RDoC Constructs: Neural Substrates, Heritability, and Relation to Psychopathology
RDoC Constructs: Neural Substrates, Heritability, and Relation to Psychopathology
批准号:
8895408
负责人:
Benjamin B Lahey
金额:
$95.8万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-12 至 2017-11-30
关键词:
AddressAdolescenceBiological AssayBrainClassificationComorbidityComplexConceptionsCuesDNAData SetDiagnosisDiagnosticDimensionsDiseaseDistressEconomic BurdenEnvironmentEnvironmental Risk FactorEquationEtiologyExhibitsFailureFrightFunctional Magnetic Resonance ImagingFunctional disorderFutureGenesGeneticGenetic studyGoalsHeritabilityHeterogeneityIndividual DifferencesInterviewLearningLinkMapsMediatingMental HealthMental disordersMindModelingMolecular GeneticsMotivationNational Institute of Mental HealthNatureNegative ValenceNeurobiologyNeurosciencesNomenclatureParticipantPathologyPatternPositive ValencePreventionPsyche structurePsychopathologyQualifyingResearchResearch Domain CriteriaResourcesRewardsSamplingStimulusSubstance abuse problemSymptomsSystemTestingTwin Multiple BirthVariantbasecognitive systemcohortdisabilitygenetic variantimprovedmotivational processesneural circuitneurobehavioralpleasurerelating to nervous systemresponseyoung adult
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The central hypothesis of the Research Domain Criteria (RDoC) project is that categorical mental disorders do not "line up" one-to-one with variations in the functioning of neural circuits. Rather, neural circuits align with narrower neurobehavioral constructs that are themselves related to psychopathology in cross-cutting fashion: Dysfunction in each construct is related to multiple forms of psychopathology and most forms of psycho- pathology are related to dysfunction in more than one construct. Failure to refocus research with this is mind will continue to obscure the neurobiology of psychopathology. We endorse these hypotheses, and propose to test them. Our first aim is to test hypotheses regarding the association between specific neural circuits and five neurobehavioral constructs in the RDoC positive and negative valence and cognitive systems domains. Using fMRI, we will assay the functioning of a mesocorticostriatal system involved in approach motivation and reward attainment (pleasure), a limbic/paralimbic system involved in anticipation and response to aversive-threatening stimuli, and control systems involved in effortful response inhibition. Thi addresses the first goal of the RDoC initiative of mapping constructs to brain circuits. RDoC's second goal is to relate constructs to psychopathology to enable a new classification of psychopathology informed by neurobiology. To advance this goal, our second aim is to test the hypothesis that RDoC constructs are associated with psychopathology in a complex but tractable cross-cutting manner. We will map RDoC constructs to empirically-defined dimensional conceptions of psychopathology based on strong evidence that prevalent mental disorders are organized by their correlations (comorbidity) into distress, fears, and externalizing
dimensions. Using structural equation modeling, we will test the hypothesis that the five selected RDoC constructs are related in cross-cutting fashion to these three dimensions of psychopathology. This reflects our hypothesis that the mental disorders that load on each broad dimension cluster together precisely because they share the same pattern of variations of these neurobiological constructs and etiologic influences. We will also test the possibility that relativ differences in the expression of RDoC constructs produces heterogeneity in the expression of symptoms within the three dimensions of psychopathology. Our third aim is to test the crucial hypothesis that variations in functioning of the neural circuits are associated with psychopathology in the same cross-cutting manner and their associations with psychopathology are mediated by the RDoC constructs. Our proposed study is based on a highly informative sample of 400 young adult twins strategically selected from a large representative cohort. Participants who exhibited psychopathology in adolescence will be steeply oversampled to greatly enrich the sample on psychopathology. Critically, the twins will allow us to determine the extent to which genetic influences are shared in common by the neural circuits, constructs, and dimensions of psychopathology.
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DOI:
10.1007/s10519-018-9907-1
发表时间:
2018-07
期刊:
Behavior genetics
影响因子:
2.6
作者:
[Van Hulle CA, Waldman I, Lahey BB]
通讯作者:
Lahey BB
A hierarchical causal taxonomy of psychopathology across the life span.
整个生命周期中精神病学的分层因果分类学。
DOI:
10.1037/bul0000069
发表时间:
2017-02
期刊:
Psychological bulletin
影响因子:
22.4
作者:
[Lahey BB, Krueger RF, Rathouz PJ, Waldman ID, Zald DH]
通讯作者:
Zald DH
DOI:
10.1037/a0033387
发表时间:
2014-01
期刊:
PSYCHOLOGICAL BULLETIN
影响因子:
22.4
作者:
[Lahey, Benjamin B.]
通讯作者:
Lahey, Benjamin B.
Validating DICOM transcoding with an open multi-format resource.
使用开放的多格式资源验证 DICOM 转码。
DOI:
10.1007/s12021-014-9230-9
发表时间:
2014
期刊:
Neuroinformatics
影响因子:
3
作者:
[Yvernault,BenjaminC, TheobaldJr,CharlesD, Smith,JolindaC, Villalta,Victoria, Zald,DavidH, Landman,BennettA]
通讯作者:
Landman,BennettA
DOI:
10.1146/annurev-clinpsy-032816-044957
发表时间:
2017-05-08
期刊:
Annual review of clinical psychology
影响因子:
18.4
作者:
[Zald DH, Treadway MT]
通讯作者:
Treadway MT
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