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Machine learning classification of ADHD and HC by multimodal serotonergic data

机译:多式二维onotonergic数据的ADHD和HC的机器学习分类

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Serotonin neurotransmission may impact the etiology and pathology of attention-deficit and hyperactivity disorder (ADHD), partly mediated through single nucleotide polymorphisms (SNPs). We propose a multivariate, genetic and positron emission tomography (PET) imaging classification model for ADHD and healthy controls (HC). Sixteen patients with ADHD and 22 HC were scanned by PET to measure serotonin transporter (SERT‘) binding potential with [11C]DASB. All subjects were genotyped for thirty SNPs within the HTR1A, HTR1B, HTR2A and TPH2 genes. Cortical and subcortical regions of interest (ROI) were defined and random forest (RF) machine learning was used for feature selection and classification in a five-fold cross-validation model with ten repeats. Variable selection highlighted the ROI posterior cingulate gyrus, cuneus, precuneus, pre-, para- and postcentral gyri as well as the SNPs HTR2A rs1328684 and rs6311 and HTR1B rs130058 as most discriminative between ADHD and HC status. The mean accuracy for the validation sets across repeats was 0.82 (±0.09) with balanced sensitivity and specificity of 0.75 and 0.86, respectively. With a prediction accuracy above 0.8, the findings underlying the proposed model advocate the relevance of the SERT as well as the HTR1B and HTR2A genes in ADHD and hint towards disease-specific effects. Regarding the high rates of comorbidities and difficult differential diagnosis especially for ADHD, a reliable computer-aided diagnostic tool for disorders anchored in the serotonergic system will support clinical decisions.
机译:血清素神经递质可能影响注意力缺陷和多动障碍(ADHD)的病因和病理,部分介导通过单一核苷酸多态性(SNP)。我们为ADHD和健康对照(HC)提出了一种多变量,遗传和正电子发射断层扫描(PET)成像分类模型。宠物扫描了16例ADHD和22hC患者,用[11C] DASB测量血清素转运蛋白转运蛋白(SERT')结合电位。所有受试者在HTR1A,HTR1B,HTR2A和TPH2基因内为三十个SNP进行基因分型。利用皮质和皮质波动区域(ROI)定义,随机森林(RF)机器学习用于具有十个重复的五倍交叉验证模型中的特征选择和分类。可变选择突出显示了ROI后刺刺刺伤过滤器,Cuneus,PriaNeus,预,Para-和后中央Gyri以及SNPS HTR2A RS1328684和RS6311和HTR1B RS130058在ADHD和HC状态之间是最判断的。重复验证组的平均精度为0.82(±0.09),分别平衡敏感性和特异性0.75和0.86。具有高于0.8的预测精度,所提出的模型的结果涉及SERT以及HTR1B和HTR2A基因在ADHD中的相关性,并提示朝向疾病特异性效果。关于合并症的高速率和难度鉴别诊断,特别是对于ADHD,用于锚定在Serotonergic系统中的可靠的计算机辅助诊断工具将支持临床决策。

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