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Vuilleumier, P.

Publications and source records attributed to Vuilleumier, P..

At least 19 recordsLinked to original sources

Higher-order topology uncovers the multidimensional dynamics of naturalistic emotion

Emotions are thought to emerge from co-activation among distributed brain systems, yet traditional fMRI analyses typically examine localized responses and pairwise connections, potentially overlooking interactions among groups of regions. Here, we use time-resolved higher-order topology to characterize these group interactions during naturalistic viewing of 14 films totaling over 2.5 h, continuously annotated across 50 affective features. The homological scaffold, representing evolving group-level topology, most closely tracks recurrent emotional states and best predicts fine-grained affective profiles. This sensitivity diminishes when emotion is compressed into dimensions of valence, arousal, and power, where pairwise connectivity captures the dominant arousal signal. Across three independent datasets, arousal predictions transfer most robustly through pairwise connectivity, while the relative geometry of broad affective states remains conserved across film narratives despite poor valence generalization. These findings reveal complementary neural representations of emotion: higher-order topology captures fine-grained affective structure, whereas pairwise connectivity provides a portable readout of broad arousal.

neuroscience↗

Individual differences of cortical and subcortical emotion-informed functional gradients

The complex interplay between brain regions that support emotional experience and their link to individual differences is a topic of active research. Additionally, there has been growing interest in using functional gradients to investigate human cortical organization during both rest and film fMRI. Among these, several studies demonstrated improved brain fingerprinting performance, reflecting greater neural identification capability of film fMRI against rest fMRI despite higher subject synchronization during film-watching than in rest. Comparably, in this work we study the relation between individual differences, in particular, state anxiety and openness scores, and brain activity during the processing of various emotional scenes in films, through functional gradients. Next to including subcortical areas, we also propose a new approach of computing functional gradients based on a subset of frames selected using emotional annotation data of films, resulting in emotion-informed functional gradients. Then we evaluate the variance in emotion-informed gradients across subjects and employ these same gradients in the prediction of individual differences. For emotion-informed functional gradients, the highest predictability of state anxiety was found for scenes of negative valence and medium-high arousal, corresponding to the typical location of anxiety within the valence-arousal-power emotional space. Additionally, predictability of state anxiety was negatively correlated to inter-subject variability. In contrast, predictability of openness was found to be highest during scenes with low arousal and positively correlated to inter-subject variability. In essence, our results first show that macroscale brain organization is affected by emotional experience, and that frame selection based on the latter can be useful to remove non-subject-specific variability while extracting subject-specific information related to the emotion experience. It also demonstrates that frame selection increases inter-subject variability allowing the extraction of more subject-specific information. Thus, expanding on the idea of brain fingerprint in film fMRI, we argue that emotional experiences enhance disentanglement of various domain of individual differences. Moreover, depending on the individual difference of interest, fMRI acquired during more or less constrained paradigms would be more suitable to reveal different properties of brain function.

neuroscience↗

Emotional modulation of visual cortical reactivation during true and false memories

Previous research revealed that memory retrieval is associated with a reactivation of sensory cortices reflecting the content of the memory. Further, such reactivation is stronger when retrieval is cued with emotional information as compared with neutral information. However, past studies focused on correct retrieval, and it remains unknown whether a similar reactivation occurs during memory errors, and whether this is enhanced in emotional contexts. Here, we hypothesized that emotion may influence memory errors due to an increase of sensory cortical reactivation at the cost of recovering episodic details (i.e. leading to incorrect retrieval of non-specific associations shared with other cues). We compared brain activations during successful memory retrieval and memory errors in 18 healthy participants who encoded unique negative or neutral scenes paired with one of four associated faces, shared with other trials. Participants were tested the next day with a scene-cued associative retrieval test, while undergoing functional magnetic resonance imaging (fMRI). Results from a face-responsive region of interest in fusiform cortex (unlike a control place-responsive region in parahippocampal cortex) showed stronger activation for both Hits ("Old" | Target) and False Alarms ("Old" | Foil), as compared with Misses ("New" | Target) and Correct Rejections ("New" | Foil). The emotional content of scene cues did not modulate activation patterns during correct retrieval but produced specific effects on Misattribution errors (incorrect "Old" | Target, i.e., retrieval of an incorrect face cued by a previously seen scene). Specifically, Misattributions were accompanied by increased fusiform activation comparable to Hits when cued by negative scenes, but low fusiform activation similar to Misses when cued by neutral scenes. Unlike Misattributions, however, Hits cued by emotional information recruited a distinctive network previously linked to personal episodic memories, including medial prefrontal, cingulate, and hippocampal regions, together with enhanced functional coupling between the latter and fusiform cortex. No implicit effect of previous face exposure was observed in the fusiform during Misses, regardless of emotion context. Our results suggest that the reactivation of sensory areas follows subjective memory experience during retrieval, and that emotion can enhance such mechanism when the cue is recognized but detailed episodic memory mediated by fronto-hippocampal circuits is absent, leading to the retrieval of inappropriate associations and false memories.

neuroscience↗

Brain neuromarkers predict self- and other-related mentalizing across adult, clinical, and developmental samples

Human social interactions rely on the ability to reflect on ones own and others internal states and traits--a process known as mentalizing. Impaired or altered mentalizing is a hallmark of multiple psychiatric and neurodevelopmental conditions. Yet, replicable and easily testable brain markers of mentalizing have so far been lacking. Here, we apply an interpretable machine learning approach to multiple datasets (total N=390) to train and validate fMRI brain signatures that predict i) mentalizing about the self, ii) mentalizing about another person, and iii) both types of mentalizing. Self-mentalizing and other-mentalizing classifiers had positive weights in anterior/medial and posterior/lateral brain areas, respectively, with accuracy rates of 82% and 77% for out-of-sample prediction. The classifier trained across both types of mentalizing showed 98% predictive accuracy and separated (mental) attributional from factual inferences. Classifier patterns revealed better self/other separation in healthy adults compared to individuals with schizophrenia and with increasing age in adolescence. Together, our findings reveal consistent and separable neural patterns subserving trait-based mentalizing about self and others--present at least from the age of adolescence and functionally altered in severe neuropsychiatric disorders. These mentalizing signatures hold promise as candidate neuromarkers of social-cognitive processes in different contexts and clinical conditions. Author NoteThis work was funded by a Starting Grant from the European Research Council (ERC, 101041087) to LKo, a German Academic Exchange Service (DAAD) doctoral grant and a Network of European Neuroscience Schools (NENS) exchange fellowship to DA, an R01 grant from the U.S. National Institutes of Mental Health (R01MH125414-01) to JAH and DAS, a Junior Leader Fellowship from "la Caixa" Foundation (LCF/BQ/PR22/11920017) to PFC, a Consolidator Grant from the European Research Council (ERC, 648082) to LKr, R37, R01 support from the U.S. National Institutes of Mental Health (R37MH076136 to TDW, MH116026 to TDW and L. Chang [PI], R01EB026549 to TDW and M. Lindquist [MPIs]), an NIMH grant (P50MH094258-01A1) to R. Adolphs, and a CIC Brain and Mental Health Chair from the Neurodis foundation to AT. LvdM acknowledges a European Science Foundation EURYI grant (044035001) that funded her doctoral studies (PI: A. Aleman). Views and opinions expressed are however those of the authors only and do not necessarily reflect those of the European Union or the European Research Council. Neither the European Union nor the granting authority can be held responsible for them. The funders had no role in study design, data analysis, manuscript preparation, or publication decisions.

neuroscience↗

Mindfulness training impacts brain network dynamics linked to stress response in young adolescents.

Mindfulness-based interventions (MBI) may lead to lower levels of psychological distress, including depression, anxiety, and stress in adolescents. Past research has advanced the discovery of neural architecture recruited by MBI. However, the brain mechanisms through which mindfulness exerts more resilient responses to social stressors in teens remain unclear. Here, we examined how MBI modulates changes in brain network dynamics following social stress with different affective valence (i.e., neutral, negative, and positive). For this aim, we carried out a longitudinal randomized controlled trial in which non-clinical adolescents underwent MBI for 8 weeks. They completed a psychosocial stress task before and following MBI. Functional magnetic resonance imaging (fMRI) and self-reported measurements of psychological distress were collected in both measurement points (i.e., "pre" and "post" MBI). We computed co-activation patterns on fMRI data to characterize dynamic functional connectivity within whole-brain networks. The results depicted how MBI modulates transient co-activation changes in dorsal medial regions of the brain default network (DN) following the experience of stress. However, these brain changes were not specific to the affective valence of stressful stimuli. The relationship between the DN dynamics and the measurements of psychological distress was mediated by MBI. Globally, our findings support a model in which MBI causally mediate brain-behavior interactions related to psychosocial stress in adolescents.

neuroscience↗

Emo-FilM: A multimodal dataset for affective neuroscience using naturalistic stimuli

The extensive Emo-FilM dataset stands for Emotion research using Films and fMRI in healthy participants. This dataset includes detailed emotion annotations by 44 raters for 14 short films with a combined duration of over 2[1/2] hours, as well as recordings of respiration, heart rate, and functional magnetic resonance imaging (fMRI) from a different sample of 30 individuals watching the same films. The detailed annotations of experienced emotion evaluated 50 items including ratings of discrete emotions and emotion components from the domains of appraisal, motivation, motor expression, physiological response, and feeling. Quality assessment for the behavioural data shows a mean inter-rater agreement of 0.38. The parallel fMRI data was acquired at 3 Tesla in four sessions, accompanied with a high-resolution structural (T1) and resting state fMRI scans for each participant. Physiological recordings during fMRI included heart rate, respiration, and electrodermal activity (EDA). Quality assessment indicators confirm acceptable quality of the MRI data. This dataset is designed, but not limited, to studying the dynamic neural processes involved in emotion experience. A particular strength of this data is the high temporal resolution of behavioural annotations, as well as the inclusion of a validation study in the fMRI sample. This high-quality behavioural data in combination with continuous physiological and MRI measurements makes this dataset a treasure trove for researching human emotion in response to naturalistic stimulation in a multimodal framework.

neuroscience↗

Emotion schema effects on associative memory differ across emotion categories at the behavioural, physiological and neural level

Previous behavioural and neuroimaging studies have consistently reported that our memory is enhanced for associations congruent or incongruent with the structure of our prior knowledge, termed as schemas. However, it remains unclear if similar effects exist if encoded associations are emotional. Do emotional schemas also facilitate learning and subsequent retrieval? Does it depend on the type of experienced emotions? Using a novel face-word pair association paradigm combined with fMRI and eye-tracking techniques, we demonstrated and replicated in two independent studies that congruency with emotion schemas and emotion category interact to affect associative memory. Overall, emotion schemas facilitated memory for associative context, paralleled by the recruitment of left inferior frontal gyrus (IFG) during successful encoding of emotionally congruent vs. incongruent pairs. However, emotion schema effects differed across two negative emotion categories: disgust and fear, with disgust remembered better than fear. The IFG engagement was higher during successful encoding of congruent vs. incongruent pairs, but only in the case of disgust, suggestive of more semantic processing involved in learning disgust-related associations. On the contrary, the encoding of congruent vs. incongruent fear-related pairs was supported by activity in right fusiform gyrus (FG), suggesting greater sensory processing of faces. Successful memory formation for congruent disgust-related pairs was associated with a higher loading of pupil dilation component related to sympathetic activation, longer gaze time on words compared to faces, and more gaze switches between the two. This was reversed for fear-related pairs where the faces attracted more attention, as reflected by longer gaze time (compared to words). Overall, our results at the behavioural, physiological, and neural level converge to suggest that emotional congruency influences memory similar to semantic schemas. However, encoding processes and neural effects vary depending on emotion category, reflecting the differential role of semantic processing and visual attention processes in the modulation of memory by disgust and fear.

neuroscience↗

Optimal confidence for unaware visuomotor deviations

Numerous studies have shown that humans can successfully correct deviations to ongoing movements without being aware of them, suggesting limited conscious monitoring of visuomotor performance. Here, we ask whether such limited monitoring impairs the capacity to judiciously place confidence ratings to reflect decision accuracy (metacognitive sensitivity). To this end, we recorded functional magnetic resonance imaging data while thirty-one participants reported visuomotor cursor deviations and rated their confidence retrospectively. We show that participants use a summary statistic of the unfolding visual feedback (the maximum cursor error) to detect deviations but that this information alone is insufficient to explain detection performance. The same summary statistics is used by participants to optimally adjust their confidence ratings, even for unaware deviations. At the neural level, activity in the ventral striatum tracked high confidence, whereas a broad network including the anterior prefrontal cortex encoded cursor error but not confidence, shedding new light on a role of the anterior prefrontal cortex for action monitoring rather than confidence. Together, our results challenge the notion of limited action monitoring and uncover a new mechanism by which humans optimally monitor their movements as they unfold, even when unaware of ongoing deviations.

neuroscience↗

Healthcare experience disrupts representational similarity between one's and others' pain in anterior insula

Medical students and professional healthcare providers often underestimate patients pain, together with decreased neural responses to pain information in the anterior insula (AI), a brain region implicated in self-pain processing and negative affect. However, the functional significance and specificity of these neural changes remains debated. Across two experiments, we recruited university medical students and emergency nurses to test the role of healthcare experience on the brain reactivity to others pain, emotions, and beliefs, using both pictorial and verbal cues. Brain responses to self-pain was also assessed and compared with those to observed pain. Our results confirmed that healthcare experience decreased the activity in AI in response to others suffering. This effect was independent from stimulus modality (pictures or texts), but specific for pain, as it did not generalize to inferences about other mental or affective states. Furthermore, representational similarity and multivariate pattern analysis revealed that healthcare experience impacted specifically a component of the neural representation of others pain that is shared with that of first-hand nociception, and related more to AI than to other pain-responsive regions. Taken together, our study suggests a decreased propensity to appraise others suffering as ones own, associated with a reduced recruitment of pain-specific information in AI. These findings provide new insights into neural mechanisms leading to pain underestimation by caregivers in clinical settings.

neuroscience↗

Differential contributions of ventral striatum subregions to the motivational and hedonic components of the affective processing of the reward

The ventral striatum is implicated in the affective processing of the reward, which can be divided into a motivational and a hedonic component. Here, we examined whether these two components rely on distinct neural substrates within the ventral striatum in humans. We used a high-resolution fMRI protocol targeting the ventral striatum combined with a Pavlovian-instrumental task and a hedonic reactivity task. Both tasks involved an olfactory reward, thereby allowing us to measure Pavlovian-triggered motivation and sensory pleasure for the same reward within the same participants. Our findings show that different subregions of the ventral striatum are dissociable in their contributions to the motivational and the hedonic component of the affective processing of the reward. Parsing the neural mechanisms and the interplay between Pavlovian incentive processes and hedonic processes might have important implications for understanding compulsive reward-seeking behaviors such as addiction, binge eating, or gambling.

neuroscience↗

Emotion Recognition in a Multi-Componential Framework: The Role of Physiology

Emotions are rich and complex experiences involving various behavioral and physiological responses. While many empirical studies have focused on discrete and dimensional representations of emotions, these representations do not fully reconcile with recent neuroscience studies that increasingly suggest a multi-process mechanism underlying emotional experience. Moreover, the latter view accords with psychological theories that consider emotions as multicomponent phenomena, such as appraisal theories. Although there is no complete consensus on the specific components of emotions and fundamental principles defining their organization, the Component Process Model (CPM) is well established framework describing an emotion as a dynamic process with five major highly interrelated components: cognitive appraisal, expression, motivation, physiology and feeling. Yet, few studies have systematically investigated a range of discrete emotions through this full multi-componential view. In the present study, we therefore elicited various emotions during movie watching and measured their manifestation across these components. Our primary goal was to investigate the relationship between physiological measures and the theoretically defined components of emotions. In addition, we also investigated whether discrete emotions could be predicted from information provided by the multicomponent response patterns, as well as the specific contributions of each component in such predictions. Results suggest that physiological features are interrelated to all other components of emotion, but the least significant predictors for emotion classification. Overall, emotion prediction was significantly higher when classifiers were trained with all five components. The findings therefore support a description of emotion as a dynamic multicomponent process, in which the emergence of a conscious feeling state requires the integration of all the components.

physiology↗

Functional dynamics of brain networks associated with carry-over effects of negative events on subsequent resting state.

Affective inertia represents the lasting impact of transient emotions at one time point on affective state at a subsequent time point. Here we describe the neural underpinnings of inertia following negative emotions elicited by sad events in movies. Using a co-activation pattern analysis of dynamic functional connectivity, we examined the temporal expression and reciprocal interactions among brain-wide networks during movies and subsequent resting periods. Our findings revealed distinctive spatiotemporal expression of visual (VIS), default mode (DMN), central executive (CEN), and frontoparietal control (FPCN) networks both in negative movies and in rest periods following these movies. We also identified different reciprocal relationships among these networks, in transitions from movie to rest. While FPCN and DMN expression increased during and after negative movies, respectively, FPCN occurrences during the movie predicted lower DMN and higher CEN expression during subsequent rest after neutral movies, but this relationship was reversed after the elicitation of negative emotions. Changes in FPCN and DMN activity correlated with more negative subjective affect. These findings provide new insights into the transient interactions of intrinsic brain networks underpinning the inertia of negative emotions. More specifically, they describe a major role of FPCN in emotion elicitation processes, with prolonged impact on DMN activity in subsequent rest, presumably involved in emotion regulation and restoration of homeostatic balance after negative events. HighlightsO_LIModulations of dynamic functional brain connectivity are associated to the temporal inertia of negative emotions. C_LIO_LIFunctional co-activations patterns (CAPs) during emotional episodes predict changes in spontaneous brain dynamics during subsequent resting state. C_LIO_LIClassical "task-rest" anticorrelations in network activity are reversed by negative emotions. C_LI

neuroscience↗

Suppressing the morning cortisol rise after memory reactivation at 4 a.m. enhances episodic memory reconsolidation in humans

Evidence from animal and human research shows that established memories can undergo changes after reactivation through a process called reconsolidation. Alterations of the level of the stress hormone cortisol may be one way of manipulating reconsolidation. Here, in a double-blind, within-subject design, we reactivated a 3-day-old memory at 3:55 a.m., immediately followed by oral administration of metyrapone vs. placebo, to examine whether metyrapone-induced suppression of the morning cortisol rise may influence reconsolidation processes during and after early morning sleep. Crucially, reactivation followed by cortisol suppression vs. placebo resulted in enhanced memory for the reactivated episode (tested four days after reactivation). This enhancement after cortisol suppression was specific for the reactivated episode vs. a non-reactivated episode. These findings suggest that when reactivation of memories is immediately followed by suppression of cortisol levels during early morning sleep, reconsolidation processes change in a way that leads to the strengthening of episodic memory traces.

neuroscience↗

Brain networks subserving functional core processes of emotions identified with componential modelling

Emotions have powerful effects on the mind, body, and behavior. Although psychology theories emphasized multi-componential characteristics of emotions, little is known about the nature and neural architecture of such components in the brain. We used a multivariate data-driven approach to decompose a wide range of emotions into functional core processes and identify their neural organization. Twenty participants watched 40 emotional clips and rated 119 emotional moments in terms of 32 component features defined by a previously validated componential model. Results show how different emotions emerge from coordinated activity across a set of brain networks coding for component processes associated with valuation appraisal, hedonic experience, novelty, goal-relevance, approach/avoidance tendencies, and social concerns. Our study goes beyond previous research that focused on either categorical or dimensional emotions and highlighting how novel methodology combined with componential modelling may allow emotion neuroscience to move forward and unveil the functional architecture of human affective experiences.

neuroscience↗

A generalizable multivariate brain pattern for interpersonal guilt

Feeling guilty when we have wronged another is a crucial aspect of prosociality, but its neurobiological bases are elusive. Although multivariate patterns of brain activity show promise for developing brain measures linked to specific emotions, it is less clear whether brain activity can be trained to detect more complex social emotional states such as guilt. Here, we identified a distributed Guilt-Related Brain Signature (GRBS) across two independent neuroimaging datasets that used interpersonal interactions to evoke guilt. This signature discriminated conditions associated with interpersonal guilt from closely matched control conditions in a cross-validated training sample (N = 24; Chinese population) and in an independent test sample (N = 19; Swiss population). However, it did not respond to observed or experienced pain, or recalled guilt. Moreover, the GRBS only exhibited weak spatial similarity with other brain signatures of social affective processes, further indicating the specificity of the brain state it represents. These findings provide a step towards developing biological markers of social emotions, which could serve as important tools to investigate guilt-related brain processes in both healthy and clinical populations.

neuroscience↗

Dissociable brain mechanisms for long-term memory of disgust- and fear- related associations

Remembering events that evoke emotions such as disgust or fear is critical to our survival. However, previous studies investigating the interplay between emotion and memory disregarded the effects of specific emotions, leading to inconsistent results. Also, the role of amygdala throughout memory stages has been poorly understood. Here, we show that after 3 weeks delay, word pairs evoking disgust were remembered better than pairs evoking fear. These two emotions distinctly modulated neural mechanisms of memory. Successful encoding of disgust-evoking information was mediated by univariate activation in amygdala and perirhinal cortex, in contrast to fear-evoking memories that engaged hippocampus and parahippocampal gyrus. Critically, univariate activation in the amygdala during encoding was correlated with memory reinstatement of individual word pairs, and more so for disgust than for fear. Together, these findings shed a new light on the role of the amygdala and medial temporal lobe regions in encoding and reinstatement of specific emotional memories.

neuroscience↗

Brain networks processing temporal information in dynamic facial expressions

Perception of emotional expressions in faces relies on the integration of distinct facial features. We used fMRI to examine the role of local and global motion information in facial movements during exposure to novel dynamic face stimuli. We found that synchronous expressions distinctively engaged medial prefrontal areas in the ventral anterior cingulate cortex (vACC), supplementary premotor areas, and bilateral superior frontal gyrus (global temporal-spatial processing). Asynchronous expressions in which one part of the face (e.g., eyes) unfolded before the other (e.g., mouth) activated more the right superior temporal sulcus (STS) and inferior frontal gyrus (local temporal-spatial processing). DCM analysis further showed that processing of asynchronous expression features was associated with a differential information flow, centered on STS, which received direct input from occipital cortex and projected to the amygdala. Moreover, STS and amygdala displayed selective interactions with vACC where the integration of both local and global motion cues (present in synchronous expressions) could take place. These results provide new evidence for a role of both local and global temporal dynamics in emotional expressions, extracted in partly separate brain pathways. Importantly, we show that dynamic expressions with synchronous movement cues may distinctively engage brain areas responsible for motor execution of expressions.

neuroscience↗

Brain functional connectivity dynamics in the aftermaths of affective and cognitive events.

Neuroimaging studies have shown carry-over effects on brain activity and connectivity following both emotional and cognitive events, persisting even during subsequent rest. Here, we investigate the functional dynamics of such effects by identifying recurring co-activation patterns (CAPs). Using the precuneus as seed region, we compare carrying-over effects on brain-wide CAPs and their modulation after both affective and cognitive challenges. Female volunteers (n=19) underwent fMRI scanning during emotional induction with sad movie clips, and executive control tasks, each followed by resting periods. Several CAPs, overlapping the default mode, salience, attention, and social cognition networks were impacted by both the preceding events (movie or task) and their valence (neutral or negative), with differential fluctuations over time. Specifically, a modulation of CAPs in posterior cingulate and ventromedial prefrontal cortex was observed after exposure to negatively valenced emotional content and predicted changes in subjective affect. Additionally, CAPs in anterior cingulate cortex and dorsal fronto-parietal areas were induced by cognitive control in a negative, but not neutral context, and amplified by the task difficulty. These findings provide new insights on the anatomical organization and temporal inertia of intrinsic functional brain networks, engaged by transient emotions and presumably involved in subsequent adaptive homeostatic processes.

neuroscience↗