Department of Psychological Sciences, Birkbeck College, University of London, London, UK.
School of Psychology, University of East Anglia, Norwich, UK.
Dev Psychopathol. 2020 Oct;32(4):1303-1322. doi: 10.1017/S0954579420000930.
Identifying developmental endophenotypes on the pathway between genetics and behavior is critical to uncovering the mechanisms underlying neurodevelopmental conditions. In this proof-of-principle study, we explored whether early disruptions in visual attention are a unique or shared candidate endophenotype of autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD). We calculated the duration of the longest look (i.e., peak look) to faces in an array-based eye-tracking task for 335 14-month-old infants with and without first-degree relatives with ASD and/or ADHD. We leveraged parent-report and genotype data available for a proportion of these infants to evaluate the relation of looking behavior to familial (n = 285) and genetic liability (using polygenic scores, n = 185) as well as ASD and ADHD-relevant temperament traits at 2 years of age (shyness and inhibitory control, respectively, n = 272) and ASD and ADHD clinical traits at 6 years of age (n = 94).Results showed that longer peak looks at the face were associated with elevated polygenic scores for ADHD (β = 0.078, p = .023), but not ASD (β = 0.002, p = .944), and with elevated ADHD traits in mid-childhood (F(1,88) = 6.401, p = .013, $\eta _p^2$=0.068; ASD: F (1,88) = 3.218, p = .076), but not in toddlerhood (ps > 0.2). This pattern of results did not emerge when considering mean peak look duration across face and nonface stimuli. Thus, alterations in attention to faces during spontaneous visual exploration may be more consistent with a developmental endophenotype of ADHD than ASD. Our work shows that dissecting paths to neurodevelopmental conditions requires longitudinal data incorporating polygenic contribution, early neurocognitive function, and clinical phenotypic variation.
确定遗传与行为之间的发育内表型对于揭示神经发育障碍的机制至关重要。在这项原理验证研究中,我们探讨了视觉注意力早期中断是否是自闭症谱系障碍 (ASD) 和注意缺陷/多动障碍 (ADHD) 的独特或共同候选内表型。我们计算了在基于数组的眼动追踪任务中,335 名 14 个月大的婴儿对面孔的最长注视时间(即注视时间峰值),这些婴儿中有些有一级亲属患有 ASD 和/或 ADHD,有些没有。我们利用这些婴儿中一部分的父母报告和基因型数据来评估注视行为与家族(n = 285)和遗传易感性(使用多基因评分,n = 185)的关系,以及 2 岁时与 ASD 和 ADHD 相关的气质特征(分别为害羞和抑制控制,n = 272)以及 6 岁时的 ASD 和 ADHD 临床特征(n = 94)。结果表明,较长的注视时间峰值与 ADHD 的多基因评分升高相关(β = 0.078,p =.023),但与 ASD 无关(β = 0.002,p =.944),并且与儿童中期的 ADHD 特征升高相关(F(1,88) = 6.401,p =.013,$\eta _p^2$=0.068;ASD:F(1,88) = 3.218,p =.076),但与幼儿期无关(p > 0.2)。当考虑整个面孔和非面孔刺激的平均注视时间峰值时,没有出现这种结果模式。因此,在自发视觉探索过程中注意力对面孔的改变可能更符合 ADHD 的发育内表型,而不是 ASD。我们的工作表明,剖析神经发育障碍的途径需要结合多基因贡献、早期神经认知功能和临床表型变化的纵向数据。