Imaging genetics of extinction of conditioned fear responses in anxiety
焦虑中条件性恐惧反应消失的影像遗传学
基本信息
- 批准号:8640968
- 负责人:
- 金额:$ 17.47万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-07-01 至 2016-03-31
- 项目状态:已结题
- 来源:
- 关键词:AffectAffectiveAllelesAmygdaloid structureAnteriorAnxietyAnxiety DisordersAreaBrainBrain regionBrain-Derived Neurotrophic FactorCandidate Disease GeneConditioned StimulusCuesDRD4 geneDataDevelopmentDopamine ReceptorDown-RegulationEmotionsExtinction (Psychology)Functional Magnetic Resonance ImagingGenesGeneticGenotypeGoalsImageImpairmentIndividualIndividual DifferencesLinkMeasuresMentorsModelingNeuroanatomyNeurobiologyParticipantPatientsPatternPrefrontal CortexPreventive InterventionProcessPsychopathologyReceptor GeneRegulationResearchResearch ActivityResearch PersonnelResearch Project GrantsRiskSamplingSpecific qualifier valueStimulusTrainingTraining ActivityVariantWorkbaseclinical anxietyconditioned fearconditioningemotion regulationemotional stimuluslearning extinctionmeetingsneural circuitneuroimagingneuromechanismpromoterpublic health relevancerelating to nervous systemresponserisk variantserotonin transporterskillstraitvalylvaline
项目摘要
DESCRIPTION (provided by applicant): Difficulty down-regulating negative affect is a prominent feature of anxiety disorders and impairment in the extinction of an aversively-conditioned response, long an important model of anxiety, is a likely mechanism underlying this form of anxiety-related emotion dysregulation. A separate line of inquiry has indicated that specific genes are associated with both extinction deficits and the functional neuroanatomy of emotion regulation. Specifically the serotonin transporter promoter gene (5-HTTLPR) is associated with greater amygdala and reduced rostral anterior cingulate activation during affective challenge and the DRD4 dopamine receptor gene has been linked with extinction learning. Imaging genetics studies of extinction will be useful for understanding the mechanisms underlying affect dysregulation in anxiety and risk for anxiety. SPECIFIC AIMS: The proposed research project will integrate findings from these domains by assessing how the 5-HTTLPR and DRD4 genes influence neural circuitry previously implicated in emotion dysregulation and extinction learning in a sample of those at risk for anxiety. CAREER DEVELOPMENT PLAN: The candidate's long term goal is to become an independent investigator in the area of imaging genetics of emotion regulation and affective psychopathology. The proposed research and training activities will focus on building expertise in three domains: 1) conditioning as a model for anxiety, 2) genetics and imaging genetics of affect-related traits, and 3) further development of previously established neuroimaging skills. The candidate will work closely with a team of mentors and consultants with expertise spanning these three domains. In addition to the proposed research project, the candidate will complete formal coursework and lab-based training, along with advisor-directed didactics in each area. SIGNIFICANCE: This project and the candidate's subsequent work will utilize the power of the imaging genetics approach to more precisely specify the mechanisms via which genes modulate emotion dysregulation and confer risk for anxiety and affective psychopathology.
PUBLIC HEALTH RELEVANCE: I will examine how specific genes influence brain regions activated when attempting to down- regulate responses to previously threatening stimuli among individuals at risk for anxiety disorders. These data will further our understanding of neurobiological factors associated with vulerability to anxiety and provide an important step toward identifying appropriate prevention and intervention measures for clinical anxiety.
描述(由申请人提供):难以下调负面情绪是焦虑症的一个突出特征,长期以来一直是焦虑症的一个重要模型的厌恶性条件反射的消退受损是这种形式的焦虑相关情绪失调的可能机制。另一项研究表明,特定的基因与灭绝缺陷和情绪调节的功能性神经解剖学有关。具体而言,5-羟色胺转运蛋白启动子基因(5-HTTLPR)与大杏仁核和减少喙前扣带回激活在情感的挑战和DRD 4多巴胺受体基因已与灭绝学习。灭绝的成像遗传学研究将有助于了解焦虑和焦虑风险的影响失调的机制。具体目标:拟议的研究项目将通过评估5-HTTLPR和DRD 4基因如何影响先前在焦虑风险样本中涉及情绪失调和消退学习的神经回路来整合这些领域的研究结果。职业发展:候选人的长期目标是成为情绪调节和情感精神病理学的成像遗传学领域的独立调查员。拟议的研究和培训活动将侧重于在三个领域建立专业知识:1)作为焦虑模型的条件反射,2)与情感相关的特征的遗传学和成像遗传学,以及3)进一步发展先前建立的神经成像技能。候选人将与一个由导师和顾问组成的团队密切合作,他们的专业知识涵盖这三个领域。除了拟议的研究项目,候选人将完成正式的课程和实验室为基础的培训,沿着与导师指导的教学法在每个领域。重要性:该项目和候选人的后续工作将利用成像遗传学方法的力量,更精确地指定基因调节情绪失调的机制,并赋予焦虑和情感精神病理学的风险。
公共卫生相关性:我将研究特定的基因如何影响大脑区域激活时,试图下调反应,以前的威胁刺激的个人在焦虑症的风险。这些数据将进一步加深我们对与焦虑易感性相关的神经生物学因素的理解,并为确定临床焦虑的适当预防和干预措施提供重要的一步。
项目成果
期刊论文数量(20)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
State anxiety carried over from prior threat increases late positive potential amplitude during an instructed emotion regulation task.
在受指导的情绪调节任务中,先前威胁带来的状态焦虑会增加后期的积极电位幅度。
- DOI:10.1037/emo0000154
- 发表时间:2016
- 期刊:
- 影响因子:0
- 作者:Pedersen,WalkerS;Larson,ChristineL
- 通讯作者:Larson,ChristineL
Visual threat detection during moderate- and high-intensity exercise.
- DOI:10.1037/a0021251
- 发表时间:2011-06
- 期刊:
- 影响因子:0
- 作者:Shields MR;Larson CL;Swartz AM;Smith JC
- 通讯作者:Smith JC
Disentangling the effects of novelty, valence and trait anxiety in the bed nucleus of the stria terminalis, amygdala and hippocampus with high resolution 7T fMRI.
- DOI:10.1016/j.neuroimage.2017.05.009
- 发表时间:2017-08-01
- 期刊:
- 影响因子:5.7
- 作者:Pedersen WS;Muftuler LT;Larson CL
- 通讯作者:Larson CL
BAS Reward Responsiveness: A unique predictor of positive psychological functioning.
BAS 奖励反应:积极心理功能的独特预测指标。
- DOI:10.1016/j.paid.2015.02.029
- 发表时间:2015
- 期刊:
- 影响因子:4.3
- 作者:Taubitz,LaurenE;Pedersen,WalkerS;Larson,ChristineL
- 通讯作者:Larson,ChristineL
Moderating Effects of Harm Avoidance on Resting-State Functional Connectivity of the Anterior Insula.
- DOI:10.3389/fnhum.2018.00447
- 发表时间:2018
- 期刊:
- 影响因子:2.9
- 作者:Huggins AA;Belleau EL;Miskovich TA;Pedersen WS;Larson CL
- 通讯作者:Larson CL
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Christine L Larson其他文献
Mental Health Disparities Following Violent Injury: A Prospective Comparison of Survivors of Violent and Nonviolent Mechanisms of Injury
暴力伤害后的心理健康差异:暴力和非暴力伤害机制幸存者的前瞻性比较
- DOI:
10.5005/jp-journals-10030-1445 - 发表时间:
2024 - 期刊:
- 影响因子:0
- 作者:
Amber Brandolino;T. deRoon;Sydney C. Timmer;C. Tomas;Timothy J. Geier;Sarah Melin;Andrew T Schramm;Christine L Larson - 通讯作者:
Christine L Larson
Christine L Larson的其他文献
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{{ truncateString('Christine L Larson', 18)}}的其他基金
Neural Mechanisms of Response Inhibition Training for Obsessive-Compulsive Disorder and Related Conditions
强迫症及相关病症反应抑制训练的神经机制
- 批准号:
10431320 - 财政年份:2022
- 资助金额:
$ 17.47万 - 项目类别:
Risk and Resilience in Urban Black American Acute Trauma Survivors
美国城市黑人急性创伤幸存者的风险和复原力
- 批准号:
10379585 - 财政年份:2021
- 资助金额:
$ 17.47万 - 项目类别:
Risk and Resilience in Urban Black American Acute Trauma Survivors
美国城市黑人急性创伤幸存者的风险和复原力
- 批准号:
10489823 - 财政年份:2021
- 资助金额:
$ 17.47万 - 项目类别:
Risk and Resilience in Urban Black American Acute Trauma Survivors
美国城市黑人急性创伤幸存者的风险和复原力
- 批准号:
10687026 - 财政年份:2021
- 资助金额:
$ 17.47万 - 项目类别:
11/21 ABCD-USA Consortium: Research Project Site at UWM
11/21 ABCD-USA 联盟:UWM 研究项目现场
- 批准号:
10379430 - 财政年份:2017
- 资助金额:
$ 17.47万 - 项目类别:
11/21 ABCD-USA Consortium: Research Project Site at UWM
11/21 ABCD-USA 联盟:UWM 研究项目现场
- 批准号:
9981163 - 财政年份:2017
- 资助金额:
$ 17.47万 - 项目类别:
11/21 ABCD-USA Consortium: Research Project Site at UWM
11/21 ABCD-USA 联盟:UWM 研究项目现场
- 批准号:
10594953 - 财政年份:2017
- 资助金额:
$ 17.47万 - 项目类别:
Acute Neurocognitive-affective Predictors of Chronic Post-trauma Outcomes
慢性创伤后结果的急性神经认知情感预测因子
- 批准号:
9279251 - 财政年份:2015
- 资助金额:
$ 17.47万 - 项目类别:
Acute Neurocognitive-affective Predictors of Chronic Post-trauma Outcomes
慢性创伤后结果的急性神经认知情感预测因子
- 批准号:
9118338 - 财政年份:2015
- 资助金额:
$ 17.47万 - 项目类别:
Imaging genetics of extinction of conditioned fear responses in anxiety
焦虑中条件性恐惧反应消失的影像遗传学
- 批准号:
8100450 - 财政年份:2010
- 资助金额:
$ 17.47万 - 项目类别:
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