有或没有自闭症谱系障碍的儿童和青少年的青春期发育、体重指数和心血管自主神经功能:一项四时点加速纵向研究

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Rachael A Muscatello, Meredith Cola, Simon Vandekar, Blythe A Corbett
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引用次数: 0

摘要

背景:自主神经系统(ANS)调节心率等“自动”功能,其改变可能对健康结果产生重大影响。自主神经功能的心血管测量,如心率变异性,是自闭症谱系障碍(ASD)的生物学标志物。ANS与身体健康之间的相互作用表明,有和没有ASD过度发育的青少年有必要检查心血管自主功能。目前的研究旨在确定自主神经功能的变化以及副交感神经和交感神经分支之间的平衡随着时间的推移与诊断、年龄、青春期发育和身体健康状况的关系。方法:研究纳入244名ASD (N = 140)或神经正常(N = 104)青少年,入组时年龄在10至13岁,随访4年。静息状态自主神经功能采用呼吸性窦性心律失常(RSA;副交感神经)和射前期(PEP;同情)。自主平衡和调节也作为结果进行了检查。线性混合模型测试了组内和组间的主要自主神经结果差异,以及青春期发育、体重和药物使用的影响。结果:基线模型在青少年ASD中显示出诊断差异,副交感神经调节较低,但在其他三个结果中没有观察到差异。添加身体质量指数(BMI)百分位数和药物使用消除了统计学上显著的诊断效果,而这两个变量都与较低的RSA和整体自主调节显著相关。副交感神经功能(RSA)随年龄和发育期稳定,而交感神经控制(PEP)随年龄和发育期明显下降。入组时的BMI百分位数能显著预测自主神经功能,而BMI随时间的变化则不能。结论:迄今为止,关于ASD的身体健康(如BMI)和自主神经预后的研究很少。目前的研究观察到很少的组间差异,但表明身体健康对ASD和神经正常青年的ANS功能有重要影响。研究结果进一步强调,有必要关注个体特征,如BMI和药物使用,以阐明自主神经差异在多大程度上与整个生命周期的健康状况相关,而不考虑诊断类别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pubertal developmental, body mass index, and cardiovascular autonomic function in children and adolescents with and without autism spectrum disorder: a four-time point accelerated longitudinal study.

Background: The Autonomic Nervous System (ANS) regulates 'automatic' functions such as heart rate, and alterations may have significant impacts on health outcomes. Cardiovascular measures of autonomic function such as heart rate variability are of interest as biological markers in autism spectrum disorder (ASD). The interplay between the ANS and physical health establishes a need to examine cardiovascular autonomic functioning in youth with and without ASD over development. The current study aimed to identify change in autonomic function and balance across the parasympathetic and sympathetic branches over time as a function of diagnosis, age, pubertal development, and physical health status.

Methods: The study included 244 ASD (N = 140) or neurotypical (NT) (N = 104) youth, ages 10 to 13 years at enrollment and followed over four years. Resting state autonomic functioning was measured using respiratory sinus arrhythmia (RSA; parasympathetic) and pre-ejection period (PEP; sympathetic). Autonomic balance and regulation were also examined as outcomes. Linear mixed models tested between- and within-group differences in the primary autonomic outcomes as well as the influence of pubertal development, body weight, and medication use.

Results: Baseline models showed diagnostic differences, with lower parasympathetic regulation, in youth with ASD, but no differences were observed for the other three outcomes. Adding body mass index (BMI) percentile and medication use removed the statistically significant diagnostic effect, while both variables were significantly related to lower RSA and overall autonomic regulation. Parasympathetic function (RSA) was stable over age and pubertal stage, while a notable decrease in sympathetic control (increased PEP) was found for age and pubertal stage. BMI percentile at enrollment significantly predicted autonomic function, while change in BMI over time did not.

Conclusions: Minimal research to date has explored physical health (e.g., BMI) and autonomic outcomes in ASD. The current study observed few group differences yet demonstrates important effects of physical health on ANS function in both ASD and neurotypical youth. Findings further emphasize a need to focus on individual traits such as BMI and medication use to elucidate the extent to which autonomic differences are related to health status, irrespective of diagnostic category, across the lifespan.

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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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