Functional connectivity patterns differ as a function of co-occurring attentional problems in preschoolers with autism.

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Alex Boxberger, Bosi Chen, Lindsay Olson, Michaela Cordova, Judy Mahmalji, Adriana Rios, Annika C Linke, Inna Fishman
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引用次数: 0

Abstract

Background: Symptoms of attention-deficit/hyperactivity disorder (ADHD) are common in children with autism spectrum disorder (ASD), and are associated with greater developmental challenges, poorer clinical outcomes, and alterations in functional connectivity (FC) of the brain. However, despite the consensus that ASD and other neurodevelopmental conditions emerge early in life, little is known about the trajectories of brain and behavioral development during the first years of life in children with ASD and co-occurring attention problems (AP).

Methods: In a sample of 122 young children (ages 1.5-5 years) with and without ASD, we examined whether toddlers and preschoolers with ASD and co-occurring AP already differ from peers with ASD without co-occurring AP on adaptive and developmental skills, ASD symptoms, and FC of the frontoparietal and salience networks, which have been previously linked to ADHD symptoms in older children with ASD and ADHD.

Results: Results of general linear model analyses revealed lower developmental and adaptive skills across multiple domains in children with ASD and elevated AP compared with their peers with lower AP, despite equivalent levels of ASD symptoms. Further, children with ASD and elevated AP showed reduced FC within the frontoparietal network (p = .027), between the frontoparietal and language networks (p = .004), and the frontoparietal and default mode networks (p = .046) in comparison to their peers with lower AP. No group differences in FC of the salience network were observed (all p > .05).

Conclusions: These findings provide evidence that neurodevelopmental and behavioral differences in children with ASD and co-occurring AP emerge very early in life, before a reliable diagnosis of ADHD is typically made. Specifically, these results demonstrate that early inattention symptoms are associated with unique connectivity patterns in executive circuitry as early as the first years of life in toddlers and preschoolers with ASD, likely contributing to the phenotypic and neural heterogeneity recognized in autism. Thus, our results underscore the importance of considering co-occurring conditions early in developmental research and clinical care, as further understanding these trajectories can inform early interventions during the critical time period when they have the greatest potential for positive impact.

Abstract Image

Abstract Image

在患有自闭症的学龄前儿童中,功能连接模式因同时发生注意力问题而有所不同。
背景:注意缺陷/多动障碍(ADHD)的症状在自闭症谱系障碍(ASD)儿童中很常见,并且与更大的发育挑战、更差的临床结果和大脑功能连接(FC)的改变有关。然而,尽管人们一致认为ASD和其他神经发育状况出现在生命早期,但对于患有ASD和并发注意力问题(AP)的儿童在生命最初几年的大脑和行为发育轨迹知之甚少。方法:在122名患有和不患有ASD的幼儿(1.5-5岁)中,我们检查了患有ASD并并发AP的幼儿和学龄前儿童在适应和发展技能、ASD症状以及额顶和显著性网络的FC方面是否已经与没有并发AP的ASD同龄人不同,这些之前与年龄较大的ASD和ADHD儿童的ADHD症状有关。结果:一般线性模型分析结果显示,尽管ASD症状水平相当,但与AP水平较低的同龄人相比,AP水平较高的ASD儿童在多个领域的发展和适应技能较低。此外,患有ASD和AP升高的儿童在额顶叶网络中显示出减少的FC (p =。027),在额顶叶和语言网络之间(p =。004),额顶叶和默认模式网络(p = 0.046)与AP较低的同龄人相比。显著性网络的FC没有组间差异(p均为0.05)。结论:这些发现提供了证据,表明患有ASD和同时发生AP的儿童在生命早期就出现了神经发育和行为差异,而这通常是在做出可靠的ADHD诊断之前。具体来说,这些结果表明,早在自闭症儿童和学龄前儿童出生后的第一年,早期注意力不集中症状就与执行回路中独特的连接模式有关,这可能有助于自闭症的表型和神经异质性。因此,我们的研究结果强调了在发育研究和临床护理早期考虑共同发生条件的重要性,因为进一步了解这些轨迹可以在关键时期为早期干预提供信息,此时它们具有最大的积极影响潜力。
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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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