Knyspel Jacob, Morneau-Vaillancourt Geneviève, Eley Thalia C
Social, Genetic & Developmental Psychiatry Centre, Memory Lane, London, SE5 8AF, UK.
Institute of Psychiatry, Psychology & Neuroscience, London, UK.
Behav Genet. 2025 Jan;55(1):1-11. doi: 10.1007/s10519-024-10204-y. Epub 2024 Oct 30.
Attention Deficit Hyperactivity Disorder (ADHD) is a common and heritable neurodevelopmental condition that has been the subject of a wealth of genetics research. Because ADHD has an early age of onset, most of this work has focused on children, meaning that less is known about the genetics of ADHD in adults. Additionally, while much research has assessed the heritability of ADHD as a general dimension, less has assessed the heritability of individual subtypes (inattention, hyperactivity) or symptoms of ADHD. It therefore remains unclear whether the genetic factors underlying ADHD symptoms conform to a unidimensional or multidimensional structure. The aim of this study was to assess the genetic and environmental dimensionality of adult ADHD symptoms. We analyzed data from 10,454 twins of the Twins Early Development Study, who provided self-reports of ADHD symptoms using the Conners scale at age 21 years. The data conformed well to a psychometric bifactor model, providing support for a general dimension of ADHD in addition to secondary dimensions for inattention and hyperactivity. However, a bifactor independent pathway twin model provided support for a general dimension only at the level of non-shared environmental effects and not additive genetic or shared environmental effects. This suggests that symptoms of ADHD cluster together under a general dimension of non-shared environmental effects, although the two subtypes of ADHD (inattention and hyperactivity) are meaningfully genetically distinct. We found the overall heritability of ADHD to be 40%, comparable with previous estimates for adult ADHD symptoms. Our results provide useful insights into the genetic and environmental architecture of specific ADHD symptoms.
注意缺陷多动障碍(ADHD)是一种常见的遗传性神经发育疾病,一直是大量遗传学研究的主题。由于ADHD发病年龄较早,大部分研究工作都集中在儿童身上,这意味着对于成人ADHD的遗传学了解较少。此外,虽然许多研究评估了ADHD作为一个总体维度的遗传性,但较少有研究评估ADHD个体亚型(注意力不集中、多动)或症状的遗传性。因此,ADHD症状背后的遗传因素是否符合单维或多维结构仍不清楚。本研究的目的是评估成人ADHD症状的遗传和环境维度。我们分析了来自双胞胎早期发育研究的10454对双胞胎的数据,他们在21岁时使用康纳斯量表对ADHD症状进行了自我报告。数据很好地符合心理测量双因素模型,除了注意力不集中和多动的次级维度外,还为ADHD的总体维度提供了支持。然而,双因素独立路径双胞胎模型仅在非共享环境效应水平上为总体维度提供了支持,而不是加性遗传或共享环境效应。这表明,ADHD症状在非共享环境效应的总体维度下聚集在一起,尽管ADHD的两种亚型(注意力不集中和多动)在遗传上有明显区别。我们发现ADHD的总体遗传率为40%,与之前对成人ADHD症状的估计相当。我们的结果为特定ADHD症状的遗传和环境结构提供了有用的见解。