Processing Of Facial Expressions Research Articles

Natural brief facial expression changes detection at a single glance: evidence from Fast Periodic Visual Stimulation

The processing of emotional facial expressions has been studied mainly with stereotypical face stimuli, but contextual information leads to drastic modulation in the categorization of facial expressions (Aviezer et al., 2017). In the human brain, brief facial expression changes are quickly read from faces (Dzhelyova et al., 2017). Yet, how reliably these changes are detected with realistic faces embedded in a natural context remain unknown. In this study, faces varied in viewpoint, identity, gender, age, ethnic origin and background context. We recorded 128-channel EEG in 17 participants while they viewed 50s sequences with a neutral-expression face at a rate of 5.99 Hz (F) at two faces orientations (upright, inverted). Every five faces, the faces changed expression to one of the six basic expression (fear, disgust, happiness, anger, surprised or sadness; Ekman, 1993), one emotion per sequence (e.g ANeutralANeutralANeutralANeutralANeutralBExpressiveANeutral …). EEG responses at 5.99 Hz reflect general visual processing, while the EEG responses at F/5 = 1.1998 Hz and its harmonics (e.g., 2F/5 = 2.3996, etc.) index detection of a brief change of natural facial expression. Despite the wide variety across images, a F/5 response was observed for each individual participant, pointing to robust facial expression categorization processes. At the group-level, the categorization response was measured over occipito-temporal sites and was largely reduced when faces were inverted, indicating that it reflects high-level processes. Despite evidence (Leleu et al., 2018; Hinojosa et al., 2015) suggesting that sad expressions are more subtle and thus lead to weaker responses than other emotions, our observations with natural expressions highlight a stronger response for this emotion, especially over the left hemisphere. Moreover, we observed a right hemisphere dominance for a shift from neutral to fearful faces and a left hemisphere dominance for a shift from neutral to happy faces.

Understanding the development of face and emotion processing under a predictive processing framework.

In the present work, we explore the development of processing of emotional facial configurations under a predictive processing (or predictive coding) framework. Predictive processing provides a new approach to brain function that has been used to explain a wide range of processes, from perception to socioemotional processing. The explanatory power of this framework for adult brain function is widely recognized, but it has yet to be systematically applied to understanding the developing brain. Studying the findings of developmental research under this framework may allow a deeper understanding of the predictive mechanisms and their ontogenetic course, and adds to knowledge on brain functions and developmental processes. Therefore, the goal of this work was to explore the potential complementarity of predictive processing and development. Specifically, we focus on how the development of facial and emotion processing may be understood under a predictive processing framework. The processing of facial expressions was selected because of the developmental relevance of these stimuli, their impact on general emotional development, as well as the large body of literature on this topic (comprised of both well-established but also incongruent findings, which a novel approach may clarify). Considering the main findings of developmental research on the processing of emotion-related facial configurations under this framework, we argue that predictive processing is consistent with developmental evidence and provides a promising avenue for developmental research, as it reveals new questions in the fields of development and emotion processing. (PsycINFO Database Record (c) 2019 APA, all rights reserved).

The influence of stimulus valence on perceptual processing of facial expressions and subsequent response inhibition.

The constant interplay between affective processing and cognitive control supports emotion regulation and appropriate social functioning. Even when affective stimuli are processed implicitly, threat-related stimuli are prioritized in the earliest stages of processing; yet, it remains unclear how implicit attention to affect influences subsequent cognitive control functions. The present study evaluated the influence of affective valence on early perceptual processes and subsequent response inhibition in a context where affective properties of the stimuli (facial expressions) were not critical for performing the task. Participants (N=32) completed an affective stop-signal task (SST) while their scalp EEGs were recorded. The SST assessed response inhibition while participants implicitly attended to happy and afraid facial expressions that were matched for level of arousal. Behavioral performance was measured via response time and accuracy while physiological response was measured via the P100, N170, and N200/P300 ERP components. Decreased gender discrimination accuracy, delayed P100 latency, and more negative N170 amplitude were observed for afraid faces compared to happy faces, suggesting a shift in processing with respect to face valence. However, differences in stopping accuracy or N200/P300 ERP components during response inhibition were not observed, pointing to top-down cognitive processes likely being recruited to override the early automatic response to prioritize threat-related stimuli. Findings highlight that, in this implicit affective attention task, threat-related stimuli are prioritized early during processing, but implicitly attending to differentially valenced stimuli did not modulate subsequent cognitive control functions.

Early life stress is associated with reduced avoidance of threatening facial expressions.

Early neglect or maltreatment has been associated with changes in children's processing of emotional facial expressions, including a hypersensitivity to the emotion of anger. This may facilitate the avoidance of danger in a maltreating environment. However, few studies have examined whether experiences of early life stress (ELS) are associated with atypical avoidance responses towards emotional facial expressions, or whether the effects of ELS can be observed in adult participants. The present study therefore examined the effects of ELS on adults' approach-avoidance tendencies towards angry, happy, and neutral facial expressions. Surprisingly, higher levels of ELS were associated with reduced avoidance of angry facial expressions among individuals with no evidence of mental illness. In contrast, there was no evidence of a relationship between ELS and avoidance of angry facial expressions among individuals with experience of mental illness. These novel findings suggest that ELS-related changes in social cognition can be observed years after the ELS itself occurred.

Neurophysiological and Interpersonal Correlates of Emotional Face Processing in Alcohol Use Disorder.

A growing literature suggests deficient emotional facial expression (EFE) processing among recently abstinent individuals with alcohol use disorders (AUDs). Further investigation is needed to clarify valence-related discrepancies and elucidate neural and psychosocial correlates. We examined neurobehavioral indices of EFE processing and interpersonal problems in treatment seekers with AUDs and healthy community controls (CCs). Thirty-four individuals with AUDs and 39 CCs completed an emotion judgment task (EJT), requiring discrimination between happy, angry, and sad EFEs. A second task requiring discrimination of male and female faces with neutral expressions served as the control task (i.e., sex judgment task, SJT). Neurophysiological (i.e., N170 and P3) and behavioral measures were analyzed using generalized linear mixed models (GLMM). Interpersonal problems were assessed with the Inventory of Interpersonal Problems-64 (IIP-64). The relationship of IIP-64 and EJT performance was investigated via within-group correlations. Analysis of the SJT revealed no group differences in behavioral measures, N170 amplitude, or P3 latency. P3 amplitudes, however, were significantly lower in the AUD group. For the EJT, initial observations of group differences in P3 amplitude were accounted for by differences in the control task. Behavioral analyses indicated that the AUD group was significantly less accurate than the CC group. Hypothesis-driven analyses using GLMM-estimated group differences indicated that anger processing was affected to a greater degree than were other emotions. Significant EJT/IIP-64 correlations were observed for anger processing within the AUD group and were confined to IIP-64 subscales with relatively high ratings on the affiliation dimension. Findings provide partial support for an emotion-specific processing deficit in persons with AUDs. Anger processing was more robustly affected than other emotions and was associated with interpersonal problems characterized by being overly needy, nonassertive, and overly accommodating. Results extend prior reports and reinforce the need for comprehensive study of emotion processing and its real-world implications.

The effects of sex and residual cannabis use on emotion processing: An event-related potential study.

Cannabis use has been shown to affect processing of emotional facial expressions as measured by the P1 and P3 event-related potential (ERP) components. These components have been shown to be related to emotion processing in particular attention to emotion. Previous research also indicates that there are sex differences in how cannabis effects males and females as well as how they process emotion. This study examined the relationship between the effects of residual cannabis use and sex differences in 144 participants (F = 80) in a facial expression emotion processing task. Both the P1 and P3 ERP components were compared in male and female participants in noncannabis user, casual cannabis user, and heavy cannabis user groupings. The task involved implicitly, explicitly, and empathically identifying emotional expressions (angry, happy, neutral, and fearful) in male and females faces. There were differences between males and females in both the P1 and P3 ERP in relation to cannabis use. Males had a larger P1 than females with cannabis use and a smaller P3. Differences in the P1 were observed in both positive and negative emotion and between tasks in relation to cannabis use patterns. Differences in the P3 were seen in heavy male users for empathy happy and casual male users implicit angry when compared to females. These differences highlight the important of considering sex differences in regard to the effects of cannabis, in particular in emotion processing. (PsycINFO Database Record (c) 2019 APA, all rights reserved).

The language context effect in facial expressions processing and its mandatory characteristic

Background visual scenes in which faces are perceived provide contextual information for facial expression processing. One type of background information, the language context, has a vital influence on facial expression processing. The current study is aimed to investigate the effect of the language context on facial expression processing by recording event-related potentials (ERPs). Experiment one adopted the facial expression categorization task to investigate the effects of different language contexts on emotional and non-emotional facial processing. Experiment two adopted the task-irrelevant paradigm to investigate whether the language context effect on facial expression processing was mandatory. The results found that (1) the language context affected facial expression processing. Facial expression processing was promoted when the language context was emotionally congruent with faces. Moreover, the language context had an evoking effect on neutral faces. To be detailed, neutral facial expressions were evoked to be judged as positive in the positive language context while as negative in the negative language context. (2) The language context effect still affected facial expression processing in a task-irrelevant paradigm. When the language context was emotionally incongruent with facial expressions, larger N170 and LPP amplitudes were elicited, indicating the inhibition of incongruent emotions. These findings prove that the language context effect on facial expression processing is mandatory.

Children with facial paralysis due to Moebius syndrome exhibit reduced autonomic modulation during emotion processing

BackgroundFacial mimicry is crucial in the recognition of others’ emotional state. Thus, the observation of others’ facial expressions activates the same neural representation of that affective state in the observer, along with related autonomic and somatic responses. What happens, therefore, when someone cannot mimic others’ facial expressions?MethodsWe investigated whether psychophysiological emotional responses to others’ facial expressions were impaired in 13 children (9 years) with Moebius syndrome (MBS), an extremely rare neurological disorder (1/250,000 live births) characterized by congenital facial paralysis. We inspected autonomic responses and vagal regulation through facial cutaneous thermal variations and by the computation of respiratory sinus arrhythmia (RSA). These parameters provide measures of emotional arousal and show the autonomic adaptation to others’ social cues. Physiological responses in children with MBS were recorded during dynamic facial expression observation and were compared to those of a control group (16 non-affected children, 9 years).ResultsThere were significant group effects on thermal patterns and RSA, with lower values in children with MBS. We also observed a mild deficit in emotion recognition in these patients.ConclusionResults support “embodied” theory, whereby the congenital inability to produce facial expressions induces alterations in the processing of facial expression of emotions. Such alterations may constitute a risk for emotion dysregulation.

Brain-based Classification of Negative Social Bias in Adolescents With Nonsuicidal Self-injury: Findings From Simulated Online Social Interaction

BackgroundInterpersonal stress and perceived rejection have been clinically observed as common triggers of nonsuicidal self-injury (NSSI), with self-injury behavior regulating both affective and social experiences. We investigated whether the subjective interpretation of social interaction in a simulated online environment might be biased in the NSSI group, and the brain mechanisms underlying the experience. MethodsThirty female adolescent patients with NSSI and thirty female age-matched controls were investigated in this case–control study. In our novel task that simulates interaction on current social media platforms, participants indicated whether they liked or disliked pictures of other players during a functional magnetic resonance imaging (fMRI) scan. Participants also viewed positive and negative feedback directed toward them by others. The task also assessed the subjective effects of the social interaction. Finally, subjects underwent a separate facial electromyography session, which measured facial expressions processing. OutcomesBehaviorally, the NSSI group showed a negative bias in processing social feedback from others. A multi-voxel pattern analysis (MVPA) identified brain regions that robustly classified NSSI subjects and controls. Regions in which mutual activity contributed to the classification included dorsomedial prefrontal cortex and subgenual anterior cingulate cortex, a region implicated in mood control. In the NSSI group, multi-voxel classification scores correlated with behavioral sensitivity to negative feedback from others. Results remained significant after controlling for medication, symptoms of depression, and symptoms of borderline personality disorder. InterpretationThis study identified behavioral and neural signatures of adolescents with NSSI during social interaction in a simulated social media environment. These findings highlight the importance of understanding social information processing in this clinical population and can potentially advance treatment approaches.

Out of Focus: Facial Feedback Manipulation Modulates Automatic Processing of Unattended Emotional Faces.

Facial expressions provide information about an individual's intentions and emotions and are thus an important medium for nonverbal communication. Theories of embodied cognition assume that facial mimicry and resulting facial feedback plays an important role in the perception of facial emotional expressions. Although behavioral and electrophysiological studies have confirmed the influence of facial feedback on the perception of facial emotional expressions, the influence of facial feedback on the automatic processing of such stimuli is largely unexplored. The automatic processing of unattended facial expressions can be investigated by visual expression-related MMN. The expression-related MMN reflects a differential ERP of automatic detection of emotional changes elicited by rarely presented facial expressions (deviants) among frequently presented facial expressions (standards). In this study, we investigated the impact of facial feedback on the automatic processing of facial expressions. For this purpose, participants (n = 19) performed a centrally presented visual detection task while neutral (standard), happy, and sad faces (deviants) were presented peripherally. During the task, facial feedback was manipulated by different pen holding conditions (holding the pen with teeth, lips, or nondominant hand). Our results indicate that automatic processing of facial expressions is influenced and thus dependent on the own facial feedback.

Double-checking emotions: Valence and emotion category in contextual integration of facial expressions of emotion

Faces showing happy, angry or fearful expressions were presented in emotionally congruent or incongruent situational contexts (short sentences describing events that would usually provoke happiness, anger or fear). The participants were assigned the task of judging whether the expression was appropriate or not to the context (congruency judgment task). Effects of emotional congruency were observed at both the behavioral and electrophysiological levels. Behavioral results showed evidence of congruency effects based on specific emotion content (e.g., less accurate and slower responses to fear faces in angry contexts). Event-related-potentials (ERP) results also showed emotional congruency effects at different post-stimulus onset latencies, beginning with the face-sensitive N170 component. An effect of emotional congruency was also shown on the N400 component that is typically sensitive to semantic congruency. Finally, a late positive potential (LPP), appearing at 450–650 ms post-stimulus onset showed a complex pattern of effects with modulations driven by the different combinations of contexts and target expressions. These results are interpreted in terms of a double process of valence and emotion checking that is supposed to underlie affective processing and contextual integration of facial expressions of emotions.

Rapid face processing for positive and negative emotions in 5-, 7-, and 12-month-old infants: An exploratory study.

Processing of positive and negative facial expressions in infancy follows a distinct course with a bias towards fearful facial expressions starting at 7months of age; however, little is known about the developmental trajectory of fear processing and other facial expressions, and if this bias is driven by specific regions of the face. This study used eye tracking to examine the processing of positive and negative emotional faces in independent groups of 5- (n=43), 7- (n=60), and 12-month-old infants (n=70). Methods: Infants were shown static images of female faces exhibiting happy, anger, and fear expressions, for one-second each. Total looking time and looking time for areas of interest (AOIs) including forehead and eyes (top), mouth and chin (bottom), and contour of each image were computed. Infants across all ages looked longer to fear faces than angry or happy faces. Negative emotions generally elicited greater looking times for the top of the face than did happy faces. In addition, we also found that at 12months of age infants looked longer for the bottom of the faces than did 5-month-olds. Our study suggests that the visual bias to attend longer to fearful faces may be in place by 5months of age, and between 5 and 12months of age, there seems to be a developmental shift towards looking more to the bottom of the faces. STATEMENT OF CONTRIBUTION: What is already known in this subject? Bias for fear face processing is present at 7months of age. Using older data collection systems, we have some idea about which facial features recruit infant attention. What the present study adds? Well-controlled paradigm that examines both positive and negative facial expressions, to different areas of interest in the face. Use of the same paradigm to test a cross-sectional sample of infants in distinct developmental stages - 5, 7, and 12months.

Viewing heterospecific facial expressions: an eye-tracking study of human and monkey viewers

Common facial expressions of emotion have distinctive patterns of facial muscle movements that are culturally similar among humans, and perceiving these expressions is associated with stereotypical gaze allocation at local facial regions that are characteristic for each expression, such as eyes in angry faces. It is, however, unclear to what extent this ‘universality’ view can be extended to process heterospecific facial expressions, and how ‘social learning’ process contributes to heterospecific expression perception. In this eye-tracking study, we examined face-viewing gaze allocation of human (including dog owners and non-dog owners) and monkey observers while exploring expressive human, chimpanzee, monkey and dog faces (positive, neutral and negative expressions in human and dog faces; neutral and negative expressions in chimpanzee and monkey faces). Human observers showed species- and experience-dependent expression categorization accuracy. Furthermore, both human and monkey observers demonstrated different face-viewing gaze distributions which were also species dependent. Specifically, humans predominately attended at human eyes but animal mouth when judging facial expressions. Monkeys’ gaze distributions in exploring human and monkey faces were qualitatively different from exploring chimpanzee and dog faces. Interestingly, the gaze behaviour of both human and monkey observers were further affected by their prior experience of the viewed species. It seems that facial expression processing is species dependent, and social learning may play a significant role in discriminating even rudimentary types of heterospecific expressions.

Human brain detection of natural brief facial expression at a single glance

Background The processing of emotional facial expressions has been studied mainly with stereotypical and posed face stimuli. In the human brain, brief facial expression changes are quickly read from faces (Dzhelyova et al., 2017). Objectives The purpose of this study is to know how reliably brief changes are detected with realistic faces embedded in a natural context. Methods In this study, faces varied in viewpoint, identity, gender, age, ethnic origin and background context. We recorded 128-channel EEG in 17 participants while they viewed 50s sequences with neutral-expression faces at a rate of 5.99 Hz (F) at two faces orientations (upright, inverted). Every five faces, the faces changed expression to one of the six basic expression (fear, disgust, happiness, anger, surprised or sadness; Ekman, 1993), one emotion per sequence. EEG responses at 5.99 Hz reflect general visual processing, while the EEG responses at F/5 = 1.1998 Hz and its harmonics (e.g., 2F/5 = 2.3996, etc.) index detection of a brief change of natural facial expression. Results At group level, the categorization response was measured over occipito-temporal sites and was largely reduced when faces were inverted, indicating that it reflects high-level processes. Our observations with natural expressions highlight a stronger response for a shift from neutral to sad faces, especially over the left hemisphere. Moreover, we observed a right hemisphere dominance for fearful faces and a left hemisphere dominance for surprised faces. Conclusion Human brain is able to detect automatically in natural scenes dynamic brief facial expression changes.

P60-F Emotional modulation of ERPs elicited by angry faces in patients with schizotypal disorder and schizophrenia

Background Emotion recognition is distorted in schizophrenia. The schizotypal disorder can be considered a mild form of schizophrenia, sharing some features but showing better preservation of prefrontal brain regions. We studied the differences in visual ERPs elicited by neutral and angry faces in patients with schizophrenia and schizotypal disorder. Materials and methods Only male participants took part in our study: 18 patients with paranoid schizophrenia, 17 patients with the schizotypal disorder, and 50 healthy volunteers. Participants had to push different buttons for photographs of neutral and angry/aggressive people (total of 80). We recorded 128-channel EEG and analyzed the evoked brain activity elicited by faces and facial expressions. The difference (p Results EM was observed at early latencies in all groups in group-specific locations. EM in components N170, N250, and P280 was quite similar in scalp topography for controls and schizotypal disorder, while it was not observed in schizophrenia for N170 and N250. The central distribution of EM was found for N450 component in all groups, and for the later latencies, EM with similar topography was found only in controls and in schizotypal disorder. Conclusions Our results indicate that EM in schizotypal disorder exhibits a general resemblance with EM in healthy controls at the latencies longer than 130 Presumably, certain stages of facial expression processing are preserved in schizotypal disorder. At the earlier latencies, the EM in schizotypal disorder has more in common with schizophrenia than with healthy controls.

What do error patterns in processing facial expressions, social interaction scenes and vocal prosody tell us about the way social cognition works in children with 22q11.2DS?

Impairments in social cognition have been frequently described in 22q11.2 deletion syndrome (22q11.2DS) and are thought to be a hallmark of difficulties in social interactions. The present study addresses aspects that are critical for everyday social cognitive functioning but have received little attention so far. Sixteen children with 22q11.2DS and 22 controls completed 1 task of facial expression recognition, 1 task of attribution of facial expressions to faceless characters involved in visually presented social interactions, and 1 task of attribution of facial expressions to characters involved in aurally presented dialogues. All three tasks have in common to involve processing of emotions. All participants also completed two tasks of attention and two tasks of visual spatial perception, and their parents completed some scales regarding behavioural problems of their children. Patients performed worse than controls in all three tasks of emotion processing, and even worse in the second and third tasks. However, they performed above chance level in all three tasks, and the results were independent of IQ, age and gender. The analysis of error patterns suggests that patients tend to coarsely categorize situations as either attractive or repulsive and also that they have difficulties in differentiating emotions that are associated with threats. An isolated association between the tasks of emotion and behaviour was found, showing that the more frequently patients with 22q11.2DS perceive happiness where there is not, the less they exhibit aggressive behaviour.

Joint Modulation of Facial Expression Processing by Contextual Congruency and Task Demands.

Faces showing expressions of happiness or anger were presented together with sentences that described happiness-inducing or anger-inducing situations. Two main variables were manipulated: (i) congruency between contexts and expressions (congruent/incongruent) and (ii) the task assigned to the participant, discriminating the emotion shown by the target face (emotion task) or judging whether the expression shown by the face was congruent or not with the context (congruency task). Behavioral and electrophysiological results (event-related potentials (ERP)) showed that processing facial expressions was jointly influenced by congruency and task demands. ERP results revealed task effects at frontal sites, with larger positive amplitudes between 250–450 ms in the congruency task, reflecting the higher cognitive effort required by this task. Effects of congruency appeared at latencies and locations corresponding to the early posterior negativity (EPN) and late positive potential (LPP) components that have previously been found to be sensitive to emotion and affective congruency. The magnitude and spatial distribution of the congruency effects varied depending on the task and the target expression. These results are discussed in terms of the modulatory role of context on facial expression processing and the different mechanisms underlying the processing of expressions of positive and negative emotions.

Widespread and lateralized social brain activity for processing dynamic facial expressions.

Dynamic facial expressions of emotions constitute natural and powerful means of social communication in daily life. A number of previous neuroimaging studies have explored the neural mechanisms underlying the processing of dynamic facial expressions, and indicated the activation of certain social brain regions (e.g., the amygdala) during such tasks. However, the activated brain regions were inconsistent across studies, and their laterality was rarely evaluated. To investigate these issues, we measured brain activity using functional magnetic resonance imaging in a relatively large sample (n = 51) during the observation of dynamic facial expressions of anger and happiness and their corresponding dynamic mosaic images. The observation of dynamic facial expressions, compared with dynamic mosaics, elicited stronger activity in the bilateral posterior cortices, including the inferior occipital gyri, fusiform gyri, and superior temporal sulci. The dynamic facial expressions also activated bilateral limbic regions, including the amygdalae and ventromedial prefrontal cortices, more strongly versus mosaics. In the same manner, activation was found in the right inferior frontal gyrus (IFG) and left cerebellum. Laterality analyses comparing original and flipped images revealed right hemispheric dominance in the superior temporal sulcus and IFG and left hemispheric dominance in the cerebellum. These results indicated that the neural mechanisms underlying processing of dynamic facial expressions include widespread social brain regions associated with perceptual, emotional, and motor functions, and include a clearly lateralized (right cortical and left cerebellar) network like that involved in language processing.

Emotion in motion: Facial dynamics affect infants' neural processing of emotions.

Research investigating the early development of emotional processing has focused mainly on infants' perception of static facial emotional expressions, likely restricting the amount and type of information available to infants. In particular, the question of whether dynamic information in emotional facial expressions modulates infants' neural responses has been rarely investigated. The present study aimed to fill this gap by recording 7-month-olds' event-related potentials to static (Study 1) and dynamic (Study 2) happy, angry, and neutral faces. In Study 1, happy faces evoked a faster right-lateralized negative central (Nc) component compared to angry faces. In Study 2, both happy and angry faces elicited a larger right-lateralized Nc compared to neutral faces. Irrespective of stimulus dynamicity, a larger P400 to angry faces was associated with higher scores on the Negative Affect temperamental dimension. Overall, results suggest that 7-month-olds are sensitive to facial dynamics, which might play a role in shaping the neural processing of facial emotional expressions. Results also suggest that the amount of attentional resources infants allocate to angry expressions is associated to their temperamental traits. These findings represent a promising avenue for future studies exploring the neurobiological processes involved in perceiving emotional expressions using dynamic stimuli.

Early processing (N170) of infant faces in mothers of children with autism spectrum disorder and its association with maternal sensitivity.

Individuals with autism spectrum disorder (ASD) exhibit impaired adult facial processing, as shown by the N170 event-related potential. However, few studies explore such processing in mothers of children with ASD, and none has assessed the early processing of infant faces in these women. Moreover, whether processing of infant facial expressions in mothers of children with ASD is related to their response to their child's needs (maternal sensitivity [MS]) remains unknown. This study explored the N170 related to infant faces in a group of mothers of children with ASD (MA) and a reference group of mothers of children without ASD. For both emotional (crying, smiling) and neutral expressions, the MA group exhibited larger amplitudes of N170 in the right hemisphere, while the reference group showed similar interhemispheric amplitudes. This lateralization effect within the MA group was not present for nonfaces and was stronger in the mothers with higher MS. We propose that mothers of ASD children use specialized perceptual resources to process infant faces, and this specialization is mediated by MS. Our findings suggest that having an ASD child modulates mothers' early neurophysiological responsiveness to infant cues. Whether this modulation represents a biological marker or a response given by experience remains to be explored. Autism Research 2019, 12: 744-758. © 2019 International Society for Autism Research, Wiley Periodicals, Inc. LAY SUMMARY: When mothers of children with autism spectrum disorder (ASD) see baby faces expressing emotions, they show a right-sided electrical response in the brain. This lateralization was stronger in mothers who were more sensitive to their children's needs. We conclude that having a child with ASD and being more attuned to their behavior generates a specialized pattern of brain activity when processing infant faces. Whether this pattern is biological or given by experience remains to be explored.