Toward the Identification of Neurodevelopmental Risk Markers of Bipolar Disorder
Toward the Identification of Neurodevelopmental Risk Markers of Bipolar Disorder
批准号:
8064708
负责人:
Cecile D. Ladouceur
金额:
$14.99万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-05-21 至 2013-04-30
关键词:
AdolescenceAdolescentAdultBipolar DisorderChildChildhoodChronicClinicalComplementDataDevelopmentDevelopment PlansEarly treatmentEmotionalEmotionsEnrollmentEthical IssuesFunctional Magnetic Resonance ImagingGenetic RiskGoalsImpairmentInterventionKnowledgeMediatingMental disordersMethodologyMethodsModelingParentsParticipantProcessPubertyRecruitment ActivityResearchRiskRisk FactorsRisk MarkerStimulusSystemTechniquesTimeTrainingadolescent offspringaffective neurosciencecareer developmentchildhood bipolar disordercognitive controldesignemotion regulationemotional stimulusendophenotypeinformation processingneuroimagingneuromechanismoffspringrelating to nervous systemresponseskills
中文摘要
描述(由申请人提供):建议的K01建议的教育目的是让申请人接受发展情感神经科学和儿童双相情感障碍方面的培训,并获得必要的技能,以表征双相情感障碍遗传风险高的青少年神经系统中的情绪调节神经发育异常。双相情感障碍是成人的一种慢性精神障碍,在儿童和青少年中更是如此。它的特征是情绪调节方面的显著障碍,这与前额叶和皮质下神经区的功能异常有关。双相情感障碍可能与这些神经区的神经发育异常有关。双相情感障碍的发病在青春期急剧增加,青春期是参与调节和调节情绪的前额叶系统发育的关键时期。对患有双相情感障碍的父母的青少年后代进行的研究,有望帮助阐明双相情感障碍发展过程中的一些神经机制。这项提议将使用功能磁共振成像(FMRI)来研究与内隐情绪信息处理和情绪认知控制相关的神经活动在双相情感障碍遗传风险高的年轻健康青少年与低风险对照组之间的差异。第二个目标是探索这些神经活动的差异在多大程度上与青春期成熟有关。该项目的中心原则是,高阶认知控制过程对情绪信息处理的调节减少是双相情感障碍的关键风险因素。该项目是对拟议的职业发展计划的补充,该计划将涉及以下方面的培训:1)研究青春期情绪调节的发展情感神经科学方法,2)与儿童双相情感障碍相关的临床问题,3)用于检查情绪调节神经系统的方法,包括在认知控制和与儿科神经成像相关的情绪和伦理问题的功能磁共振成像方面增加神经系统的知识和技能,4)纵向研究中使用的设计和方法,以及用于对神经发育轨迹进行建模的高级统计技术。这项研究的发现将有助于识别双相情感障碍潜在的神经发育风险标记物,并建立双相情感障碍特有的内表型,这将有助于制定早期干预策略。
英文摘要
DESCRIPTION (provided by applicant): The educational aim of the proposed K01 proposal is to allow the applicant to train in developmental affective neuroscience and pediatric bipolar disorder and acquire the skills necessary to characterize neurodevelopmental abnormalities in neural systems of emotion regulation in young adolescents at high genetic risk of bipolar disorder. Bipolar disorder is a chronic and debilitating psychiatric disorder in adults and even more so in children and adolescents. It is characterized by significant impairments in emotion regulation, which have been associated with functional abnormalities in prefrontal and subcortical neural regions. Bipolar disorder may be mediated by neurodevelopmental abnormalities in these neural regions. The onset of bipolar disorder increases dramatically in adolescence, which is a key period for the development of prefrontal systems involved in modulating and regulating emotions. Studies in adolescent offspring of parents with bipolar disorder, who are significantly at risk of developing the illness, promise to help elucidate some of the neural mechanisms involved in the development of bipolar disorder. This proposal will use functional magnetic resonance imaging (fMRI) to investigate differences in neural activity associated with implicit emotional information processing and emotional cognitive control in young healthy adolescents at high genetic risk of bipolar disorder compared to low-risk controls. The secondary goal is to explore to what extent these differences in neural activity are associated with pubertal maturation. The central tenet of the proposed project is that reduced modulation of emotional information processing by higher-order cognitive control processes represents a key risk factor for bipolar disorder. This project complements the proposed career development plan that will involve obtaining training in: 1) developmental affective neuroscience approaches to the study of emotion regulation in adolescence, 2) clinical issues associated with pediatric bipolar disorder, 3) methodology used to examine neural systems of emotion regulation, including increased knowledge and skills in fMRI of neural systems at the interface of cognitive control and emotion and ethical issues associated with pediatric neuroimaging, 4) design and methods used in longitudinal research and advanced statistical techniques for modeling neurodevelopmental trajectories. Findings from this study will contribute to identifying potential neurodevelopmental risk markers for bipolar disorder and establishing endophenotypes of emotion dysregulation specific to bipolar disorder, which will facilitate the development of early intervention strategies.
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会议论文
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海外基金