The neural basis of social interaction perception and its disruption in autism spectrum disorder
The neural basis of social interaction perception and its disruption in autism spectrum disorder
批准号:
10432589
负责人:
Leyla Isik
金额:
$26.09万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
已结题
起止时间:
2022-03-11 至 2024-02-29
关键词:
AdultAgeAreaBehavioralBiologicalBrainBrain regionChildClinicalCognitionDiagnosisFaceFunctional Magnetic Resonance ImagingFutureGoalsHostilityHumanIndividualInvestigationKnowledgeLightLocationMeasuresMethodsMindModelingMotionNeurodevelopmental DisorderPerceptionPersonsPopulationPublishingResearchSocial InteractionSocial PerceptionSocial statusStimulusStructure of superior temporal sulcusValidationWorkadult with autism spectrum disorderaffectionautism spectrum disorderautisticbasecomputerized toolsexperimental studyimprovedindividual variationindividuals with autism spectrum disorderinnovationmachine learning methodmovierelating to nervous systemresponsesocialsocial communicationsocial deficitssocial neurosciencetheoriestrait
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary
Autism spectrum disorder (ASD) is characterized largely by deficits in social interaction and communication.
However, despite these clear behavioral differences it has been difficult to isolate differences in high-level social
brain regions in ASD. One important area that has been under-studied is the perception of others’ social
interactions. Recognizing others’ social interactions—directed, contingent actions between two or more people—
is a core area of human cognition. Humans quickly and effortlessly extract a wealth of information when viewing
a social interaction and use this information to guide their own actions. Social interaction perception is notably
disrupted in autism, but the brain basis of these deficits are still unknown. Recently a region in the posterior
superior temporal sulcus in neurotypical (NT) adults has been identified that is selectively engaged when viewing
others’ social interactions in both controlled stimuli and during natural movie viewing. Critically, social interaction
selectivity in the brain has never been studied in ASD. The long-term goal of this research is to understand the
brain basis of social interaction perception in controlled and naturalistic contexts, and its disruption in autism.
Our overall objective is to identify differences in neural response to social interactions in high-functioning
individuals with ASD using both controlled and movie stimuli. Our central hypotheses are that social interactions
engage the same region of the pSTS in NT subjects in both controlled and naturalistic settings, and that this
activity is significantly decreased in autism. Aim 1 will identify the brain regions that selectively respond to social
interactions in NT subjects using both controlled and natural movie fMRI paradigms. Advanced machine learning
methods will isolate the unique neural contribution of social interactions during movie viewing, allowing the first
direct comparison between controlled stimuli, the status quo in social neuroscience, and natural movie stimuli,
an exciting new paradigm that is more ecologically relevant, better drives neural responses, and opens the door
to studies of new populations, including children and more impacted individuals with autism
. Aim 2 will identify
the brain regions that are selective to social interactions in ASD subjects in controlled and movie stimuli and how
they differ from neurotypical brain responses identified in Aim 1. The proposed study will provide us with a direct
comparison of the neural basis of social interaction perception in controlled and naturalistic settings, as well as
a clear understanding of the neural basis of social interaction perception in ASD. This work will also pioneer the
use of natural stimuli for studies of neurodevelopmental disorders, creating a new framework to understand the
neural basis of high-level social perception in a range of clinical populations.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
The neural computations underlying human social interaction recognition
-
批准号:10637982
-
项目类别:
-
资助金额:$66.36万
-
财政年份:2023
-
负责人:Leyla Isik
-
依托单位:
The neural basis of social interaction perception and its disruption in autism spectrum disorder
-
批准号:10589804
-
项目类别:
-
资助金额:$20.4万
-
财政年份:2022
-
负责人:Leyla Isik
-
依托单位:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
-
批准号:JCZRQN202500010
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
-
批准号:2025JJ70209
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
-
批准号:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
-
批准号:2023JJ50274
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
-
批准号:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
-
批准号:81973577
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
-
批准号:81602908
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: