Neural Mechanisms for Early Development of Pervasive Anger and Irritability
普遍愤怒和易怒早期发展的神经机制
基本信息
- 批准号:8162711
- 负责人:
- 金额:$ 15.39万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2011
- 资助国家:美国
- 起止时间:2011-06-20 至 2015-04-30
- 项目状态:已结题
- 来源:
- 关键词:9 year oldAffectiveAgeAmygdaloid structureAngerAnteriorAttentionBehaviorBehavioralBiological MarkersBrainCaregiversCategoriesChildChild BehaviorChild Behavior ChecklistChild PsychiatryClinicClinicalClinical ServicesClinical SkillsDSM-VDevelopmentDiagnosisDiagnosticDiseaseDorsalEmotionalEmotionsFunctional Magnetic Resonance ImagingFunctional disorderFutureGoalsKnowledgeMeasuresMediatingMental HealthMood DisordersNatureParentsPsychiatric DiagnosisPsychiatristPsychopathologyPublicationsQuestionnairesRelative (related person)ReportingResearchResearch TrainingRiskSamplingScanningScheduleSchool-Age PopulationScientistSecureSeveritiesStagingSupport SystemSymptomsSystemTherapeutic InterventionTrainingaffective neurosciencebasebehavior measurementcareerclinical Diagnosisclinical carecognitive neurosciencedevelopmental psychologyearly onsetemotion regulationexperiencemeetingsneuroimagingneuromechanismnovel diagnosticspsychosocialrelating to nervous systemresearch clinical testingteacher
项目摘要
DESCRIPTION (provided by applicant): The goal of this research is to use functional magnetic resonance imaging (fMRI) to study the neural basis of attentional dyscontrol and emotion dysregulation in a sample of young children (ages 6-9) who are displaying early onset pervasive anger and irritability. These symptoms represent a significant mental health concern that some say requires a new diagnostic category in the DSM-V revision in order to secure the research and clinical services that these children require. The proposed study will be the first to examine brain mechanisms for attentional dyscontrol and emotion dysregulation, which signify key behavioral deficits, in these young school-age, unmedicated children upon first clinic presentation. Obtaining these measures of functional abnormalities in attentional control and emotion regulatory neural systems in young children presenting with pervasive anger and irritability relative to age-matched healthy counterparts will first help us to identify which children show greater levels of dysfunction within these neural systems. It is also a first step toward the longer term goal of examining the extent to which these neural system abnormalities may represent biological markers that can help distinguish relevant developmental trajectories of psychopathology, so that different treatments can be applied at this early stage of symptomatology. Well-validated experimental paradigms, including one paradigm developed by the PI, and behavioral measures will be employed. Primary analyses will probe the neural activity within specific regions related to attentional dyscontrol and emotion dysregulation, and connectivity amongst them, in order to define brain deficits for this illness. Exploratory analyses will examine the extent to which these neural system abnormalities may predict symptom severity and clinical diagnosis by correlating activity in these neural systems with parent reported symptom severity and clinician diagnostic report. Finally, long term plans for this research include a future proposal to complete a longitudinal neuroimaging study in which young children presenting with pervasive anger and irritability will be scanned yearly to increase our understanding of the neural and clinical trajectories of these symptoms. The P.I. already possesses general knowledge of developmental psychology with specific emphasis on emotional development and has extensive experience in the neuroimaging of young children, but lacks the clinical skill set necessary to become an independent scientist in the field of child psychiatry. Therefore, the proposed training plan is aimed at acquiring the relevant clinical skill set necessary to conduct neurodevelopmental research regarding early risk for child psychopathology. The P.I. will complete coursework, train with experts in the field, and author empirical and theoretical publications in order to develop an understanding of child clinical issues. This cross-disciplinary research and training plan, therefore, allows for a stepwise approach to a career in the cognitive and affective neuroscience of child psychopathology.
描述(由申请人提供):本研究的目的是使用功能性磁共振成像(fMRI)来研究幼儿(6-9岁)样本中注意力控制障碍和情绪调节障碍的神经基础,这些儿童表现出早期发作的普遍愤怒和易怒。这些症状代表了一个重要的心理健康问题,有人说需要在DSM-V修订版中建立一个新的诊断类别,以确保这些儿童所需的研究和临床服务。这项拟议的研究将是第一个研究注意力控制障碍和情绪调节障碍的大脑机制,这意味着这些年轻的学龄儿童在首次临床表现时存在关键的行为缺陷。获得这些措施的注意力控制和情绪调节神经系统的功能异常的幼儿普遍愤怒和易怒相对于年龄匹配的健康同行将首先帮助我们确定哪些孩子表现出更大的水平在这些神经系统的功能障碍。这也是迈向长期目标的第一步,即检查这些神经系统异常可能代表的生物标志物的程度,这些生物标志物可以帮助区分精神病理学的相关发展轨迹,以便在精神病理学的早期阶段应用不同的治疗方法。 将采用经过充分验证的实验范例,包括PI开发的一个范例和行为测量。初步分析将探测与注意力控制障碍和情绪调节障碍相关的特定区域内的神经活动,以及它们之间的连接,以确定这种疾病的大脑缺陷。探索性分析将通过将这些神经系统中的活动与父母报告的症状严重程度和临床医生诊断报告相关联,检查这些神经系统异常可预测症状严重程度和临床诊断的程度。最后,这项研究的长期计划包括一个未来的建议,以完成纵向神经影像学研究,其中表现出普遍愤怒和易怒的幼儿将每年进行扫描,以增加我们对这些症状的神经和临床轨迹的理解。 私家侦探已经拥有发展心理学的一般知识,特别强调情感发展,并在幼儿神经成像方面拥有丰富的经验,但缺乏成为儿童精神病学领域独立科学家所需的临床技能。因此,拟议的培训计划的目的是获得必要的相关临床技能集进行神经发育研究有关儿童精神病理学的早期风险。私家侦探将完成课程,与该领域的专家一起培训,并撰写经验和理论出版物,以发展对儿童临床问题的理解。这种跨学科的研究和培训计划,因此,允许在儿童精神病理学的认知和情感神经科学的职业生涯的逐步方法。
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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Susan B Perlman其他文献
Susan B Perlman的其他文献
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{{ truncateString('Susan B Perlman', 18)}}的其他基金
Dyadic Synchrony as a Mechanism of Parent-Child Interaction Therapy (PCIT): A Neuroscience-Based Approach
二元同步作为亲子互动治疗(PCIT)的机制:一种基于神经科学的方法
- 批准号:
9614022 - 财政年份:2018
- 资助金额:
$ 15.39万 - 项目类别:
Dyadic Synchrony as a Mechanism of Parent-Child Interaction Therapy (PCIT): A Neuroscience-Based Approach
二元同步作为亲子互动治疗(PCIT)的机制:一种基于神经科学的方法
- 批准号:
9982657 - 财政年份:2018
- 资助金额:
$ 15.39万 - 项目类别:
From Irritability to Impairment: How Neurodevelopment of Executive Function and Parent-Child Neural Synchrony Influence the Transition from Normal to Abnormal Functioning.
从易怒到受损:执行功能的神经发育和亲子神经同步如何影响从正常功能到异常功能的转变。
- 批准号:
8950905 - 财政年份:2015
- 资助金额:
$ 15.39万 - 项目类别:
From Irritability to Impairment: How Neurodevelopment of Executive Function and Parent-Child Neural Synchrony Influence the Transition from Normal to Abnormal Functioning.
从易怒到受损:执行功能的神经发育和亲子神经同步如何影响从正常功能到异常功能的转变。
- 批准号:
9137708 - 财政年份:2015
- 资助金额:
$ 15.39万 - 项目类别:
From Irritability to Impairment: How Neurodevelopment of Executive Function and Parent-Child Neural Synchrony Influence the Transition from Normal to Abnormal Functioning.
从易怒到受损:执行功能的神经发育和亲子神经同步如何影响从正常功能到异常功能的转变。
- 批准号:
9244172 - 财政年份:2015
- 资助金额:
$ 15.39万 - 项目类别:
A Study of Preschool Irritability: Brain Imaging in the Clinic Setting
学龄前烦躁的研究:临床环境中的脑成像
- 批准号:
8635101 - 财政年份:2014
- 资助金额:
$ 15.39万 - 项目类别:
A Study of Preschool Irritability: Brain Imaging in the Clinic Setting
学龄前烦躁的研究:临床环境中的脑成像
- 批准号:
8807943 - 财政年份:2014
- 资助金额:
$ 15.39万 - 项目类别:
Neural Mechanisms for Early Development of Pervasive Anger and Irritability
普遍愤怒和易怒早期发展的神经机制
- 批准号:
8464802 - 财政年份:2011
- 资助金额:
$ 15.39万 - 项目类别:
Neural Mechanisms for Early Development of Pervasive Anger and Irritability
普遍愤怒和易怒早期发展的神经机制
- 批准号:
8656145 - 财政年份:2011
- 资助金额:
$ 15.39万 - 项目类别:
Neural Mechanisms for Early Development of Pervasive Anger and Irritability
普遍愤怒和易怒早期发展的神经机制
- 批准号:
8287552 - 财政年份:2011
- 资助金额:
$ 15.39万 - 项目类别:
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