Mapping Dimensional Aspects of Biobehavioral Threat Reactivity in Young, Violence-Exposed Children: Linkages to Fear and Distress

绘制遭受暴力的幼儿生物行为威胁反应的维度:与恐惧和痛苦的联系

基本信息

项目摘要

PROJECT SUMMARY: Interpersonal violence (IV) affects more than 1 in 5 young children in the United States annually. For young children, IV exposure most commonly occurs within the family context in the forms of partner violence and harsh/abusive parenting. Children exposed to IV represent a heterogeneous group. A portion of children develop psychological problems that cut across multiple diagnostic categories characterized by fear and distress symptoms. Existing models broadly implicate disruptions in biological stress systems in the etiology of violence-associated symptoms, but lack specificity for explaining heterogeneous symptom presentations in young children. Advancing this science requires novel laboratory and analytic methods for assessing and synthesizing threat reactivity across multiple biobehavioral levels. Inspired by the Research Domain Criteria (RDoC) initiative, we propose to achieve this by leveraging person-centered methods to identify unique profiles of threat reactivity across multiple levels of biobehavioral functioning never before studied together in young children: observed behavior, attention bias, autonomic reactivity, startle, event-related brain potentials. The fundamental scientific premise of the proposed work is that threat reactivity is a central intermediate phenotype linking early IV to this clinical vulnerability in young children. The proposed sample will include 360 children, ages 4 to 6 years, with (n = 240) and without (n = 120) IV exposure followed over 1 year. We advance three aims. Aim 1 is to map biobehavioral threat reactivity profiles to dimensional patterns of fear and distress in IV exposed and non-exposed young children. We hypothesize that we will identify hyper- and hypo-reactive profiles that link to greater symptoms relative to a non-extreme profile, and that hyper-reactivity will relate to fear, whereas hypo-reactivity will relate to distress at baseline and over 1 year. Aim 2 is to test whether threat reactivity profiles serve as intermediate phenotypes in explaining the link between violence exposure and symptoms over time. We hypothesize that children exposed to more severe IV will more likely be classified as hyper- or hypo-reactive and that profile type will mediate the link between IV and symptoms at baseline and 1 year later. Further, given high dependency of young children’s self-regulation on caregiving relationships and threats to regulatory capacity in violent environments, we hypothesize that mothers’ ability to co-regulate their children’s negative affect will shape these risk pathways. Thus, Aim 3 is to test the hypothesis that maternal responsiveness to child negative affect will play a unique role in shaping threat reactivity pathways over time. We hypothesize that emotionally-responsive parenting (assessed with a multi-method protocol) will buffer the associations between IV and threat reactivity profiles and between exposure and symptom trajectories over 1 year. This study will provide critical insight into the etiology of violence-related psychopathology with key implications for developing novel approaches for identification, prevention, and intervention for these highly vulnerable young children.
项目总结:

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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

{{ 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 }}

Margaret J Briggs-Gowan其他文献

Margaret J Briggs-Gowan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('Margaret J Briggs-Gowan', 18)}}的其他基金

Impact of Perinatal Pandemic-Related Stress on the Early Caregiving Environment, Infant Functioning, DNA Methylation, and Telomere Length
围产期流行病相关压力对早期护理环境、婴儿功能、DNA 甲基化和端粒长度的影响
  • 批准号:
    10371155
  • 财政年份:
    2021
  • 资助金额:
    $ 75.34万
  • 项目类别:
Impact of Perinatal Pandemic-Related Stress on the Early Caregiving Environment, Infant Functioning, DNA Methylation, and Telomere Length
围产期流行病相关压力对早期护理环境、婴儿功能、DNA 甲基化和端粒长度的影响
  • 批准号:
    10199458
  • 财政年份:
    2021
  • 资助金额:
    $ 75.34万
  • 项目类别:
Impact of Perinatal Pandemic-Related Stress on the Early Caregiving Environment, Infant Functioning, DNA Methylation, and Telomere Length
围产期流行病相关压力对早期护理环境、婴儿功能、DNA 甲基化和端粒长度的影响
  • 批准号:
    10619507
  • 财政年份:
    2021
  • 资助金额:
    $ 75.34万
  • 项目类别:
Impact of Perinatal Pandemic-Related Stress on the Early Caregiving Environment, Infant Functioning, DNA Methylation, and Telomere Length
围产期流行病相关压力对早期护理环境、婴儿功能、DNA 甲基化和端粒长度的影响
  • 批准号:
    10728403
  • 财政年份:
    2021
  • 资助金额:
    $ 75.34万
  • 项目类别:
Mapping Dimensional Aspects of Biobehavioral Threat Reactivity in Young, Violence-Exposed Children: Linkages to Fear and Distress
绘制遭受暴力的幼儿生物行为威胁反应的维度:与恐惧和痛苦的联系
  • 批准号:
    10469567
  • 财政年份:
    2018
  • 资助金额:
    $ 75.34万
  • 项目类别:
Mapping Dimensional Aspects of Biobehavioral Threat Reactivity in Young, Violence-Exposed Children: Linkages to Fear and Distress
绘制遭受暴力的幼儿生物行为威胁反应的维度:与恐惧和痛苦的联系
  • 批准号:
    10248455
  • 财政年份:
    2018
  • 资助金额:
    $ 75.34万
  • 项目类别:
Early Traumatic Stress Exposure: Neurodevelopmental Mechanisms of Clinical Risk
早期创伤性应激暴露:临床风险的神经发育机制
  • 批准号:
    8544532
  • 财政年份:
    2012
  • 资助金额:
    $ 75.34万
  • 项目类别:
Early Traumatic Stress Exposure: Neurodevelopmental Mechanisms of Clinical Risk
早期创伤性应激暴露:临床风险的神经发育机制
  • 批准号:
    8139152
  • 财政年份:
    2010
  • 资助金额:
    $ 75.34万
  • 项目类别:
Early Traumatic Stress Exposure: Neurodevelopmental Mechanisms of Clinical Risk
早期创伤性应激暴露:临床风险的神经发育机制
  • 批准号:
    8469761
  • 财政年份:
    2010
  • 资助金额:
    $ 75.34万
  • 项目类别:
Early Traumatic Stress Exposure: Neurodevelopmental Mechanisms of Clinical Risk
早期创伤性应激暴露:临床风险的神经发育机制
  • 批准号:
    8644902
  • 财政年份:
    2010
  • 资助金额:
    $ 75.34万
  • 项目类别:

相似海外基金

Hormone therapy, age of menopause, previous parity, and APOE genotype affect cognition in aging humans.
激素治疗、绝经年龄、既往产次和 APOE 基因型会影响老年人的认知。
  • 批准号:
    495182
  • 财政年份:
    2023
  • 资助金额:
    $ 75.34万
  • 项目类别:
Investigating how alternative splicing processes affect cartilage biology from development to old age
研究选择性剪接过程如何影响从发育到老年的软骨生物学
  • 批准号:
    2601817
  • 财政年份:
    2021
  • 资助金额:
    $ 75.34万
  • 项目类别:
    Studentship
RAPID: Coronavirus Risk Communication: How Age and Communication Format Affect Risk Perception and Behaviors
RAPID:冠状病毒风险沟通:年龄和沟通方式如何影响风险认知和行为
  • 批准号:
    2029039
  • 财政年份:
    2020
  • 资助金额:
    $ 75.34万
  • 项目类别:
    Standard Grant
Neighborhood and Parent Variables Affect Low-Income Preschool Age Child Physical Activity
社区和家长变量影响低收入学龄前儿童的身体活动
  • 批准号:
    9888417
  • 财政年份:
    2019
  • 资助金额:
    $ 75.34万
  • 项目类别:
The affect of Age related hearing loss for cognitive function
年龄相关性听力损失对认知功能的影响
  • 批准号:
    17K11318
  • 财政年份:
    2017
  • 资助金额:
    $ 75.34万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    9320090
  • 财政年份:
    2017
  • 资助金额:
    $ 75.34万
  • 项目类别:
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    10166936
  • 财政年份:
    2017
  • 资助金额:
    $ 75.34万
  • 项目类别:
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    9761593
  • 财政年份:
    2017
  • 资助金额:
    $ 75.34万
  • 项目类别:
How age dependent molecular changes in T follicular helper cells affect their function
滤泡辅助 T 细胞的年龄依赖性分子变化如何影响其功能
  • 批准号:
    BB/M50306X/1
  • 财政年份:
    2014
  • 资助金额:
    $ 75.34万
  • 项目类别:
    Training Grant
Inflamm-aging: What do we know about the effect of inflammation on HIV treatment and disease as we age, and how does this affect our search for a Cure?
炎症衰老:随着年龄的增长,我们对炎症对艾滋病毒治疗和疾病的影响了解多少?这对我们寻找治愈方法有何影响?
  • 批准号:
    288272
  • 财政年份:
    2013
  • 资助金额:
    $ 75.34万
  • 项目类别:
    Miscellaneous Programs
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了