Wadsworth Sally J, DeFries John C, Willcutt Erik G, Pennington Bruce F, Olson Richard K
Institute for Behavioral Genetics,University of Colorado,Boulder,CO,USA.
Twin Res Hum Genet. 2015 Dec;18(6):755-61. doi: 10.1017/thg.2015.66. Epub 2015 Nov 5.
Approximately 60% of children with reading difficulties (RD) meet criteria for at least one co-occurring disorder. The most common of these, attention deficit-hyperactivity disorder (ADHD), occurs in 20-40% of individuals with RD. Recent studies have suggested that genetic influences are responsible. To assess the genetic etiologies of RD and the comorbidity of RD and two ADHD symptom dimensions -- inattention (IN) and hyperactivity/impulsivity (H/I) -- we are conducting the first longitudinal twin study of RD and ADHD. Data from twin pairs in which at least one member of the pair met criteria for proband status for RD at initial assessment, and were reassessed 5 years later, were subjected to DeFries-Fulker (DF) analysis. Analyses of reading composite data indicated that over 60% of the proband deficit at initial assessment was due to genetic influences, and that reading deficits at follow-up were due substantially to the same genetic influences. When a bivariate DF model was fitted to reading performance and IN data, genetic influences accounted for 60% of contemporaneous comorbidity and over 60% of the longitudinal relationship. In contrast, analysis of the comorbidity between reading performance and H/I indicated that common genetic influences accounted for only about 20% of the contemporaneous and about 10% of the longitudinal relationships. Results indicate that (1) genetic influences on RD are substantial and highly stable; (2) the comorbidity between RD and IN is due largely to genetic influences, both contemporaneously and longitudinally; and (3) genetic influences contribute significantly less to the comorbidity between RD and H/I.
约60%有阅读障碍(RD)的儿童符合至少一种共病障碍的标准。其中最常见的是注意缺陷多动障碍(ADHD),在20%-40%的RD个体中出现。近期研究表明这是由遗传影响所致。为评估RD的遗传病因以及RD与ADHD的两个症状维度——注意力不集中(IN)和多动/冲动(H/I)——的共病情况,我们正在开展第一项关于RD和ADHD的纵向双生子研究。对双生子的数据进行了DeFries-Fulker(DF)分析,这些双生子中至少有一名成员在初始评估时符合RD先证者状态标准,并在5年后接受了重新评估。阅读综合数据的分析表明,初始评估时超过60%的先证者缺陷是由遗传影响导致的,随访时的阅读缺陷在很大程度上也归因于相同的遗传影响。当对阅读表现和IN数据拟合双变量DF模型时,遗传影响占同期共病的60%以及纵向关系的60%以上。相比之下,阅读表现与H/I之间共病情况的分析表明,共同遗传影响仅占同期关系的约20%以及纵向关系的约10%。结果表明:(1)遗传对RD的影响很大且高度稳定;(2)RD与IN之间的共病在同期和纵向方面在很大程度上都归因于遗传影响;(3)遗传影响对RD与H/I之间共病的贡献要小得多。