EPHA5基因多态性与注意缺陷多动障碍:基于“基因-脑-认知”模型的关联性分析

The Association Between EPHA5 Gene Polymorphism and Attention-Deficit/Hyperactivity Disorder Based on the "Gene-Brain-Cognition" Model

  • 摘要:
    目的 基于“基因-脑-认知”模型,探讨EPHA5基因rs4860671位点多态性与注意缺陷多动障碍(attention-deficit/hyperactivity disorder,ADHD)的关联性,并分析其对患儿执行功能及静息态脑功能的影响。
    方法 本研究为病例对照研究,以2015—2020年北京大学第六医院门诊ADHD患儿及同期北京市普通中小学在读健康儿童为研究对象。两组均测定EPHA5基因rs4860671位点基因型;通过静息态功能磁共振成像评估脑自发活动;此外,分别采用ADHD评定量表和执行功能行为评定量表评价ADHD核心症状与执行功能。使用遗传关联分析、协方差分析和中介分析等方法,系统探究rs4860671位点多态性与ADHD临床症状、执行功能及脑功能活动的关联性。
    结果 共纳入244例ADHD患儿,83名健康儿童。其中,188例ADHD患儿和70名健康儿童完成了MRI扫描。等位基因分析发现,rs4860671位点的G等位基因在ADHD患儿中的分布频率显著高于健康儿童(77.5%比69.9%, P=0.049);基因型分析结果显示,在显性模型下,rs4860671位点基因型分布频率在两组间亦存在显著差异(P=0.031)。在执行功能的关联分析中,携带rs4860671位点GG基因型儿童相较于携带A等位基因(AA+AG)的儿童,情绪控制分数更高(15.99±4.62)分比(14.53±4.03)分,P=0.017,提示其情绪控制能力较差;进一步中介分析显示,情绪控制在rs4860671位点基因型与ADHD核心症状之间发挥完全中介效应。脑影像学分析发现,在ADHD患儿中,rs4860671位点GG基因型携带者右侧枕下回和左侧枕中回的脑自发活动较A等位基因携带者减弱。
    结论 EPHA5基因rs4860671多态性可能通过影响情绪控制能力和视觉网络功能活动进而参与ADHD发病,该发现为深入理解ADHD神经生物学机制提供了新的科学依据。

     

    Abstract:
    Objective Based on the "gene-brain-cognition" model, this study aimed to investigate the association between the rs4860671 polymorphism of the EPHA5 gene and attention-deficit/hyperactivity disorder (ADHD), and to analyze its impact on executive function and resting-state brain activity in affected children.
    Methods This was a case-control study. Children with ADHD attending the outpatient clinic of Peking University Sixth Hospital from 2015 to 2020 and typically developing children from general primary and secondary schools in Beijing during the same period were enrolled as subjects. Genotypes of the EPHA5 rs4860671 polymorphism were determined in both groups. Resting-state functional magnetic resonance imaging was used to assess spontaneous brain activity. In addition, the ADHD Rating Scale and the Behavior Rating Inventory of Executive Function were administered to evaluate ADHD core symptoms and executive function, respectively. Genetic association analysis, analysis of covariance, and mediation analysis were systematically performed to explore the associations of the rs4860671 polymorphism with ADHD clinical symptoms, executive function, and brain functional activity.
    Results A total of 244 children with ADHD and 83 healthy controls were included. Among them, 188 children with ADHD and 70 healthy controls completed MRI scanning. Allelic analysis revealed that the frequency of the G allele of rs4860671 was significantly higher in children with ADHD than in healthy controls (77.5% vs. 69.9%, P=0.049). Genotype distribution analysis also demonstrated a significant difference between the two groups under the dominant model (P=0.031). Regarding executive function, children carrying the GG genotype of rs4860671 had higher scores in emotion control compared with those carrying the A allele (AA+AG) (15.99±4.62 vs. 14.53±4.03, P=0.017), indicating poorer emotion regulation ability. Further mediation analysis showed that emotion control fully mediated the relationship between rs4860671 genotype and core symptoms of ADHD. Neuroimaging analysis revealed that among children with ADHD, carriers of the GG genotype exhibited decreased spontaneous brain activity in the right inferior occipital gyrus and left middle occipital gyrus compared with A allele carriers.
    Conclusions The rs4860671 polymorphism of the EPHA5 gene may be involved in the pathogenesis of ADHD by influencing emotion regulation ability and visual network functional activity. This finding provides new scientific evidence for a deeper understanding of the neurobiological mechanisms underlying ADHD.

     

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