Decreased attention in 10- and 14-month-olds with neurofibromatosis type 1 and association with later ADHD traits.

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Tessel Bazelmans, Francesca Penza, Jannath Begum-Ali, Chloe Taylor, Mark H Johnson, Tony Charman, Jonathan Green, Shruti Garg, Emily J H Jones
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引用次数: 0

Abstract

Background: Identifying precursors to ADHD, which affects up to 5% of children, is crucial for early identification and support. To this end, we used a prospective sample to investigate endogenous attention and activity level in infants with and without an elevated likelihood (EL) for ADHD and investigated associations with ADHD traits at 3-years. EL status was based on a family history of autism and/or ADHD or a diagnosis of neurofibromatosis type 1 (NF1), a genetic condition associated with higher rates of ADHD.

Methods: Infants (n = 26 typical likelihood (TL), n = 70 EL-autism, n = 28 EL-ADHD, n = 18 EL-autism + ADHD, and n = 29 NF1) participated in a live puppet task at 10 and/or 14 months. Mixed-effect models compared groups on behaviourally coded Focused Attention and Vigilance (i.e. Sustained Attention) and Movement, which was measured concurrently using an accelerometer to capture activity during these distinct attention states. Finally, we examined the bivariate associations of Attention and Movement, and their interaction, with 3-year parent-reported ADHD traits.

Results: Infants with NF1 exhibited less Focused Attention and Vigilance than EL-ADHD [t (1,170) = 3.53, p = .005] or EL-autism [t (1,170) = 5.43, p < .001] infants and this did not differ across age. There were no Attention differences between the EL and TL groups and no Group or age differences in Movement, however Movement did vary by Attention type: [Formula: see text](2) = 215.25, p < .001 (Focused Attention < Vigilance < Looking elsewhere). Across the cohort, less Focused Attention at 10 months (rs = -.27, p = .008) was associated with more ADHD traits at 3-years. During Vigilance at 14 months, there was a significant Attention-by-Movement interaction effect (z = 25.65, p < .001), showing that the association between more Vigilance and fewer ADHD traits was most pronounced in infants showing less Movement.

Conclusions: Reduced attention was observed from 10 months onwards in those with NF1, but not in those with a familial likelihood of ADHD. Moreover, early focused attention and the ability to modulate activity level by attentive state (i.e. more vigilant, less movement) may be important emerging features associated with later ADHD traits. We consider implications for early detection and early support strategies.

患有1型神经纤维瘤病的10和14个月大婴儿的注意力下降与后来的ADHD特征有关。
背景:ADHD影响多达5%的儿童,识别其前体对于早期识别和支持至关重要。为此,我们使用前瞻性样本来调查有和没有ADHD可能性升高(EL)的婴儿的内源性注意力和活动水平,并在3岁时调查与ADHD特征的关系。EL状态是基于自闭症和/或ADHD的家族史或1型神经纤维瘤病(NF1)的诊断,这是一种与较高的ADHD发病率相关的遗传病。方法:在10和/或14个月时,对26名典型似然(TL)婴儿、70名典型似然(EL-autism)婴儿、28名典型似然(EL-ADHD)婴儿、18名典型似然(EL-autism + ADHD)婴儿和29名非典型似然(NF1)婴儿进行真人木偶实验。混合效应模型比较各组的行为编码集中注意力和警惕性(即持续注意力)和运动,同时使用加速计来捕捉这些不同注意状态下的活动。最后,我们检查了注意力和运动的双变量关联,以及它们与3年父母报告的ADHD特征的相互作用。结果:NF1患儿的注意力和警惕性低于EL-ADHD [t (1170) = 3.53, p =。[005]或el -自闭症[t (1,170) = 5.43, p]结论:在NF1患者中观察到10个月后注意力下降,但在具有ADHD家族可能性的患者中则没有。此外,早期集中注意力和通过注意状态调节活动水平的能力(即更警惕,更少运动)可能是与后期ADHD特征相关的重要新特征。我们考虑早期发现和早期支持策略的影响。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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