Genetic by Context Influence on Trajectories of Adolescent Health Risk Behaviors
Genetic by Context Influence on Trajectories of Adolescent Health Risk Behaviors
批准号:
7655674
负责人:
VANGIE A FOSHEE
金额:
$72.83万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2011-08-31
关键词:
AddressAdolescenceAdolescentAdolescent DevelopmentAgeAggressive behaviorAlcohol consumptionAlcohol or Other Drugs useAreaBehaviorBehavioralBiologicalBudgetsBuffersCandidate Disease GeneCatechol O-MethyltransferaseCensusesChromosomes, Human, Pair 15Cohort StudiesCollectionDataData CollectionDevelopmentDopamine ReceptorDrug usageEffect Modifiers (Epidemiology)EnvironmentEtiologyExposure toFamilyFamily StudyGenderGenesGeneticGenetic MarkersGenotypeGrowthHazard ModelsHealthIllicit DrugsInfluentialsInterventionLifeManuscriptsMeasurementMeasuresMethyltransferase GeneModelingMonoamine Oxidase ANeighborhoodsNicotinePaperParentsPatient Self-ReportPhysical aggressionPrincipal InvestigatorProceduresProspective StudiesPsychometricsPublic HealthReceptor GeneResearchReview LiteratureRisk BehaviorsSalivaSample SizeSamplingSchoolsScienceSeriesSocial ControlsSocial EnvironmentSocial NetworkStressTechniquesTestingTimeTobacco useValidationWhole Bloodaggression preventionalcohol misuseanti socialbasebehavior changebehavior influencecohortcontextual factorsdata managementdesigngene environment interactioninnovationpeerpreventprogramsprospectivepublic health relevancereceptorserotonin transportersocial cognitive theorytheoriesvalidation studiesyoung adult
中文摘要
描述(由申请人提供):了解青少年健康基因-环境相互作用对酒精使用、物质使用和攻击行为风险行为的病因学的发展,需要检查遗传和环境变量及其相互作用。本研究旨在测试来自5个精心选择区域的遗传标记之间的相互作用- 5-羟色胺转运基因(SLC6A4),单胺氧化酶A基因(MAOA),儿茶酚- o -甲基转移酶基因(COMT), 4型多巴胺受体基因(DRD4),以及15号染色体上重叠三种尼古丁受体(CHRNA5-CHRNA3-CHRNB5)的高LD区域的一系列标签snp和基于理论的背景变量(压力,健康风险行为模型,和社会控制)从四个关键的社会背景(家庭,同伴,学校和社区)对青少年烟草使用,酒精滥用,非法药物使用和攻击(一般和对同伴和约会)的轨迹。目的1是确定这些遗传标记和健康风险行为轨迹之间的关联是否在假设的方向上受到基于理论的背景变量的调节。该研究还旨在阐明哪些理论结构(目标2)和社会背景(目标3)在调节遗传标记与风险行为轨迹之间的关联方面最重要,以及哪些健康风险行为最受基因-环境相互作用的影响(目标4)。一项7波前瞻性队列研究(n = 4000)已经提供了数据,用于测量11至19岁的健康风险行为和环境变量。在该研究中,使用了创新的测量技术,包括社会网络分析来测量同伴和学校背景,美国人口普查数据在街区组水平(n = 58)和青少年和父母自我报告来测量社区背景。在拟议的研究中,将从现在的年轻人身上收集全血并进行基因分型。这些数据将与前瞻性研究的数据合并,以解决四个具体目标。该研究从先前的研究中扩展了几个概念,包括评估相互作用对青少年健康风险行为轨迹的影响,而不是点估计,允许检查基因-环境相互作用对整个青春期健康风险行为变化的影响,使用基于理论的背景调节因子,以及检查除主要研究的家庭背景之外的背景调节因子。拟议的研究还解决了候选基因环境研究的显着方法局限性,通过对背景变量进行强有力的测量,选择有限数量的经验证明的候选基因进行研究,使用前瞻性设计,结合K-fold交叉验证程序,控制祖先遗传,并且具有足够的能力来检测适度性,即使按性别分层。了解非延展性基因型之间的关联加剧或消除的条件,对于制定有效的公共卫生和个性化计划以促进健康的青少年发展至关重要。公共卫生相关性:遗传环境对青少年健康风险行为轨迹的影响项目摘要-相关性烟草使用,酒精滥用,非法药物使用和攻击是重大的公共卫生问题。这项研究将有助于理解在哪些条件下,不可延展性基因型和这些健康风险行为之间的关联被加剧或消除,这种理解对于制定有效的公共卫生和个性化计划来预防这些公共卫生问题和促进健康的青少年发展至关重要。
英文摘要
DESCRIPTION (provided by applicant): Understanding the development of adolescent health gene-environment interactions on the etiology of alcohol use, substance use, and aggressive behavior risk behaviors requires examination of both genetic and environmental variables and their interactions. This study proposes to test interactions between genetic markers from five carefully selected regions - the serotonin transporter gene (SLC6A4), the monoamine oxidase A gene (MAOA), the catechol-O-methyltransferase gene (COMT), the type 4 dopamine receptor gene (DRD4), and a series of tag SNPs in a high LD region on chromosome 15 overlapping three nicotine receptors (CHRNA5-CHRNA3-CHRNB5) and theoretically-based contextual variables (stress, models of health risk behaviors, and social controls) from four key social contexts (family, peer, school, and neighborhood) on trajectories of adolescent tobacco use, alcohol misuse, illicit drug use, and aggression (in general and against peers and dates). Aim 1 is to determine if associations between these genetic markers and trajectories of health risk behaviors are moderated by theoretically-based contextual variables in the directions hypothesized. The study is intended also to illuminate which theoretical constructs (aim 2) and social contexts (aim 3) are most important in moderating associations between genetic markers and trajectories of risk behaviors, and which health risk behaviors are most influenced by gene-by-environment interactions (aim 4). Data are already available from a seven- wave prospective cohort study (n = 4000) for measuring the health risk behaviors and contextual variables from ages 11 through 19. In that study innovative measurement techniques were used including social network analyses to measure the peer and school context and U.S. Census data at the block group level (n = 58) and adolescent and parent self-reports to measure neighborhood context. For the proposed study, whole blood will be collected from the now young adults and genotyped. Those data will be merged with data from the prospective study to address the four specific aims. The study features several conceptual extensions from prior studies including assessing the influence of interactions on trajectories rather than point estimates of adolescent health risk behaviors, allowing for an examination of how the influence of gene-by-environment interactions on health risk behaviors change across adolescence, use of theoretically- based contextual moderators, and examination of moderators from contexts besides the predominately studied family context. The proposed study also addresses notable methodological limitations of candidate gene-by- environment studies by having strong measures of the contextual variables, selecting a limited number of empirically justified candidate genes to study, using a prospective design, incorporating a K-fold cross- validation procedure, controlling for ancestral heritage, and having sufficient power for detecting moderation, even when stratifying by gender. Understanding the conditions under which the associations between non- malleable genotypes are exacerbated or neutralized is crucial for developing effective public health and individualized programs to promote healthy adolescent development. PUBLIC HEALTH RELEVANCE: Genetic by Context Influence on Trajectories of Adolescent Health Risk Behaviors Project Summary - Relevance Tobacco use, alcohol misuse, illicit drug use, and aggression are significant public health problems. The study will contribute toward understanding the conditions under which the associations between non-malleable genotypes and these health risk behaviors are exacerbated or neutralized and this understanding is crucial for developing effective public health and individualized programs for preventing these public health problems and for promoting healthy adolescent development.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
A Randomized Efficacy Trial of Moms and Teens for Safe Dates
-
批准号:8304109
-
项目类别:
-
资助金额:$40.0万
-
财政年份:2010
-
负责人:VANGIE A FOSHEE
-
依托单位:
A Randomized Efficacy Trial of Moms and Teens for Safe Dates
-
批准号:8142247
-
项目类别:
-
资助金额:$39.9万
-
财政年份:2010
-
负责人:VANGIE A FOSHEE
-
依托单位:
Genetic by Context Influence on Trajectories of Adolescent Health Risk Behaviors
-
批准号:7937710
-
项目类别:
-
资助金额:$72.3万
-
财政年份:2009
-
负责人:VANGIE A FOSHEE
-
依托单位:
Grants for vilence-related injury prevention research ipv & sv
-
批准号:7151104
-
项目类别:
-
资助金额:$29.72万
-
财政年份:2003
-
负责人:VANGIE A FOSHEE
-
依托单位:
Grants for violence-related injury prevention research: IPV & SV
-
批准号:7151105
-
项目类别:
-
资助金额:$25.78万
-
财政年份:2003
-
负责人:VANGIE A FOSHEE
-
依托单位:
海外基金