5:1. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  17. Onan A. Bidirectional convolutional recurrent neural network architecture with group-wise enhancement mechanism for text sentiment classification. J King Saud Univ - Comput Inf Sci. 2022; 34(5):2098-117. DOI
  18. Roberts RE, Anderson EJ, Husain M. Expert cognitive control and individual differences associated with frontal and parietal white matter microstructure. J Neurosci. 2010; 30(50):17063-7. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  19. Dedovic K, D’Aguiar C, Pruessner JC, Van Stegeren AH. What stress does to your brain: A review of neuroimaging studies: Imaging stress effects on memory: A review of neuroimaging studies. Can J Psychiatry. 2008; 53(12):A1-2. DOI
  20. Jalalvandi M, ZahediNiya M, Kargar J, Karimi SA, Sharini H, Goodarzi N. Brain Functional Mechanisms in Attentional Processing Following Modified Conflict Stroop Task. J Biomed Phys Eng. 2020; 10(4):493-506. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  21. Onan A. Consensus clustering‐based undersampling approach to imbalanced learning. Scientific Programming. 2019; 2019(1):5901087. DOI
  22. Yu M, Liu Y. Differences in executive function of the attention network between athletes from interceptive and strategic sports. J Mot Behav. 2021; 53(4):419-30. DOI | PubMed
  23. MacDonald AW 3rd, Cohen JD, Stenger VA, Carter CS. Dissociating the role of the dorsolateral prefrontal and anterior cingulate cortex in cognitive control. Science. 2000; 288(5472):1835-8. DOI | PubMed
  24. Coulthard EJ, Nachev P, Husain M. Control over conflict during movement preparation: role of posterior parietal cortex. Neuron. 2008; 58(1):144-57. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  25. Derrfuss J, Brass M, Neumann J, Von Cramon DY. Involvement of the inferior frontal junction in cognitive control: meta-analyses of switching and Stroop studies. Hum Brain Mapp. 2005; 25(1):22-34. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  26. Carter CS, Macdonald AM, Stenger VA, Cohen JD. 11. Dissociating the contributions of DLPFC and anterior cingulate to executive control: an event-related fMRI study. Brain Cogn. 2001; 47(1-2):66-9.
  27. Yousef Pour M, Masjoodi S, Fooladi M, Jalalvandi M, Vosoughi R, Vejdani Afkham B, Khabiri H. Identification of the Cognitive Interference Effect Related to Stroop Stimulation: Using Dynamic Causal Modeling of Effective Connectivity in Functional Near-Infrared Spectroscopy (fNIRS). J Biomed Phys Eng. 2020; 10(4):467-78. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  28. Brass M, Ruge H, Meiran N, Rubin O, Koch I, Zysset S, et al. When the same response has different meanings: recoding the response meaning in the lateral prefrontal cortex. Neuroimage. 2003; 20(2):1026-31. DOI | PubMed
  29. Coderre EL, Smith JF, Van Heuven WJ, Horwitz B. The Functional Overlap of Executive Control and Language Processing in Bilinguals. Biling (Camb Engl). 2016; 19(3):471-88. Publisher Full Text | DOI | PubMed [ PMC Free Article ]
  30. Mackworth JF. Vigilance, arousal, and habituation. Psychol Rev. 1968; 75(4):308-22. DOI | PubMed