GENETICS, THE ADOLESCENT BRAIN, AND ADDICTION LIABILITY: A LONGITUDINAL TWIN STUDY
GENETICS, THE ADOLESCENT BRAIN, AND ADDICTION LIABILITY: A LONGITUDINAL TWIN STUDY
批准号:
9243301
负责人:
Andrey P. Anokhin
金额:
$62.21万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-03-15 至 2021-02-28
关键词:
AchievementAddressAdolescenceAdolescentAdolescent DevelopmentAgeAlcohol or Other Drugs useBehaviorBrainBrain imagingBrain regionComorbidityCorpus striatum structureCorrelation StudiesDataDevelopmentDevelopmental CourseElectroencephalographyElectrophysiology (science)EnvironmentEtiologyExposure toFunctional Magnetic Resonance ImagingFunctional disorderGeneticGenetic RiskGoalsGrowthHeritabilityImageImpulsive BehaviorImpulsivityIndividualIndividual DifferencesInfluentialsKnowledgeLaboratoriesLongitudinal StudiesMediatingMethodsModelingNeuroanatomyNeurocognitivePathway interactionsPatternPopulation GrowthPreventive InterventionPsychopathologyRecruitment ActivityRegistriesResearchResearch DesignResolutionResourcesRewardsRisk MarkerRisk-TakingRoleSamplingSubstance abuse problemSubstance of AbuseSymptomsSystemTestingTwin Multiple BirthTwin StudiesValidationaddictionadolescent brain developmentadolescent substance usebasebehavior testbrain behaviorbrain pathwaycognitive controlcognitive functiondesigndevelopmental geneticsfollow-upimaging biomarkerimaging modalityimaging studyinsightlongitudinal designneurodevelopmentnotch proteinprospectivepublic health relevancerelating to nervous systemresiliencereward processingsubstance misusesuccesstheories
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The overall goal of the proposed study is to elucidate etiological mechanisms of adolescent substance use and abuse through the integration of developmental and genetic research designs. Previous studies have substantially advanced our understanding of adolescent brain development and the neural basis for impulsive and risk-taking behaviors. An influential neurodevelopmental model posits that accelerated development of reward-related brain regions combined with relative immaturity of the cognitive control regions predisposes adolescents to impulsive behavior and substance abuse. However, the majority of functional magnetic resonance imaging (fMRI) studies have relied on small samples and cross-sectional designs, precluding a direct test of the "maturational asynchrony" hypothesis. Furthermore, cross-sectional correlational studies are unable to delineate pre-existing determinants of substance misuse and its consequences for the brain. Another significant gap in knowledge is the lack of fMRI heritability studies of neural systems underlying reward-related behaviors and inhibitory control, precluding the identification and validation of endophenotypic markers of risk for addictions. A better understanding of the interplay between etiological factors
and pathways to addiction and their dynamic changes across adolescent development requires an integration of genetic and developmental research, but so far this approach has been implemented only using electrophysiological markers of brain function (EEG, ERP) that provide limited insight into the underlying functional neuroanatomy of reward processing and cognitive control. These gaps in knowledge create critical barriers to further progress in understanding the etiology of addictive disorders. To address them, we propose a longitudinal (age 13 to 18) study of a large sample (n=320) of adolescent MZ and DZ twins involving multilevel, interdisciplinary, theory- driven assessments of the brain and behavior. The proposed integrative approach capitalizes on the availability of a unique recruitment resource (state-wide twin registry), top-notch imaging methods, and our prior success of recruiting a large sample of adolescent twins into a laboratory-based longitudinal study. The following Specific Aims will be pursued: 1) To examine developmental trajectories of two brain networks implicated in pathophysiology of addiction: the reward network (RN) and the cognitive control network (CCN) across adolescence, and to determine whether substance use interferes with normal brain development; 2) To estimate the heritability of fMRI markers of RN and CCN functioning throughout adolescence and overlap of genetic influences on RN and CCN across development; 3) To determine whether heritable individual differences in RN and CCN functioning and their relative maturation rates prospectively predict impulsivity, substance misuse, and a broader spectrum of externalizing problems. The achievement of these aims will substantially advance our understanding of the determinants and consequences of adolescent substance misuse and comorbid psychopathology.
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财政年份:2017
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TEST-RETEST RELIABILITY OF PUTATIVE FMRI ENDOPHENOTYPES FOR SUBSTANCE ABUSE RISK
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资助金额:$17.16万
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GENETICS, THE ADOLESCENT BRAIN, AND ADDICTION LIABILITY: A LONGITUDINAL TWIN STUDY
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资助金额:$63.29万
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财政年份:2016
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依托单位:
TEST-RETEST RELIABILITY OF PUTATIVE FMRI ENDOPHENOTYPES FOR SUBSTANCE ABUSE RISK
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批准号:9035991
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项目类别:
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资助金额:$20.59万
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财政年份:2016
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负责人:Andrey P. Anokhin
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依托单位:
THE FUNCTIONAL NEUROANATOMY OF RESPONSE INHIBITION: INTEGRATING ERP AND FMRI DATA
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资助金额:$22.8万
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负责人:Andrey P. Anokhin
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依托单位:
Linking Genetics, Brain, and Behavior to Understand Addiiction Vulnerability
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资助金额:$11.77万
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财政年份:2009
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负责人:Andrey P. Anokhin
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依托单位:
NEUROCOGNITIVE EFFECTS OF NICOTINE DEPRIVATION AND DOPAMINE GENES
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项目类别:
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资助金额:$22.8万
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财政年份:2009
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负责人:Andrey P. Anokhin
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依托单位:
Linking Genetics, Brain, and Behavior to Understand Addiiction Vulnerability
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项目类别:
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资助金额:$11.77万
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财政年份:2009
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负责人:Andrey P. Anokhin
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依托单位:
Linking Genetics, Brain, and Behavior to Understand Addiiction Vulnerability
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项目类别:
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资助金额:$9.22万
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财政年份:2009
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依托单位:
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资助金额:$11.42万
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依托单位:
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项目类别:
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资助金额:$38.46万
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负责人:Andrey P. Anokhin
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依托单位:
NEUROCOGNITIVE EFFECTS OF NICOTINE DEPRIVATION AND DOPAMINE GENES
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资助金额:$18.56万
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资助金额:$11.77万
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财政年份:2009
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依托单位:
NEUROCOGNITIVE PREDICTORS OF SMOKING CESSATION
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资助金额:$37.08万
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负责人:Andrey P. Anokhin
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依托单位:
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资助金额:$33.69万
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财政年份:2008
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依托单位:
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海外基金