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Social Cognition in Williams Syndrome: Relations between Performance on the Social Attribution Task and Cognitive and Behavioral Characteristics

机译:威廉姆斯综合症中的社会认知:社会归因任务的表现与认知和行为特征之间的关系

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Williams syndrome (WS) is a developmental disorder of genetic origin, with characteristic cognitive and personality profiles. Studies of WS point to an outgoing and gregarious personality style, often contrasted with autism spectrum disorders; however, recent research has uncovered underlying social reciprocity difficulties in people with WS. Social information processing difficulties that underlie these social reciprocity difficulties have been sparsely examined. Participants in the current study included 24 children with WS ages 8 through 15. A lab-based measure of social perception and social cognition was administered (Social Attribution Test), as well as an intellectual functioning measure (KBIT-II) and parent reports of communication and reciprocal social skills (Social Communication Questionnaire, Social Responsiveness Scale). Relations between social cognition, cognitive abilities, and social-communication were examined. Results demonstrated relations between parent-reported social reciprocity and the typicality of the responses provided in the lab-based measure, even once variability in intellectual functioning was taken into account. Specifically, those individuals who produced narratives in response to the social attribution task (SAT) that were more similar to those described in previous studies of typically developing individuals were also reported to have fewer social reciprocity difficulties in the real world setting as reported by parents. In addition, a significant improvement in performance on the SAT was seen with added scaffolding, particularly for participants with stronger intellectual functioning. These findings indicate that difficulties interpreting the social dynamics between others in ambiguous situations may contribute to the social relationship difficulties observed in people with WS, above and beyond the role of intellectual functioning. Exploratory analyses indicated that performance by individuals with stronger intellectual functioning is improved with additional structure to a greater degree than for those with weaker intellectual functioning. Interventions that specifically target these social information processing of individuals with WS would likely be beneficial.
机译:威廉姆斯综合征(WS)是遗传起源的发育障碍,具有特征性的认知和性格特征。对WS的研究指出了一种外向和群居的人格风格,通常与自闭症谱系障碍形成对比。但是,最近的研究发现了WS患者潜在的社会互惠困难。稀疏地研究了构成这些社会互惠困难基础的社会信息处理困难。本研究的参与者包括24名WS年龄在8至15岁之间的儿童。该研究采用了基于实验室的社交知觉和社交认知测评(社会归因测试),以及一项智力功能测评(KBIT-II)和家长的报告。沟通和互惠的社交技能(社交沟通问卷,社交反应量表)。研究了社会认知,认知能力和社交沟通之间的关系。结果表明,即使考虑到智力功能的变异性,父母报告的社交互惠与基于实验室的措施所提供的回应的典型性之间也存在关系。具体而言,据父母报道,那些响应社会归因任务(SAT)而产生叙事的个体与先前针对典型发展中个体的研究中描述的个体更为相似,据报道,他们在现实世界中的社交互惠困难也较少。此外,通过增加脚手架,可以显着提高SAT的表现,特别是对于具有较强智力功能的参与者。这些发现表明,在模棱两可的情况下,难以理解他人之间的社会动态可能会导致WS人群中社交功能上的困难,而超越了智力功能的作用。探索性分析表明,与智力功能较弱的人相比,具有较强智力功能的人的绩效通过附加结构得到了更大程度的改善。专门针对WS个人的这些社会信息处理的干预措施可能会有所帮助。

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