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Salmi, J.

Publications and source records attributed to Salmi, J..

3 recordsLinked to original sources

Autistic traits modulate neural responses to social signals during natural vision

Impairments in social perception, a hallmark of autism spectrum disorder (ASD), are also evident at subclinical levels in the general population. However, it remains unclear how such variation in autistic traits modulate neural processing of different types of social information. Here, we investigated whether autistic traits in neurotypical individuals are associated with neural responses to a broad array of social perceptual features during viewing naturalistic stimuli using functional magnetic resonance imaging (fMRI). We also tested the generalizability of these effects across two experiments. Ninety-seven participants completed the Autism Spectrum Quotient (AQ) and watched a set of 96 movie clips and a full movie during an fMRI scan. Intensity of 126 social features in the movie stimuli was continuously annotated by independent observers, and 44 most reliably rated features were used to model neural responses. We examined how consistently the responses to each social feature were dependent on the participants AQ scores. Replicable AQ-dependent neural responses to social features were found in both datasets. The temporal cortex and especially the superior temporal gyrus (STG), served as a central "hub" where autistic traits consistently modulated responses to social features across datasets. Different AQ subscales also revealed distinct association patterns in other brain regions. These findings indicate that autism-related traits broadly influence neural processing of naturalistic social signals, providing insight into how characteristics of autistic symptoms relate to socioemotional processing.

neuroscience↗

Reduced inter-subject functional connectivity during movies in autism: Replicability across cross-national fMRI datasets

BackgroundAutism is a neurodevelopmental disorder characterized by repetitive behaviors and difficulties in social communication and interaction. Previous research has shown that these symptoms are linked to idiosyncratic behavioral and brain activity patterns while viewing natural social events in movies. This study aimed to investigate the replicability of brain activity idiosyncrasy in autistic individuals by comparing their inter-subject functional connectivity (ISFC) with that of neurotypical individuals. MethodsWe tested for ISFC differences between autistic and neurotypical groups using functional magnetic resonance imaging (fMRI) data from two independent datasets from Germany (Nneurotypical = 25, 7 Males, 18 Females; Nautism = 22, 12 Males, 10 Females) and Finland (Nneurotypical = 19, Nautism = 18; All males). Participants watched short movie stimuli, and pairwise ISFCs were computed across 273 brain regions. Group differences were evaluated using subject-wise permutation tests for each dataset. ResultsIn both datasets, the autistic group showed lower ISFCs compared to the neurotypical group, specifically between visual regions (e.g., occipital gyrus, cuneus) and parietal regions (e.g., superior and inferior parietal lobules), as well as between visual regions and frontal regions (e.g., inferior frontal gyrus, precentral gyrus). ISFC was higher in the Finnish autistic group in temporal regions associated with sound and speech processing. ConclusionsThe study confirmed the replicability of reduced ISFCs in autistic individuals during naturalistic movie-watching, especially between visual and parietal/frontal brain regions. These findings reinforce the utility of ISFC and naturalistic movie-watching paradigm in studying neural connectivity alterations in autism.

neuroscience↗

Dopamine D2R and opioid MOR availability in autism spectrum disorder

Opioid and dopamine receptor systems are implicated in the pathoetiology of autism, but in vivo human brain imaging evidence for their role remains elusive. Here, we investigated regional type 2 dopamine and mu-opioid receptor (D2R and MOR, respectively) availabilities and regional interactions between the two neuromodulatory systems associated with autism spectrum disorder (ASD). In vivo positron emission tomography (PET) with radioligands [11C]raclopride (D2R) and [11C]carfentanil (MOR) was carried out in 16 adult males with high functioning ASD and 19 age and sex matched controls. Regional group differences in D2R and MOR receptor availabilities were tested with linear mixed models and associations between regional receptor availabilities were examined with correlations. There were no group differences in whole-brain voxel-wise analysis of DR2 but ROI analysis presented a lower overall mean D2R availability in striatum of the ASD versus control group. Post hoc regional analysis revealed reduced D2R availability in nucleus accumbens of the ASD group. The whole-brain voxel-wise analysis of MOR revealed precuneal up-regulation in the ASD group, but there was no overall group difference in the ROI analysis for MOR. MOR down-regulation was observed in the hippocampi of the ASD group in a post hoc analysis. Regional correlations between D2R and MOR availabilities were weaker in the ASD group versus control group in the amygdala and nucleus accumbens. These alterations may translate to disrupted modulation of social motivation and reward in ASD.

neuroscience↗