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Straube, T.

Publications and source records attributed to Straube, T..

11 recordsLinked to original sources

Differential modulation of the neurocomputational signature of early and late mismatch responses to spoken words by awareness and task relevance

Mismatch responses (MMRs), including the mismatch negativity (MMN) and the P3, are a hallmark of the brains capacity to detect unexpected events. They are discussed to be generated by two main processes: adaptation and prediction error (PE). However, MMR research on underlying mechanisms has mostly relied on simple, non-linguistic stimuli such as tones, and it remains unknown how awareness and attentional conditions affect MMRs to auditory verbal stimuli, that, unlike tones, carry lexical-semantic meaning. Here, we conducted a preregistered EEG study that disentangled influences of awareness, general task-relevance of word stimuli, and specific target-relevance of word oddballs on the MMN and P3. In addition, single-trial neurocomputational models were applied to uncover the underlying generative models of the MMRs. Results show that word-related MMN and P3 were only elicited when words were task-relevant, and the P3 increased with target-relevance. Crucially, no word-related MMN emerged under inattention, in contrast to the pre-attentive MMN typically reported for tonal deviants. Neurocomputational modeling revealed that the early part of the task-relevant MMN reflects adaptation processes. PE processes generated later parts of the MMN under task-relevance, and the entire MMN under target-relevance, as well as the P3 independent of relevance conditions. This suggests that the same temporal generation pattern of adaptation and PE underlie mismatch responses to both words and tones, but that, unlike tonal MMRs, eliciting MMRs to words requires the allocation of attention. This attentional dependency may reflect the additional lexical-semantic and multi-level representational demands that spoken words impose on the auditory system.

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Identifying neural correlates of auditory perceptual awareness and deviance using a no-report inattentional deafness paradigm

The relationship between neural processes supporting perception, deviance processing, and post-perceptual task demands during auditory processing is not well understood. We used multitone masking and a no-report inattentional deafness paradigm to dissociate neural correlates of auditory perceptual awareness, deviance processing, and task demands. Evoked responses to physically identical target-tone pairs were recorded across three phases differing only in task instructions. In Phase A, human participants remained nave to (and thus unaware of) the target tones. In Phase B, participants were informed about (and thus aware of) the target tones. In Phase C, participants remained aware of the target tones and judged the duration of the silent gap between them, rendering them task-relevant. When participants were aware of them, target tones elicited an auditory awareness negativity and an increased positivity in the P3 window), with larger responses when target tones were additionally task-relevant. Furthermore, though largest in Phase C, deviant stimuli elicited a mismatch negativity across all task conditions, while a significant P3 to deviants was only observed in Phase C. Thus, early and late responses can be independently modulated by awareness, deviance, and task-relevance, indicating that they do not necessarily rely on shared neural mechanisms despite overlapping spatiotemporal profiles.

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Neural correlates of consciousness in an auditory no-report fMRI study

In the search for neural correlates of consciousness (NCC), prominent theories disagree about the role of sensory versus wide-spread fronto-parietal brain activity. Research on auditory awareness has been widely neglected, and isolating NCC from correlates of task-related post-perceptual processes (e.g., report) is an ongoing challenge. The present study addressed these issues using functional magnetic resonance imaging (fMRI) during a no-report inattentional deafness paradigm. Sixty-three participants performed an auditory distractor task while supra-threshold but task-irrelevant sounds were presented in the background. Whereas one group was aware of these stimuli, another group remained unaware. Comparing brain responses to the critical sounds between aware and unaware participants while controlling for correlates of sensory and postperceptual processing revealed that auditory awareness was associated with significantly increased activity in secondary auditory but not in fronto-parietal areas. These findings suggest a dominant role of stimulus-specific sensory processing rather than widespread fronto-parietal information broadcasting in conscious perception.

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Early neural responses to nonconscious fearful and neutral faces - an ERP study

Prioritized processing of fearful compared to neutral faces is reflected in differential event-related potentials (ERPs). There is an ongoing debate about the extent to which faces in general and fearful faces in particular enhance specific ERPs if they are not consciously perceived. Specifically, the N170 has been suggested as the most likely candidate for enhanced processing of nonconscious fearful faces. In this pre-registered study, we tested in a large sample based on sequential Bayesian sampling (N = 64) whether early components of the ERP (P1, N170, and early posterior negativity; EPN) discriminate between fearful faces, neutral faces, and non-facial control stimuli. Consciousness was manipulated by presenting stimuli for 17 ms in a backward masking design, with the mask following immediately or after a delay of 200 ms. Participants rated their subjective perception on a perceptual awareness scale in each trial. Importantly, only trials in which nothing but the mask was perceived were considered for the analysis of nonconscious effects. The results showed strong evidence for an increased N170 in response to nonconscious fearful compared to neutral faces; however, this difference was significantly smaller than in the conscious condition. Furthermore, we obtained strong evidence for N170 differences between nonconscious faces and no-faces. For P1 and EPN amplitudes, no significant effects were observed in the nonconscious conditions, although exploratory analyses of the P1 peak interval suggest nonconscious face-no-face differentiation. These results support the notion that nonconscious emotion and face processing are detectable in early neural responses and show that these nonconscious effects are considerably weaker than the corresponding conscious effects.

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Specific amygdala and hippocampal subfield volumes in social anxiety disorder and their relation to clinical characteristics; an international mega-analysis

Social anxiety disorder (SAD) has been associated with alterations in amygdala and hippocampal volume but there is mixed evidence for the direction of volumetric alterations. Additionally, little is known about the involvement of the distinct subfields in the pathophysiology of SAD. Volumetric data from a large multi-centre sample of 107 adult individuals with SAD and 140 healthy controls (HCs) was segmented using FreeSurfer to produce 9 amygdala and 12 hippocampal subfield volumes. Volumes were compared between groups using linear mixed-effects models adjusted for age, age-squared, sex, site and whole amygdala and hippocampal volumes. Subgroup analyses examined subfield volumes in relation to comorbid anxiety disorder, and comorbid major depressive disorder (MDD), psychotropic medication status, and symptom severity. In the full sample, SAD was associated with smaller amygdala volumes in the basal (d=-0.32, pFDR=0.022), accessory basal (d=- 0.42, pFDR=0.005) and corticoamygdaloid transition area (d=-0.37, pFDR=0.014), and larger hippocampal volume in the CA3 (d=0.34, pFDR=0.024), CA4 (d=0.44, pFDR=0.007), dentate gyrus (d=0.35, pFDR=0.022) and molecular layer (d=0.28, pFDR= 0.033), compared to HCs. SAD without comorbid anxiety, in addition, demonstrated smaller lateral amygdala (d=-0.30, pFDR=0.037) and hippocampal amygdala transition area (d=-0.33, pFDR=0.027) relative to HCs. In SAD without comorbid MDD, only the smaller accessory basal amygdala remained significant (d=-0.41, pFDR=0.017). No association was found between subfield volume and medication status or symptom severity. In conclusion, we observed distinct patterns of volumetric differences across specific amygdala and hippocampal subfields, regions that are associated with sensory information processing, threat evaluation and fear generalization. These findings suggest a possible disruption in information flow between the amygdala and hippocampal formation for fear processing in SAD.

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A Comparison of Methods to Harmonize Cortical Thickness Measurements Across Scanners and Sites

Results of neuroimaging datasets aggregated from multiple sites may be biased by site- specific profiles in participants demographic and clinical characteristics, as well as MRI acquisition protocols and scanning platforms. We compared the impact of four different harmonization methods on results obtained from analyses of cortical thickness data: (1) linear mixed-effects model (LME) that models site-specific random intercepts (LMEINT), (2) LME that models both site-specific random intercepts and age-related random slopes (LMEINT+SLP), (3) ComBat, and (4) ComBat with a generalized additive model (ComBat-GAM). Our test case for comparing harmonization methods was cortical thickness data aggregated from 29 sites, which included 1,343 cases with posttraumatic stress disorder (PTSD) (6.2-81.8 years old) and 2,067 trauma-exposed controls without PTSD (6.3-85.2 years old). We found that, compared to the other data harmonization methods, data processed with ComBat-GAM were more sensitive to the detection of significant case-control differences in regional cortical thickness (X2(3) = 34.339, p < 0.001), and case-control differences in age-related cortical thinning (X2(3) = 15.128, p = 0.002). Specifically, ComBat-GAM led to larger effect size estimates of cortical thickness reductions (corrected p-values < 0.001), smaller age-appropriate declines (corrected p-values < 0.001), and lower female to male contrast (corrected p-values < 0.001) in cases compared to controls relative to other harmonization methods. Harmonization with ComBat-GAM also led to greater estimates of age-related declines in cortical thickness (corrected p-values < 0.001) in both cases and controls compared to other harmonization methods. Our results support the use of ComBat-GAM for harmonizing cortical thickness data aggregated from multiple sites and scanners to minimize confounds and increase statistical power.

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The effects of emotional valence and intensity on cognitive and affective empathy after insula lesions

The insula plays a central role in empathy. However, the complex structure of empathic deficits following insular damage is not fully understood. While previous lesion research has shown variable deficits in patients with insular damage on basic discrimination tasks or self-report measures, it is unclear in how far patients with insular damage are impaired in cognitive (CE) and affective empathy (AE) functions depending on valence and arousal of stimuli using an ecologically valid paradigm. In the present study, patients with insular lesions (n = 20) and demographically-matched healthy controls (n = 24) viewed 16 videos (duration: 60 sec each) that varied in terms of valence and emotional intensity. The videos showed a person (target) reporting on a personal life event. In CE conditions, subjects continuously rated the affective state of the target, while in AE conditions they continuously rated their own affect. Mean Squared Error (MSE) assessed deviations between subject and target ratings (CE: deviation between targets and participants ratings of targets emotions; AE: deviation between targets and participants self-ratings of emotion). Patients differed from controls only in negative, low intensity AE, rating their own affective state less negative than the target rated his/her affect. This deficit was not related to trait empathy, neuropsychological or clinical parameters, or laterality of lesion. Our findings provide important insights into the profile of social cognition impairment after insular damage. Empathic functions may be widely spared after insular damage in a naturalistic, dynamic setting, potentially due to the intact interpretation of social context cues by residual networks outside the lesion. The particular role of the insula in AE for negative states may evolve specifically in situations that bear higher uncertainty, which points to a threshold role of the insula in online ratings of AE.

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Lateralized deficits in arousal processing after insula lesions: behavioral and autonomic evidence

A large body of evidence ascribes a pivotal role in emotion processing to the insular cortex. However, the complex structure and lateralization of emotional deficits following insular damage are not understood. Here, we investigated emotional ratings of valence and arousal and skin conductance responses (SCR) to a graded series of emotionally arousing scenes in patients with left (n = 10) or right (n = 9) insular damage and in healthy controls (n = 18). We found a significant reduction in overall SCRs, arousal ratings and valence extremity scores in right-lesioned patients, as compared to left-lesioned patients and healthy controls. Additional analyses of correlations between subjective arousal ratings resp. SCR and normative arousal ratings revealed that both lesion groups had evaluative and physiological difficulties to discover changes in stimulus arousal. Although no group differences emerged on overall ratings of valence, analysis of correlations between subjective and normative valence ratings displayed markedly reduced accuracy in right-lesioned patients, as compared to left-lesioned patients and healthy controls. Our findings support the hypothesis that the left and right insulae subserve different functions in emotion processing, potentially due to asymmetrical representations of autonomic information in the left and right human forebrain. The right insula may serve as integral node for sympathetic arousal and cognitive affective processing.

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Effects of awareness and task relevance on neurocomputational models of mismatch negativity generation

Detection of regularities and their violations in sensory input is key to perception. Violations are indexed by an early EEG component called the mismatch negativity (MMN) - even if participants are distracted or unaware of the stimuli. On a mechanistic level, two dominant models have been suggested to contribute to the MMN: adaptation and prediction. Whether and how context conditions, such as awareness and task relevance, modulate the mechanisms of MMN generation is unknown. We conducted an EEG study disentangling influences of task relevance and awareness on the visual MMN. Then, we estimated different computational models for the generation of single-trial amplitudes in the MMN time window. Amplitudes were best explained by a prediction error model when stimuli were task-relevant but by an adaptation model when task-irrelevant and unaware. Thus, mismatch generation does not rely on one predominant mechanism but mechanisms vary with task relevance of stimuli.

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Differential effects of prediction and adaptation along the cortical hierarchy during deviance processing

Neural mismatch responses have been proposed to rely on different mechanisms, including prediction error-related activity and adaptation to frequent stimuli. However, the cortical hierarchical structure of these mechanisms is unknown. To investigate this question, we used functional magnetic resonance imaging (fMRI) and an auditory oddball design with a suited control condition that enabled us to delineate the contributions of prediction error- or adaptation-related brain activation during deviance processing. We found that while prediction-error related processes increased with the hierarchical position of the brain area, adaptation declined. This suggests that the relative contribution of different mechanisms in deviance processing varies across the cortical hierarchy.

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Reward Prediction Error Signaling during Reinforcement Learning in Social Anxiety Disorder is altered by Social Observation

BACKGROUNDDysfunctional expectations of impending social or performance outcomes are core features of Social Anxiety Disorder (SAD) but often lack formal definition in clinical research. Reinforcement learning (RL) models offer a framework to define changes in outcome expectations in a formal way by computing the prediction error (PE). This study quantifies the updating of expectations by PEs in SAD and investigates alterations in RL regions associated with PE signaling.\n\nMETHOD48 adult participants (24 diagnosed with SAD and 24 age-, gender-, and education- matched healthy controls (HC)) underwent event-related functional magnetic resonance imaging while learning from probabilistic feedback. Crucially, both groups completed two parallel versions of the task: one in which they learned under scrutiny (social observation) and one in which they learned without being overtly evaluated (non-social control condition).\n\nRESULTSCoupling to prediction errors in SAD was elevated in dorsomedial prefrontal cortex (DMPFC) when learning under observation. These findings provide the first evidence that PE signaling during social performance situations in SAD is associated with hypersensitive response signatures in DMPFC, a brain region associated with using others value standards as a proxy for ones own value standards. Dynamic Causal Modelling further revealed that RPE-modulated connectivity from ventral pallidum to DMPFC during observation was reduced in SAD.\n\nCONCLUSIONSThe present results corroborate a crucial role of DMPFC in SAD, which corresponds to dysfunctional expectations about others alleged performance standards that play a prominent role in current models of the disorder.

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