Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach.

IF 6.3 1区 医学 Q1 GENETICS & HEREDITY Molecular Autism Pub Date : 2023-05-23 DOI:10.1186/s13229-023-00549-2
Nicholas Donnelly, Adam Cunningham, Sergio Marco Salas, Matthew Bracher-Smith, Samuel Chawner, Jan Stochl, Tamsin Ford, F Lucy Raymond, Valentina Escott-Price, Marianne B M van den Bree
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Abstract

Background: Genomic conditions can be associated with developmental delay, intellectual disability, autism spectrum disorder, and physical and mental health symptoms. They are individually rare and highly variable in presentation, which limits the use of standard clinical guidelines for diagnosis and treatment. A simple screening tool to identify young people with genomic conditions associated with neurodevelopmental disorders (ND-GCs) who could benefit from further support would be of considerable value. We used machine learning approaches to address this question.

Method: A total of 493 individuals were included: 389 with a ND-GC, mean age = 9.01, 66% male) and 104 siblings without known genomic conditions (controls, mean age = 10.23, 53% male). Primary carers completed assessments of behavioural, neurodevelopmental and psychiatric symptoms and physical health and development. Machine learning techniques (penalised logistic regression, random forests, support vector machines and artificial neural networks) were used to develop classifiers of ND-GC status and identified limited sets of variables that gave the best classification performance. Exploratory graph analysis was used to understand associations within the final variable set.

Results: All machine learning methods identified variable sets giving high classification accuracy (AUROC between 0.883 and 0.915). We identified a subset of 30 variables best discriminating between individuals with ND-GCs and controls which formed 5 dimensions: conduct, separation anxiety, situational anxiety, communication and motor development.

Limitations: This study used cross-sectional data from a cohort study which was imbalanced with respect to ND-GC status. Our model requires validation in independent datasets and with longitudinal follow-up data for validation before clinical application.

Conclusions: In this study, we developed models that identified a compact set of psychiatric and physical health measures that differentiate individuals with a ND-GC from controls and highlight higher-order structure within these measures. This work is a step towards developing a screening instrument to identify young people with ND-GCs who might benefit from further specialist assessment.

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识别与智力障碍相关的基因组疾病的神经发育和精神特征:一种机器学习方法。
背景:基因组疾病可能与发育迟缓、智力障碍、自闭症谱系障碍以及身心健康症状有关。这些基因组疾病各自都很罕见,表现形式也千差万别,这就限制了标准临床指南在诊断和治疗方面的应用。如果能有一种简单的筛查工具来识别患有与神经发育障碍相关的基因组疾病(ND-GCs)的青少年,并为他们提供进一步的支持,这将具有相当大的价值。我们采用机器学习方法来解决这一问题:我们共纳入了 493 人:389人患有ND-GC,平均年龄=9.01岁,66%为男性)和104名无已知基因组状况的兄弟姐妹(对照组,平均年龄=10.23岁,53%为男性)。主要照护者完成了行为、神经发育和精神症状以及身体健康和发育的评估。利用机器学习技术(惩罚逻辑回归、随机森林、支持向量机和人工神经网络)开发了 ND-GC 状态分类器,并确定了能提供最佳分类性能的有限变量集。探索性图表分析用于了解最终变量集的关联性:所有机器学习方法都确定了分类准确率较高的变量集(AUROC 在 0.883 和 0.915 之间)。我们确定了 30 个最能区分 ND-GCs 患儿和对照组患儿的变量子集,这 30 个变量组成了 5 个维度:行为、分离焦虑、情境焦虑、沟通和运动发育:本研究使用了一项队列研究中的横断面数据,这些数据在 ND-GC 状态方面是不平衡的。在临床应用之前,我们的模型需要在独立数据集和纵向随访数据中进行验证:在这项研究中,我们建立的模型确定了一套紧凑的精神和身体健康测量指标,可将 ND-GC 患者与对照组区分开来,并突出了这些测量指标的高阶结构。这项工作为开发筛查工具迈出了一步,该工具可用于识别患有 ND-GC 的年轻人,他们可能会从进一步的专家评估中受益。
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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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