基于扩散张量成像的发展预测模型揭示了儿童早期自闭症大脑中年龄依赖性的异质性。

IF 6.3 1区 医学 Q1 GENETICS & HEREDITY
Xinyue Huang, Yating Ming, Weixing Zhao, Rui Feng, Yuanyue Zhou, Lijie Wu, Jia Wang, Jinming Xiao, Lei Li, Xiaolong Shan, Jing Cao, Xiaodong Kang, Huafu Chen, Xujun Duan
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引用次数: 0

摘要

目的:越来越多的证据表明自闭症患者存在非典型白质(WM)微观结构,但研究结果存在分歧。自闭症患者在儿童早期的发展受到同时快速大脑生长的影响,这可能导致自闭症中非典型WM微观结构的不一致发现。在这里,我们旨在揭示自闭症儿童的发展本质,并在考虑发展因素的同时,描绘整个幼儿期非典型WM微观结构。方法:在本研究中,从两个独立的队列中获得扩散张量成像,包括91名自闭症儿童和100名4-7岁的典型发育中儿童(TDC)。基于TDC参与者,使用支持向量回归进行发展预测建模,以估计自闭症儿童的WM非典型发展指数。然后,使用k-means聚类方法确定自闭症儿童的亚组,并使用双样本t检验在人口统计学信息、WM非典型发展指数和自闭症特征的基础上相互比较。WM非典型发展指数和年龄的关系用偏相关估计。此外,我们对自闭症儿童各亚组与TDC亚组的WM微观结构进行了基于无阈值聚类增强的双样本t检验。结果:我们根据WM非典型发育指数将自闭症儿童分为两个亚组。这两个亚组表现出不同的发育阶段和年龄依赖性的多样性。WM非典型发育指数与年龄呈负相关。此外,在这两个阶段中,非典型WM微观结构和不同临床表现的相反模式被揭示,亚组1表现出过度生长,具有低水平的自闭症特征,而亚组2表现出延迟成熟,具有高水平的自闭主义特征。结论:本研究阐明了儿童早期自闭症儿童的年龄依赖性异质性,并描绘了从过度生长模式到延迟模式的发育阶段特异性差异。试验注册本研究已于2016年6月21日在ClinicalTrials.gov(标识符:NCT02807766)上注册(https://clinicaltrials.gov/ct2/show/NCT02807766)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Developmental prediction modeling based on diffusion tensor imaging uncovering age-dependent heterogeneity in early childhood autistic brain.

Developmental prediction modeling based on diffusion tensor imaging uncovering age-dependent heterogeneity in early childhood autistic brain.

Developmental prediction modeling based on diffusion tensor imaging uncovering age-dependent heterogeneity in early childhood autistic brain.

Developmental prediction modeling based on diffusion tensor imaging uncovering age-dependent heterogeneity in early childhood autistic brain.

Objective: There has been increasing evidence for atypical white matter (WM) microstructure in autistic people, but findings have been divergent. The development of autistic people in early childhood is clouded by the concurrently rapid brain growth, which might lead to the inconsistent findings of atypical WM microstructure in autism. Here, we aimed to reveal the developmental nature of autistic children and delineate atypical WM microstructure throughout early childhood while taking developmental considerations into account.

Method: In this study, diffusion tensor imaging was acquired from two independent cohorts, containing 91 autistic children and 100 typically developing children (TDC), aged 4-7 years. Developmental prediction modeling using support vector regression based on TDC participants was conducted to estimate the WM atypical development index of autistic children. Then, subgroups of autistic children were identified by using the k-means clustering method and were compared to each other on the basis of demographic information, WM atypical development index, and autistic trait by using two-sample t-test. Relationship of the WM atypical development index with age was estimated by using partial correlation. Furthermore, we performed threshold-free cluster enhancement-based two-sample t-test for the group comparison in WM microstructures of each subgroup of autistic children with the rematched subsets of TDC.

Results: We clustered autistic children into two subgroups according to WM atypical development index. The two subgroups exhibited distinct developmental stages and age-dependent diversity. WM atypical development index was found negatively associated with age. Moreover, an inverse pattern of atypical WM microstructures and different clinical manifestations in the two stages, with subgroup 1 showing overgrowth with low level of autistic traits and subgroup 2 exhibiting delayed maturation with high level of autistic traits, were revealed.

Conclusion: This study illustrated age-dependent heterogeneity in early childhood autistic children and delineated developmental stage-specific difference that ranged from an overgrowth pattern to a delayed pattern. Trial registration This study has been registered at ClinicalTrials.gov (Identifier: NCT02807766) on June 21, 2016 ( https://clinicaltrials.gov/ct2/show/NCT02807766 ).

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来源期刊
Molecular Autism
Molecular Autism GENETICS & HEREDITY-NEUROSCIENCES
CiteScore
12.10
自引率
1.60%
发文量
44
审稿时长
17 weeks
期刊介绍: Molecular Autism is a peer-reviewed, open access journal that publishes high-quality basic, translational and clinical research that has relevance to the etiology, pathobiology, or treatment of autism and related neurodevelopmental conditions. Research that includes integration across levels is encouraged. Molecular Autism publishes empirical studies, reviews, and brief communications.
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