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首页> 外文期刊>Journal of abnormal child psychology >The Genetic Overlap of Attention-Deficit/Hyperactivity Disorder and Autistic-like Traits: an Investigation of Individual Symptom Scales and Cognitive markers
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The Genetic Overlap of Attention-Deficit/Hyperactivity Disorder and Autistic-like Traits: an Investigation of Individual Symptom Scales and Cognitive markers

机译:注意缺陷/多动障碍和自闭样特征的遗传重叠:个人症状量表和认知标记的调查。

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Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorders (ASDs) frequently co-occur. However, due to previous exclusionary diagnostic criteria, little is known about the underlying causes of this covariation. Twin studies assessing ADHD symptoms and autistic-like traits (ALTs) suggest substantial genetic overlap, but have largely failed to take into account the genetic heterogeneity of symptom subscales. This study aimed to clarify the phenotypic and genetic relations between ADHD and ASD by distinguishing between symptom subscales that characterise the two disorders. Moreover, we aimed to investigate whether ADHD-related cognitive impairments show a relationship with ALT symptom subscales; and whether potential shared cognitive impairments underlie the genetic risk shared between the ADHD and ALT symptoms. Multivariate structural equation modelling was conducted on a population-based sample of 1312 twins aged 7-10. Social-communication ALTs correlated moderately with both ADHD symptom domains (phenotypic correlations around 0.30) and showed substantial genetic overlap with both inattention and hyperactivity-impulsivity (genetic correlation = 0.52 and 0.44, respectively). In addition to previously reported associations with ADHD traits, reaction time variability (RTV) showed significant phenotypic (0.18) and genetic (0.32) association with social-communication ALTs. RTV captured a significant proportion (24 %) of the genetic influences shared between inattention and social-communication ALTs. Our findings suggest that social-communication ALTs underlie the previously observed phenotypic and genetic covariation between ALTs and ADHD symptoms. RTV is not specific to ADHD symptoms, but is also associated with social-communication ALTs and can, in part, contribute to an explanation of the co-occurrence of ASD and ADHD.
机译:注意缺陷/多动障碍(ADHD)和自闭症谱系障碍(ASD)经常并发。但是,由于先前的排除性诊断标准,对该协变的根本原因了解甚少。评估ADHD症状和自闭症样特征(ALTs)的双胞胎研究表明存在大量的遗传重叠,但是在很大程度上没有考虑到症状分量表的遗传异质性。这项研究旨在通过区分两种疾病的特征症状量表来阐明ADHD和ASD之间的表型和遗传关系。此外,我们旨在调查与ADHD相关的认知障碍是否与ALT症状分量表相关。以及潜在的共有认知障碍是否是ADHD和ALT症状之间共享的遗传风险的基础。多变量结构方程模型是对1312个7-10岁的双胞胎进行基于人群的抽样研究。社交交流ALTs与两个ADHD症状域均呈中等程度的相关性(表型相关性约为0.30),并且与注意力不集中和多动性冲动表现出显着的遗传重叠(遗传相关性分别为0.52和0.44)。除了先前报道的与多动症性状的关联外,反应时间变异性(RTV)还显示出与社交交流ALT的显着表型(0.18)和遗传(0.32)关联。 RTV捕获了注意力不集中和社交交流ALT之间共享的大部分遗传影响(24%)。我们的发现表明,社交交流型ALT是先前观察到的ALT和ADHD症状之间的表型和遗传共变的基础。 RTV并非特定于ADHD症状,但也与社交交流ALT相关,并且在一定程度上有助于解释ASD和ADHD的同时发生。

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