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The separation of ADHD inattention and hyperactivity-impulsivity symptoms: pathways from genetic effects to cognitive impairments and symptoms

机译:多动症注意力不集中和多动冲动症状的分离:从遗传效应到认知障碍和症状的途径

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摘要

Both shared and unique genetic risk factors underlie the two symptom domains of attention deficit hyperactivity disorder (ADHD): inattention and hyperactivity-impulsivity. The developmental course and relationship to co-occurring disorders differs across the two symptom domains, highlighting the importance of their partially distinct etiologies. Familial cognitive impairment factors have been identified in ADHD, but whether they show specificity in relation to the two ADHD symptom domains remains poorly understood. We aimed to investigate whether different cognitive impairments are genetically linked to the ADHD symptom domains of inattention versus hyperactivity-impulsivity. We conducted multivariate genetic model fitting analyses on ADHD symptom scores and cognitive data, from goo-go and fast tasks, collected on a population twin sample of 1312 children aged 7-10. Reaction time variability (RTV) showed substantial genetic overlap with inattention, as observed in an additive genetic correlation of 0.64, compared to an additive genetic correlation of 0.31 with hyperactivity-impulsivity. Commission errors (CE) showed low additive genetic correlations with both hyperactivity-impulsivity and inattention (genetic correlations of 0.17 and 0.11, respectively). The additive genetic correlation between RTV and CE was also low and non-significant at −0.10, consistent with the etiological separation between the two indices of cognitive impairments. Overall, two key cognitive impairments phenotypically associated with ADHD symptoms, captured by RTV and CE, showed different genetic relationships to the two ADHD symptom domains. The findings extend a previous model of two familial cognitive impairment factors in combined subtype ADHD by separating pathways underlying inattention and hyperactivity-impulsivity symptoms.
机译:注意缺陷多动障碍(ADHD)的两个症状域是共有的和独特的遗传危险因素:注意力不集中和冲动过度。在两个症状域中,发展过程和与同时发生的疾病的关系不同,这突显了其部分不同病因的重要性。在ADHD中已经鉴定出家族性认知障碍因子,但是它们是否相对于两个ADHD症状域显示出特异性仍知之甚少。我们旨在调查是否不同的认知障碍与注意力不集中与多动症冲动的ADHD症状域遗传相关。我们对来自/不通过和快速任务的ADHD症状评分和认知数据进行了多变量遗传模型拟合分析,这些数据是从1312名7-10岁儿童的双胞胎样本中收集的。反应时间变异性(RTV)显示出明显的遗传重叠和疏忽,如0.64的加性遗传相关性与0.31的多动性冲动性相关。佣金错误(CE)显示出与活动过度冲动和注意力不集中的加性遗传相关性较低(遗传相关性分别为0.17和0.11)。 RTV和CE之间的加性遗传相关性也很低,在-0.10时无显着性,与认知障碍两个指标之间的病因学分离相一致。总体而言,RTV和CE捕获的两个与ADHD症状在表型上相关的关键认知障碍表现出与两个ADHD症状域的不同遗传关系。这些发现通过分离注意力不集中和过度冲动症状的潜在途径,扩展了合并的多动症亚型中两个家族性认知障碍因素的先前模型。

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