Maternal prenatal distress exposure negatively associates with the stability of neonatal frontoparietal network.

IF 2.6 4区 心理学 Q2 BEHAVIORAL SCIENCES Stress-The International Journal on the Biology of Stress Pub Date : 2024-01-01 Epub Date: 2023-12-09 DOI:10.1080/10253890.2023.2275207
Jetro J Tuulari, Olli Rajasilta, Joana Cabral, Morten L Kringelbach, Linnea Karlsson, Hasse Karlsson
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Abstract

Maternal prenatal distress (PD), frequently defined as in utero prenatal stress exposure (PSE) to the developing fetus, influences the developing brain and numerous associations between PSE and brain structure have been described both in neonates and in older children. Previous studies addressing PSE-linked alterations in neonates' brain activity have focused on connectivity analyses from predefined seed regions, but the effects of PSE at the level of distributed functional networks remains unclear. In this study, we investigated the impact of prenatal distress on the spatial and temporal properties of functional networks detected in functional MRI data from 20 naturally sleeping, term-born (age 25.85 ± 7.72 days, 11 males), healthy neonates. First, we performed group level independent component analysis (GICA) to evaluate an association between PD and the identified functional networks. Second, we searched for an association with PD at the level of the stability of functional networks over time using leading eigenvector dynamics analysis (LEiDA). No statistically significant associations were detected at the spatial level for the GICA-derived networks. However, at the dynamic level, LEiDA revealed that maternal PD negatively associated with the stability of a frontoparietal network. These results imply that maternal PD may influence the stability of frontoparietal connections in neonatal brain network dynamics and adds to the cumulating evidence that frontal areas are especially sensitive to PSE. We advocate for early preventive intervention strategies regarding pregnant mothers. Nevertheless, future research venues are required to assess optimal intervention timing and methods for maximum benefit.

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母亲产前窘迫暴露与新生儿额顶叶网络稳定性负相关。
母体产前窘迫(PD),通常被定义为发育中胎儿的宫内产前应激暴露(PSE),影响发育中的大脑,新生儿和年龄较大的儿童都有PSE与大脑结构之间的许多联系。先前针对新生儿大脑活动中PSE相关变化的研究主要集中在预定义种子区域的连接分析上,但PSE在分布式功能网络层面的影响尚不清楚。在这项研究中,我们调查了产前窘迫对20名自然睡眠、足月出生(年龄25.85)的功能MRI数据中检测到的功能网络的空间和时间特性的影响 ± 7.72天,11名男性),健康新生儿。首先,我们进行了组级独立分量分析(GICA),以评估PD与功能网络的空间配置之间的关联。其次,我们使用领先特征向量动力学分析(LEiDA)在函数网络随时间的稳定性水平上搜索与PD的关联。对于GICA衍生的网络,在空间水平上没有检测到统计学上显著的关联。然而,在动态水平上,LEiDA显示,母体帕金森病显著降低了额顶网络的稳定性。这些结果表明,母体帕金森病可能影响新生儿脑网络动力学中额顶连接的稳定性,并增加了额叶区域对PSE特别敏感的累积证据。我们提倡对孕妇采取早期预防性干预策略。然而,未来的研究场所需要评估最佳干预时机和方法,以获得最大效益。
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来源期刊
CiteScore
5.60
自引率
0.00%
发文量
25
审稿时长
6-12 weeks
期刊介绍: The journal Stress aims to provide scientists involved in stress research with the possibility of reading a more integrated view of the field. Peer reviewed papers, invited reviews and short communications will deal with interdisciplinary aspects of stress in terms of: the mechanisms of stressful stimulation, including within and between individuals; the physiological and behavioural responses to stress, and their regulation, in both the short and long term; adaptive mechanisms, coping strategies and the pathological consequences of stress. Stress will publish the latest developments in physiology, neurobiology, molecular biology, genetics research, immunology, and behavioural studies as they impact on the understanding of stress and its adverse consequences and their amelioration. Specific approaches may include transgenic/knockout animals, developmental/programming studies, electrophysiology, histochemistry, neurochemistry, neuropharmacology, neuroanatomy, neuroimaging, endocrinology, autonomic physiology, immunology, chronic pain, ethological and other behavioural studies and clinical measures.
期刊最新文献
Inhibition of prefrontal cortex parvalbumin interneurons mitigates behavioral and physiological sequelae of chronic stress in male mice. Maternal prenatal distress exposure negatively associates with the stability of neonatal frontoparietal network. Decreased amygdala-sensorimotor connectivity mediates the association between prenatal stress and broad autism phenotype in young adults: Project Ice Storm. Accumbal μ-opioid receptors and salt taste-elicited hedonic responses in a rodent model of prenatal adversity, and their correlates using human functional genomics. Behavior, synaptic mitochondria, and microglia are differentially impacted by chronic adolescent stress and repeated endotoxin exposure in male and female rats.
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