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Core-Symptom-Defined Cortical Gyrification Differences in Autism Spectrum Disorder

机译:核心症状定义的自闭症谱系疾病中的皮质改变差异

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Autism spectrum disorder (ASD) is a heterogeneous disease that is characterized by abnormalities in social communication and interaction as well as repetitive behaviors and restricted interests. Structural brain imaging has identified significant cortical folding alterations in ASD; however, relatively less known is whether the core symptoms are related to neuroanatomical differences. In this study, we aimed to explore core-symptom-anchored gyrification alterations and their developmental trajectories in ASD. We measured the cortical vertex-wise gyrification index (GI) in 321 patients with ASD (aged 7–39 years) and 350 typically developing (TD) subjects (aged 6–33 years) across 8 sites from the Autism Brain Imaging Data Exchange I (ABIDE I) repository and a longitudinal sample (14 ASD and 7 TD, aged 9–14 years in baseline and 12–18 years in follow-up) from ABIDE II. Compared with TD, the general ASD patients exhibited a mixed pattern of both hypo- and hyper- and different developmental trajectories of gyrification. By parsing the ASD patients into three subgroups based on the subscores of the Autism Diagnostic Interview—Revised (ADI-R) scale, we identified core-symptom-specific alterations in the reciprocal social interaction (RSI), communication abnormalities (CA), and restricted, repetitive, and stereotyped patterns of behavior (RRSB) subgroups. We also showed atypical gyrification patterns and developmental trajectories in the subgroups. Furthermore, we conducted a meta-analysis to locate the core-symptom-anchored brain regions (circuits). In summary, the current study shows that ASD is associated with abnormal cortical folding patterns. Core-symptom-based classification can find more subtle changes in gyrification. These results suggest that cortical folding pattern encodes changes in symptom dimensions, which promotes the understanding of neuroanatomical basis, and clinical utility in ASD.
机译:自闭症谱系障碍(ASD)是一种异质疾病,其特征是社会沟通和互动的异常以及重复行为和限制利益。结构脑成像在ASD中确定了显着的皮质折叠改变;然而,相对较小的是核心症状是否与神经杀菌差异有关。在这项研究中,我们旨在探索核心症状固定的热化改变及其在ASD中的发育轨迹。我们测量了321名患有ASD(7-39岁)患者的皮质顶点 - 明智的引物指数(GI),350名通常在8位点的350名典型的发展(6-33岁),来自自闭症脑成像数据交换的8个站点(恪守i)储存库和纵向样本(14吨和7吨,在基线9-14岁,随访中为12-18岁)。与TD相比,一般ASD患者表现出一种混合模式,具有多种和不同发育轨迹的热化。通过将ASD患者解析为三个亚组,基于自闭症诊断访谈修订的(ADI-R)规模,我们确定了循环症状特定于互惠社会互动(RSI),通信异常(CA)和受限制,重复和刻板的行为模式(RRSB)子组。我们还在亚组中展示了非典型的热化模式和发育轨迹。此外,我们进行了荟萃分析以定位核心静态锚定的脑区(电路)。总之,目前的研究表明,ASD与异常的皮质折叠模式相关联。基于核心症状的分类可以找到更细微的变化。这些结果表明皮质折叠模式编码症状尺寸的变化,促进了对神经杀菌基础的理解和ASD的临床效用。

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