Department of Psychiatry & Behavioral Sciences, the MIND Institute, University of California, Davis, CA, USA.
AI in Medical Imaging, German Center for Neurodegenerative Diseases, Bonn, Germany.
Mol Psychiatry. 2024 Nov;29(11):3440-3451. doi: 10.1038/s41380-024-02592-8. Epub 2024 May 16.
Previous studies have reported alterations in cortical thickness in autism. However, few have included enough autistic females to determine if there are sex specific differences in cortical structure in autism. This longitudinal study aimed to investigate autistic sex differences in cortical thickness and trajectory of cortical thinning across childhood. Participants included 290 autistic (88 females) and 139 nonautistic (60 females) individuals assessed at up to 4 timepoints spanning ~2-13 years of age (918 total MRI timepoints). Estimates of cortical thickness in early and late childhood as well as the trajectory of cortical thinning were modeled using spatiotemporal linear mixed effects models of age-by-sex-by-diagnosis. Additionally, the spatial correspondence between cortical maps of sex-by-diagnosis differences and neurotypical sex differences were evaluated. Relative to their nonautistic peers, autistic females had more extensive cortical differences than autistic males. These differences involved multiple functional networks, and were mainly characterized by thicker cortex at ~3 years of age and faster cortical thinning in autistic females. Cortical regions in which autistic alterations were different between the sexes significantly overlapped with regions that differed by sex in neurotypical development. Autistic females and males demonstrated some shared differences in cortical thickness and rate of cortical thinning across childhood relative to their nonautistic peers, however these areas were relatively small compared to the widespread differences observed across the sexes. These results support evidence of sex-specific neurobiology in autism and suggest that processes that regulate sex differentiation in the neurotypical brain contribute to sex differences in the etiology of autism.
先前的研究报告称自闭症患者存在皮质厚度改变。然而,很少有研究纳入足够数量的自闭症女性患者,以确定自闭症患者的皮质结构是否存在性别特异性差异。本纵向研究旨在探究自闭症患者的性别差异,以及在儿童期皮质变薄的轨迹。参与者包括 290 名自闭症患者(88 名女性)和 139 名非自闭症患者(60 名女性),他们在 2-13 岁期间接受了多达 4 次的评估(共 918 个 MRI 时间点)。使用时空线性混合效应模型,根据年龄、性别和诊断对早期和晚期儿童的皮质厚度以及皮质变薄的轨迹进行了建模。此外,还评估了性别-诊断差异和神经典型性别差异的皮质图之间的空间对应关系。与非自闭症同龄人相比,自闭症女性的皮质差异比自闭症男性更广泛。这些差异涉及多个功能网络,主要表现为 3 岁时皮质较厚,以及自闭症女性皮质变薄的速度较快。在性别之间存在自闭症改变的皮质区域与神经典型发育中存在性别的区域显著重叠。自闭症女性和男性与非自闭症同龄人相比,在儿童期的皮质厚度和皮质变薄率方面存在一些共同的差异,但与跨性别观察到的广泛差异相比,这些差异相对较小。这些结果支持自闭症存在性别特异性神经生物学的证据,并表明调节神经典型大脑性别分化的过程有助于自闭症病因的性别差异。