Disrupted development of neural connections by alcohol initiation in adolescence

青春期酒精引发的神经连接发育受到破坏

基本信息

批准号：
8693876
负责人：
Monica Luciana
金额：
$ 52.64万
依托单位：
UNIVERSITY OF MINNESOTA
依托单位国家：
美国
项目类别：
财政年份：
2011
资助国家：
美国
起止时间：
2011-09-20 至 2016-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8693876
关键词：
Adolescence Adolescent Adult Adverse effects Age Alcohol consumption Alcoholic beverage heavy drinker Alcohols Anterior Atrophic Attention Automobile Driving Basal Ganglia Behavior Behavior Control Behavioral Brain Brain region Child Chronic Clinical Communities Complex Corpus striatum structure Corticospinal Tracts Critical Pathways Cues Data Data Collection Decision Making Development Developmental Process Diffusion Disease Drug usage Education Electrophysiology (science)Enrollment Esthesia Fiber Functional Magnetic Resonance Imaging Funding General Population Genetic Health behavior Heavy Drinking Incentives Individual Justice Legal Longitudinal Studies Magnetic Resonance Imaging Measures Medial Mediating Memory Methods Modeling National Institute on Alcohol Abuse and Alcoholism Nature Neurocognitive Neurosciences Nucleus Accumbens Parahippocampal Gyrus Parents Parietal Participant Pathway interactions Patient Self-Report Pattern Play Predisposition Prefrontal Cortex Pregnancy in Adolescence Prevention Problem behavior Process Protocols documentation Psychiatry Public Health Questionnaires Reporting Research Research Personnel Resistance Rest Rewards Risk Role Sampling Scanning Societies Structure Substance abuse problem Testing Thick Time Touch sensation Weight adolescent alcohol initiation adverse outcome age related alcohol effect alcohol exposure alcohol use disorder alcohol use initiation behavior test cognitive control critical period discounting early adolescence emerging adult executive function follow-up frontal lobe functional disability gray matter indexing meetings memory process neurodevelopment neuroimaging neuropsychological peer influence relating to nervous system response social substance abuse prevention trait underage drinking white matter

项目摘要

DESCRIPTION (provided by applicant): This application is a resubmitted R01 proposal in response to PA-09-097 Alcohol, Decision- Making, and Adolescent Brain Development (NIAAA). The project capitalizes upon an existing longitudinal sample of adolescents who were enrolled starting in 2004 in a longitudinal brain development study. Participants, ages 9 to 23, underwent an extensive structural neuroimaging protocol that included T1-weighted and diffusion-weighted scans, and also completed a comprehensive behavioral testing battery and a set of self- report questionnaires. Most participants were free of alcohol and drug use at study enrollment. Participants completed one follow-up assessment, two years after the baseline enrollment, using similar data collection methods as at baseline. [A third assessment wave was completed on approximately half the sample since this proposal was reviewed]. Here, funds are requested to conduct two additional longitudinal assessments of the full sample (n=170), many of whom have transitioned from no alcohol use to significant use over time. To date, found age-related improvements were found in numerous frontal lobe-mediated functions, including planning, delay discounting, inhibitory control, and motivated decision making. These functions are associated with white matter integrity throughout the brain, but particularly within tracts that connect the frontal lobe with striatal brain regions. Preliminary findings indicate that individuals who initiated alcohol use, and/or increased their use over time, showed signs of reduced white matter development, specifically with respect to fiber pathways that provide connectivity among cortical regions (superior parietal, anterior temporal, prefrontal) involved in high-level associative processes as well as inhibitory cognitive and behavioral control. Additionally, longitudinal effects of alcohol use include reduced volume of neural fibers connecting the key subcortical structure involved in mediating incentive-reward activation, the nucleus accumbens, with the key cortical region involved in providing descending inhibitory control over behavioral responses to reward cues, the medial orbitofrontal cortex. [Preliminary findings from the partial Time 3 data collection include reductions in white matter integrity of brain regions directly involved in memory processes (hippocampal gyrus, temporal polar cortex) in association with escalating alcohol use from Time 2 to Time 3.] Additional longitudinal assessment will permit a more sophisticated modeling, using linear mixed models, of the effects of adolescent alcohol initiation on ongoing neural connectivity development, together with parallel analyses on associations between behavioral and brain development and how alcohol initiation impacts them. Within the proposed study, the investigators will be able to assess brain connectivity via structural MRI, electrophysiology, resting state fMRI, and a broad range of behavioral tasks. Thus, this application meets NIAAA funding objectives, because the scientific inquiry into the question of alcohol's effects on the developing brain will be advanced.

描述（由申请人提供）：本申请是针对 PA-09-097 酒精、决策和青少年大脑发育 (NIAAA) 重新提交的 R01 提案。该项目利用了从 2004 年开始参加纵向大脑发育研究的现有青少年纵向样本。年龄在 9 至 23 岁之间的参与者接受了广泛的结构神经影像检查，其中包括 T1 加权和弥散加权扫描，并完成了全面的行为测试和一套自我报告问卷。大多数参与者在研究登记时没有饮酒和吸毒。参与者在基线入组两年后使用与基线类似的数据收集方法完成了一项后续评估。 [自审查该提案以来，已对大约一半的样本完成了第三次评估]。在此，需要资金对整个样本（n = 170）进行两次额外的纵向评估，其中许多人随着时间的推移已经从不饮酒转变为大量饮酒。迄今为止，我们发现许多额叶介导的功能都与年龄相关，包括计划、延迟贴现、抑制控制和动机性决策。这些功能与整个大脑的白质完整性有关，特别是在连接额叶和纹状体大脑区域的脑束内。初步研究结果表明，开始饮酒和/或随着时间的推移增加饮酒的个体，表现出白质发育减少的迹象，特别是在参与大脑皮质区域（顶上叶、前颞叶、前额叶）之间提供连接的纤维通路方面。高级联想过程以及抑制性认知和行为控制。此外，饮酒的纵向影响包括神经纤维体积减少，该神经纤维连接参与介导激励-奖励激活的关键皮层下结构（伏隔核）和关键皮层区域，该区域涉及对奖励线索的行为反应提供下行抑制控制，即内侧眶额皮质。 [部分时间 3 数据收集的初步发现包括直接参与记忆过程的大脑区域（海马回、颞极皮层）的白质完整性降低，与从时间 2 到时间 3 的饮酒量增加有关。]额外的纵向评估将允许使用线性混合模型对青少年饮酒对持续神经连接发展的影响进行更复杂的建模，同时对行为和大脑发育之间的关联以及饮酒对它们的影响进行并行分析。在拟议的研究中，研究人员将能够通过结构 MRI、电生理学、静息状态 fMRI 和广泛的行为任务来评估大脑连接性。因此，该申请符合 NIAAA 的资助目标，因为将推进对酒精对发育中大脑的影响问题的科学探究。