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单核苷酸多态性可预测自闭症谱系障碍的症状严重程度。

Single nucleotide polymorphisms predict symptom severity of autism spectrum disorder.

机构信息

Key Laboratory of Child Development and Learning Science, Ministry of Education, Southeast University, Nanjing, 210096 Jiangsu, China.

出版信息

J Autism Dev Disord. 2012 Jun;42(6):971-83. doi: 10.1007/s10803-011-1327-5.

Abstract

Autism is widely believed to be a heterogeneous disorder; diagnosis is currently based solely on clinical criteria, although genetic, as well as environmental, influences are thought to be prominent factors in the etiology of most forms of autism. Our goal is to determine whether a predictive model based on single-nucleotide polymorphisms (SNPs) can predict symptom severity of autism spectrum disorder (ASD). We divided 118 ASD children into a mild/moderate autism group (n = 65) and a severe autism group (n = 53), based on the Childhood Autism Rating Scale (CARS). For each child, we obtained 29 SNPs of 9 ASD-related genes. To generate predictive models, we employed three machine-learning techniques: decision stumps (DSs), alternating decision trees (ADTrees), and FlexTrees. DS and FlexTree generated modestly better classifiers, with accuracy = 67%, sensitivity = 0.88 and specificity = 0.42. The SNP rs878960 in GABRB3 was selected by all models, and was related associated with CARS assessment. Our results suggest that SNPs have the potential to offer accurate classification of ASD symptom severity.

摘要

自闭症被广泛认为是一种异质性疾病;目前的诊断仅基于临床标准,尽管遗传和环境因素被认为是大多数自闭症形式发病的重要因素。我们的目标是确定基于单核苷酸多态性 (SNP) 的预测模型是否可以预测自闭症谱系障碍 (ASD) 的症状严重程度。我们根据儿童自闭症评定量表 (CARS) 将 118 名 ASD 儿童分为轻度/中度自闭症组 (n = 65) 和重度自闭症组 (n = 53)。对于每个孩子,我们获得了 9 个与 ASD 相关基因的 29 个 SNP。为了生成预测模型,我们采用了三种机器学习技术:决策树桩 (DS)、交替决策树 (ADTree) 和 FlexTree。DS 和 FlexTree 生成了稍好的分类器,准确率 = 67%,灵敏度 = 0.88,特异性 = 0.42。所有模型都选择了 GABRB3 中的 SNP rs878960,并且与 CARS 评估相关。我们的结果表明,SNP 有可能提供 ASD 症状严重程度的准确分类。

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