Abstract
Despite broad evidence suggesting that adversity exposed youth experience an impaired ability to recognize emotion in others, the underlying biological mechanisms remains elusive. This study uses a multi-method approach to target the neurological substrates of this phenomenon in a well-phenotyped sample of youth meeting diagnostic criteria for post-traumatic stress disorder. 21 PTSD-afflicted youth and 23 typically developing controls completed clinical interview schedules, an emotion recognition task with eye-tracking, and an implicit emotion processing task during functional magnetic resonance imaging. PTSD was associated with decreased accuracy in identification of angry, disgust, and neutral faces as compared to TD youth. Notably, these impairments occurred despite the normal deployment of visual attention in youth with PTSD relative to TD youth. Correlation with a related fMRI task revealed a group by accuracy interaction for amygdala-hippocampus functional connectivity (FC) for angry expressions, where TD youth showed a positive relationship between anger accuracy and amygdala-hippocampus FC, this relationship was reversed in youth with PTSD. These findings are a novel characterization of impaired threat recognition within a well-phenotyped population of severe pediatric PTSD. Further, the differential amygdala-hippocampus FC identified in youth with PTSD may imply aberrant efficiency of emotional contextualization circuits.
Keywords: Posttraumatic Stress Disorders, Emotion, Adolescent, Functional Neuroimaging
INTRODUCTION
Pediatric posttraumatic stress disorder (pPTSD) is a detrimental neurodevelopmental disorder that affects an estimated 5% of youth by the age of 18 (McLaughlin et al., 2013). PTSD has a significant impact on cognitive, emotional, and psychosocial development in youth, is highly comorbid with other psychiatric illnesses (Brady, 1997; Donnelly & Amaya-Jackson, 2002; Famularo, Fenton, Kinscherff, & Augustyn, 1996; Kessler, Sonnega, Bromet, Hughes, & Nelson, 1995; Lamberg, 2001), and carries the highest risk of all mental illnesses for first suicide attempt (Miché et al., 2018). The development of new treatments for pPTSD have been hampered by a limited understanding of its underlying neurobehavioral mechanisms which occur on the backdrop of ongoing neurodevelopment. A crucial aspect of psychosocial development is the ability to accurately recognize the emotional expression of others, and deficits in this process may contribute to psychopathology such as PTSD (Abhang, Gawali, & Mehrotra, 2016). While prior research indicates impairments in emotion recognition in maltreated youth, there has been little investigation of such abilities within pediatric PTSD across all trauma types. The identification and characterization of these deficits and their underlying behavioral, physiological, and neurobiological mechanisms may elucidate novel and intervenable treatment targets.
Facial emotion recognition, or the general ability to infer emotional meaning from a facial expression(Izard et al., 2001), is well conserved, begins in the first few years of life, and undergoes normative development from childhood and adolescence through adulthood (Herba & Phillips, 2004; Philippot & Feldman, 1990; Tottenham, Hare, & Casey, 2011). On the other hand, impairments in emotion recognition during childhood and adolescence are detrimental to the development of positive social interactions and can contribute to emotional and behavioral difficulties(Izard et al., 2001). Emotion recognition impairments may be influenced by a number of environmental factors during childhood, including exposure to maltreatment (Pollak, 2008; Pollak, Messner, Kistler, & Cohn, 2009; Pollak & Sinha, 2002). While still understudied, a recent systematic review found preliminary support for an association between childhood maltreatment and a global impairment in facial emotion recognition in younger children and further suggests that maltreated youth are able to identify threat at lower intensities than non-maltreated youth (da Silva Ferreira, Crippa, & de Lima Osório, 2014).
However, emotion recognition deficits specific to youth with PTSD remain unclear. To our knowledge, there have been two studies which have begun to characterize emotion recognition in cohorts of trauma-exposed youth with differing rates of PTSD. One study of maltreated children with and without PTSD who underwent a recognition task with happy, fearful, and neutral faces found faster recognition of fearful faces as compared to non-maltreated children, but with no effect of PTSD status (Masten et al., 2008). In contrast, a sample of adolescent boys enrolled in therapeutic day school with and without PTSD completed a recognition task using only sad, angry, and fearful expressions found that continuous PTSD symptom severity was associated with less accurate recognition of angry relative to fearful faces (Javdani et al., 2017). In response to these contradictory findings within clinically mixed samples, there is a clear need to characterize emotion recognition deficits within a sample of pPTSD subsequent to any index trauma type and their relationship to symptom severity measures.
When investigating emotion recognition abnormalities in pPTSD, it is also important to investigate its underlying neurobehavioral substrates. One proposed mechanism of emotion recognition impairments lies in visual attention or arousal during the recognition task (Ralph Adolphs et al., 2005). A recent study of emotion recognition using eye tracking in healthy adults found emotion-specific patterns of eye fixations across positive, negative, and neutral conditions (Eisenbarth, Link to external site, Alpers, & Link to external site, 2011). Abnormal visual attention patterns during emotion recognition have been found in adults with prefrontal lesions (Wolf, Philippi, Motzkin, Baskaya, & Koenigs, 2014), autism spectrum disorders (Black et al., 2017), adults with PTSD (Wolf, 2016), and comorbid borderline personality disorder (BPD) and PTSD (Kaiser et al., 2019). Within the maltreatment literature, previous studies have shown both that childhood trauma severity is positively correlated with attentional bias toward angry faces (Lakshman et al., 2020) and conversely that maltreated youth exhibit an attentional bias away from threatening faces as compared to non-maltreated youth (Pine et al., 2005). To date, however, no studies have examined visual attention during emotional face recognition in youth with PTSD as compared to typically developing youth.
Another possible mechanism of altered recognition may be in underlying neurobiological circuitry of facial emotion recognition. One model of facial emotion recognition suggests a three-part process (Ralph Adolphs, 2002). First, visual cortices, such as the inferior occipital gyrus, fusiform gyrus, and superior temporal gyrus, are responsible for initial perceptual processing of a face (Haxby, Hoffman, & Gobbini, 2000). Second, the response to emotionally salient stimuli in visual cortices are modulated by feedback from the prefrontal cortex and amygdala providing a conceptual analysis of the emotion. Human lesion studies of the amygdala consistently identify deficits in recognition of negative emotional faces, including fear, anger, disgust, and sadness in adults with bilateral lesions (R Adolphs et al., 1999; Broks et al., 1998; Calder, 1996; Calder, Lawrence, & Young, 2001; Schmolck & Squire, 2001) and unilateral lesions to the right amygdala (Ralph Adolphs, Tranel, & Damasio, 2001; A. K. Anderson, Spencer, Fulbright, & Phelps, 2000). Finally, the amygdala and prefrontal cortices may then trigger the hippocampus in order to retrieve conceptual knowledge about the identified emotion (Ralph Adolphs, 2002).
In line with studies of adults with PTSD and adolescents/adults with childhood trauma exposure that have reported functional abnormalities in the amygdala (Cisler, Scott Steele, Smitherman, Lenow, & Kilts, 2013; Etkin & Wager, 2007; Hayes, Hayes, & Mikedis, 2012; Hein & Monk, 2017; Patel, Spreng, Shin, & Girard, 2012), functional deficits in amygdala circuitry may also play a role in the emotion processing impairments in pPTSD. This is evidenced by previous reports in which youth with PTSD symptoms have exhibited amygdala hyperactivation during emotional faces tasks (Garrett et al., 2012; Keding & Herringa, 2016) as well as cross-sectional and longitudinal abnormalities in amygdala-prefrontal functional connectivity (Cisler et al., 2013; Heyn et al., 2019; Wolf & Herringa, 2016). To our knowledge, abnormalities in amygdala function during emotional face viewing have yet to be linked to specific emotion recognition processes in pediatric PTSD.
The current study uses a well-defined clinical cohort of youth with PTSD and age- and sex-matched non-traumatized typically developing (TD) youth in order to address these knowledge gaps. Here, we investigated (1) accuracy and reaction time of facial emotion recognition spanning positive, negative, and neutral expressions, (2) physiological correlates of recognition abnormalities using pupil diameter and eye-tracking, and (3) the relationship between recognition abnormalities and amygdala functional connectivity during emotional face viewing due to the well-characterized role of the amygdala in emotion processing and its functional abnormalities in pPTSD. In line with the previous studies of emotion processing in youth with PTSD (Javdani et al., 2017; Keding & Herringa, 2016; Pine et al., 2005), we hypothesize youth with PTSD to show impaired recognition, in combination with attentional avoidance, of negative or threat-related emotions.
METHODS
Table 1 provides participant demographic information. Recruitment and assessment details have been previously described (Heyn et al., 2019; Keding & Herringa, 2015, 2016; Wolf & Herringa, 2016) but are briefly summarized here. The Youth PTSD Study recruited 96 youth (TD, n=48; PTSD, n = 48) ranging from 7 to 17 years. Youth with PTSD were recruited from local mental health facilities and age- and sex-matched TD youth were recruited from the community using social media, University emails, flyers, etc.
Table 1.
Full Sample Participant Characteristics.
| Typically Developing | PTSD | Group Comparisons | ||
|---|---|---|---|---|
|
| ||||
| Demographic Information | t/X2 | P | ||
|
| ||||
| n (Female) | 23 (18) | 21 (14) | ||
| Age | 14.66 ± 2.52 | 14.59 ± 2.85 | 0.09 | 0.93 |
| IQ | 111.13 ± 11.60 | 96.71 ± 13.36 | 3.83 | <0.005 * |
| Tanner | 3.66 ± 1.15 | 3.21 ± 1.8 | 0.99 | 0.33 |
| Parental Education | Junior High (1) High School/GED (2) Some College/Associates (4) 4-Year College Degree (6) Graduate/Professional School (10) Unknown (0) |
Junior High (2) High School/GED (5) Some College/Associates (11) 4-Year College Degree (1) Graduate/Professional School (0) Unknown (2) |
20.41 | 0.001 * |
| MFQ | 2.85 ± 2.55 | 28.40 ± 12.82 | −9.37 | <0.005 * |
| SCARED | 6.80 ± 3.74 | 39.14 ± 15.49 | −9.72 | <0.005 * |
|
| ||||
| Trauma and Clinical Variables | ||||
|
| ||||
| CTQ | 34.91 ± 15.49 | 59.33 ± 19.11 | −5.77 | <0.005 * |
| CAPS-CA | - | 73.21 ± 16.75 | - | - |
| PTSD-RI | - | 49.95 ± 15.35 | - | - |
| Age of Index Trauma | - | 6.43 ± 4.02 | ||
| Number of KSADS Trauma Types | - | 3.76 ± 2.30 | ||
| Index Trauma | - | - | - | |
| Traumatic News | 2 | |||
| Traumatic Accident | 4 | |||
| Sexual Abuse | 11 | |||
| Witness Domestic Violence | 4 | |||
| Co-Morbid Disorders | - | |||
| Major Depressive Disorder | 15 | |||
| Anxiety Disorder | 12 | |||
| ADHD | 5 | |||
| History of Psychiatric Medication | - | - | - | |
| Stimulant | 8 | |||
| SSRI/SNRI/NRI | 12 | |||
| Lithium | 1 | |||
| Anticonvulsant | 1 | |||
| Antipsychotic | 1 | |||
| Benzodiazepine | 1 | |||
| Other | 5 | |||
Typically developing and PTSD youth did not significantly differ in sex distribution, age, or pubertal stage. The PTSD group had significantly lower IQ scores, and significantly higher MFQ, SCARED, and CTQ scores. The CAPS-CA score was not obtained on the first five PTSD participants.
Abbreviations: MFQ, Mood and Feelings Questionnaire; SCARED, Screen for Child Anxiety Related Mood Disorders; CAPS-CA, Clinician-Administered PTSD Scale Child and Adolescent version; PTSD-RI, PTSD Reaction Index; AHDH, attention deficit hyperactivity disorder; SSRI/SNRI/NRI, selective serotonin/norepinephrine reuptake inhibitor.
All youth participants and their parent/caregiver completed the Kiddie Schedule for Affective Disorders and Schizophrenia (KSADS) (Kaufman et al., 1997) in order to assess the youth for current and past psychopathology. In addition, all youth were assessed for childhood abuse severity (Childhood Trauma Questionnaire – Abuse subscale, CTQ), depression (Mood and Feelings Questionnaire, MFQ) (Costello & Angold, 1988), and anxiety symptom severity (Screen for Child Anxiety Related Emotional Disorders, (SCARED) (Birmaher et al., 1997), as well as IQ using the Wechsler Abbreviated Scale of Intelligence-II (Wechsler, 2011), pubertal stage using the Tanner Sexual Maturation Scale (Marshall & Tanner, 1969, 1970), and lifetime load of stressful events using the Stressful Life Events Schedule (Williamson et al., 2003). Within the clinical group, a PTSD diagnosis was determined using DSM-IV criteria using a combination of the KSADS and the Clinician-Administered PTSD Scale for Children and Adolescents (CAPS-CA) (Weathers, Keane, & Davidson, 2001). The number of KSADS trauma types endorsed was used as a proxy for trauma load. PTSD symptom severity was assessed using the UCLA PTSD Reaction Index (PTSD-RI) (Steinberg, Brymer, Decker, & Pynoos, 2004).
Exclusion criteria included IQ<70, history of psychotic/bipolar/obsessive compulsive disorders, active suicidality, substance abuse or dependence, psychotropic medication usage in 8 the past 4 weeks (6 weeks for fluoxetine), unstable neurological or other medical condition, MRI contraindication, and/or pregnancy in females. Youth were not taken off psychotropic medication for the purpose of study enrollment. All participants gave written informed consent from a legally acceptable representative and a youth assent when appropriate. All study procedures were approved by the University of Wisconsin Health Sciences IRB.
Emotion Recognition Task and Statistical Analyses
Full details regarding the emotion recognition task can be found in Supplementary Materials and Methods and are briefly summarized here. The emotion recognition task consisted of participants viewing faces with six different expressions (happy, sad, angry, fearful, disgust, and neutral) selected from Karolinska Directed Emotional Faces set (Lundqvist, Flykt, & Öhman, 1998). The face stimuli consisted of ten white male and ten white female actors, with each actor presenting two emotions. The stimulus set included images from all 20 actors, and each participant was presented with the same stimulus set. For homogeneity, all actors chosen for this task were of the same race, images were converted to grayscale, cropped in order to remove hair and ears, and matched for size and luminescence. Before beginning the task, youth were given instructions that they would see a series of faces that would display on the screen for a few seconds and then would be asked to identify which emotion they believe was on the face. An identical control task using the same set of faces was completed by all participants in which they were instead asked to identify the gender of the face presented. The presentation order of the gender and emotion identification task was counterbalanced across participants. During each facial stimulus presentation, pupillary diameter, fixation count, and fixation duration were estimated. One fixation was defined as any time a gaze coordinate remained within a 1° visual angle for 100ms or greater (Karsh & Breitenbach, 1983; Lambert, Monty, & Hall, 1974), and identified offline using automated software. Finally, each face was divided into four areas of interest for eye-tracking analyses: eyes, mouth, face, and outside. Due to limited availability of eye tracking equipment, 45 youth completed the behavioral emotion and gender identification tasks (TD, n=23; PTSD, n=21).
All statistical analyses were completed in R (R Core Team, 2016) and RStudio (RSTudio Team, 2012). General linear models and linear mixed-effect modeling on the trial-wise data for all participants was used to identify group (TD, PTSD) x emotion (happy, sad, angry, fearful, disgust, neutral) interactions, adjusting for age, sex, trial number, and subject as a random effect across three dependent variables: accuracy, reaction time, and pupil diameter. Following any significant interactions, independent-sample t-tests were used in order to compare groups for each emotion. In order to identify group- and emotion-related differences within the eye-tracking data, group x emotion x face region interactions were modeled against fixation duration and fixation count, adjusting for age, sex, trial number, and subject as a random effect. Multiple-comparison correction was applied using false-discovery rate (FDR) (Benjamini & Hochberg, 1995) at pFDR<0.05 across all models in the emotion and gender recognition tasks.
Functional MRI Task and Statistical Analyses
In order to relate any abnormalities in emotion identification accuracy with implicit emotion processing, we analyzed functional connectivity differences during a separate dynamic face task. Details regarding this task have been previously reported (Keding & Herringa, 2016) and are briefly summarized here. During fMRI, all participants completed an implicit cognitive-emotional processing task which required them to identify the color of a semi-transparent overlay atop a face changing from neutral to emotional (angry, happy) over a 1-second period. Examples of the emotional stimuli used in this task are included in Figure 2. Youth completed three blocks, each consisting of 12 faces, presented pseudorandomly based on emotion condition. Control shape blocks displaying a morphing oval with the colored overlay was intermixed between face blocks in order to ensure no emotion blocks were encountered sequentially. Please see Supplementary Material and Methods for details on image acquisition and preprocessing. One youth with PTSD was excluded from final analyses due to motion artifact.
Figure 2. Aberrant amygdala-hippocampus functional connectivity to angry faces viewing relative to anger accuracy in the recognition task.
Angry and happy fMRI trial schematics represent the one second face presentation in which the faces morphed from neutral to angry or happy, and youth were asked to report what color the face was presented over. Significant group x anger accuracy effect using the amygdala in a seed-based whole-brain functional connectivity analysis, covaried for age and sex (pFDR < 0.05). Scatterplots represent extracted cluster averages per subject. Accuracy was defined relative to total recognition accuracy per subject, to account for individual variation in global recognition ability. Also shown is the extracted cluster average from amygdala-hippocampus region identified in the angry trials applied to the happy viewing trials for reference.
Abbreviations: TD, typically developing; PTSD, posttraumatic stress disorder; FC, functional connectivity.
In first-level analyses, functional data for individual subjects were analyzed using general linear models within AFNI’s 3dDeconvolve. Variables modeled included three blocks for each emotion condition, and a shape condition as a fixed-effect regressor, with a gamma hemodynamic response function (HRF) of 1-second duration. Also included were six motion parameters and their derivatives as nuisance regressors and four polynomial drift terms. Using AFNI’s 3dCalc, we used the average activation and bilateral amygdala functional connectivity across the three angry blocks, due to abnormalities identified in recognition of anger in the preceding behavioral analyses. Finally, a general linear test was used from these average activation and connectivity templates in order to create an angry-shape contrast for each subject to be used in subsequent group analyses.
In second-level analyses, between-subject analyses were conducted to examine group differences in the relationship between average anger accuracy as quantified by results of the behavioral in recognition task and activation/bilateral amygdala functional connectivity in this dynamic face task. This a priori analysis was chosen to quantify possible neurobiological underpinnings of aberrant emotion processing identified in the first set of behavioral analyses. In order to control for the ability to identify any emotion, anger identification accuracy is defined as the ratio between accuracy to only angry faces and accuracy across all emotions. Each of the three models were fit using AFNI’s 3dttest++. Age and sex were also included as covariates. We completed both whole-brain analyses and analyses within an a priori limbic search region comprising the amygdala and hippocampus using masks generated from the AFNI standard template. Whole-brain multiple-comparison correction was preformed using Monte Carlo simulation in AFNI’s 3dClustSim with voxel-wise p < 0.005 and pFWE < 0.05. The identified cluster threshold was 32 voxels in the amygdala/hippocampus and 283 for whole-brain correction. Peak coordinates are based in the MNI atlas in LPI orientation.
Secondary Analyses
First, in order to compare sample characteristics between the PTSD and TD groups, independent t-tests and chi-squared tests were conducted across demographic and clinical variables. Second, exploratory analyses assessing the role of PTSD symptom severity and identified behavioral and activation/connectivity abnormalities were conducted within the PTSD group using general linear mixed effect models and symptom severity measures (PTSD-RI total score, PTSD-RI B/C/D subscores, MFQ, and SCARED). Each symptom measure was evaluated in a separate linear regression, adjusting for age and sex, with multiple-comparison correction across all symptom models. Symptom results that survive FDR correction are reported (pFDR < 0.05). Third, in order to investigate the mechanisms underlying recognition deficits between groups, the proportion of each erroneous emotion label to total incorrect trials was calculated per emotion per group. Two-sample tests for equality of proportions between groups with continuity correction were then run to compare PTSD and TD erroneous emotion attribution. Finally, regression analyses were conducted to investigate the impact of the following demographic variables on behavioral and neural abnormalities: IQ, Tanner stage, age at index trauma, stressful life events, trauma load, childhood abuse severity, presence of current or previous clinical depressive or anxiety disorder, previous use of psychotropic medication, or history of therapy. All secondary analyses were conducted in R (R Core Team, 2016) and RStudio (RSTudio Team, 2012).
RESULTS
Demographic and Clinical Characteristics
TD and PTSD youth did not significantly differ on age (t(42) = 0.09, p = 0.93), sex (χ2(1) = 0.01, p = 0.92), or pubertal stage (Tanner; t(42) = 0.99, p = 0.33). However, youth with PTSD did on average have lower IQ scores than TD youth (t(42) = 3.83, p < 0.005). As expected, PTSD youth scored significantly higher than TD youth on overall childhood maltreatment exposure severity (CTQ; t(42) = −5.77, p < 0.005), as well as depression (MFQ; t(42) = −9.37, p < 0.005) and anxiety symptom severity (SCARED; t(42) = −9.72, p < 0.005). As a whole, the PTSD cohort was exposed to high levels of trauma. On average, each youth with PTSD experienced 3.8 ± 2.3 KSADS trauma types; interpersonal violence represented the majority of index trauma. The average age of index trauma was 6.4 ± 4.0 years. Finally, rates of current comorbidity were high with just over 71% of PTSD youth diagnosed with major depression and 57% with an anxiety disorder. Demographic and clinical characteristics are further summarized in Table 1.
Emotion Recognition Performance
When youth were explicitly instructed to process and identify emotion, PTSD youth overall performed worse at emotion identification than TD youth (χ2 = 271.85, pFDR < 0.001). Average emotion identification accuracy was 84.3% (± SD 0.364) correct identification for PTSD youth and 87.6% (± SD 0.330) correct identification for TD youth. We also found a significant group by emotion interaction on identification accuracy (χ2 = 20.33, pFDR = 0.003). Specifically, PTSD youth performed significantly worse than TD youth for anger, disgust, and neutral accuracy (Figure 1). A detailed breakdown of the average accuracy and standard deviation for each emotion and group can be found in Supplementary Materials and Methods. Importantly, when youth were instructed only to attend to the gender rather than the emotion of the face presented, the groups performed equally well (Figure S1; F(5,40)=1.49, pFDR = 0.69). Further details regarding gender recognition task performance can be found in Supplementary Material and Methods.
Figure 1. Emotion recognition deficits and symptom correlates in youth with PTSD.
(A) Line chart representing mean accuracy across all trials per participant per group, based upon emotion of the face presented. Error bars represent the standard error. (B) Scatterplot represents average angry accuracy plotted by PTSD symptom severity, as measured by the PTSD-RI total score. The bar chart visualizes the average accuracy by group, median-splitting the PTSD youth into high and low PTSD-RI symptom severity. Angry and symptom correlates are one representative symptom relationship identified. * pFDR < 0.05
Abbreviations: TD, typically developing; PTSD, posttraumatic stress disorder.
Importantly, these group-related abnormalities in identifying threat-related emotions could not be explained by any other behavioral or physiological measure tested. This is evidenced by the absence of any significant group by emotion interactions in reaction time (F(5,6788) = 1.09, pFDR = 0.54), fixation count (F(5,6917) = 1.18, pFDR = 0.49), fixation duration (F(5, 6917) = 1.57, pFDR = 0.32), or pupil diameter (F(5,6953) = 0.31, pFDR = 0.99). More specifically, PTSD youth showed no differences in overall fixation duration to the eyes, mouth, or face compared to TD youth across all emotion conditions. PTSD youth did show decreased fixation counts to the face region across all emotions in both the emotion and gender identification tasks (Figure S2; F(3, 6917) = 27.69, pFDR < 0.001). These differences in fixation count were unaccompanied by emotion-specific differences.
Within the PTSD group, anger accuracy was positively associated with symptom severity across numerous domains (Figure 1B) (PTSD: PTSD-RI Total, t = 3.44, pFDR=0.002; Re-experiencing, PTSD-RI B, t = 2.50, pFDR = 0.03; Avoidance, PTSD-RI C, t = 3.33, pFDR = 0.003; Hyperarousal, PTSD-RI D, t = 4.03, pFDR < 0.005; Anxiety, SCARED, t = 3.18, pFDR = 0.004). All emotion recognition and symptom relationships are detailed in Supplementary Materials and Methods. In an effort to understand why accuracy would increase with symptom severity, the PTSD group was separated into high and low PTSD severity based upon a median split in total PTSD-RI score. Youth with low PTSD symptom severity had significantly lower threat-related emotion identification accuracy than both high PTSD severity youth and TD youth (Figure 1C).
As an additional step we then carried out an analysis of the errors made by youth in the emotion recognition task. In general, when youth incorrectly identified an emotion, they were most prone to say they saw disgust. Among the trials in which the participant chose the wrong emotion, we found that the incorrect use of an emotion was dependent on group status (χ2 = 23.44, p < 0.005). Two-sample tests for equality of proportions between groups with continuity correction were then run across all incorrect trials to identify which misattributions are driving this effect (Table 2). Altogether, these results suggest differential processing of positive and negative in pediatric PTSD. PTSD youth more often attributed happy when presented disgust faces (χ2= 5.41, p = 0.02), as well as a trending misattribution of happy when viewing neutral faces (χ2 = 3.53, p = 0.06) as compared TD youth. Youth with PTSD were more likely than TD youth to label fear when presented with the majority of other emotions, including happy (χ2 = 4.44, p = 0.04), angry (χ2 = 11.67, p < 0.001), and disgust (χ2 = 9.14, p = 0.003) faces.
Table 2.
Erroneous response patterns within the typically developing and posttraumatic stress disorder groups during incorrect identification trials.
| Emotion Presented | Erroneous Emotion Response (%) | |||||
|---|---|---|---|---|---|---|
| Happy | Sad | Anger | Fear | Disgust | Neutral | |
|
| ||||||
| TD | ||||||
|
| ||||||
| Happy | - | 0.00 | 0.00 | 0.00 | 0.00 | 100.00 |
| Sad | 5.23 | - | 5.23 | 57.89 | 15.79 | 15.79 |
| Anger | 11.11 | 27.78 | - | 0.00 | 44.44 | 16.67 |
| Fear | 0.00 | 13.89 | 8.33 | - | 72.22 | 5.56 |
| Disgust | 0.00 | 22.22 | 77.78 | 0.00 | - | 0.00 |
| Neutral | 0.00 | 80.00 | 20.00 | 0.00 | 0.00 | - |
|
| ||||||
| PTSD | ||||||
|
| ||||||
| Happy | - | 0.00 | 20.00 | 40.00 | 20.00 | 20.00 |
| Sad | 5.89 | - | 5.89 | 41.18 | 41.18 | 5.89 |
| Anger | 10.00 | 30.00 | - | 16.67 | 31.67 | 20.00 |
| Fear | 3.13 | 28.13 | 21.89 | - | 40.63 | 6.23 |
| Disgust | 6.45 | 6.45 | 74.19 | 9.68 | - | 3.23 |
| Neutral | 22.22 | 33.33 | 22.22 | 11.11 | 11.11 | - |
“Emotion presented” indicates the emotion of the face that the youth was viewing and “erroneous emotion response” indicates the incorrect label chose by the youth. Values are shown as a percentage of total incorrect trial per emotion. Colored cells show significantly (red, p<0.05) or trending (yellow, p<0.10) differences in proportion between groups using a two-sample equality test of proportions using continuity correction.
Abbreviations: TD, typically developing; PTSD, posttraumatic stress disorder.
Emotion Identification Accuracy and Amygdala Function
In an effort to understand the neural underpinnings of deficits in threat-related emotion processing, we investigated the relationship between amygdala activation/functional connectivity and average anger recognition accuracy. This average accuracy was estimated from results of the behavioral emotion recognition task. No significant group x accuracy interactions were identified in activation nor in the whole-brain analyses of amygdala functional connectivity. However, amygdala functional connectivity analyses in the a priori search region revealed a significant group x accuracy interaction between right amygdala and right hippocampus (peak F= −3.62; k=49; x=32, y=16, z=−11). In this case, PTSD youth showed decreased amygdala-hippocampus connectivity with identification accuracy, the reverse pattern of TD youth (Figure 2). This group by accuracy interaction was not identified in the happy condition (pFDR > 0.05). There was no significant relationship identified between amygdala-hippocampus functional connectivity and any measure of symptom severity.
Confound Analyses
The significant primary behavioral and connectivity results (group by emotion and group by anger identification accuracy interactions, respectively) remained significant when adjusted for the following potential confounds: IQ, Tanner stage, age at index trauma, stressful life events, trauma load, childhood abuse severity, presence of current and previous clinical depressive or anxiety disorder, previous use of psychotropic medication, or history of therapy. Details of confound analyses can be found in Supplementary Materials and Methods Table 2.
DISCUSSION
To our knowledge, this is the first reported study to comprehensively characterize emotion recognition in pediatric PTSD, including behavioral performance, visual attention, and functional brain measures. In summary, we found: (1) youth with PTSD exhibit decreased accuracy in identifying threat-related and neutral expressions, (2) emotion recognition deficits were identified in the absence of visual attention and gender identification deficits, (3) recognition accuracy was positively (and unexpectedly) related to PTSD, anxiety, and depression symptom severity, (4) youth with PTSD exhibit unique patterns of incorrectly labeling negative and positive emotional expressions, and (5) recognition accuracy deficits were further related to aberrant right amygdala-hippocampus functional connectivity. Altogether, this preliminary study works to clarify behavioral deficits in threat recognition in youth with PTSD, discusses these findings within the context of a broader model of trauma exposure and risk for PTSD, and suggests one potential mechanism may be abnormalities in emotional contextualization circuits implicated in the appraisal of threat-related stimuli.
We detected valence-specific abnormalities in facial emotion recognition in youth with PTSD, who exhibited decreased accuracy to threat-related emotions as compared to TD youth. Curiously, we further found that within the PTSD group, symptom severity was positively associated with accuracy recognizing these emotions. While previous studies, along with a systematic review, have identified a link between childhood maltreatment exposure and more sensitive (earlier) detection of threat (da Silva Ferreira et al., 2014; Iffland & Neuner, 2020; Pollak et al., 2009; Pollak & Sinha, 2002), there is little consensus as to how threat recognition is related to pediatric PTSD. One study detected no deficits in recognizing fear, happy, or neutral faces in a cohort of maltreated youth, about half of whom had PTSD (Masten et al., 2008), while a separate study found that PTSD symptom severity was associated with a decreased ability to recognize anger relative to fear and sadness (Javdani et al., 2017). The discordance of findings in these prior studies as well as the current study could be due to a number of factors including differences in tasks (what emotions were presented and how responses were elicited), outcome measures (overall and relative recognition accuracy, intensity of emotion when recognition occurred, etc.), and the inclusion of trauma-exposed youth with mixed diagnostic status.
Despite these differences, in line with a recent meta-analysis hypothesizing a link between deficits in social cognition and PTSD risk (Stevens & Jovanovic, 2019), we propose a synthesis of our findings and previous studies detailed above into a parsimonious model of trauma exposure and emotion recognition in youth vulnerable to psychopathology. Specifically, we posit that emotion recognition processes mediate the relationship between trauma exposure and PTSD. Here, trauma exposure may induce threat-related emotion recognition deficits in youth vulnerable to the development of PTSD leading, in turn, to the emergence of PTSD. Conversely, the emergence of PTSD may serve to counteract these emotion recognition deficits through increasing hypervigilance processes. While this study is unable to directly test the causal relationships between these variables, it is imperative that future studies use prospective longitudinal designs, recruiting youth prior to trauma exposure, to further explore these hypotheses.
In order to understand the interaction of perception and recognition in this study, we also had youth complete a control task in which they were only asked to identify the sex of the face and collected eye fixation patterns during both tasks. All results indicate that neither visual perception nor attention underlie emotion recognition deficits in pediatric PTSD. Both TD and PTSD youth were able to perceive other aspects of the facial stimuli at comparable levels, as evidenced by similarly high accuracies of gender recognition during the control task. Eye tracking analyses of fixation data further revealed no evidence of visual attention differences. Youth with PTSD completed recognition tasks at the same pace of TD youth in both emotion and gender recognition and further did not exhibit any abnormal eye fixation behavior specific to emotion type, altogether suggesting no deficiencies in basic face perception. Finally, although pupillary response has been identified as a useful proxy of emotional arousal (Aboyoun & Dabbs, 1998; Bradley, Miccoli, Escrig, & Lang, 2008; Hess & Polt, 1960; Libby, Lacey, & Lacey, 1973), we did not detect any differences in pupil diameter between PTSD and TD youth during threat-related emotion identification. While this may provide evidence suggesting that differences in arousal during viewing of emotional expressions was not an underlying mechanism of aberrant emotion recognition, future research may find evidence of underlying arousal differences using a different proxy.
Due to this lack of behavioral or visual attention mechanisms underlying detected threat-related deficiencies, we conducted post-hoc exploratory analyses in order to investigate neurobiological correlates of recognition accuracy during a similar emotional face processing task. Functional connectivity analyses revealed an abnormal relationship between right amygdala-hippocampal circuitry and anger accuracy. While TD youth showed a positive relationship between anger accuracy and right amygdala-hippocampus FC, this relationship was reversed in youth with PTSD. Previous studies have found that interactions between the amygdala and hippocampus are crucial to the creation of emotionally salient representations and interpretations of your environment (Phelps, 2004). Further, this circuit has been already implicated in both rodents (Herry et al., 2008; Pitkänen, Pikkarainen, Nurminen, & Ylinen, 2000; Senn et al., 2014) and humans (de Voogd, Fernández, & Hermans, 2016; Hermans et al., 2017) during emotion and threat processing tasks. Maltreated adults without psychiatric illness have previously shown exhibited increased recruitment between the amygdala and hippocampus during an emotional matching task, providing initial evidence that childhood maltreatment may be due to underlying inefficiency in the neural processing of emotions (Demers et al., 2018). Expanding this model into youth with trauma exposure and PTSD, it could be that increased connectivity in lower accuracies mimic these network inefficiencies previously characterized. This may further be evidenced by better threat recognition accuracy as a reflection of increasing network efficiency. Altogether, this evidence suggests the presence of a threat-related contextual modulation model within the basal amygdala and hippocampus whose efficiency be disrupted in youth with trauma exposure and PTSD. However, these are preliminary links between behavioral and neural correlates and future research is needed to further explore these hypotheses.
We then investigated patterns of emotion labeling during incorrect trials in order to further understand the behavioral deficits. First, youth with PTSD were more likely than TD youth to use the fear label regardless of the emotional valence of the face being shown. Behaviorally, adult PTSD has been associated with the overgeneralization of fear associations, hypersensitivity to threat, and difficulties in fear extinction (Blechert, Michael, Vriends, Margraf, & Wilhelm, 2007; Ehlers et al., 2010; Milad et al., 2008; Pole et al., 2009; Shin & Handwerger, 2009). When combined with our findings that youth with PTSD are more likely to identify fear in their surroundings, regardless of the emotion they are presented, lends additional support that a primary clinical manifestation of PTSD may be the overgeneralization of fear perception in both youth and adults.
Finally, we detected patterns within the misidentifications of facial expressions. While our sample size warrants cautious interpretation, we nonetheless detected that during the presentation of negative facial expressions (fear, anger, and disgust), youth with PTSD were statistically more likely to identify the face as being happy than TD youth. To supplement this finding of paradoxical reversal of positive and negative stimuli in emotion identification, we further explored whether similar patterns were present in the functional connectivity analyses. To do so, we compared the right amygdala-hippocampus circuitry while viewing an angry face, which we found to be significantly related to anger identification accuracy, with how the same circuitry during the viewing of happy faces was related to happy identification accuracy. Unsurprisingly, TD and PTSD youth seemed to exhibit no differences in right amygdala-hippocampal recruitment with happy accuracy, suggesting less contextual modulation is needed in non-threatening conditions. This finding of entangled positive and negative emotion processing in the right amygdala are supported by converging evidence that the amygdala encodes across multiple emotional valences (Mattavelli et al., 2014; Tovote, Fadok, & Lüthi, 2015) and previously identified differential coupling between the amygdala-PFC to happy versus angry facial emotion presentation (Keding & Herringa, 2016). Together, these findings further suggest valence-inappropriate emotion recognition and right amygdala-hippocampal recruitment in pediatric PTSD. Future investigation of emotion recognition including both positive and negative stimuli in prospective studies prior to trauma exposure would be helpful in delineating the onset and causal relationship of these abnormalities with the emergence of PTSD in youth.
While the present study has helped to characterize behavioral, physiological, and neurobiological emotion recognition impairments in youth with PTSD, this novel study has several limitations should be noted. First, the clinical sample recruited for this study was diverse and included a high proportion of youth with past and/or present comorbid disorders such as anxiety and depression. While confound analyses revealed that comorbidity was not a significant explanatory factor of any of the behavioral or imaging findings, many of these effects were significantly correlated with comorbid symptom severity. This sample is also highly representative of our study population, which commonly presents with high rates of comorbidity (Kessler et al., 1995). Second, the cross-sectional nature of our data and use of non-trauma exposed TD youth as a comparison precludes any investigation of the causal effects of trauma and PTSD on emotion recognition in youth. Next, all facial stimuli viewed by youth in the current study were adult faces. The literature surrounding the own-age bias in facial perception and recognition is mixed (Picci & Scherf, 2016; Vetter, Drauschke, Thieme, & Altgassen, 2018), however it remains unclear whether this bias is present in pPTSD especially in the wake of interpersonal violence perpetrated by adults. Additionally, the current study related behavioral metrics derived from one task and related those metrics to neuroimaging measures collected during a related yet separate task which precludes this study from making any definitive inferences underlying abnormal emotion recognition processes and pPTSD. Although the amygdala is consistently regarded as important in the pathophysiology of PTSD (Henigsberg, Kalember, Petrović, & Šečić, 2019), whole-brain rather than seed-based functional connectivity analyses could identify other regions and networks involved in abnormal emotion recognition. Finally, previous research has suggested that IQ may account for some variance in emotion recognition performance in other disorders, such autism spectrum disorder (M. Anderson & Miller, 1998; Harms, Martin, & Wallace, 2010; Jones et al., 2011; Wright et al., 2008) and may mediate the relationship between childhood maltreatment and future emotion processing deficits (Young & Widom, 2014). For these reasons we chose to investigate the IQ confound analyses and importantly all of those effects identified remained significant. Altogether, the limitations mentioned above together warrant future studies prospective studies with larger samples that are able to interrogate across trauma types to further investigate emotion recognition processes and pPTSD.
In conclusion, the present study found that youth with PTSD exhibit deficits in facial emotion recognition for threat and neutral expressions. We posit that impaired differentiation between threatening and non-threatening facial expressions may be related to the onset of pediatric PTSD and that increasing PTSD severity may be a compensatory response to counteract deficits in threat-safety emotion recognition through enhanced neural processing of threat. Notably, while these impairments could not be explained by reaction time differences, fixation time to different regions of the face, or arousal via pupil diameter, they may be related to abnormal communication between the right amygdala and hippocampus. Furthermore, youth with PTSD exhibit patterns of emotion misidentification that suggest confusion of positively and negatively valanced emotions. Together, these data point to emotion identification deficits as a potentially novel and modifiable treatment target for youth with PTSD. Future studies would be warranted to replicate the current findings in larger prospective samples of youth, and test whether novel therapies such as emotion recognition training may help prevent or treat symptoms of PTSD and other comorbid disorders in youth.
Supplementary Material
Abbreviations.
- PTSD
posttraumatic stress disorder
- TD
typically developing
- MRI
magnetic resonance imaging
REFEERENCES
- Abhang PA, Gawali BW, & Mehrotra SC (2016). Chapter 5—Emotion Recognition. In Abhang PA, Gawali BW, & Mehrotra SC (Eds.), Introduction to EEG- and Speech-Based Emotion Recognition (pp. 97–112). Academic Press. 10.1016/B978-0-12-804490-2.00005-1 [DOI] [Google Scholar]
- Aboyoun DC, & Dabbs JM (1998). THE HESS PUPIL DILATION FINDINGS: SEX OR NOVELTY? Social Behavior and Personality: An International Journal, 26(4), 415–419. 10.2224/sbp.1998.26.4.415 [DOI] [Google Scholar]
- Adolphs R, Tranel D, Hamann S, Young AW, Calder AJ, Phelps EA, … Damasio AR (1999). Recognition of facial emotion in nine individuals with bilateral amygdala damage. Neuropsychologia, 37(10), 1111–1117. 10.1016/S0028-3932(99)00039-1 [DOI] [PubMed] [Google Scholar]
- Adolphs Ralph. (2002). Neural systems for recognizing emotion. Current Opinion in Neurobiology, 12(2), 169–177. 10.1016/S0959-4388(02)00301-X [DOI] [PubMed] [Google Scholar]
- Adolphs Ralph, Gosselin F, Buchanan TW, Tranel D, Schyns P, & Damasio AR (2005). A mechanism for impaired fear recognition after amygdala damage. Nature, 433(7021), 68. 10.1038/nature03086 [DOI] [PubMed] [Google Scholar]
- Adolphs Ralph, Tranel D, & Damasio H (2001). Emotion recognition from faces and prosody following temporal lobectomy. Neuropsychology, 15(3), 396–404. 10.1037/0894-4105.15.3.396 [DOI] [PubMed] [Google Scholar]
- Anderson AK, Spencer DD, Fulbright RK, & Phelps EA (2000). Contribution of the anteromedial temporal lobes to the evaluation of facial emotion. Neuropsychology, 14(4), 526–536. 10.1037/0894-4105.14.4.526 [DOI] [PubMed] [Google Scholar]
- Anderson M, & Miller KL (1998). Modularity, mental retardation and speed of processing. Developmental Science, 1(2), 239–245. 10.1111/1467-7687.00037 [DOI] [Google Scholar]
- Benjamini Y, & Hochberg Y (1995). Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing. Journal of the Royal Statistical Society. Series B (Methodological), 57(1), 289–300. 10.2307/2346101 [DOI] [Google Scholar]
- Birmaher B, Khetarpal S, Brent D, Cully M, Balach L, Kaufman J, & Neer SM (1997). The Screen for Child Anxiety Related Emotional Disorders (SCARED): Scale construction and psychometric characteristics. Journal of the American Academy of Child and Adolescent Psychiatry, 36(4), 545–553. 10.1097/00004583-199704000-00018 [DOI] [PubMed] [Google Scholar]
- Black MH, Chen NTM, Iyer KK, Lipp OV, Bölte S, Falkmer M, … Girdler S (2017). Mechanisms of facial emotion recognition in autism spectrum disorders: Insights from eye tracking and electroencephalography. Neuroscience & Biobehavioral Reviews, 80, 488–515. 10.1016/j.neubiorev.2017.06.016 [DOI] [PubMed] [Google Scholar]
- Blechert J, Michael T, Vriends N, Margraf J, & Wilhelm FH (2007). Fear conditioning in posttraumatic stress disorder: Evidence for delayed extinction of autonomic, experiential, and behavioural responses. Behaviour Research and Therapy, 45(9), 2019–2033. 10.1016/j.brat.2007.02.012 [DOI] [PubMed] [Google Scholar]
- Bradley MM, Miccoli L, Escrig MA, & Lang PJ (2008). The pupil as a measure of emotional arousal and autonomic activation. Psychophysiology, 45(4), 602–607. 10.1111/j.1469-8986.2008.00654.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brady KT (1997). Posttraumatic stress disorder and comorbidity: Recognizing the many faces of PTSD. The Journal of Clinical Psychiatry, 58(Suppl 9), 12–15. [PubMed] [Google Scholar]
- Broks P, Young AW, Maratos EJ, Coffey PJ, Calder AJ, Isaac CL, … Hadley D (1998). Face processing impairments after encephalitis: Amygdala damage and recognition of fear. Neuropsychologia, 36(1), 59–70. 10.1016/S0028-3932(97)00105-X [DOI] [PubMed] [Google Scholar]
- Calder AJ (1996). Facial Emotion Recognition after Bilateral Amygdala Damage: Differentially Severe Impairment of Fear. Cognitive Neuropsychology, 13(5), 699–745. 10.1080/026432996381890 [DOI] [Google Scholar]
- Calder AJ, Lawrence AD, & Young AW (2001). Neuropsychology of fear and loathing. Nature Reviews Neuroscience, 2(5), 352. 10.1038/35072584 [DOI] [PubMed] [Google Scholar]
- Cisler JM, Scott Steele J, Smitherman S, Lenow JK, & Kilts CD (2013). Neural processing correlates of assaultive violence exposure and PTSD symptoms during implicit threat processing: A network-level analysis among adolescent girls. Psychiatry Research, 214(3), 238–246. 10.1016/j.pscychresns.2013.06.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Costello EJ, & Angold A (1988). Scales to assess child and adolescent depression: Checklists, screens, and nets. Journal of the American Academy of Child and Adolescent Psychiatry, 27(6), 726–737. 10.1097/00004583-198811000-00011 [DOI] [PubMed] [Google Scholar]
- da Silva Ferreira GC, Crippa JAS, & de Lima Osório F (2014). Facial emotion processing and recognition among maltreated children: A systematic literature review. Frontiers in Psychology, 5. 10.3389/fpsyg.2014.01460 [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Voogd LD, Fernández G, & Hermans EJ (2016). Awake reactivation of emotional memory traces through hippocampal–neocortical interactions. NeuroImage, 134, 563–572. 10.1016/j.neuroimage.2016.04.026 [DOI] [PubMed] [Google Scholar]
- Demers LA, McKenzie KJ, Hunt RH, Cicchetti D, Cowell RA, Rogosch FA, … Thomas KM (2018). Separable Effects of Childhood Maltreatment and Adult Adaptive Functioning on Amygdala Connectivity During Emotion Processing. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, 3(2), 116–124. 10.1016/j.bpsc.2017.08.010 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Donnelly C. l., & Amaya-Jackson L (2002). Post-Traumatic Stress Disorder in Children and Adolescents: Epidemiology, Diagnosis and Treatment Options. Pediatric Drugs, 4(3), 159–170. 10.2165/00148581-200204030-00003 [DOI] [PubMed] [Google Scholar]
- Ehlers A, Suendermann O, Boellinghaus I, Vossbeck-Elsebusch A, Gamer M, Briddon E, … Glucksman E (2010). Heart rate responses to standardized trauma-related pictures in acute posttraumatic stress disorder. International Journal of Psychophysiology, 78(1), 27–34. 10.1016/j.ijpsycho.2010.04.009 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisenbarth H, Link to external site, this link will open in a new window, Alpers GW, & Link to external site, this link will open in a new window. (2011). Happy mouth and sad eyes: Scanning emotional facial expressions. Emotion, 11(4), 860–865. http://dx.doi.org.ezproxy.library.wisc.edu/10.1037/a0022758 [DOI] [PubMed] [Google Scholar]
- Etkin A, & Wager TD (2007). Functional neuroimaging of anxiety: A meta-analysis of emotional processing in PTSD, social anxiety disorder, and specific phobia. The American Journal of Psychiatry, 164(10), 1476–1488. 10.1176/appi.ajp.2007.07030504 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Famularo R, Fenton T, Kinscherff R, & Augustyn M (1996). Psychiatric comorbidity in childhood post traumatic stress disorder. Child Abuse & Neglect, 20(10), 953–961. [DOI] [PubMed] [Google Scholar]
- Garrett AS, Carrion V, Kletter H, Karchemskiy A, Weems CF, & Reiss A (2012). Brain activation to facial expressions in youth with PTSD symptoms. Depression and Anxiety, 29(5), 449–459. 10.1002/da.21892 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harms MB, Martin A, & Wallace GL (2010). Facial Emotion Recognition in Autism Spectrum Disorders: A Review of Behavioral and Neuroimaging Studies. Neuropsychology Review, 20(3), 290–322. 10.1007/s11065-010-9138-6 [DOI] [PubMed] [Google Scholar]
- Haxby JV, Hoffman EA, & Gobbini MI (2000). The distributed human neural system for face perception. Trends in Cognitive Sciences, 4(6), 223–233. 10.1016/S1364-6613(00)01482-0 [DOI] [PubMed] [Google Scholar]
- Hayes JP, Hayes SM, & Mikedis AM (2012). Quantitative meta-analysis of neural activity in posttraumatic stress disorder. Biology of Mood & Anxiety Disorders, 2(1), 9. 10.1186/2045-5380-2-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hein TC, & Monk CS (2017). Research Review: Neural response to threat in children, adolescents, and adults after child maltreatment – a quantitative meta-analysis. Journal of Child Psychology and Psychiatry, 58(3), 222–230. 10.1111/jcpp.12651 [DOI] [PubMed] [Google Scholar]
- Henigsberg N, Kalember P, Petrović ZK, & Šečić A (2019). Neuroimaging research in posttraumatic stress disorder – Focus on amygdala, hippocampus and prefrontal cortex. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 90, 37–42. 10.1016/j.pnpbp.2018.11.003 [DOI] [PubMed] [Google Scholar]
- Herba C, & Phillips M (2004). Annotation: Development of facial expression recognition from childhood to adolescence: behavioural and neurological perspectives. Journal of Child Psychology and Psychiatry, 45(7), 1185–1198. 10.1111/j.1469-7610.2004.00316.x [DOI] [PubMed] [Google Scholar]
- Hermans EJ, Kanen JW, Tambini A, Fernández G, Davachi L, & Phelps EA (2017). Persistence of Amygdala-Hippocampal Connectivity and Multi-Voxel Correlation Structures During Awake Rest After Fear Learning Predicts Long-Term Expression of Fear. Cerebral Cortex (New York, N.Y.: 1991), 27(5), 3028–3041. 10.1093/cercor/bhw145 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Herry C, Ciocchi S, Senn V, Demmou L, Müller C, & Lüthi A (2008). Switching on and off fear by distinct neuronal circuits. Nature, 454(7204), 600–606. 10.1038/nature07166 [DOI] [PubMed] [Google Scholar]
- Hess EH, & Polt JM (1960). Pupil Size as Related to Interest Value of Visual Stimuli. Science, 132(3423), 349–350. 10.1126/science.132.3423.349 [DOI] [PubMed] [Google Scholar]
- Heyn SA, Keding TJ, Ross MC, Cisler JM, Mumford JA, & Herringa RJ (2019). Abnormal Prefrontal Development in Pediatric Posttraumatic Stress Disorder: A Longitudinal Structural and Functional Magnetic Resonance Imaging Study. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, 4(2), 171–179. 10.1016/j.bpsc.2018.07.013 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Iffland B, & Neuner F (2020). Varying Cognitive Scars – Differential Associations Between Types of Childhood Maltreatment and Facial Emotion Processing. Frontiers in Psychology, 11. 10.3389/fpsyg.2020.00732 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Izard C, Fine S, Schultz D, Mostow A, Ackerman B, & Youngstrom E (2001). Emotion Knowledge as a Predictor of Social Behavior and Academic Competence in Children at Risk. Psychological Science, 12(1), 18–23. 10.1111/1467-9280.00304 [DOI] [PubMed] [Google Scholar]
- Javdani S, Sadeh N, Donenberg GR, Emerson EM, Houck C, & Brown LK (2017). Affect recognition among adolescents in therapeutic schools: Relationships with posttraumatic stress disorder and conduct disorder symptoms. Child and Adolescent Mental Health, 22(1), 42–48. 10.1111/camh.12198 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jones CRG, Pickles A, Falcaro M, Marsden AJS, Happé F, Scott SK, … Charman T (2011). A multimodal approach to emotion recognition ability in autism spectrum disorders. Journal of Child Psychology and Psychiatry, 52(3), 275–285. 10.1111/j.1469-7610.2010.02328.x [DOI] [PubMed] [Google Scholar]
- Kaiser D, Jacob GA, van Zutphen L, Siep N, Sprenger A, Tuschen-Caffier B, … Domes G (2019). Biased Attention to Facial Expressions of Ambiguous Emotions in Borderline Personality Disorder: An Eye-Tracking Study. Journal of Personality Disorders, 1–28. 10.1521/pedi_2019_33_363 [DOI] [PubMed] [Google Scholar]
- Karsh RB, & Breitenbach FW (1983). Looking at looking: The amorphous fixation measure.
- Kaufman J, Birmaher B, Brent D, Rao U, Flynn C, Moreci P, … Ryan N (1997). Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): Initial reliability and validity data. Journal of the American Academy of Child and Adolescent Psychiatry, 36(7), 980–988. 10.1097/00004583-199707000-00021 [DOI] [PubMed] [Google Scholar]
- Keding TJ, & Herringa RJ (2015). Abnormal structure of fear circuitry in pediatric post-traumatic stress disorder. Neuropsychopharmacology: Official Publication of the American College of Neuropsychopharmacology, 40(3), 537–545. 10.1038/npp.2014.239 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keding TJ, & Herringa RJ (2016). Paradoxical Prefrontal-Amygdala Recruitment to Angry and Happy Expressions in Pediatric Posttraumatic Stress Disorder. Neuropsychopharmacology: Official Publication of the American College of Neuropsychopharmacology, 41(12), 2903–2912. 10.1038/npp.2016.104 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kessler RC, Sonnega A, Bromet E, Hughes M, & Nelson CB (1995). Posttraumatic stress disorder in the National Comorbidity Survey. Archives of General Psychiatry, 52(12), 1048–1060. [DOI] [PubMed] [Google Scholar]
- Lakshman M, Murphy L, Mekawi Y, Carter S, Briscione M, Bradley B, … Powers A (2020). Attention bias towards threat in African American children exposed to early life trauma. Behavioural Brain Research, 383, 112513. 10.1016/j.bbr.2020.112513 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lamberg L (2001). Psychiatrists Explore Legacy of Traumatic Stress in Early Life. JAMA, 286(5), 523–526. 10.1001/jama.286.5.523-JMN0801-2-1 [DOI] [PubMed] [Google Scholar]
- Lambert RH, Monty RA, & Hall RJ (1974). High-speed data processing and unobtrusive monitoring of eye movements. Behavior Research Methods & Instrumentation, 6(6), 525–530. 10.3758/BF03201340 [DOI] [Google Scholar]
- Libby WL, Lacey BC, & Lacey JI (1973). Pupillary and Cardiac Activity During Visual Attention. Psychophysiology, 10(3), 270–294. 10.1111/j.1469-8986.1973.tb00526.x [DOI] [PubMed] [Google Scholar]
- Lundqvist D, Flykt A, & Öhman A (1998). The Karolinska Directed Emotional Faces—KDEF [CD ROM]. Department of Clinical Neuroscience, Psychology section, Karolinska Institutet. [Google Scholar]
- Marshall WA, & Tanner JM (1969). Variations in pattern of pubertal changes in girls. Archives of Disease in Childhood, 44(235), 291–303. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marshall WA, & Tanner JM (1970). Variations in the Pattern of Pubertal Changes in Boys. Archives of Disease in Childhood, 45(239), 13–23. 10.1136/adc.45.239.13 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Masten CL, Guyer AE, Hodgdon HB, McClure EB, Charney DS, Ernst M, … Monk CS (2008). Recognition of facial emotions among maltreated children with high rates of post-traumatic stress disorder. Child Abuse & Neglect, 32(1), 139–153. 10.1016/j.chiabu.2007.09.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mattavelli G, Sormaz M, Flack T, Asghar AUR, Fan S, Frey J, … Andrews TJ (2014). Neural responses to facial expressions support the role of the amygdala in processing threat. Social Cognitive and Affective Neuroscience, 9(11), 1684–1689. 10.1093/scan/nst162 [DOI] [PMC free article] [PubMed] [Google Scholar]
- McLaughlin KA, Koenen KC, Hill ED, Petukhova M, Sampson NA, Zaslavsky AM, & Kessler RC (2013). Trauma exposure and posttraumatic stress disorder in a national sample of adolescents. Journal of the American Academy of Child and Adolescent Psychiatry, 52(8), 815–830.e14. 10.1016/j.jaac.2013.05.011 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miché M, Hofer PD, Voss C, Meyer AH, Gloster AT, Beesdo-Baum K, & Lieb R (2018). Mental disorders and the risk for the subsequent first suicide attempt: Results of a community study on adolescents and young adults. European Child & Adolescent Psychiatry, 27(7), 839–848. 10.1007/s00787-017-1060-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Milad MR, Orr SP, Lasko NB, Chang Y, Rauch SL, & Pitman RK (2008). Presence and acquired origin of reduced recall for fear extinction in PTSD: Results of a twin study. Journal of Psychiatric Research, 42(7), 515–520. 10.1016/j.jpsychires.2008.01.017 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Patel R, Spreng RN, Shin LM, & Girard TA (2012). Neurocircuitry models of posttraumatic stress disorder and beyond: A meta-analysis of functional neuroimaging studies. Neuroscience and Biobehavioral Reviews, 36(9), 2130–2142. 10.1016/j.neubiorev.2012.06.003 [DOI] [PubMed] [Google Scholar]
- Phelps EA (2004). Human emotion and memory: Interactions of the amygdala and hippocampal complex. Current Opinion in Neurobiology, 14(2), 198–202. 10.1016/j.conb.2004.03.015 [DOI] [PubMed] [Google Scholar]
- Philippot P, & Feldman RS (1990). Age and social competence in preschoolers’ decoding of facial expression. British Journal of Social Psychology, 29(1), 43–54. 10.1111/j.2044-8309.1990.tb00885.x [DOI] [PubMed] [Google Scholar]
- Picci G, & Scherf KS (2016). From Caregivers to Peers: Puberty Shapes Human Face Perception. Psychological Science, 27(11), 1461–1473. 10.1177/0956797616663142 [DOI] [PubMed] [Google Scholar]
- Pine DS, Mogg K, Bradley BP, Montgomery L, Monk CS, McClure E, … Kaufman J (2005). Attention bias to threat in maltreated children: Implications for vulnerability to stress-related psychopathology. The American Journal of Psychiatry, 162(2), 291–296. 10.1176/appi.ajp.162.2.291 [DOI] [PubMed] [Google Scholar]
- Pitkänen A, Pikkarainen M, Nurminen N, & Ylinen A (2000). Reciprocal Connections between the Amygdala and the Hippocampal Formation, Perirhinal Cortex, and Postrhinal Cortex in Rat: A Review. Annals of the New York Academy of Sciences, 911(1), 369–391. 10.1111/j.1749-6632.2000.tb06738.x [DOI] [PubMed] [Google Scholar]
- Pole N, Neylan TC, Otte C, Henn-Hasse C, Metzler TJ, & Marmar CR (2009). Prospective Prediction of Posttraumatic Stress Disorder Symptoms Using Fear Potentiated Auditory Startle Responses. Biological Psychiatry, 65(3), 235–240. 10.1016/j.biopsych.2008.07.015 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pollak SD (2008). Mechanisms Linking Early Experience and the Emergence of Emotions: Illustrations From the Study of Maltreated Children. Current Directions in Psychological Science, 17(6), 370–375. 10.1111/j.1467-8721.2008.00608.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pollak SD, Messner M, Kistler DJ, & Cohn JF (2009). Development of perceptual expertise in emotion recognition. Cognition, 110(2), 242–247. 10.1016/j.cognition.2008.10.010 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pollak SD, & Sinha P (2002). Effects of early experience on children’s recognition of facial displays of emotion. Developmental Psychology, 38(5), 784–791. http://dx.doi.org.ezproxy.library.wisc.edu/10.1037/0012-1649.38.5.784 [DOI] [PubMed] [Google Scholar]
- R Core Team. (2016). R: A Language and Environment for Statistical Computing. Vienna, Austria: R Foundation for Statistical Computing. Retrieved from https://www.R-project.org [Google Scholar]
- Team RSTudio. (2012). RStudio: Integrated Development for R. Boston, MA: RStudio, Inc. [Google Scholar]
- Schmolck H, & Squire LR (2001). Impaired perception of facial emotions following bilateral damage to the anterior temporal lobe. Neuropsychology, 15(1), 30–38. http://dx.doi.org.ezproxy.library.wisc.edu/10.1037/0894-4105.15.1.30 [PubMed] [Google Scholar]
- Senn V, Wolff SBE, Herry C, Grenier F, Ehrlich I, Gründemann J, … Lüthi A (2014). Long-range connectivity defines behavioral specificity of amygdala neurons. Neuron, 81(2), 428–437. 10.1016/j.neuron.2013.11.006 [DOI] [PubMed] [Google Scholar]
- Shin LM, & Handwerger K (2009). Is posttraumatic stress disorder a stress-induced fear circuitry disorder? Journal of Traumatic Stress, 22(5), 409–415. 10.1002/jts.20442 [DOI] [PubMed] [Google Scholar]
- Steinberg AM, Brymer MJ, Decker KB, & Pynoos RS (2004). The University of California at Los Angeles Post-traumatic Stress Disorder Reaction Index. Current Psychiatry Reports, 6(2), 96–100. [DOI] [PubMed] [Google Scholar]
- Stevens JS, & Jovanovic T (2019). Role of social cognition in post-traumatic stress disorder: A review and meta-analysis. Genes, Brain, and Behavior, 18(1), e12518. 10.1111/gbb.12518 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tottenham N, Hare TA, & Casey BJ (2011). Behavioral Assessment of Emotion Discrimination, Emotion Regulation, and Cognitive Control in Childhood, Adolescence, and Adulthood. Frontiers in Psychology, 2. 10.3389/fpsyg.2011.00039 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tovote P, Fadok JP, & Lüthi A (2015). Neuronal circuits for fear and anxiety. Nature Reviews Neuroscience, 16(6), 317–331. 10.1038/nrn3945 [DOI] [PubMed] [Google Scholar]
- Vetter NC, Drauschke M, Thieme J, & Altgassen M (2018). Adolescent Basic Facial Emotion Recognition Is Not Influenced by Puberty or Own-Age Bias. Frontiers in Psychology, 9. 10.3389/fpsyg.2018.00956 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weathers FW, Keane TM, & Davidson JR (2001). Clinician-administered PTSD scale: A review of the first ten years of research. Depression and Anxiety, 13(3), 132–156. [DOI] [PubMed] [Google Scholar]
- Wechsler D (2011). Wechsler Abbreviated Scale of Intelligence–Second Edition Manual. Bloomington, MN: Pearson. [Google Scholar]
- Williamson DE, Birmaher B, Ryan ND, Shiffrin TP, Lusky JA, Protopapa J, … Brent DA (2003). The stressful life events schedule for children and adolescents: Development and validation. Psychiatry Research, 119(3), 225–241. [DOI] [PubMed] [Google Scholar]
- Wolf RC (2016). A role for ventromedial prefrontal cortex in facial emotion recognition (Ph.D., The University of Wisconsin - Madison). The University of Wisconsin - Madison, United States -- Wisconsin. Retrieved from https://search.proquest.com/docview/1811945642/abstract/6DB38A4EE27F4A48PQ/1 [Google Scholar]
- Wolf RC, & Herringa RJ (2016). Prefrontal-Amygdala Dysregulation to Threat in Pediatric Posttraumatic Stress Disorder. Neuropsychopharmacology: Official Publication of the American College of Neuropsychopharmacology, 41(3), 822–831. 10.1038/npp.2015.209 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wolf RC, Philippi CL, Motzkin JC, Baskaya MK, & Koenigs M (2014). Ventromedial prefrontal cortex mediates visual attention during facial emotion recognition. Brain: A Journal of Neurology, 137(Pt 6), 1772–1780. 10.1093/brain/awu063 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wright B, Clarke N, Jordan J, Young AW, Clarke P, Miles J, … Williams C (2008). Emotion recognition in faces and the use of visual context Vo in young people with high-functioning autism spectrum disorders. Autism, 12(6), 607–626. 10.1177/1362361308097118 [DOI] [PubMed] [Google Scholar]
- Young JC, & Widom CS (2014). Long-term effects of child abuse and neglect on emotion processing in adulthood. Child Abuse & Neglect, 38(8), 1369–1381. 10.1016/j.chiabu.2014.03.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
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