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自闭症谱系障碍青少年皮质厚度的纵向变化及其与受限和重复行为的关系。

Longitudinal Changes in Cortical Thickness in Adolescents with Autism Spectrum Disorder and Their Association with Restricted and Repetitive Behaviors.

机构信息

Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital, Goethe University, Deutschordenstrasse 50, 60528 Frankfurt, Germany.

Brain Imaging Center, Schleusenweg 2-16, Haus 95H, Goethe University, 60528 Frankfurt, Germany.

出版信息

Genes (Basel). 2021 Dec 20;12(12):2024. doi: 10.3390/genes12122024.

Abstract

The neuroanatomy of autism spectrum disorder (ASD) shows highly heterogeneous developmental trajectories across individuals. Mapping atypical brain development onto clinical phenotypes, and establishing their molecular underpinnings, is therefore crucial for patient stratification and subtyping. In this longitudinal study we examined intra- and inter-individual differences in the developmental trajectory of cortical thickness (CT) in childhood and adolescence, and their genomic underpinnings, in 33 individuals with ASD and 37 typically developing controls (aged 11-18 years). Moreover, we aimed to link regional atypical CT development to intra-individual variations in restricted and repetitive behavior (RRB) over a two-year time period. Individuals with ASD showed significantly reduced cortical thinning in several of the brain regions functionally related to wider autism symptoms and traits (e.g., fronto-temporal and cingulate cortices). The spatial patterns of the neuroanatomical differences in CT were enriched for genes known to be associated with ASD at a genetic and transcriptomic level. Further, intra-individual differences in CT correlated with within-subject variability in the severity of RRBs. Our findings represent an important step towards characterizing the neuroanatomical underpinnings of ASD across development based upon measures of CT. Moreover, our findings provide important novel insights into the link between microscopic and macroscopic pathology in ASD, as well as their relationship with different clinical ASD phenotypes.

摘要

自闭症谱系障碍(ASD)的神经解剖结构显示,个体之间存在高度异质的发育轨迹。因此,将非典型大脑发育映射到临床表型,并确定其分子基础,对于患者分层和亚型划分至关重要。在这项纵向研究中,我们研究了 33 名 ASD 患者和 37 名正常发育对照者(年龄 11-18 岁)在儿童和青少年时期皮质厚度(CT)发育轨迹的个体内和个体间差异,以及它们的基因组基础。此外,我们旨在将区域异常 CT 发育与两年时间内个体内受限和重复行为(RRB)的个体内变化联系起来。与更广泛的自闭症症状和特征相关的大脑区域(例如额颞叶和扣带回皮层)中,ASD 患者的皮质变薄明显减少。CT 神经解剖差异的空间模式在基因和转录组水平上与 ASD 相关的基因富集。此外,CT 的个体内差异与 RRBs 严重程度的个体内变异性相关。我们的研究结果代表了根据 CT 测量值描述 ASD 跨发展的神经解剖基础的重要一步。此外,我们的研究结果为 ASD 中小观和宏观病理学之间的联系以及它们与不同的 ASD 临床表型之间的关系提供了重要的新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18e1/8701312/5602425210fe/genes-12-02024-g001.jpg

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