Neural and behavioral trajectories of the overcontrolled phenotype: Associations with development, social context and psychiatric symptoms in early childhood
过度控制表型的神经和行为轨迹:与幼儿期发育、社会背景和精神症状的关联
基本信息
- 批准号:10443029
- 负责人:
- 金额:$ 69.15万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-07-01 至 2027-04-30
- 项目状态:未结题
- 来源:
- 关键词:6 year old9 year oldAdolescenceAdultAgeAnorexia NervosaAttenuatedBehavioralBehavioral MechanismsChildChild RearingChildhoodChronicCognitiveCommunitiesCrystallizationDataDevelopmentDimensionsDiseaseEarly InterventionEarly identificationElectroencephalogramEvaluationEvent-Related PotentialsExhibitsFrequenciesFunctional disorderGoalsGrainImpairmentInterventionInvestigationKnowledgeLongevityMental disordersMentored Patient-Oriented Research Career Development AwardMethodsMonitorNeurobiologyNeuronal PlasticityObsessive-Compulsive DisorderOnset of illnessOutcomePerformancePhenotypeProcessPsychopathologyPublic HealthResearchResearch Domain CriteriaResistanceRiskSamplingSchool-Age PopulationSchoolsSeveritiesSocial Anxiety DisorderSocial DevelopmentSocial EnvironmentSocial ProcessesSymptomsTechniquesTimeagedcognitive controlcognitive developmentcognitive processcomorbiditycontextual factorscontrol theorycost effectivedesignearly childhoodexperiencehigh riskimprovedindexinginsightneurobiological mechanismneurodevelopmentnovelpeerpsychiatric symptomrecruitrelating to nervous systemresponsesevere psychiatric disordersocialsocial influence
项目摘要
PROJECT SUMMARY
Heightened performance monitoring and overcontrol (HPM/OC) is a transdiagnostic phenotype comprised of
perfectionism, extreme concern for errors, cognitive inflexibility and excessive need for control. There is
increasing evidence that the HPM/OC phenotype is identifiable in early childhood and underlies obsessive-
compulsive disorder (OCD), social anxiety disorder (SAD) and anorexia nervosa (AN). These psychiatric
disorders are severe, chronic, and treatment-resistant disorders with high rates of comorbidity. However, there
is surprisingly little research examining the neurobiological and behavioral mechanisms that make up the
HPM/OC phenotype in early school-age childhood in relation to the development of transdiagnostic psychiatric
symptoms. Moreover, it is unknown how the HPM/OC phenotype interacts with rapid developmental
progression during this age or is influenced by social-contextual features, such as social evaluation, peer
rejection or parenting styles. Determining answers to these fundamental questions could provide insight into
the emergence of the HPM/OC phenotype and provide novel treatment targets for early intervention. The goal
of the current proposal is to improve understanding of the HPM/OC phenotype in early childhood in relation to
early markers of OCD and SAD by assessing the developmental progression of cognitive facets of
performance monitoring and reactive versus proactive cognitive control and the influence of social-contextual
features on psychiatric outcomes. We posit that cognitive processes that make up the HPM/OC phenotype,
including heightened performance monitoring and more reactive versus proactive cognitive control, interact
with various social contexts to differentiate early school-age children with impairing HPM/OC. The early school-
age period is when HPM/OC is first evident and is a time of rapid cognitive and social development, making it a
pivotal time to understand the developmental psychopathology of this presentation. We will employ cutting-
edge and cost-effective electroencephalogram (EEG) event-related potential (ERP) and time-frequency (TF)
analyses to examine multiple Research Domain Criteria (RDoC) constructs across three repeated yearly
assessments in a sample of 300 community children oversampled for elevated dimensional HPM/OC, ages
spanning 4 - 9 years. This fine-grained evaluation will provide an opportunity to characterize 1) how HPM/OC
impacts normative neurodevelopmental trajectories of RDoC constructs during an age of high neural plasticity,
2) the developmental progression of cognitive facets of the HPM/OC phenotype in relation to transdiagnostic
psychiatric impairment and 3) the impact of social-contextual features that may influence these relationships.
This knowledge could have far-reaching effects on our understanding of the early neurodevelopment of the
HPM/OC phenotype prior to disorder onset, which could inform early identification of high-risk children and
targeted early interventions that could lessen the severity, course and impairment of multiple psychiatric
disorders across the lifespan.
项目总结
增强型性能监控和过度控制(HPM/OC)是一种跨诊断表型,包括
完美主义、对错误的极端关注、认知上的僵化和对控制的过度需求。的确有
越来越多的证据表明,HPM/OC表型在儿童早期就可以识别出来,并成为强迫症的基础。
强迫症(OCD)、社交焦虑症(SAD)和神经性厌食症(AN)。这些精神病患者
疾病是严重的、慢性的、难治性疾病,具有很高的共患率。然而,在那里
令人惊讶的是,几乎没有研究来检验构成
学龄儿童HPM/OC表型与跨诊断精神病学发展的关系
症状。此外,HPM/OC表型如何与快速发育相互作用尚不清楚
在这个年龄段的进步或受社会背景特征的影响,如社会评价、同伴
拒绝或养育方式。确定这些基本问题的答案可以提供对
HPM/OC表型的出现,为早期干预提供了新的治疗靶点。目标是
目前的建议是提高对儿童早期HPM/OC表型与以下方面的理解
强迫症和自闭症的早期标志物评估认知方面的发展
绩效监控、反应性认知控制与主动性认知控制以及社会语境的影响
关于精神结果的特写。我们假设构成HPM/OC表型的认知过程,
包括更高的性能监控和更具反应性的主动认知控制、交互
通过不同的社会背景来区分患有HPM/OC受损的早期学龄儿童。早期的学校-
年龄段是HPM/OC首次出现的时期,是认知和社会快速发展的时期,使其成为
这是理解这一陈述的发展精神病理学的关键时刻。我们将使用切割-
边缘和经济实惠的脑电(EEG)事件相关电位(ERP)和时频(Tf)
分析以检查三年重复的多个研究领域标准(RDoC)结构
对300名年龄段HPM/OC升高的社区儿童进行过度抽样的评估
时间跨度为4-9年。这一精细的评估将提供一个机会来描述1)HPM/OC
在神经可塑性很高的时代影响RDoC结构的标准神经发育轨迹,
2)HPM/OC表型认知方面的发展与跨诊断的关系
精神障碍和3)可能影响这些关系的社会背景特征的影响。
这一知识可能会对我们理解儿童早期神经发育产生深远的影响。
疾病发作前的HPM/OC表型,这可能有助于早期识别高危儿童和
有针对性的早期干预,可以减轻多发性精神病患者的严重程度、病程和损害
一生中都会出现疾病。
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)
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Kirsten Gilbert其他文献
Kirsten Gilbert的其他文献
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{{ truncateString('Kirsten Gilbert', 18)}}的其他基金
Attention-Related Neural Circuitry in Pediatric Anxiety and ADHD
小儿焦虑症和多动症中的注意力相关神经回路
- 批准号:
10561956 - 财政年份:2023
- 资助金额:
$ 69.15万 - 项目类别:
Neural and behavioral trajectories of the overcontrolled phenotype: Associations with development, social context and psychiatric symptoms in early childhood
过度控制表型的神经和行为轨迹:与幼儿期发育、社会背景和精神症状的关联
- 批准号:
10654803 - 财政年份:2022
- 资助金额:
$ 69.15万 - 项目类别:
Heightened Performance Monitoring and Overcontrol: Neural Markers and Caregiving Processes in Developmental Risk Trajectories
加强绩效监控和过度控制:发育风险轨迹中的神经标记和护理过程
- 批准号:
10299265 - 财政年份:2021
- 资助金额:
$ 69.15万 - 项目类别:
Heightened Performance Monitoring and Overcontrol: Neural Markers and Caregiving Processes in Developmental Risk Trajectories
加强绩效监控和过度控制:发育风险轨迹中的神经标记和护理过程
- 批准号:
10251873 - 财政年份:2017
- 资助金额:
$ 69.15万 - 项目类别:
Heightened Performance Monitoring and Overcontrol: Neural Markers and Caregiving Processes in Developmental Risk Trajectories
加强绩效监控和过度控制:发育风险轨迹中的神经标记和护理过程
- 批准号:
9751968 - 财政年份:2017
- 资助金额:
$ 69.15万 - 项目类别:
Developmental Pathways to Borderline Personality Disorder: Longitudinal Observational, Clinical, and Neural Predictors From Early Childhood to Young Adulthood
边缘性人格障碍的发展途径:从幼儿期到青年期的纵向观察、临床和神经预测因素
- 批准号:
10734460 - 财政年份:2010
- 资助金额:
$ 69.15万 - 项目类别:
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