Methods of Plasticity Research, Department of Psychology, University of Zurich.
J Psychopathol Clin Sci. 2024 Nov;133(8):667-677. doi: 10.1037/abn0000914.
Autism spectrum disorder ("autism") is a neurodevelopmental condition characterized by substantial behavioral and neuroanatomical heterogeneity. This poses significant challenges to understanding its neurobiological mechanisms and developing effective interventions. Identifying phenotypically more homogeneous subgroups and shifting the focus from average group differences to individuals is a promising approach to addressing heterogeneity. In the present study, we aimed to parse clinical and neuroanatomical heterogeneity in autism by combining clustering of clinical features with normative modeling based on neuroanatomical measures (cortical thickness [CT] and subcortical volume) within the Autism Brain Imaging Data Exchange data sets (N autism = 861, N nonautistic individuals [N NAI] = 886, age range = 5-64). First, model-based clustering was applied to autistic symptoms as measured by the Autism Diagnostic Observation Schedule to identify clinical subgroups of autism (N autism = 499). Next, we ran normative modeling on CT and subcortical parcellations (N autism = 690, N NAI = 744) and examined whether clinical subgrouping resulted in increased neurobiological homogeneity within the subgroups compared to the entire autism group by comparing their spatial overlap of neuroanatomical deviations. We further investigated whether the identified subgroups improved the accuracy of autism classification based on the neuroanatomical deviations using supervised machine learning with cross-validation. Results yielded two clinical subgroups primarily differing in restrictive and repetitive behaviors (RRBs). Both subgroups showed increased homogeneity in localized deviations with the high-RRB subgroup showing increased volume deviations in the cerebellum and the low-RRB subgroup showing decreased CT deviations predominantly in the postcentral gyrus and fusiform cortex. Nevertheless, substantial within-group heterogeneity remained highlighted by the lack of improvement of the classifier's performance when distinguishing between the subgroups and NAI. Future research should aim to further reduce heterogeneity incorporating additional neuroanatomical clustering in even larger samples. This will eventually pave the way for more tailored behavioral interventions and improving clinical outcomes. (PsycInfo Database Record (c) 2024 APA, all rights reserved).
自闭症谱系障碍(“自闭症”)是一种神经发育障碍,其特征是行为和神经解剖学的显著异质性。这对理解其神经生物学机制和开发有效的干预措施构成了重大挑战。通过将临床特征聚类与基于神经解剖学测量(皮质厚度[CT]和皮质下体积)的规范建模相结合,确定表型上更同质的亚组,并将重点从平均组间差异转移到个体,是解决异质性的一种很有前途的方法。在本研究中,我们旨在通过将临床特征聚类与基于神经解剖学测量(皮质厚度[CT]和皮质下体积)的规范建模相结合,解析自闭症中的临床和神经解剖学异质性,这些数据来自自闭症脑成像数据交换(Autism Brain Imaging Data Exchange,ABIDE)数据集(自闭症患者 N = 861,非自闭症个体 N = 886,年龄范围 5-64 岁)。首先,我们应用基于模型的聚类方法对自闭症诊断观察量表(Autism Diagnostic Observation Schedule,ADOS)测量的自闭症症状进行聚类,以确定自闭症的临床亚组(自闭症患者 N = 499)。接下来,我们对 CT 和皮质下分区进行规范建模(自闭症患者 N = 690,非自闭症个体 N = 744),通过比较神经解剖学偏差的空间重叠,检查临床亚组划分是否导致亚组内的神经生物学同质性增加,与整个自闭症组相比。我们还进一步研究了基于神经解剖学偏差的监督机器学习分类器,通过交叉验证,是否可以通过识别亚组来提高自闭症的分类准确性。结果得出了两个主要在受限和重复行为(RRB)上存在差异的临床亚组。两个亚组在局部偏差上的一致性都有所提高,高 RRB 亚组在小脑显示出体积偏差增加,低 RRB 亚组在中央后回和梭状回显示出 CT 偏差减少。然而,当区分亚组和非自闭症个体时,分类器性能的提高并不明显,这突出表明了组内仍存在很大的异质性。未来的研究应旨在进一步减少异质性,在更大的样本中纳入额外的神经解剖学聚类。这最终将为更有针对性的行为干预措施和改善临床结果铺平道路。(PsycInfo 数据库记录(c)2024 APA,保留所有权利)。