Neurocognitive Risk For Alcoholism Into Adulthood
Neurocognitive Risk For Alcoholism Into Adulthood
批准号:
8896367
负责人:
Mary M Heitzeg
金额:
$59.29万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-06-01 至 2017-07-31
关键词:
AddressAdolescenceAdultAgeAlcohol abuseAlcohol consumptionAlcohol or Other Drugs useAlcoholismAmygdaloid structureAnimalsAttentionBackBehaviorBehavior ControlBehavioralBiological Neural NetworksBrainCommunitiesConsumptionCuesDevelopmentDistalDrug usageEarly identificationEarly treatmentEnvironmental Risk FactorFamily StudyFunctional Magnetic Resonance ImagingGamblingGoalsHeavy DrinkingHumanImageImpairmentIncentivesIndividualIndividual DifferencesInterventionInvestigationIowaKnowledgeLifeLife Cycle StagesLongevityLongitudinal StudiesMapsMedialMediatingMediationMediator of activation proteinMichiganNeighborhoodsNeural PathwaysNeurocognitionNeurocognitiveNeurophysiology - biologic functionOutcomeParticipantPatternPersonalityPersonality AssessmentPlayPopulationPredispositionPreventionProcessPublic HealthRegulationRewardsRiskRisk-TakingRoleSamplingServicesShort-Term MemorySocial EnvironmentSocial NetworkSocial PoliciesSocial supportStagingSubstance Use DisorderSystemTemperamentTimeVentral StriatumWorkalcohol involvementalcohol riskalcohol use disorderbasecareercritical developmental perioddiscountingdrinkingdrinking behaviorearly adolescenceearly childhoodemerging adulthigh riskneural circuitneuropsychologicaloperationpeerpreventprogramspsychologicreinforcerrelating to nervous systemresilienceresponsesocialyoung adult
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The scientific issues of this project are focused around four core developmental phenomena of the 18-23 year old period: 1) this period is normatively the highest alcohol consumption interval in the life course; 2) toward the end of this interval, for the majority of young adults, a decrease in consumption begins to take place; 3) for a higher risk subset of the population, the high consumption pattern continues; and 4) while these critical behavioral shifts are occurring, the neural networks responsible for effortful control and reward response/incentive reactivity are also maturing, albeit at different rates. Three corollary, as yet unanswered questions critical to both social policy about youthful drinking and intervention, are to be addressed: A) To what degree are the changes in drinking behavior taking place over this developmental interval attributable to the maturation of these neural networks?; B) Does heavy alcohol consumption influence the maturation of these networks?; C) How do social environmental reinforcers and prior individual differences in risk mediate or moderate both of these outcomes? During the past 5 years, this project has investigated neurocognitive and functional brain indicators of later problem alcohol use, identifying trajectories of problem use and neural indicators of risk and resilience. This revised continuation project builds on this prior work by extending the investigation into early adulthood and identifying effects of heavy drinking on personality, neurocognition and brain function as well as the interactions between early risk, heavy drinking, and social context (social supports, peer drinking, environmental insults) throughout adolescence and early adulthood. Subjects are participants in the Michigan Longitudinal Study, a high risk for alcohol use disorder family study that has been characterizing temperament, behavioral risk and social context since early childhood and neurocognitive risk since early adolescence. Associated brain function has been studied using fMRI since late adolescence in a subset of these participants. Over the next 5 years, the study will probe the two domains of Effortful Control, and Incentive Reactivity, assessed at the levels of brain function (Regulation/dysregulation of frontostriatal and frontolimbic circuitry and connectivity), neurocognition, and personality. Neurocognitive and personality assessments will continue at 3 year intervals (N= 1456), starting at age 12; a subset of participants (N = 225) will continue to be assessed yearly via fMRI starting at age 18. An important new focus of the imaging work is the interaction between frontal and subcortical processes, to be explored longitudinally using a delayed discounting task, and frontostriatal and frontolimbic functional connectivity analyses. Results will developmentally characterize the relationship between drinking behavior, social environment, and brain function and connectivity change. A special focus is the extent to which drinking behavior lags brain change or leads it, and the role that social environment plays in moderating such change.
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The developmental behavior genetics of drug involvement: overview and comments.
药物参与的发育行为遗传学:概述和评论。
DOI:
10.1007/s10519-006-9070-y
发表时间:
2006
期刊:
Behavior genetics
影响因子:
2.6
作者:
[Zucker,RobertA]
通讯作者:
Zucker,RobertA
DOI:
10.1016/j.biopsych.2010.02.020
发表时间:
2010-08-01
期刊:
BIOLOGICAL PSYCHIATRY
影响因子:
10.6
作者:
[Heitzeg, Mary M., Nigg, Joel T., Yau, Wai-Ying Wendy, Zucker, Robert A., Zubieta, Jon-Kar]
通讯作者:
Zubieta, Jon-Kar
Inattention/hyperactivity and aggression from early childhood to adolescence: heterogeneity of trajectories and differential influence of family environment characteristics.
从幼儿期到青春期的注意力不集中/多动和攻击性:轨迹的异质性和家庭环境特征的差异影响。
DOI:
10.1017/50954579405050066
发表时间:
2005
期刊:
Development and psychopathology
影响因子:
3.3
作者:
[Jester,JenniferM, Nigg,JoelT, Adams,Kenneth, Fitzgerald,HiramE, Puttler,LeonI, Wong,MariaM, Zucker,RobertA]
通讯作者:
Zucker,RobertA
DOI:
10.1016/j.sleep.2008.06.015
发表时间:
2009-08
期刊:
SLEEP MEDICINE
影响因子:
4.8
作者:
[Wong, Maria M., Brower, Kirk J., Zucker, Robert A.]
通讯作者:
Zucker, Robert A.
Sleep problems, suicidal ideation, and self-harm behaviors in adolescence.
青春期的睡眠问题、自杀意念和自残行为。
DOI:
10.1016/j.jpsychires.2010.09.005
发表时间:
2011-04
期刊:
JOURNAL OF PSYCHIATRIC RESEARCH
影响因子:
4.8
作者:
[Wong, Maria M., Brower, Kirk J., Zucker, Robert A.]
通讯作者:
Zucker, Robert A.
共 8 条
9/21 ABCD-USA CONSORTIUM: RESEARCH PROJECT SITE AT U MICHIGAN
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批准号:10595054
-
项目类别:
-
资助金额:$208.8万
-
财政年份:2015
-
负责人:Mary M Heitzeg
-
依托单位:
9/21 ABCD-USA CONSORTIUM: RESEARCH PROJECT SITE AT U MICHIGAN
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批准号:10378527
-
项目类别:
-
资助金额:$209.39万
-
财政年份:2015
-
负责人:Mary M Heitzeg
-
依托单位:
9/21 ABCD-USA CONSORTIUM: RESEARCH PROJECT SITE AT U MICHIGAN
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批准号:9980077
-
项目类别:
-
资助金额:$207.8万
-
财政年份:2015
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负责人:Mary M Heitzeg
-
依托单位:
Sleep homeostasis and neural circuitry of risky behavior in adolescents
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批准号:8880081
-
项目类别:
-
资助金额:$10.18万
-
财政年份:2014
-
负责人:Mary M Heitzeg
-
依托单位:
Longitudinal fMRI Study of Youth at Risk for Drug Abuse
-
批准号:7097989
-
项目类别:
-
资助金额:$14.53万
-
财政年份:2005
-
负责人:Mary M Heitzeg
-
依托单位:
Longitudinal fMRI Study of Youth at Risk for Drug Abuse
-
批准号:7270680
-
项目类别:
-
资助金额:$14.53万
-
财政年份:2005
-
负责人:Mary M Heitzeg
-
依托单位:
Longitudinal fMRI Study of Youth at Risk for Drug Abuse
-
批准号:7483200
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项目类别:
-
资助金额:$14.65万
-
财政年份:2005
-
负责人:Mary M Heitzeg
-
依托单位:
Longitudinal fMRI Study of Youth at Risk for Drug Abuse
-
批准号:7667428
-
项目类别:
-
资助金额:$14.94万
-
财政年份:2005
-
负责人:Mary M Heitzeg
-
依托单位:
Longitudinal fMRI Study of Youth at Risk for Drug Abuse
-
批准号:6962469
-
项目类别:
-
资助金额:$14.53万
-
财政年份:2005
-
负责人:Mary M Heitzeg
-
依托单位:
Neurocognitive Risk For Alcoholism Into Adulthood
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批准号:8522246
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项目类别:
-
资助金额:$59.9万
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财政年份:2000
-
负责人:Mary M Heitzeg
-
依托单位:
Neurocognitive Risk For Alcoholism Into Adulthood
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批准号:8705323
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项目类别:
-
资助金额:$60.95万
-
财政年份:2000
-
负责人:Mary M Heitzeg
-
依托单位:
Neurocognitive Risk For Alcoholism Into Adulthood
-
批准号:8104832
-
项目类别:
-
资助金额:$69.85万
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财政年份:2000
-
负责人:Mary M Heitzeg
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依托单位:
Neurocognitive Risk For Alcoholism Into Adulthood
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批准号:8323558
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项目类别:
-
资助金额:$66.51万
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财政年份:2000
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负责人:Mary M Heitzeg
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依托单位:
Family Study of Risk for Alcoholism Over the Life Course
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批准号:8576562
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项目类别:
-
资助金额:$69.95万
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财政年份:1987
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负责人:Mary M Heitzeg
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依托单位:
Family Study of Risk for Alcoholism Over the Life Course
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批准号:8707907
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项目类别:
-
资助金额:$66.8万
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财政年份:1987
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负责人:Mary M Heitzeg
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依托单位:
Family Study of Risk for Alcoholism Over the Life Course
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批准号:8901829
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项目类别:
-
资助金额:$65.64万
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财政年份:1987
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负责人:Mary M Heitzeg
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依托单位:
海外基金