- Research article
- Open Access
Altered connectivity within the salience network during direct eye gaze in PTSD
© Thome et al.; licensee BioMed Central Ltd. 2014
Received: 14 May 2014
Accepted: 19 September 2014
Published: 25 November 2014
Posttraumatic stress (PTSD) disorder has been associated with heightened threat sensitivity. Evidence suggests that direct eye gaze leads to sustained activation of the superior colliculus/periaqueductal grey within individuals with PTSD. The present analysis investigated functional connectivity within the salience network (SN) in the same sample as presented in a prior publication during direct versus averted gaze in adults with PTSD related to childhood maltreatment as compared to healthy individuals.
Functional connectivity within the SN was examined using functional magnetic resonance imaging while participants viewed avatars positioned in direct versus averted gaze relative to the participant in 16 individuals with PTSD related to childhood maltreatment and 16 healthy control subjects. Connectivity within the SN was assessed via Independent Component Analysis (ICA). Associations with symptom severity were explored with multiple regression analyses on individual subject components.
Temporal multiple regression analyses revealed higher connectivity within the SN during direct versus averted gaze which was more pronounced in individuals with PTSD as compared to healthy controls. Compared to controls, individuals with PTSD showed increased integration of the left amygdala and the right insula within the SN. PTSD symptom severity was positively associated with connectivity of the right mid-cingulate cortex within the SN in PTSD subjects only.
Participants with PTSD showed enhanced coupling of the amygdala and the insula within the SN as compared to healthy control subjects during gaze processing. Our results provide evidence for an increased sensitivity of the salience network to direct versus averted gaze in individuals with PTSD related to childhood maltreatment.
The investigation of social cognition is particularly pertinent because PTSD is often associated with significant interpersonal problems, including interpersonal violence and difficulties forming and maintaining intimate and non-intimate relationship [1–6]. Regulating emotional arising states in a flexible and socially tolerable way are necessary for a successful social interaction. Increasing evidence points to insufficient emotion regulation skills in PTSD subjects [7, 8]. It is important to note that heightened states of fear and anxiety in addition to high levels of social emotions, including guilt and shame weigh heavily on the everyday life of these patients [for review see . However, little is known about the underlying neural mechanism of the latter, e.g. disturbances within early information processing versus higher order information processing.
The majority of behavioural studies investigating social cognition in PTSD focused on deficits in empathic responding, emotion recognition, and theory of mind [9–14]. The capacity to be aware of and comprehend others’ emotions, behaviours, and intentions, that is, theory of mind, may be an important determinant of emotion recognition and empathic responding [15–17].
Response to mutual eye-contact represents one paradigm for studying social cognitive/theory of mind processes in PTSD. Eye contact enables individuals to adopt the perspective of others [18, 19] as it provides a basis for communication and social interaction. A recent review by Senju and colleagues  proposed that eye contact modulates cognition and attention. One theory supporting the latter argument is the “communicative intention detector model”  which suggests that direct eye contact aims at communicating with the perceiver, resulting in an opportunity to grasp the intentions and emotions of others [21–27]. Steuwe and colleagues  investigated the neural underpinnings of response to male avatars, displayed as expressing neutral, happy, or angry expressions, in either direct versus averted gaze relative to the participant. Direct versus averted gaze lead to greater BOLD response within the dorsomedial prefrontal cortex (DMPFC), left temperoparietal junction (TPJ), and right temporal pole (TP) within healthy controls as compared to individuals with PTSD, independent of the emotional expression of the avatar. By contrast, individuals with PTSD demonstrated increased BOLD response within subcortical structures, specifically, the superior colliculus and periaqueductal gray. Enhanced sensitivity of subcortical regions during eye contact processing may compromise a person’s capacity for higher order social cognition. In fact, this subcortical route was described as an “innate alarm system”  that facilitates defensive responses, including exaggerated startle, hypervigilance, cowering, and escape . Over activation of this “innate alarm system” may decrease an individual’s capacity for theory of mind and affiliative interaction.
Consistent with the idea of enhanced alarm signaling, a recently published meta-analysis of neuroimaging studies of PTSD demonstrated increased activation across different task types (symptom-provocation and cognitive-emotional tasks) within regions of the salience network, including the right (mid) dorsal anterior cingulate cortex (dACC), and bilateral amygdalae . The authors suggested that increased response within brain regions comprising the salience network may lead to an allocation of cognitive resources to a broad range of external stimuli, thus leading to symptoms of hypervigilance and aberrant goal directed activity.
Three investigations have examined resting state SN connectivity in PTSD [31–33] (for review see also ). Generally speaking, these studies demonstrated increased coupling between key nodes of the SN. Specifically, PTSD patients showed an increased coupling between the anterior insula and peri-insula/superior temporal gyrus, hippocampus and amygdala when compared to a combined control group consisting of combat and healthy control subjects . The same investigators also found an increased connectivity between the amygdala seed and the insula in PTSD subjects as compared to combat controls only .
Given that previous research indicated enhanced coupling between key nodes of the salience network during resting state in PTSD patients [31–33] combined with our recent findings of enhanced alarm signaling during direct versus averted gaze in this population , which may be further related to enhanced downstream activation of the salience network, we were interested in investigating SN associated activation pattern in response to direct versus averted gaze perception in individuals with PTSD related to prolonged childhood abuse, a sample we previously described in Steuwe and colleagues . As a first step, we were interested in examining salience network activation during gaze processing within this sample in general. We therefore applied independent component analysis (ICA). It is a powerful method to characterize large-scale brain networks. So far, ICA based studies have identified components representing different functionally relevant cortical networks such as the SN, the default mode network (DMN), and the central executive network (CEN). Based on the findings described above, we hypothesized enhanced connectivity within the SN during mutual eye contact in patients with PTSD.
Participants and measures
Demographic and clinical information
Mean (s.d.) age
% employed (full or part time)
Mean (s.d.) CAPS
Mean (s.d.) present number
Mean (s.d.) lifetime
Panic Disorder w/wo A goraphobia
Generalized Anxiety Disorder
Undifferentiated Somatoform Disorder
Childhood Trauma History
Mean (s.d.) on CTQ-PA
Mean (s.d.) on CTQ-EA
Mean (s.d.) on CTQ-SA
Mean (s.d.) on CTQ-PN
Mean (s.d.) on CTQ-EN
Behavioral task description and procedure
The stimuli consisted of three-dimensional dynamic animations of four different avatars who moved from horizontally across a computer screen . The experimental set up was modeled on a paradigm by Schrammel et al. (for a detailed description of stimulus material and development, see ). The stimulus material consisted of silent video sequences, each 8.8 s, displaying a male avatar moving in profile to the middle of the screen (2 s), then turning either toward the observer directly or at 30° to the left or right, whilst displaying direct or averted gaze, and then moving to exit the screen (2 s). The virtual character either displayed a happy, angry, or neutral facial expression during the period of direct or averted gaze (4.8 s), whereas while entering and exiting the character expressed only a neutral expression. In the case of equally oriented body posture and gaze, this combination was labelled as congruent. In total, 48 video sequences were displayed with four clips for each combination of within-subject factors [gaze direction (two levels: direct versus avert) × congruency (two levels: congruent versus incongruent) × emotion (three levels: happy versus angry versus neutral)] in random order. The male characters were always presented in front of a grey background with only head and shoulders visible. The hair colour (light or dark) as well as the direction of the character’s entrance (from left or right) were counterbalanced. Participants were instructed to pay attention while watching the scenes.
Overall, video sequences were presented in 48 blocks, separated into two runs of 8 min and 54s each; acquiring 178 3 s whole brain imaged volumes. Each run started with a 30-s resting scan and included 24 blocks consisting of 4.7-s arrow condition (an arrow indicated the gaze direction of the avatar), 8.8-s video clip and 7.5-s fixation cross. Video sequences were displayed via an external projector and viewed via a mirror system.
After the scanning procedure, participants were asked to rate the facial expressions of the male characters. The following questions were asked: “What emotion is the character expressing?” and “How do you feel while watching this character?”. Each stimulus was rated on a one to nine (negative to positive) Likert scale.
All imaging data were collected using a 3.0 T whole-body MRI scanner (Magnetom Tim Trio, Siemens Medical Solution, Erlangen, Germany) with a manufacturer‘s 32-channel phased array head coil. Scanning parameters and preprocessing procedures were previously described (please see ).
Orthogonal scout images were collected and used to prescribe a three-dimensional T1-weighted anatomical image of the whole head with 1 mm isotropic resolution (MP-RAGE, TR/TE/TI = 2300 ms/2.98 ms/900 ms, flip angle = 9°, FOV (X, Y, Z) = 256 mm × 240 mm × 192 mm, acc. Factor = 4, total acq. time 3 min 12 s). The anatomical volume was used to determine the angle of the transverse plane passing though both the anterior and posterior commeasures midsagittally and as the source image for interindividual spatial normalization. A set of 64 contagious, 2 mm-thick imaging planes for blood oxygenation level-dependent (BOLD) fMRI were prescribed parallel to the AC-PC plane and positioned to ensure coverage of the top of the brain.
BOLD fMRI images were acquired with the manufacturer’s standard gradient-echo EPI pulse sequence (single-shot blipped EPI) using an interleaved slice acquisition order and tridimensional prospective acquisition correction. EPI volumes were acquired with 2 mm isotropic resolution and the following parameters: FOV = 192 mm × 192 mm × 94 × 94 matrix, TR/TE = 3000 ms/20 ms, flip angle = 90°, 64 slices, 178 measurements.
Imaging data were preprocessed using Statistical Parametric Mapping 2 (Wellcome Trust Centre for Neuroimaging, London, UK) implemented in MATLAB 7.2 (Mathworks Inc., Sherbon, MA).
To reduce the effects of head motion, each subject’s images were realigned to the first volume of each series. The realigned functional images were then spatially normalized to a standard echo-planar imaging template supplied by SPM2. All images were then spatially smoothed with an 8 mm FWHM Gaussian smoothing kernel.
fMRI connectivity analysis
Independent component analysis (ICA) is a powerful method to discover the hidden factors from a set of observed data in such a way that they are maximally independent . Previous work implemented ICA successfully to discover either task- or resting-state-related imaging data, suggesting that it is possible to examine temporal coherent networks (TCN) which are associated with more or less external triggered cognitive load ).
Hence, group spatial ICA (group-ICA) was conducted for all 32 subjects using the infomax algorithm  within the GIFT software (http://icatb.sourceforge.net/, version v2.0e) implemented in MATLAB R2011a (Mathworks Inc., Sherbon, MA). A detailed review of group ICA fMRI analyses can be reviewed in Calhoun et al. 2008, 2009 [40, 41] (see also [43, 44]).
We ran group-ICA on the pooled dataset (all 356 acquired data volumes, concatenated across two runs). In this study, the optimal number of independent components was found to be 20 using modified minimum description length criteria [44, 45]. We applied the ICASSO algorithm implemented in GIFT to increase the robustness of our independent components to initial algorithm conditions by repeating the ICA estimation 20 times. Single subjects’ spatial maps and corresponding time courses were then computed and converted to z-scores for display and use in further statistical analyses. Each voxel in the brain has a z-score representing the strength of its contribution to the component‘s time course [41–46].
The component related to the SN was automatically detected using the spatial sorting function implemented in the GIFT software. In detail, this procedure resulted in a set of spatially independent components, which were correlated with a binary SN mask derived from a previous study . The mask mainly included the ACC, mPFC, mid cingulate gyrus, bilateral STG and, bilateral insular cortices and amygdalae. We selected the component with the highest correlation for further analyses.
Statistical comparison of spatial maps
For all subjects, z-score spatial maps of the component of interest were imported into SPM8 (http://www.fil.ion.ucl.ac.uk/spm/) for two-sample t-tests. We employed region-of-interest (ROI) analyses for FWE-correction based on the hypothesized effects within the salience network. In particular, we focused on brain regions that have been previously associated with the salience network: cingulate gyrus (MNI coordinates: x = 4, y = −6, z = 34; ), amygdala (MNI coordinates: x = −24, y = −4, z = −26;  and insula (x = 42, y =10, z = −12; ) with a sphere from 6 – 10 mm radius. Statistical significance was assessed using small volume correction  at a threshold of P < 0.05 (FWE corrected) for those clusters that also passed a whole-brain uncorrected threshold of P < 0.005 and a cluster threshold of k = 10 .
Statistical comparison of time courses
Multiple regression analysis using the temporal sorting function in GIFT was performed on the ICA time course with the general linear model (GLM) design matrix taken from SPM8. The design matrix contained six regressors: 1) happy facial expression direct; 2) happy facial expression avert; 3) neutral facial expression direct; 4) neutral facial expression avert; 5) angry facial expression direct; and 6) angry facial expression avert. Only congruent body posture and gaze direction was modeled based on our prior analysis reported in Steuwe et al. . This approach leads to a set of beta weights for each regressor, subject and component. To draw inference about the degree of task-relatedness, the utility “stats on beta-weights” implemented within the GIFT software was applied.
Here, beta-weights associated with the component as well as regressors of interest were entered into second-level analyses. To test whether there are differences between groups regarding emotional facial expression and gaze direction, we ran a 2 (PTSD vs Controls) × 3 (happy vs angry vs neutral) × 2 (avert vs direct) ANOVA. In case of significant effects, post hoc t-tests corrected for multiple comparisons were applied. Given that our previous findings focused on direct gaze processing , we only report post hoc comparisons for direct greater than avert gaze within the results section.
Multiple regression analyses of spatial maps
We conducted second-level multiple regression analyses in SPM8 on individual z-score spatial maps within the PTSD group only to assess whether the integration of specific brain regions within the SN is related to symptom severity. The same significance thresholds as described above were applied.
Perception of facial expression
Analysis of the reported feelings while watching the virtual characters also revealed a significant main effect of group (F1,30 = 17.15, P < 0.001) which traced back to the differences in feelings regarding angry (t24.11 = 3.01, P < 0.006) and happy facial expressions (t30 = 2.63, P < 0.013). In addition, a main effect of facial expression (F1.35, 40.57 = 50.83, P < 0.001) indicated that all subjects felt more positive while observing happy expressions when compared with neutral (t31 = 5.58, P < 0.001) and angry faces (t31 = −7.89, P < 0.001), and participants felt more positive during neutral as compared to angry facial expression (t31 = −6.29, P < 0.001).
Statistical comparison of spatial maps
Symptom severity and spatial distribution
Statistical comparison of time courses
The aim of the present study was to gain insight into SN activity in response to direct versus avert gaze perception in individuals with PTSD related to childhood maltreatment. Overall, analyses revealed an increased coupling within the SN during direct versus averted gaze which was more pronounced in patients with PTSD as compared to healthy control subjects. Specifically, the left amygdala and right insula showed greater integration within the SN in individuals with PTSD.
Moreover, symptom severity as assessed with the CAPS was positively correlated with the coupling of the right mid cingulate cortex within the SN in PTSD subjects.
It has been suggested that the salience network is involved in the detection, identification, and integration of internal and external stimuli which are most relevant for the individual in order to guide behavior that is most suited to maintain homeostasis. It comprises paralimbic structures including the dorsal anterior cingulate cortex (dACC) and orbital frontoinsula , brain regions known to be involved in interoceptive-autonomic processing [54–56]. Increased activation in regions associated with the salience network has been associated with the processing of the emotional component of pain , empathic responses to pain , the experience of metabolic stress, hunger, or pleasurable touch , and social rejection [59, 60].
Increased connectivity within the SN during direct gaze may aid the enhanced processing of relevant external cues, i.e., facial expressions, as the activation of this network is associated with heightened attention processing in order to identify relevant cues whether they are cognitive, emotional or homeostatic in nature [50, 54, 61, 62]. In this regard, it is interesting to note that studies demonstrated direct facial expression of anger and happiness to be associated with better performance in emotion recognition tasks as compared to avert facial expression [24, 63–65]. Furthermore, direct gaze when compared to avert gaze seems to increase reaction times for emotion detection . Assuming that increased activation of the SN is triggered by gaze perception, enhanced recruitment of this network may lead to better performance in emotion recognition of facial expressions. The present findings, however, cannot be linked to behavioral performance because participants were instructed to pay attention to the avatars rather than evaluating their emotional expression. Thus, future studies should additionally assess behavioral responses, including the labeling of displayed emotions directly after watching the videos. Interestingly, we found the strongest increase in SN activation in response to neutral direct facial expression. There is evidence that neutral faces are not perceived without an affective component , and subjects tend to evaluate such stimuli as negative . Thus, neutral faces may capture more salience processes due to their ambiguous nature.
PTSD subjects appeared to recruit the right insula and left amygdala within the SN more, suggesting increased salience processing during direct gaze perception as compared to healthy control subjects. Healthy participants did not seem to activate structures within the SN more as compared to PTSD subjects as indicated by non-significant spatial results. The latter findings add to the hypothesis that gaze perception triggers the activation of the SN in both groups, although more so in individuals with PTSD related to childhood maltreatment. These results are in line with previous studies showing increased SN coupling during resting-state in subjects with PTSD [31–33] (for review see also ). Since the presented sample experienced prolonged exposure to interpersonal violence during childhood, we speculate that the finding of increased connectivity within the SN during direct gaze in trauma survivors may have developed as an adaptive response to interpersonal violence by facilitating enhanced processing of relevant external cues involving facial expression, thus facilitating appropriate survival responses.
Symptom severity as assessed by the CAPS  was associated with a higher coupling of the mid cingulate cortex within the SN in PTSD subjects. The mid cingulate cortex is thought to be involved in error detection and attention to behaviorally relevant stimuli [68–72] and has been shown to have functional connections with the insula [50, 73, 74]. Taylor and colleagues  examined two systems of connectivity between subdivisions of the insular and cingulate cortices. The authors suggest that one system is involved in emotional salience monitoring and is thought to comprise the anterior insula, posterior anterior cingulate cortex (pACC), and the anterior mid cingulate cortex (aMCC). The second system includes the mid cingulate (MCC) and the entire insular cortex and has been suggested to play a key role in general salience monitoring, including monitoring of the environment, selecting appropriate responses as well as the mapping of skeletomotor body orientation. One may therefore hypothesize a positive association between the latter system and PTSD symptom severity. Future research should examine the functional connectivity between the midcingulate and insular cortex during direct eye gaze in people with PTSD.
Several limitations of the present study are worth noting. Firstly, ICA does not provide information about a direct task related connectivity between unique brain structures but rather enables a characterization of large scale brain networks hidden in a dataset. Here, as a first step, we were interested in an exploration of potential salience network activation within a gaze processing task in general. Future research will need to examine effective connectivity and context sensitive changes in effective connectivity. For this purpose, either psychophysiological interaction analyses  which focus on changes in the contribution one brain region has to another while the experimental and/or psychological context is changing or dynamic causal modeling  which is also a model-based approach aiming to identify an appropriate neuronal model of interacting brain structures should be employed in future studies. Secondly, only women participated and only male avatars were utilized; future investigations should examine the effects of participant gender in interaction with the gender of the avatars viewed. Based on the present data, we cannot conclude whether the examined salience network connectivity is due to mutual eye contact solely and/or might also be associated with state arousal. Thus, future research should also examine state arousal to disentangle the effects of interpersonal cues and current level of arousal. In addition, eye tracking and pupillary reactivity data during gaze processing should be examined. It will also be beneficial to study a trauma-exposed control group without PTSD in the future; however, we have found it to be very difficult to recruit trauma-exposed subjects who have similar CTQ scores to PTSD groups but who also do not report a history of psychopathology. Finally, the implications of abnormalities in gaze processing for social functioning should be examined in traumatized persons.
In summary, enhanced coupling of the amygdala and the insula within the SN was observed in individuals with PTSD related to childhood maltreatment during direct versus avert eye contact. These findings suggest increased sensitivity of the salience network during direct eye contact in this population. The behavioral and treatment implications of these findings deserve attention in future research.
We would like to thank Stephanie Nevill and Suzy Southwell for their help with subject recruitment and assessment. Funding for this study was received from the Canadian Institutes of Health Research and the International Association for Analytical Psychology under the auspices of President Joe Cambray.
- Lanius RA, Bluhm RL, Frewen PA: How understanding the neurobiology of complex post-traumatic stress disorder can inform clinical practice: a social cognitive and affective neuroscience approach. Acta Psychiatr Scand 2011, 124: 331–348.PubMedView ArticleGoogle Scholar
- Ahrens CE, Aldana E: The ties that bind: understanding the impact of sexual assault disclosure on survivors' relationships with friends, family, and partners. J Trauma Dissociation 2012, 13: 226–243.PubMedView ArticleGoogle Scholar
- Babcock RL, Deprince AP: Factors contributing to ongoing intimate partner abuse: childhood betrayal trauma and dependence on one's perpetrator. J Interpers Violence 2013, 28: 1385–1402.PubMedView ArticleGoogle Scholar
- Dorahy MJ, Corry M, Shannon M, Webb K, McDermott B, Ryan M, Dyer KF: Complex trauma and intimate relationships: the impact of shame, guilt and dissociation. J Affect Disord 2013, 147: 72–79.PubMedView ArticleGoogle Scholar
- Owen J, Quirk K, Manthos M: I get no respect: the relationship between betrayal trauma and romantic relationship functioning. J Trauma Dissociation 2012, 13: 175–189.PubMedView ArticleGoogle Scholar
- Gobin RL: Partner preferences among survivors of betrayal trauma. J Trauma Dissociation 2012, 13: 152–174.PubMedView ArticleGoogle Scholar
- Shepherd L, Wild J: Emotion regulation, physiological arousal and PTSD symptoms in trauma-exposed individuals. J Behav Ther Exp Psychiatry 2014, 45: 360–367.PubMedPubMed CentralView ArticleGoogle Scholar
- Xiong K, Zhang Y, Qiu M, Zhang J, Sang L, Wang L, Xie B, Wang J, Li M: Negative emotion regulation in patients with posttraumatic stress disorder. PLoS One 2013, 8: e81957.PubMedPubMed CentralView ArticleGoogle Scholar
- Mazza M, Giusti L, Albanese A, Mariano M, Pino MC, Roncone R: Social cognition disorders in military police officers affected by posttraumatic stress disorder after the attack of An-Nasiriyah in Iraq 2006. Psychiatry Res 2012, 198: 248–252.PubMedView ArticleGoogle Scholar
- Nazarov A, Frewen P, Parlar M, Oremus C, Macqueen G, McKinnon M, Lanius R: Theory of mind performance in women with posttraumatic stress disorder related to childhood abuse. Acta Psychiatr Scand 2014, 129: 193–20.PubMedView ArticleGoogle Scholar
- Nietlisbach G, Maercker A: Social cognition and interpersonal impairments in trauma survivors with PTSD. J Aggress Maltreat Trauma 2009, 18: 382–402.View ArticleGoogle Scholar
- Nietlisbach G, Maercker A, Rossler W, Haker H: Are empathic abilities impaired in posttraumatic stress disorder? Psychol Rep 2010, 106: 832–844.PubMedView ArticleGoogle Scholar
- Shenk CE, Putnam FW, Noll JG: Predicting the accuracy of facial affect recognition: the interaction of child maltreatment and intellectual functioning. J Exp Child Psychol 2013, 114: 229–242.PubMedPubMed CentralView ArticleGoogle Scholar
- Plana I, Lavoie MA, Battaglia M, Achim AM: A meta-analysis and scoping review of social cognition performance in social phobia, posttraumatic stress disorder and other anxiety disorders. J Anxiety Disord 2014, 28: 169–177.PubMedView ArticleGoogle Scholar
- Carrington SJ, Bailey AJ: Are there theory of mind regions in the brain? A review of the neuroimaging literature. Hum Brain Mapp 2009, 30: 2313–2335.PubMedView ArticleGoogle Scholar
- Gallagher HL, Frith CD: Functional imaging of 'theory of mind'. Trends Cogn Sci 2003, 7: 77–83.PubMedView ArticleGoogle Scholar
- Siegal M, Varley R: Neural systems involved in "theory of mind". Nat Rev Neurosci 2002, 3: 463–471.PubMedGoogle Scholar
- Baron-Cohen S: Mindblindness: An Essay on Autism and Theory of Mind. Cambridge: MIT Press; 1995.Google Scholar
- Tomasello M, Carpenter M: Shared intentionality. Dev Sci 2007, 10: 121–125.PubMedView ArticleGoogle Scholar
- Senju A, Johnson MH: The eye contact effect: mechanisms and development. Trends Cogn Sci 2009, 13: 127–134.PubMedView ArticleGoogle Scholar
- Bockler A, van der Wel RP, Welsh TN: Catching eyes: effects of social and nonsocial cues on attention capture. Psychol Sci 2014, 7: 7.Google Scholar
- Freeth M, Foulsham T, Kingstone A: What affects social attention? Social presence, eye contact and autistic traits. PLoS One 2013, 8: 9.View ArticleGoogle Scholar
- Wicker B, Perrett DI, Baron-Cohen S, Decety J: Being the target of another's emotion: a PET study. Neuropsychologia 2003, 41: 139–146.PubMedView ArticleGoogle Scholar
- Conty L, N'Diaye K, Tijus C, George N: When eye creates the contact! ERP evidence for early dissociation between direct and averted gaze motion processing. Neuropsychologia 2007, 45: 3024–3037.PubMedView ArticleGoogle Scholar
- Pelphrey KA, Viola RJ, McCarthy G: When strangers pass: processing of mutual and averted social gaze in the superior temporal sulcus. Psychol Sci 2004, 15: 598–603.PubMedView ArticleGoogle Scholar
- Schilbach L, Wohlschlaeger AM, Kraemer NC, Newen A, Shah NJ, Fink GR, Vogeley K: Being with virtual others: neural correlates of social interaction. Neuropsychologia 2006, 44: 718–730.PubMedView ArticleGoogle Scholar
- Kampe KK, Frith CD, Frith U: "Hey John": signals conveying communicative intention toward the self activate brain regions associated with "mentalizing," regardless of modality. J Neurosci 2003, 23: 5258–5263.PubMedGoogle Scholar
- Steuwe C, Daniels JK, Frewen PA, Densmore M, Pannasch S, Beblo T, Reiss J, Lanius RA: Effect of direct eye contact in PTSD related to interpersonal trauma: an fMRI study of activation of an innate alarm system. Soc Cogn Affect Neurosci 2012, 25: 25.Google Scholar
- Liddell BJ, Brown KJ, Kemp AH, Barton MJ, Das P, Peduto A, Gordon E, Williams LM: A direct brainstem-amygdala-cortical 'alarm' system for subliminal signals of fear. Neuroimage 2005, 24: 235–243.PubMedView ArticleGoogle Scholar
- Hayes JP, Hayes SM, Mikedis AM: Quantitative meta-analysis of neural activity in posttraumatic stress disorder. Biol Mood Anxiety Disord 2012, 2: 2045–5380.View ArticleGoogle Scholar
- Sripada RK, King AP, Garfinkel SN, Wang X, Sripada CS, Welsh RC, Liberzon I: Altered resting-state amygdala functional connectivity in men with posttraumatic stress disorder. J Psychiatry Neurosci 2012, 37: 241–249.PubMedPubMed CentralView ArticleGoogle Scholar
- Sripada RK, King AP, Welsh RC, Garfinkel SN, Wang X, Sripada CS, Liberzon I: Neural dysregulation in posttraumatic stress disorder: evidence for disrupted equilibrium between salience and default mode brain networks. Psychosom Med 2012, 74: 904–911.PubMedPubMed CentralView ArticleGoogle Scholar
- Rabinak CA, Angstadt M, Welsh RC, Kenndy AE, Lyubkin M, Martis B, Phan KL: Altered amygdala resting-state functional connectivity in post-traumatic stress disorder. Front Psychiatr 2011., 2:Google Scholar
- Peterson A, Thome J, Frewen RA, Lanius RA: Resting State neuroimaging studies: a new way of identifying differences and similarities among anxiety disorders? Can J Psychiatry 2014. in pressGoogle Scholar
- Blake DD, Weathers FW, Nagy LM, Kaloupek DG, Gusman FD, Charney DS, Keane TM: The development of a clinician-administered PTSD scale. J Trauma Stress 1995, 8: 75–90.PubMedView ArticleGoogle Scholar
- Association AP: Diagnostic and Statistical Manual of Mental Disorders. 4th edition. Washington DC: American Psychiatric Press; 2000.Google Scholar
- First MB, Spitzer RL, Gibbon M, Williams JBW: Structured Clinical Interview for DSM-IV Axis Disorders, Clinician Version (SCID-CV). Washington, DC: American Psychiatric Press; 1996.Google Scholar
- Bernstein DP, Stein JA, Newcomb MD, Walker E, Pogge D, Ahluvalia T, Stokes J, Handelsman L, Medrano M, Desmond D, Zule W: Development and validation of a brief screening version of the Childhood Trauma Questionnaire. Child Abuse Negl 2003, 27: 169–190.PubMedView ArticleGoogle Scholar
- Schrammel F, Pannasch S, Graupner ST, Mojzisch A, Velichkovsky BM: Virtual friend or threat? The effects of facial expression and gaze interaction on psychophysiological responses and emotional experience. Psychophysiology 2009, 46: 922–931.PubMedView ArticleGoogle Scholar
- Calhoun VD, Liu J, Adali T: A review of group ICA for fMRI data and ICA for joint inference of imaging, genetic, and ERP data. Neuroimage 2009, 45: 13.View ArticleGoogle Scholar
- Calhoun VD, Kiehl KA, Pearlson GD: Modulation of temporally coherent brain networks estimated using ICA at rest and during cognitive tasks. Hum Brain Mapp 2008, 29: 828–838.PubMedPubMed CentralView ArticleGoogle Scholar
- Bell AJ, Sejnowski TJ: An information-maximization approach to blind separation and blind deconvolution. Neural Comput 1995, 7: 1129–1159.PubMedView ArticleGoogle Scholar
- Calhoun VD, Adali T, Pearlson GD, Pekar JJ: A method for making group inferences from functional MRI data using independent component analysis. Hum Brain Mapp 2001, 14: 140–151.PubMedView ArticleGoogle Scholar
- Li YO, Adali T, Calhoun VD: Estimating the number of independent components for functional magnetic resonance imaging data. Hum Brain Mapp 2007, 28: 1251–1266.PubMedView ArticleGoogle Scholar
- Himberg J, Hyvarinen A, Esposito F: Validating the independent components of neuroimaging time series via clustering and visualization. Neuroimage 2004, 22: 1214–1222.PubMedView ArticleGoogle Scholar
- Beckmann CF, DeLuca M, Devlin JT, Smith SM: Investigations into resting-state connectivity using independent component analysis. Philos Trans R Soc Lond B Biol Sci 2005, 360: 1001–1013.PubMedPubMed CentralView ArticleGoogle Scholar
- Kluetsch RC, Ros T, Theberge J, Frewen PA, Calhoun VD, Schmahl C, Jetly R, Lanius RA: Plastic modulation of PTSD resting-state networks and subjective wellbeing by EEG neurofeedback. Acta Psychiatr Scand 2013.Google Scholar
- Patel R, Spreng RN, Shin LM, Girard TA: Neurocircuitry models of posttraumatic stress disorder and beyond: a meta-analysis of functional neuroimaging studies. Neurosci Biobehav Rev 2012, 36: 2130–2142.PubMedView ArticleGoogle Scholar
- Aupperle RL, Ravindran L, Tankersley D, Flagan T, Stein NR, Simmons AN, Stein MB, Paulus MP: Pregabalin influences insula and amygdala activation during anticipation of emotional images. Neuropsychopharmacology 2011, 36: 1466–1477.PubMedPubMed CentralView ArticleGoogle Scholar
- Seeley WW, Menon V, Schatzberg AF, Keller J, Glover GH, Kenna H, Reiss AL, Greicius MD: Dissociable intrinsic connectivity networks for salience processing and executive control. J Neurosci 2007, 27: 2349–2356.PubMedPubMed CentralView ArticleGoogle Scholar
- Worsley KJ, Marrett S, Neelin P, Vandal AC, Friston KJ, Evans AC: A unified statistical approach for determining significant signals in images of cerebral activation. Hum Brain Mapp 1996, 4: 58–73.PubMedView ArticleGoogle Scholar
- Lieberman MD, Cunningham WA: Type I and Type II error concerns in fMRI research: re-balancing the scale. Soc Cogn Affect Neurosci 2009, 4: 423–428.PubMedPubMed CentralView ArticleGoogle Scholar
- Ham T, Leff A, de Boissezon X, Joffe A, Sharp DJ: Cognitive control and the salience network: an investigation of error processing and effective connectivity. J Neurosci 2013, 33: 7091–7098.PubMedView ArticleGoogle Scholar
- Craig AD: How do you feel? Interoception: the sense of the physiological condition of the body. Nat Rev Neurosci 2002, 3: 655–666.PubMedView ArticleGoogle Scholar
- Damoiseaux JS, Rombouts SA, Barkhof F, Scheltens P, Stam CJ, Smith SM, Beckmann CF: Consistent resting-state networks across healthy subjects. Proc Natl Acad Sci U S A 2006, 103: 13848–13853.PubMedPubMed CentralView ArticleGoogle Scholar
- Critchley HD, Tang J, Glaser D, Butterworth B, Dolan RJ: Anterior cingulate activity during error and autonomic response. Neuroimage 2005, 27: 885–895.PubMedView ArticleGoogle Scholar
- Peyron R, Laurent B, Garcia-Larrea L: Functional imaging of brain responses to pain. A review and meta-analysis (2000). Neurophysiol Clin 2000, 30: 263–288.PubMedView ArticleGoogle Scholar
- Singer T, Seymour B, O'Doherty J, Kaube H, Dolan RJ, Frith CD: Empathy for pain involves the affective but not sensory components of pain. Science 2004, 303: 1157–1162.PubMedView ArticleGoogle Scholar
- Eisenberger NI, Lieberman MD, Williams KD: Does rejection hurt? An FMRI study of social exclusion. Science 2003, 302: 290–292.PubMedView ArticleGoogle Scholar
- Domsalla M, Koppe G, Niedtfeld I, Vollstadt-Klein S, Schmahl C, Bohus M, Lis S: Cerebral processing of social rejection in patients with borderline personality disorder. Soc Cogn Affect Neurosci 2013. epub ahead of printGoogle Scholar
- Menon V: Developmental pathways to functional brain networks: emerging principles. Trends Cogn Sci 2013, 31: 00219–00212.Google Scholar
- Menon V, Uddin LQ: Saliency, switching, attention and control: a network model of insula function. Brain Struct Funct 2010, 214: 655–667.PubMedPubMed CentralView ArticleGoogle Scholar
- Adams RB Jr, Kleck RE: Effects of direct and averted gaze on the perception of facially communicated emotion. Emotion 2005, 5: 3–11.PubMedView ArticleGoogle Scholar
- N'Diaye K, Sander D, Vuilleumier P: Self-relevance processing in the human amygdala: gaze direction, facial expression, and emotion intensity. Emotion 2009, 9: 798–806.PubMedView ArticleGoogle Scholar
- Pinkham AE, Loughead J, Ruparel K, Overton E, Gur RE, Gur RC: Abnormal modulation of amygdala activity in schizophrenia in response to direct- and averted-gaze threat-related facial expressions. Am J Psychiatry 2011, 168: 293–301.PubMedView ArticleGoogle Scholar
- Carvajal F, Rubio S, Serrano JM, Rios-Lago M, Alvarez-Linera J, Pacheco L, Martin P: Is a neutral expression also a neutral stimulus? A study with functional magnetic resonance. Exp Brain Res 2013, 228: 467–479.PubMedView ArticleGoogle Scholar
- Said CP, Haxby JV, Todorov A: Brain systems for assessing the affective value of faces. Philos Trans R Soc Lond B Biol Sci 2011, 366: 1660–1670.PubMedPubMed CentralView ArticleGoogle Scholar
- Davis KD, Taylor KS, Hutchison WD, Dostrovsky JO, McAndrews MP, Richter EO, Lozano AM: Human anterior cingulate cortex neurons encode cognitive and emotional demands. J Neurosci 2005, 25: 8402–8406.PubMedView ArticleGoogle Scholar
- Fair DA, Dosenbach NU, Church JA, Cohen AL, Brahmbhatt S, Miezin FM, Barch DM, Raichle ME, Petersen SE, Schlaggar BL: Development of distinct control networks through segregation and integration. Proc Natl Acad Sci U S A 2007, 104: 13507–13512.PubMedPubMed CentralView ArticleGoogle Scholar
- Kucyi A, Hodaie M, Davis KD: Lateralization in intrinsic functional connectivity of the temporoparietal junction with salience- and attention-related brain networks. J Neurophysiol 2012, 108: 3382–3392.PubMedView ArticleGoogle Scholar
- Rushworth MF, Buckley MJ, Behrens TE, Walton ME, Bannerman DM: Functional organization of the medial frontal cortex. Curr Opin Neurobiol 2007, 17: 220–227.PubMedView ArticleGoogle Scholar
- Weissman-Fogel I, Moayedi M, Taylor KS, Pope G, Davis KD: Cognitive and default-mode resting state networks: do male and female brains "rest" differently? Hum Brain Mapp 2010, 31: 1713–1726.PubMedGoogle Scholar
- Van Hoesen GW, Norecraft RJ, Vogt BA, Gabriel M: Connections of the monkey cingulate cortex. In Neuropsychiatry: A comprehensive textbook. Edited by: Fogel B, Schiffer RB, Roa SM. Baltimore, MD: William & Wilkins; 1996:113–143.Google Scholar
- Vogt BA, Vogt L, Farber NB: Cingulate Cortex and Disease Models. In The Rat Nervous System. 3rd edition. Edited by: Paxinos G. San Diego, California: Elsevier Academic Press; 2004:705–727.Google Scholar
- Taylor KS, Seminowicz DA, Davis KD: Two systems of resting state connectivity between the insula and cingulate cortex. Hum Brain Mapp 2009, 30: 2731–2745.PubMedView ArticleGoogle Scholar
- Friston KJ, Buechel C, Fink GR, Morris J, Rolls E, Dolan RJ: Psychophysiological and modulatory interactions in neuroimaging. Neuroimage 1997, 6: 218–229.PubMedView ArticleGoogle Scholar
- Friston KJ, Harrison L, Penny W: Dynamic causal modelling. Neuroimage 2003, 19: 1273–1302.PubMedView ArticleGoogle Scholar
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