婴儿期兴奋/抑制平衡与执行注意力相互作用,可预测儿童期自闭症特征。

IF 6.3 1区 医学 Q1 GENETICS & HEREDITY Molecular Autism Pub Date : 2022-12-08 DOI:10.1186/s13229-022-00526-1
Virginia Carter Leno, Jannath Begum-Ali, Amy Goodwin, Luke Mason, Greg Pasco, Andrew Pickles, Shruti Garg, Jonathan Green, Tony Charman, Mark H Johnson, Emily J H Jones
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引用次数: 0

摘要

背景:自闭症的特征被认为是大脑皮层兴奋和抑制(E/I)的非典型平衡。然而,大多数研究都是对年龄较大的自闭症患者的E/I改变进行研究,这意味着研究结果可能部分反映了同态复仇。为了评估影响的方向性,有必要在自闭症症状出现之前的生命早期研究 E/I 平衡的改变。最近的解释框架认为,还必须考虑早期风险特征如何与后期发展的调节因素相互作用,以预测自闭症的结果:方法:我们通过提取脑电图(EEG)功率谱斜率的非周期性指数("1/f")来确定婴儿早期的E/I平衡指数。为了验证我们的 E/I 平衡指数,我们测试了 10 个月大的神经纤维瘤病 1 型(NF1)婴儿(22 人)和非神经纤维瘤病 1 型婴儿(27 人)的非周期性指数差异。然后,我们在一个更大的异质性纵向队列中检测了E/I的改变,该队列包括有神经发育疾病家族史和无家族史的婴儿(n = 150),这些婴儿一直被跟踪到幼儿期。我们通过评估10个月的非周期性斜率与36个月的神经发育特征之间的关联是否会被24个月的执行注意力所调节,从而检验了E/I平衡的改变与我们提出的调节因子--执行注意力的相关性。分析对脑电图评估时的年龄、性别和脑电图试验次数进行了调整:结果:患有 NF1 的婴儿具有较高的非周期性指数,表明其抑制能力较强,这支持了我们的婴儿 E/I 测量方法。纵向分析表明,非周期性斜率与执行注意力之间存在显著的交互作用,因此较高的非周期性指数预示着较强的儿童自闭症特征,但这只适用于执行功能能力较弱的婴儿:局限性:目前的研究依赖于家长对婴儿执行功能型能力的报告;未来的工作需要用客观的认知测量方法来复制效果:研究结果表明,E/I平衡的改变是自闭症结局的发展途径,较高的执行功能能力可能会缓冲早期皮质非典型性的影响,这与较强的执行功能能力可能会改变各种风险因素的影响的建议是一致的。
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Infant excitation/inhibition balance interacts with executive attention to predict autistic traits in childhood.

Background: Autism is proposed to be characterised by an atypical balance of cortical excitation and inhibition (E/I). However, most studies have examined E/I alterations in older autistic individuals, meaning that findings could in part reflect homeostatic compensation. To assess the directionality of effects, it is necessary to examine alterations in E/I balance early in the lifespan before symptom emergence. Recent explanatory frameworks have argued that it is also necessary to consider how early risk features interact with later developing modifier factors to predict autism outcomes.

Method: We indexed E/I balance in early infancy by extracting the aperiodic exponent of the slope of the electroencephalogram (EEG) power spectrum ('1/f'). To validate our index of E/I balance, we tested for differences in the aperiodic exponent in 10-month-old infants with (n = 22) and without (n = 27) neurofibromatosis type 1 (NF1), a condition thought to be characterised by alterations to cortical inhibition. We then tested for E/I alterations in a larger heterogeneous longitudinal cohort of infants with and without a family history of neurodevelopmental conditions (n = 150) who had been followed to early childhood. We tested the relevance of alterations in E/I balance and our proposed modifier, executive attention, by assessing whether associations between 10-month aperiodic slope and 36-month neurodevelopmental traits were moderated by 24-month executive attention. Analyses adjusted for age at EEG assessment, sex and number of EEG trials.

Results: Infants with NF1 were characterised by a higher aperiodic exponent, indicative of greater inhibition, supporting our infant measure of E/I. Longitudinal analyses showed a significant interaction between aperiodic slope and executive attention, such that higher aperiodic exponents predicted greater autistic traits in childhood, but only in infants who also had weaker executive functioning abilities.

Limitations: The current study relied on parent report of infant executive functioning-type abilities; future work is required to replicate effects with objective measures of cognition.

Conclusions: Results suggest alterations in E/I balance are on the developmental pathway to autism outcomes, and that higher executive functioning abilities may buffer the impact of early cortical atypicalities, consistent with proposals that stronger executive functioning abilities may modify the impact of a wide range of risk factors.

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来源期刊
Molecular Autism
Molecular Autism GENETICS & HEREDITY-NEUROSCIENCES
CiteScore
12.10
自引率
1.60%
发文量
44
审稿时长
17 weeks
期刊介绍: Molecular Autism is a peer-reviewed, open access journal that publishes high-quality basic, translational and clinical research that has relevance to the etiology, pathobiology, or treatment of autism and related neurodevelopmental conditions. Research that includes integration across levels is encouraged. Molecular Autism publishes empirical studies, reviews, and brief communications.
期刊最新文献
Auditory N1 event-related potential amplitude is predictive of serum concentration of BPN14770 in fragile X syndrome. Characterizing genetic pathways unique to autism spectrum disorder at multiple levels of biological analysis. Developmental trajectories in infants and pre-school children with Neurofibromatosis 1. Superior temporal sulcus folding, functional network connectivity, and autistic-like traits in a non-clinical population. Structure-function coupling in white matter uncovers the hypoconnectivity in autism spectrum disorder.
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