Doyle-Thomas Krissy A R, Duerden Emma G, Taylor Margot J, Lerch Jason P, Soorya Latha V, Wang A Ting, Fan Jin, Hollander Eric, Anagnostou Evdokia
Bloorview Research Institute, Holland Bloorview Kids Rehabilitation Hospital, 150 Kilgour Road, Toronto, Ontario, M4G 1R8, Canada.
Res Autism Spectr Disord. 2013 Jan;7(1):141-150. doi: 10.1016/j.rasd.2012.08.004.
Several brain regions show structural and functional abnormalities in individuals with autism spectrum disorders (ASD), but the developmental trajectory of abnormalities in these structures and how they may relate to social and communicative impairments are still unclear. We assessed the effects of age on cortical thickness in individuals with ASD, between the ages of 7 and 39 years in comparison to typically developing controls. Additionally, we examined differences in cortical thickness in relation to symptomatology in the ASD group, and their association with age. Analyses were conducted using a general linear model, controlling for sex. Social and communication scores from the Autism Diagnostic Interview-Revised (ADI-R) were correlated with the thickness of regions implicated in those functions. Controls showed widespread cortical thinning relative to the ASD group. Within regions-of-interest, increased thickness in the rostral anterior cingulate cortex was associated with poorer social scores. Additionally, a significant interaction between age and social impairment was found in the orbitofrontal cortex, with more impaired younger children having decreased thickness in this region. These results suggest that differential neurodevelopmental trajectories are present in individuals with ASD and some differences are associated with diagnostic behaviours.
在患有自闭症谱系障碍(ASD)的个体中,几个脑区显示出结构和功能异常,但这些结构异常的发育轨迹以及它们与社交和沟通障碍的关系仍不清楚。我们评估了年龄对7至39岁ASD个体皮质厚度的影响,并与正常发育的对照组进行了比较。此外,我们研究了ASD组中与症状学相关的皮质厚度差异及其与年龄的关联。分析采用一般线性模型,对性别进行了控制。来自自闭症诊断访谈修订版(ADI-R)的社交和沟通得分与涉及这些功能的脑区厚度相关。与ASD组相比,对照组显示出广泛的皮质变薄。在感兴趣的区域内,喙前扣带回皮质厚度增加与较差的社交得分相关。此外,在眶额皮质中发现年龄与社交障碍之间存在显著交互作用,年龄较小且社交受损更严重的儿童该区域厚度减小。这些结果表明,ASD个体存在不同的神经发育轨迹,一些差异与诊断行为相关。