Development of Respiratory Sinus Arrhythmia in Young Infants With Autism Spectrum Disorder, Preterm Birth, and Typical Development.

IF 5.6
Jessica Bradshaw, John E Richards, Julia Yurkovic-Harding, Eilis McLaughlin
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Abstract

Respiratory sinus arrhythmia (RSA) is a key index of parasympathetic function and environmental adaptability. Lower resting RSA has been linked to preterm (PT) birth in infancy and autism spectrum disorder (ASD) in childhood, yet RSA across the first 2 years in young infants born PT or later diagnosed with ASD remains unknown. This study examined resting RSA and mean interbeat interval (IBI) development from 1 to 24 months in infants at varying ASD likelihoods, including infant siblings of children with ASD and those born PT. A longitudinal design tracked resting RSA and mean IBI in 137 infants from 1 to 24 months. Infants were classified as elevated likelihood for ASD (EL), low likelihood for ASD (LL), or PT and later classified by developmental outcome as ASD, neurodivergent (ND), or typically developing (TD). Mixed-effects models examined developmental trajectories and group differences. Results indicated that both RSA and mean IBI increased across all groups from 1 to 24 months, with the most rapid growth observed in the first 6 months. PT infants exhibited lower RSA and mean IBI initially, but aligned with LL infants when age was corrected for prematurity. Infants later diagnosed with ASD showed no early RSA differences, but exhibited elevated RSA from 9 to 24 months, distinguishing them from TD and ND infants. Elevated resting RSA in ASD from 9 to 24 months may reflect reduced social monitoring, increased attentional regulation, or decreased stress during a resting period free of structured tasks. These findings contrast with lower RSA in older children with ASD, highlighting developmental shifts in autonomic function and the need for further research into RSA as an early biomarker for ASD.

患有自闭症谱系障碍、早产和典型发育的婴幼儿呼吸窦性心律失常的发展。
呼吸性窦性心律失常(RSA)是副交感神经功能和环境适应性的重要指标。较低的静息RSA与婴儿期早产(PT)和儿童期自闭症谱系障碍(ASD)有关,但在出生为PT或后来被诊断为ASD的幼儿中,前2年的RSA仍不清楚。本研究对不同ASD可能性的婴儿进行了1 - 24个月的静息RSA和平均间歇期(IBI)发育检查,包括患有ASD的婴儿的兄弟姐妹和出生时患有PT的婴儿。纵向设计追踪了137名1 - 24个月婴儿的静息RSA和平均间歇期(IBI)发育情况。婴儿被分为ASD的高可能性(EL),低可能性(LL),或PT,后来根据发育结果分为ASD,神经发散性(ND)或典型发展性(TD)。混合效应模型检验了发育轨迹和群体差异。结果表明,RSA和平均IBI在1至24个月期间均有所增加,其中前6个月增长最快。PT婴儿最初表现出较低的RSA和平均IBI,但当年龄校正为早产时,与LL婴儿一致。后来被诊断为ASD的婴儿没有早期RSA差异,但在9至24个月期间RSA升高,这与TD和ND婴儿区分开来。9至24个月ASD患者的静息期RSA升高可能反映出在无结构化任务的静息期社会监测减少、注意力调节增加或压力减少。这些发现与年龄较大的ASD儿童的低RSA形成对比,突出了自主神经功能的发育变化,以及RSA作为ASD早期生物标志物的进一步研究的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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