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Predicting attention-deficit/hyperactivity disorder severity from psychosocial stress and stress-response genes: a random forest regression approach

机译:从社会心理压力和压力反应基因预测注意力缺陷/多动障碍的严重程度:随机森林回归方法

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Identifying genetic variants contributing to attention-deficit/hyperactivity disorder (ADHD) is complicated by the involvement of numerous common genetic variants with small effects, interacting with each other as well as with environmental factors, such as stress exposure. Random forest regression is well suited to explore this complexity, as it allows for the analysis of many predictors simultaneously, taking into account any higher-order interactions among them. Using random forest regression, we predicted ADHD severity, measured by Conners’ Parent Rating Scales, from 686 adolescents and young adults (of which 281 were diagnosed with ADHD). The analysis included 17?374 single-nucleotide polymorphisms (SNPs) across 29 genes previously linked to hypothalamic–pituitary–adrenal (HPA) axis activity, together with information on exposure to 24 individual long-term difficulties or stressful life events. The model explained 12.5% of variance in ADHD severity. The most important SNP, which also showed the strongest interaction with stress exposure, was located in a region regulating the expression of telomerase reverse transcriptase ( TERT ). Other high-ranking SNPs were found in or near NPSR1, ESR1 , GABRA6, PER3 , NR3C2 and DRD4 . Chronic stressors were more influential than single, severe, life events. Top hits were partly shared with conduct problems. We conclude that random forest regression may be used to investigate how multiple genetic and environmental factors jointly contribute to ADHD. It is able to implicate novel SNPs of interest, interacting with stress exposure, and may explain inconsistent findings in ADHD genetics. This exploratory approach may be best combined with more hypothesis-driven research; top predictors and their interactions with one another should be replicated in independent samples.
机译:由于众多常见的遗传变异涉及很小的作用,相互影响以及与环境因素(如压力暴露)的相互作用,因此识别导致注意力缺陷/多动障碍(ADHD)的遗传变异变得复杂。随机森林回归非常适合探索这种复杂性,因为它允许同时分析许多预测变量,并考虑到它们之间的任何高级交互作用。使用随机森林回归,我们根据Conners的父母等级量表预测了686名青少年(其中281名被诊断为ADHD)的ADHD严重程度。该分析包括跨越29个先前与下丘脑-垂体-肾上腺(HPA)轴活动相关的基因的17–374个单核苷酸多态性(SNP),以及有关暴露于24个个体长期困难或压力性生活事件的信息。该模型解释了多动症严重程度变异的12.5%。最重要的SNP,也表现出与压力暴露的最强相互作用,位于调节端粒酶逆转录酶(TERT)表达的区域。在NPSR1,ESR1,GABRA6,PER3,NR3C2和DRD4或附近发现了其他高级SNP。慢性应激源比单个严重事件有更大的影响力。热门歌曲部分与行为问题有关。我们得出的结论是,可以使用随机森林回归来研究多种遗传和环境因素如何共同促进多动症。它能够暗示感兴趣的新型SNP,并与压力暴露相互作用,并可能解释ADHD遗传学中不一致的发现。最好将这种探索性方法与更多假设驱动的研究相结合。最佳预测变量及其相互之间的相互作用应在独立样本中进行复制。

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