了解自闭症的异质性:识别临床亚群和神经解剖学偏差。

IF 3.1 Q2 PSYCHIATRY Journal of psychopathology and clinical science Pub Date : 2024-11-01 DOI:10.1037/abn0000914
Jente Meijer, Bruno Hebling Vieira, Camille Elleaume, Zofia Baranczuk-Turska, Nicolas Langer, Dorothea L Floris
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引用次数: 0

摘要

自闭症谱系障碍("自闭症")是一种神经发育性疾病,其特点是行为和神经解剖异质性很大。这给了解其神经生物学机制和制定有效的干预措施带来了巨大挑战。识别表型上更为同质的亚组,并将关注点从平均群体差异转移到个体身上,是解决异质性问题的一种很有前景的方法。在本研究中,我们的目标是在自闭症脑成像数据交换数据集(自闭症患者人数 = 861,非自闭症患者人数 [N NAI] = 886,年龄范围 = 5-64)中,将临床特征聚类与基于神经解剖测量(皮质厚度 [CT] 和皮质下体积)的常模相结合,从而解析自闭症的临床和神经解剖异质性。首先,对自闭症诊断观察表所测量的自闭症症状进行基于模型的聚类,以确定自闭症的临床亚组(自闭症人数 = 499)。接下来,我们对 CT 和皮层下细胞群(N autism = 690,N NAI = 744)进行了规范建模,并通过比较神经解剖学偏差的空间重叠,考察了临床亚组与整个自闭症群体相比是否会导致亚组内神经生物学同质性的增加。我们进一步研究了已识别的亚组是否提高了基于神经解剖学偏差的自闭症分类的准确性,方法是使用带交叉验证的监督机器学习。结果发现了两个临床亚组,主要在限制性和重复性行为(RRBs)方面存在差异。两个亚组在局部偏差方面的同质性都有所提高,高RRB亚组小脑体积偏差增大,低RRB亚组CT偏差减小,主要集中在中央后回和纺锤形皮层。然而,在区分亚组和 NAI 时,分类器的性能没有提高,这突出表明组内仍存在大量异质性。未来的研究应着眼于进一步减少异质性,在更大的样本中纳入更多的神经解剖聚类。这最终将为更有针对性的行为干预和改善临床结果铺平道路。(PsycInfo Database Record (c) 2024 APA, 版权所有)。
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Toward understanding autism heterogeneity: Identifying clinical subgroups and neuroanatomical deviations.

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).

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