AUTONOMIC NERVOUS SYSTEM FUNCTIONING IN THE HUMAN FETUS

人类胎儿自主神经系统的功能

基本信息

  • 批准号:
    2872836
  • 负责人:
  • 金额:
    $ 10.74万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1995
  • 资助国家:
    美国
  • 起止时间:
    1995-02-01 至 2000-01-31
  • 项目状态:
    已结题

项目摘要

A number of developmental disorders in children, including learning disabilities, can be traced to deficits in attention and abnormalities in autonomic nervous system (ANS) functioning. A vagally-mediated decrease in heart rate is used as a marker of attention in infants, and an association between prestimulus respiratory sinus arrhythmia (RSA) and the magnitude of the heart rate deceleration has been demonstrated. Evaluation of ANS functioning and information processing capabilities are particularly well- suited for assessing central nervous system (CNS) status in utero: the ANS can be examined in human fetuses noninvasively using spectral decomposition techniques, and human fetuses are capable of displaying a heart rate deceleratory response to certain acoustic stimuli. After identifying acoustic parameters which consistently elicit a heart rate deceleration in normal human term fetuses, we will examine the relationship between prestimulus RSA and the magnitude of the cardiac deceleratory response and determine if there is a decrease in respiratory frequency and heart rate variability (HRV) concomitant with the heart rate deceleration. Furthermore, we will determine if fetuses categorized as sympathetic-dominant exhibit a different type of cardiac response to low- intensity acoustic stimuli than fetuses categorized as parasympathetic- dominant and whether these characteristics are stable over time. Special emphasis will be placed on identifying parameters which are capable of distinguishing growth-restricted fetuses and fetuses with CNS structural anomalies from normal fetuses. An important aspect of the proposed study plan is that subjects examined as fetuses will be examined again as neonates and will be followed prospectively to two years of age. The fetal electrocardiogram will be captured noninvasively using standard cardiac electrodes positioned on the mother's abdomen. Adaptive signal processing methodology will be used to extract fetal R-waves from the raw data. Sympathetic-parasympathetic balance will be evaluated by applying spectral decomposition techniques to the analysis of fetal and neonatal HRV data. The heart rate response to low-intensity acoustic stimuli will be related to ANS functioning in both fetuses and neonates. We believe that differences in intrinsic ANS activity and cardiac responsivity may ultimately help to identify the fetus at-risk for neurobehavioral abnormalities and hence facilitate the implementation of appropriate intervention protocols early in the course of development.
儿童的一些发育障碍,包括学习 残疾,可以追溯到注意力不足和 自主神经系统(ANS)功能。一种由迷宫调节的减少 心率被用作婴儿注意力的标志,并与 刺激前呼吸性窦性心律失常与心率变异性的关系 已经证实了心率减速的可能性。对ANS的评估 运作和信息处理能力尤其出色- 适合于评估子宫内中枢神经系统(CNS)状态的ANS 可利用光谱技术在人类胎儿体内进行无创检测 分解技术,人类胎儿能够显示出 心率对某些声音刺激的减速反应。之后 识别持续引起心率的声学参数 正常足月胎儿的减速,我们将检查 刺激前RSA与心脏大小的关系 减速反应,并确定呼吸是否减少 频率和心率变异性(HRV)伴随着心率 减速。此外,我们将确定胎儿是否被归类为 交感神经优势型表现出一种不同类型的心脏反应 比被归类为副交感神经的胎儿更强烈的声刺激- 以及这些特征是否随着时间的推移而稳定。特价 重点将放在确定能够 中枢神经系统结构障碍胎儿与生长受限胎儿的鉴别 正常胎儿的异常。拟议研究的一个重要方面 计划是,被检查为胎儿的受试者将再次接受检查 新生儿,并将前瞻性地跟踪到两岁。这个 胎儿心电图将使用标准的无创采集 放置在母亲腹部的心脏电极。自适应信号 将使用处理方法从原始数据中提取胎儿R波 数据。交感-副交感神经平衡将通过应用 光谱分解技术在胎儿和新生儿分析中的应用 心率变异性数据。心率对低强度声刺激的反应将 与ANS在胎儿和新生儿中的功能有关。我们相信 固有的ANS活性和心脏反应性的差异可能 最终帮助确定神经行为的高危胎儿 异常情况,从而便利执行适当的 在开发过程中的早期干预方案。

项目成果

期刊论文数量(6)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Heart rate dynamics in low risk human fetuses.
低风险人类胎儿的心率动态。
  • DOI:
    10.1203/00006450-199807000-00018
  • 发表时间:
    1998
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Mooney,DM;Groome,LJ;Holland,SB;Smith,YD
  • 通讯作者:
    Smith,YD
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

LYNN J GROOME其他文献

LYNN J GROOME的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('LYNN J GROOME', 18)}}的其他基金

AUTONOMIC NERVOUS SYSTEM FUNCTIONING IN THE HUMAN FETUS
人类胎儿自主神经系统的功能
  • 批准号:
    2205997
  • 财政年份:
    1995
  • 资助金额:
    $ 10.74万
  • 项目类别:
AUTONOMIC NERVOUS SYSTEM FUNCTIONING IN THE HUMAN FETUS
人类胎儿自主神经系统的功能
  • 批准号:
    2655141
  • 财政年份:
    1995
  • 资助金额:
    $ 10.74万
  • 项目类别:
AUTONOMIC NERVOUS SYSTEM FUNCTIONING IN THE HUMAN FETUS
人类胎儿自主神经系统的功能
  • 批准号:
    2205998
  • 财政年份:
    1995
  • 资助金额:
    $ 10.74万
  • 项目类别:
AUTONOMIC NERVOUS SYSTEM FUNCTIONING IN THE HUMAN FETUS
人类胎儿自主神经系统的功能
  • 批准号:
    2332282
  • 财政年份:
    1995
  • 资助金额:
    $ 10.74万
  • 项目类别:

相似海外基金

Say Yes to NO: The Next Generation Scaffolds with Localized and Sustained Nitric Oxide (NO) Delivery for Central Nervous System Regeneration
对“否”说“是”:具有局部和持续一氧化氮 (NO) 输送的下一代支架,用于中枢神经系统再生
  • 批准号:
    EP/X027198/2
  • 财政年份:
    2024
  • 资助金额:
    $ 10.74万
  • 项目类别:
    Fellowship
Elucidation of metabolic control mechanism by FGF21-mediated central nervous system signaling in neonatal period
阐明新生儿期 FGF21 介导的中枢神经系统信号传导的代谢控制机制
  • 批准号:
    23K10836
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Strategy to Attack Coronavirus Infections Brain Fog-Central Nervous System Sequelae Using a Novel Patented Technology
利用新型专利技术对抗冠状病毒感染脑雾-中枢神经系统后遗症的策略
  • 批准号:
    23K10453
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Identification of immune cells protecting from lethal viral infection in the central nervous system
鉴定中枢神经系统免受致命病毒感染的免疫细胞
  • 批准号:
    22KJ1176
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
    Grant-in-Aid for JSPS Fellows
Discovery of novel nodal antibodies in the central nervous system demyelinating diseases and elucidation of the mechanisms through an optic nerve demyelination model
发现中枢神经系统脱髓鞘疾病中的新型节点抗体并通过视神经脱髓鞘模型阐明其机制
  • 批准号:
    23K14783
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Central nervous system inflammation due to a high-fat diet and changes in exercise volume - effects on obesity
高脂肪饮食和运动量变化引起的中枢神经系统炎症——对肥胖的影响
  • 批准号:
    23K10646
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Central Nervous System Reprogramming of the Control of Blood Pressure Induced by Early Life Stress
早期生活压力引起的血压控制的中枢神经系统重新编程
  • 批准号:
    10555126
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
2023 Central Nervous System Injury and Repair Gordon Research Conference and Seminar
2023中枢神经系统损伤与修复戈登研究会议暨研讨会
  • 批准号:
    10753737
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
Maladaptive Remodeling of the Neuromuscular Synapse Following Central Nervous System Injury
中枢神经系统损伤后神经肌肉突触的适应不良重塑
  • 批准号:
    10569935
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
Effects of Central Nervous System Agents on Next Generation Development via Changes in Sperm DNA Methylation
中枢神经系统药物通过精子 DNA 甲基化的变化对下一代发育的影响
  • 批准号:
    23K19438
  • 财政年份:
    2023
  • 资助金额:
    $ 10.74万
  • 项目类别:
    Grant-in-Aid for Research Activity Start-up
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了