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Neurodevelopmental heterogeneity and computational approaches for understanding autism

机译:理解孤独症的神经发育异质性和计算方法

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In recent years, the emerging field of computational psychiatry has impelled the use of machine learning models as a means to further understand the pathogenesis of multiple clinical disorders. In this paper, we discuss how autism spectrum disorder (ASD) was and continues to be diagnosed in the context of its complex neurodevelopmental heterogeneity. We review machine learning approaches to streamline ASD’s diagnostic methods, to discern similarities and differences from comorbid diagnoses, and to follow developmentally variable outcomes. Both supervised machine learning models for classification outcome and unsupervised approaches to identify new dimensions and subgroups are discussed. We provide an illustrative example of how computational analytic methods and a longitudinal design can improve our inferential ability to detect early dysfunctional behaviors that may or may not reach threshold levels for formal diagnoses. Specifically, an unsupervised machine learning approach of anomaly detection is used to illustrate how community samples may be utilized to investigate early autism risk, multidimensional features, and outcome variables. Because ASD symptoms and challenges are not static within individuals across development, computational approaches present a promising method to elucidate subgroups of etiological contributions to phenotype, alternative developmental courses, interactions with biomedical comorbidities, and to predict potential responses to therapeutic interventions.
机译:近年来,计算精神病学的新兴领域促使人们使用机器学习模型作为进一步了解多种临床疾病发病机理的手段。在本文中,我们讨论了自闭症谱系障碍(ASD)在复杂的神经发育异质性背景下如何并且将继续得到诊断。我们回顾了机器学习方法,以简化ASD的诊断方法,辨别合并症诊断的相似之处和不同之处,并跟踪发展变化的结果。讨论了用于分类结果的监督机器学习模型和用于识别新维度和子组的无监督方法。我们提供了一个说明性示例,说明了计算分析方法和纵向设计如何提高我们的推理能力,以检测可能无法达到正式诊断阈值水平的早期功能失调行为。具体而言,使用异常检测的无监督机器学习方法来说明如何使用社区样本来调查早期自闭症风险,多维特征和结果变量。由于ASD症状和挑战在整个发展过程中并不是一成不变的,因此计算方法提供了一种有前途的方法,可阐明病因对表型,替代发展过程,与生物医学合并症的相互作用以及预测对治疗干预措施的潜在作用的亚组。

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