Stress Regulation, Working Memory, and Cognitive Disorganization In Adolescence
Stress Regulation, Working Memory, and Cognitive Disorganization In Adolescence
批准号:
8942877
负责人:
Aysenil Belger
金额:
$61.29万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-07-20 至 2020-05-31
关键词:
16 year oldAdolescenceAdolescentAffectAffectiveAgeAmygdaloid structureAnteriorAnxietyAphasiaArousalAttentionBehaviorBehavioralBiologicalBrainCategoriesClinicalCognitionCognitiveCognitive deficitsDevelopmentDiagnosticDiagnostic and Statistical Manual of Mental DisordersDimensionsDiseaseEatingElectroencephalographyEpidemiologyEtiologyFunctional Magnetic Resonance ImagingFunctional disorderGenetic studyGoalsHormonesHydrocortisoneImageImpairmentIndividualInsula of ReilMeasurementMeasuresMedialMediatingMemory impairmentModelingMolecular GeneticsNeurobiologyPatient Self-ReportPerformancePhenotypePhysiologicalPlayPrefrontal CortexPsychopathologyPsychotic DisordersRecoveryRegulationReportingResearch Domain CriteriaRestRiskRoleSalivarySeveritiesSex CharacteristicsShort-Term MemoryStagingStressStress TestsSymptomsSystemTimeTranscendbehavior measurementbehavioral constructbiological adaptation to stresscingulate cortexclinical riskcognitive systemcritical periodexperiencefunctional outcomesheart rate variabilityneurobiological mechanismneuroimagingneuropsychologicalpsychosocialpublic health relevancerelating to nervous systemsexsexual dimorphism
中文摘要
描述(由申请人提供):青春期是精神病理学核心症状出现的高峰期。认知紊乱(CD)是精神病的一个关键症状维度,最常见于青春期,反映了思维的紊乱,并由怪异行为、失语症和注意力受损的存在来定义。CD超越了DSM的诊断范畴,可预测精神障碍的发作和严重程度,并与神经心理障碍相关。遗传学研究已经报道CD是高度可遗传的,因此已经被提出作为分子遗传学研究的有希望的表型。尽管它在预示精神病风险方面起着关键作用,但对青少年CD的神经生物学基础知之甚少。然而,据报道,经历混乱的青少年在工作记忆容量(WMC)和唤醒/压力调节(ASR)方面存在显着缺陷。这两种行为结构在青少年时期表现出显著的成熟变化,这是向更高层次认知、情感调节和心理社会适应过渡所必需的。尽管有强有力的流行病学证据表明压力在精神病病因学中的作用,以及工作记忆障碍在精神病中的中心地位,但对其在青春期对CD的贡献知之甚少。检查与青春期工作记忆和压力调节相关的神经和生理系统,以及它们对CD严重程度的影响,提供了关键的一步
阐明导致精神病发作的病理生理机制。这种方法与RDoC框架一致,该框架鼓励使用收敛测量来研究域的基础神经生物学(本提案中的认知系统和唤醒调节),以及代表具有精神病临床风险症状的个体所表达的基本行为的结构(工作记忆容量和压力调节)。我们将使用多模态方法整合功能神经影像学,电生理学和行为措施,以确定收敛措施的工作记忆和唤醒/压力调节结构的神经,生理和行为单位,并表征的贡献,非典型ASR和受损的WMC CD症状的严重程度通过临床量表测量。目的1:研究180名青少年(9-16岁)的工作记忆障碍和非典型唤醒/应激调节对CD症状严重程度的影响。在AIM 2中,我们将对WM和ASR结构之间的关系及其对CD严重程度的影响进行建模。在AIM 3中,我们将研究CD症状严重程度的纵向轨迹,WM和ASR的行为和电生理测量,以及它们与AIM 1和2中获得的基线神经,行为和生理测量的相关性。对于每个目标,我们将探讨性别差异和青春期成熟对青春期压力调节和工作记忆的调节作用,以及它们在确定功能结果方面的影响。影响:了解与青春期工作记忆容量和压力调节相关的神经和生理系统及其对CD严重程度的贡献,是阐明促进精神病出现和恶化的核心病理生理机制的关键一步。
英文摘要
DESCRIPTION (provided by applicant): Adolescence is a peak time for the emergence of the core symptoms of psychopathology. Cognitive disorganization (CD) is a key symptom dimension of psychosis that emerges most commonly in adolescence, reflects a disorganization of thought and is defined by the presence of bizarre behavior, alogia, and impaired attention. CD transcends DSM diagnostic categories, predicts the onset and severity of psychotic disorders, and is associated with neuropsychological impairment. Genetic studies have reported that CD is highly heritable, and therefore has been proposed as a promising phenotype for molecular genetic studies. Despite its critical role in heralding risk for psychosis, little is knon about the neurobiological underpinnings of CD in adolescents. It has been reported however that adolescents experiencing disorganization have significant deficits in working memory capacity (WMC) and arousal/stress regulation (ASR). These two behavioral constructs show dramatic maturational changes during adolescence, which are necessary for the transition to higher-level cognition, affect regulation and psychosocial adaptation. Despite the strong epidemiologic evidence for the role of stress in the etiology of psychosis, and the centrality of working memory impairments in psychosis, little is known about their contribution to CD in adolescence. Examining the neural and physiological systems associated with working memory and stress regulation in adolescence, and their contribution to CD severity, offers a critical step
in elucidating the pathophysiological mechanisms that contribute to the onset of psychosis. This approach is consistent with the RDoC framework, which encourages using converging measurements to study the underlying neurobiology of domains (Cognitive System and Arousal Regulation in this proposal), and constructs (working memory capacity and stress regulation) that represent fundamental behaviors expressed by individuals with clinical risk symptoms for psychosis. We will use a multimodal approach integrating functional neuroimaging, electrophysiological, and behavioral measures to ascertain converging measures of working memory and arousal/stress regulation constructs across neural, physiological, and behavioral units, and to characterize the contributions of atypical ASR and impaired WMC in the severity of CD symptoms measured through clinical scales. In Aim 1, we will evaluate the contributions of working memory impairments and atypical arousal/stress regulation in 180 adolescents (ages 9-16) to the severity of CD symptom. In AIM 2 we will model the relationship between WM and ASR constructs and their impact on CD severity. In AIM 3, we will examine the longitudinal trajectory of CD symptom severity, behavioral and electrophysiological measures of WM and ASR, and their associations with baseline neural, behavioral, and physiological measures acquired in AIMs 1 and 2. For each aim, we will explore the modulatory role of sex differences and pubertal maturation on stress-regulation and working memory during adolescence, and their influence in determining functional outcomes. IMPACT: Understanding the neural and physiological systems associated with working memory capacity and stress regulation in adolescence, and their contribution to CD severity, is a crucial step for elucidating the core pathophysiological mechanisms that promote the emergence and exacerbation of psychosis.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Developmental Pathophysiology of Adverse Patterns of Substance Use in Adolescents with Anxiety
-
批准号:10566213
-
项目类别:
-
资助金额:$70.68万
-
财政年份:2023
-
负责人:Aysenil Belger
-
依托单位:
Clinical Translational Core
-
批准号:10673844
-
项目类别:
-
资助金额:$43.65万
-
财政年份:2020
-
负责人:Aysenil Belger
-
依托单位:
Clinical Translational Core
-
批准号:10224309
-
项目类别:
-
资助金额:$43.65万
-
财政年份:2020
-
负责人:Aysenil Belger
-
依托单位:
Clinical Translational Core
-
批准号:10455488
-
项目类别:
-
资助金额:$43.65万
-
财政年份:2020
-
负责人:Aysenil Belger
-
依托单位:
Stress Regulation, Working Memory, and Cognitive Disorganization In Adolescence
-
批准号:9249221
-
项目类别:
-
资助金额:$13.04万
-
财政年份:2015
-
负责人:Aysenil Belger
-
依托单位:
Stress Regulation, Working Memory, and Cognitive Disorganization In Adolescence
-
批准号:9111064
-
项目类别:
-
资助金额:$58.72万
-
财政年份:2015
-
负责人:Aysenil Belger
-
依托单位:
THE ROLE OF DOPAMINE IN NORMAL BRAIN FUNCTION
-
批准号:7716846
-
项目类别:
-
资助金额:$0.05万
-
财政年份:2008
-
负责人:Aysenil Belger
-
依托单位:
BIRN-GENETIC FACTORS
-
批准号:7716853
-
项目类别:
-
资助金额:$0.02万
-
财政年份:2008
-
负责人:Aysenil Belger
-
依托单位:
Project 2-Mapping Cortical Circuit Maturation in High Risk Adolescents
-
批准号:7333006
-
项目类别:
-
资助金额:$34.48万
-
财政年份:2007
-
负责人:Aysenil Belger
-
依托单位:
THE ROLE OF DOPAMINE IN NORMAL BRAIN FUNCTION
-
批准号:7625641
-
项目类别:
-
资助金额:$0.13万
-
财政年份:2006
-
负责人:Aysenil Belger
-
依托单位:
FIRST BIRN
-
批准号:7625619
-
项目类别:
-
资助金额:$0.11万
-
财政年份:2006
-
负责人:Aysenil Belger
-
依托单位:
BIRN-GENETIC FACTORS
-
批准号:7625652
-
项目类别:
-
资助金额:$0.11万
-
财政年份:2006
-
负责人:Aysenil Belger
-
依托单位:
MAPPING OF BRAIN FUNCTIONS
-
批准号:7377431
-
项目类别:
-
资助金额:$0.02万
-
财政年份:2005
-
负责人:Aysenil Belger
-
依托单位:
THE ROLE OF DOPAMINE IN NORMAL BRAIN FUNCTION
-
批准号:7377588
-
项目类别:
-
资助金额:$0.02万
-
财政年份:2005
-
负责人:Aysenil Belger
-
依托单位:
MAPPING OF BRAIN FUNCTIONS
-
批准号:7200232
-
项目类别:
-
资助金额:$0.31万
-
财政年份:2004
-
负责人:Aysenil Belger
-
依托单位:
Mapping of Brain Functions
-
批准号:6980666
-
项目类别:
-
资助金额:$0.25万
-
财政年份:2003
-
负责人:Aysenil Belger
-
依托单位:
NEUROIMAGING OF SOCIAL AND COGNITIVE DEFICITS IN AUTISM
-
批准号:6560407
-
项目类别:
-
资助金额:$26.12万
-
财政年份:2002
-
负责人:Aysenil Belger
-
依托单位:
Project 2-Mapping Cortical Circuit Maturation in High Risk Adolescents
-
批准号:8307511
-
项目类别:
-
资助金额:$30.42万
-
财政年份:2002
-
负责人:Aysenil Belger
-
依托单位:
Project 2-Mapping Cortical Circuit Maturation in High Risk Adolescents
-
批准号:7902020
-
项目类别:
-
资助金额:$33.55万
-
财政年份:2002
-
负责人:Aysenil Belger
-
依托单位:
Functional Neuroimaging In Turner Syndrome
-
批准号:6435385
-
项目类别:
-
资助金额:$7.28万
-
财政年份:2002
-
负责人:Aysenil Belger
-
依托单位:
海外基金