Central Autonomic Network and heart rate variability in premature neonates.

IF 2.3 4区 医学 Q2 DEVELOPMENTAL BIOLOGY Developmental Neuroscience Pub Date : 2024-02-06 DOI:10.1159/000536513
Kelsey Christoffel, Josepheen De Asis-Cruz, Rathinaswamy B Govindan, Jung Hoon Kim, Kevin Michael Cook, Kushal Kapse, Nickie Andescavage, Sudeepta Basu, Emma Spoehr, Catherine Limperopoulos, Adre Du Plessis
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Abstract

Introduction: The Central Autonomic Network (CAN) is a hierarchy of brain structures that collectively influence cardiac autonomic input, mediating the majority of brain-heart interactions, but has never been studied in premature neonates. In this study, we use heart rate variability (HRV), which has been described as the "primary output" of the CAN, and resting state functional MRI to characterize brain-heart relationships in premature neonates.

Methods: We studied premature neonates who underwent resting state functional MRI (rsfMRI) at term, (37-weeks postmenstrual age [PMA] or above) and had HRV data recorded during the same week of their MRI. HRV was derived from continuous electrocardiogram data during the week of the rsfMRI scan. For rsfMRI, a seed-based approach was used to define regions of interest (ROI) pertinent to the CAN, and blood oxygen level-dependent signal was correlated between each ROI as a measure of functional connectivity. HRV was correlated with CAN connectivity (CANconn) for each region, and sub-group analysis was performed based on sex and clinical comorbidities.

Results: Forty-seven premature neonates were included in this study, with a mean gestational age at birth of 28.1 +/- 2.6 weeks. Term CANconn was found to be significantly correlated with HRV in approximately one-fifth of CAN connections. Two distinct patterns emerged among these HRV-CANconn relationships. In the first, increased HRV was associated with stronger CANconn of limbic regions. In the second pattern, stronger CANconn at the precuneus was associated with impaired HRV maturation. These patterns were especially pronounced in male premature neonates.

Conclusion: We report for the first time evidence of brain-heart relationships in premature neonates and an emerging CAN, most striking in male neonates, suggesting that the brain-heart axis may be more vulnerable in male premature neonates. Signatures in the heart rate may eventually become an important non-invasive tool to identify premature males at highest risk for neurodevelopmental impairment.

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早产新生儿的中枢自主神经网络和心率变异性。
引言中央自主神经网络(CAN)是大脑结构的一个层次,它共同影响心脏的自主神经输入,介导了大部分的脑-心相互作用,但从未在早产新生儿中进行过研究。在这项研究中,我们利用心率变异性(HRV)和静息状态功能磁共振成像来描述早产新生儿的脑心关系:我们研究了在足月(月经后 37 周或以上)接受静息状态功能磁共振成像(rsfMRI)并在磁共振成像的同一周记录心率变异数据的早产新生儿。心率变异是从 rsfMRI 扫描当周的连续心电图数据中得出的。对于 rsfMRI,采用基于种子的方法来定义与 CAN 相关的感兴趣区 (ROI),并在每个感兴趣区之间关联血氧水平相关信号,作为功能连通性的衡量标准。心率变异与每个区域的CAN连通性(CANconn)相关,并根据性别和临床合并症进行分组分析:本研究共纳入 47 名早产新生儿,出生时的平均胎龄为 28.1 +/- 2.6 周。研究发现,在大约五分之一的 CAN 连接中,CANconn 术语与心率变异显著相关。在这些心率变异与 CANconn 的关系中出现了两种不同的模式。第一种模式是,心率变异的增加与边缘区域更强的 CANconn 相关。在第二种模式中,楔前区较强的 CAN 连接与心率变异成熟受损有关。这些模式在男性早产新生儿中尤为明显:我们首次报告了早产新生儿脑-心关系的证据,以及在男性早产新生儿中最显著的新兴 CAN,这表明男性早产新生儿的脑-心轴可能更脆弱。心率特征最终可能成为一种重要的非侵入性工具,用于识别神经发育障碍风险最高的早产男性。
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来源期刊
Developmental Neuroscience
Developmental Neuroscience 医学-发育生物学
CiteScore
4.00
自引率
3.40%
发文量
49
审稿时长
>12 weeks
期刊介绍: ''Developmental Neuroscience'' is a multidisciplinary journal publishing papers covering all stages of invertebrate, vertebrate and human brain development. Emphasis is placed on publishing fundamental as well as translational studies that contribute to our understanding of mechanisms of normal development as well as genetic and environmental causes of abnormal brain development. The journal thus provides valuable information for both physicians and biologists. To meet the rapidly expanding information needs of its readers, the journal combines original papers that report on progress and advances in developmental neuroscience with concise mini-reviews that provide a timely overview of key topics, new insights and ongoing controversies. The editorial standards of ''Developmental Neuroscience'' are high. We are committed to publishing only high quality, complete papers that make significant contributions to the field.
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