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额外一条X染色体儿童的社会认知及潜在认知机制:与自闭症谱系障碍的比较

Social cognition and underlying cognitive mechanisms in children with an extra X chromosome: a comparison with autism spectrum disorder.

作者信息

van Rijn S, Stockmann L, van Buggenhout G, van Ravenswaaij-Arts C, Swaab H

机构信息

Clinical Child and Adolescent Studies, Leiden University.

Leiden Institute for Brain and Cognition.

出版信息

Genes Brain Behav. 2014 Jun;13(5):459-67. doi: 10.1111/gbb.12134. Epub 2014 May 7.

Abstract

Individuals with an extra X chromosome are at increased risk for autism symptoms. This study is the first to assess theory of mind and facial affect labeling in children with an extra X chromosome. Forty-six children with an extra X chromosome (29 boys with Klinefelter syndrome and 17 girls with Trisomy X), 56 children with autism spectrum disorder (ASD) and 88 non-clinical controls, aged 9-18 years, were included. Similar to children with ASD, children with an extra X chromosome showed significant impairments in social cognition. Regression analyses showed that different cognitive functions predicted social cognitive skills in the extra X and ASD groups. The social cognitive deficits were similar for boys and girls with an extra X chromosome, and not specific for a subgroup with high Autism Diagnostic Interview Revised autism scores. Thus, children with an extra X chromosome show social cognitive deficits, which may contribute to social dysfunction, not only in children showing a developmental pattern that is 'typical' for autism but also in those showing mild or late presenting autism symptoms. Our findings may also help explain variance in type of social deficit: children may show similar social difficulties, but these may arise as a consequence of different underlying information processing deficits.

摘要

拥有一条额外X染色体的个体出现自闭症症状的风险增加。本研究首次评估了拥有额外X染色体的儿童的心理理论和面部表情识别能力。研究纳入了46名拥有额外X染色体的儿童(29名患有克兰费尔特综合征的男孩和17名患有X三体综合征的女孩)、56名患有自闭症谱系障碍(ASD)的儿童以及88名年龄在9至18岁的非临床对照儿童。与患有ASD的儿童相似,拥有额外X染色体的儿童在社会认知方面存在显著缺陷。回归分析表明,不同的认知功能可预测拥有额外X染色体的儿童组和ASD儿童组的社会认知技能。拥有额外X染色体的男孩和女孩的社会认知缺陷相似,且并非特定于自闭症诊断访谈修订版自闭症得分较高的亚组。因此,拥有额外X染色体的儿童存在社会认知缺陷,这可能导致社会功能障碍,不仅在呈现“典型”自闭症发展模式的儿童中如此,在那些呈现轻度或迟发性自闭症症状的儿童中也是如此。我们的研究结果也可能有助于解释社会缺陷类型的差异:儿童可能表现出相似的社会困难,但这些困难可能是由不同的潜在信息处理缺陷导致的。

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