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Brain imaging results in children with ASD. In these lateral views of the brain, regions in green are those that differ significantly in children with autism compared to controls in A) rest regional blood flow measured by PET and in B) concentration of gray matter measured by MRI. 

Brain imaging results in children with ASD. In these lateral views of the brain, regions in green are those that differ significantly in children with autism compared to controls in A) rest regional blood flow measured by PET and in B) concentration of gray matter measured by MRI. 

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Results on brain imaging studies have led to a better understanding of the neural circuits involved in social cognition and its implication in autism spectrum dis- orders (ASD). It has been shown that the superior temporal sulcus (STS) is highly implicated in social processes, from perception of socially relevant information, such as body movements...

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... children with autism, PET (positron emission tomo- graphy) and SPECT (single photon emission tomography) studies have described localized bilateral temporal hy- poperfusion. These rest functional abnormalities were centered in the STS and superior temporal gyrus [10,14] ( Figure 2A). In both studies, participants with autism and control groups were matched for age and develop- mental quotients. ...
Context 2
... team per- formed a MRI study using VBM and high-resolution 3D- T1-weighted images acquired from 21 children with au- tism and 12 healthy control children. A significant bilat- eral decrease of grey matter was found in the STS of children with autism [11] (Figure 2B). The major find- ing of this study was the remarkable consistency between the bilateral temporal abnormalities found in autistic children by three independent MRI, PET [14] and SPECT studies [10]. ...

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... Increases in the superior temporal gyrus (STG) have been commonly reported in autism 30,31,35,54,132-141 . STG and surrounding cortical regions are also repeatedly implicated in autism and known to be involved in cognitive functions that are often impacted (e.g., language) in autistic individuals 25, [142][143][144][145][146] . The present results in ADHD were much more widespread and less localised than in autism. ...
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... This heterogeneity at the behavioral level could be the consequence of a distinct cortical network of MSI, as all studies using neuroimaging techniques demonstrated that sensory merging in ASD occurred at different topographies and latencies compared to control participants (Brandwein et al., 2013(Brandwein et al., , 2015Molholm et al., 2020;Russo et al., 2010;Stefanou et al., 2020). In addition, structural, anatomic, and functional differences in the superior temporal sulcus, an important site of audiovisual multisensory integration (for a review, see Beauchamp, 2010), have been demonstrated in participants with ASD compared to control participants (for a review, see Zilbovicius et al., 2013). We can add that the authors of the enhanced perceptual functioning model, a well-established ASD model (Mottron and Burack, 2001;Mottron et al., 2006), proposed that cerebral plasticity in low-level brain areas in ASD leads to enhanced activation in these specific brain areas, referred to as 'areas of strength', generating a preference toward a low level of processing. ...
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... Presence of areas involved in voice and face recognition, gaze perception, and theory of mind confirms the importance of the right superior temporal cortex in social cognition (25). Right hemispheric dominance for language and autistic children who previously have been reported to show anatomical and functional abnormalities in the STS (26). Asymmetry in the development of the temporal lobe has been demonstrated anatomically and with MRI, with the right side developing earlier than the left (27). ...
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... In humans, the posterior superior temporal sulcus (pSTS) is a cortical locus for processing the dynamic aspects of faces [18]. The pSTS in the right hemisphere plays an important role in social perception [19]. In ASD, a neuroimaging study indicated that the right pSTS was abnormally activated during emotion perception [20]. ...
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... Also, analysis revealed no relationship between the latency of N1 at P8 when the participants viewed the AW video and SATQ scores. A previous study examined a relationship between cerebral blood flow and neural activity and they showed that the more severe autistic syndrome is, the lower regional cerebral blood flow is in left superior temporal region [17]. The present result might related the low regional cerebral blood flow around left superior temporal sulcus. ...
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... Results from eye-tracking studies 1.4. Voice and face: audiovisual integration 49 objectively demonstrate abnormalities in the processing of social information in ASD (Zilbovicius et al., 2013;Wang et al., 2015). ...
Thesis
Emotions are the fuel of human survival and social development. Not only do we undergo primitive reflexes mediated by ancient brain structures, but we also consciously and unconsciously regulate our emotions in social con- texts, affiliating with friends and distancing from foes. One of our main tools for emotion regulation is facial expression and, in particular, smiles. Smiles are deeply grounded in human behavior: they develop early, and are used across cultures to communicate affective states. The mechanisms that under- lie their cognitive processing include interactions not only with visual, but also emotional and motor systems. Smiles, trigger facial imitation in their observers, reactions thought to be a key component of the human capacity for empathy.Smiles, however, are not only experienced visually, but also have audible consequences. Although visual smiles have been widely studied, almost nothing is known about the cognitive processing of their auditory counter- part. This is the aim of this dissertation. In this work, we characterise and model the smile acousitc fingerprint, and use it to probe how auditory smiles are processed cognitively. We give here evidence that (1) auditory smiles can trigger unconscious facial imitation, that (2) they are cognitively integrated with their visual counterparts during perception, and that (3) the develop- ment of these processes does not depend on pre-learned visual associations. We conclude that the embodied mechanisms associated to the visual process- ing of facial expressions of emotions are in fact equally found in the auditory modality, and that their cognitive development is at least partially indepen- dent from visual experience.
... Results from eye-tracking studies 1.4. Voice and face: audiovisual integration 49 objectively demonstrate abnormalities in the processing of social information in ASD (Zilbovicius et al., 2013;Wang et al., 2015). ...
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Emotions are the fuel of human survival and social development. Not onlydo we undergo primitive reflexes mediated by ancient brain structures, butwe also consciously and unconsciously regulate our emotions in social contexts,affiliating with friends and distancing from foes. One of our main toolsfor emotion regulation is facial expression and, in particular, smiles. Smilesare deeply grounded in human behavior: they develop early, and are usedacross cultures to communicate affective states. The mechanisms that underlietheir cognitive processing include interactions not only with visual, butalso emotional and motor systems. Smiles, trigger facial imitation in theirobservers, reactions thought to be a key component of the human capacityfor empathy.Smiles, however, are not only experienced visually, but also have audibleconsequences. Although visual smiles have been widely studied, almostnothing is known about the cognitive processing of their auditory counterpart.This is the aim of this dissertation. In this work, we characterise andmodel the smile acousitc fingerprint, and use it to probe how auditory smilesare processed cognitively. We give here evidence that (1) auditory smiles cantrigger unconscious facial imitation, that (2) they are cognitively integratedwith their visual counterparts during perception, and that (3) the developmentof these processes does not depend on pre-learned visual associations.We conclude that the embodied mechanisms associated to the visual processingof facial expressions of emotions are in fact equally found in the auditorymodality, and that their cognitive development is at least partially independentfrom visual experience.
... Abnormal activity in this structure was previously related to the social cognition deficits observed in autism. It was shown that this brain area is underactive in ASD subjects during face perception, especially when the face stimulus is dynamic (gaze and facial expression shifts) (Redcay 2008, Saitovitch et al. 2012, Zilbovicius et al. 2013. In our study, faces were static but they differed in respect to their expressions, possibly causing the increase of activity in the posterior STS in a majority of the control participants and the lack of such activity in PK. ...
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... NeuroImage: Clinical 19 (2018) 38-46 harbors reciprocal neural connections to multiple limbic, paralimbic, and sensory association areas of the brain (Barnes and Pandya, 1992;Seltzer and Pandya, 1994), including the insular cortex Mufson and Mesulam, 1982). The activity of this region of the anterior STS has been associated with multiple processes relevant to social function such as face perception, biological motion perception, and higher-order aspects of social cognition (Adolphs, 2001;Allison et al., 2000;Grossman et al., 2010;Hein and Knight, 2008), all of which are frequently impaired in individuals with ASD Zilbovicius et al., 2013). In the present study, a greater degree of taste reactivity in ASD was predicted by greater food-related activity of the aSTS and greater functional connectivity between the aSTS and gustatory regions of the dorsal mid-insular cortex. ...
... The prominent involvement of the anterior STS, a region associated with functional deficits in other areas of ASD symptomatology (Boddaert et al., 2004;Verhoeven et al., 2010;Zilbovicius et al., 2013), suggests that multiple seemingly distinct symptoms of ASD may share a common neural etiology. Interventions, such as non-invasive brain stimulation or neurofeedback training, specifically targeting the anterior STS (Ramot et al., 2017) might thus prove beneficial for treating a variety of behaviors associated with ASD. ...
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Selective or ‘picky’ eating habits are common among those with autism spectrum disorder (ASD). These behaviors are often related to aberrant sensory experience in individuals with ASD, including heightened reactivity to food taste and texture. However, very little is known about the neural mechanisms that underlie taste reactivity in ASD. In the present study, food-related neural responses were evaluated in 21 young adult and adolescent males diagnosed with ASD without intellectual disability, and 21 typically-developing (TD) controls. Taste reactivity was assessed using the Adolescent/Adult Sensory Profile, a clinical self-report measure. Functional magnetic resonance imaging was used to evaluate hemodynamic responses to sweet (vs. neutral) tastants and food pictures. Subjects also underwent resting-state functional connectivity scans. The ASD and TD individuals did not differ in their hemodynamic response to gustatory stimuli. However, the ASD subjects, but not the controls, exhibited a positive association between self-reported taste reactivity and the response to sweet tastants within the insular cortex and multiple brain regions associated with gustatory perception and reward. There was a strong interaction between diagnostic group and taste reactivity on tastant response in brain regions associated with ASD pathophysiology, including the bilateral anterior superior temporal sulcus (STS). This interaction of diagnosis and taste reactivity was also observed in the resting state functional connectivity between the anterior STS and dorsal mid-insula (i.e., gustatory cortex). These results suggest that self-reported heightened taste reactivity in ASD is associated with heightened brain responses to food-related stimuli and atypical functional connectivity of primary gustatory cortex, which may predispose these individuals to maladaptive and unhealthy patterns of selective eating behavior. Trial registration (clinicaltrials.gov identifier) NCT01031407. Registered: December 14, 2009.