Linking Biological and Social Pathways to Adolescent Health and Well-Being

将生物和社会途径与青少年健康和福祉联系起来

• 批准号: 8430135
• 负责人: Jodi Ford
• 金额: $ 25.52万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-07-15 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8430135
• 关键词: Adherence; Adolescent; Adolescent Risk Behavior; Adrenal Glands; African American; Alcohol or Other Drugs use; Behavioral; Biological; Biological Markers; Chronic; Chronic stress; Cohort Studies; Collection; Community Surveys; Computer Assisted; County; Crime; Data; Data Collection; Data Quality; Data Sources; Development; Discipline; Disease; Exposure to; Foundations; Funding; Future; Grant; Hair; Health; Health Benefit; Health behavior; Household and Family; Human Herpesvirus 4; Hydrocortisone; Hypothalamic structure; Impaired health; Individual; Interview; Lead; Length; Life; Life Cycle Stages; Link; Mails; Measurement; Measures; Mediating; Mental Health; Methodology; Neighborhoods; Neurosecretory Systems; Not Hispanic or Latino; Ohio; Outcome; Pathway interactions; Personal Satisfaction; Pituitary Gland; Population; Population Research; Population Study; Positioning Attribute; Protocols documentation; Psychosocial Factor; Psychosocial Stress; Research; Respondent; Retrieval; Risk; Risk Behaviors; Role; Saliva; Salivary; Sampling; Schools; Shapes; Social Impacts; Social Network; Stress; System; Techniques; Testing; Time; United States National Institutes of Health; Validity and Reliability; Variant; Victimization; Violence; abstracting; aged; cost effective; cost effectiveness; design; environmental stressor; health disparity; immune function; multilevel analysis; physical conditioning; prospective; psychosocial; public health relevance; racial and ethnic; research study; response; sample collection; social; socioeconomics; stressor; trait; viral DNA

DESCRIPTION (provided by applicant): Linking Biological and Social Pathways to Adolescent Health and Well-Being Abstract Research across disciplines provides strong evidence that exposure to chronic stress contributes to poor physical and mental health outcomes across the life course. Consequently, large-scale population studies have increasingly integrated the collection of biomarkers of hypothalamus-pituitary-adrenal (HPA) activity (e.g. cortisol) to investigate the extent to which the neuroendocrine pathway explicates the role of chronic stress in shaping poor health outcomes and racial/ethnic and socioeconomic health disparities. However, few population studies have collected cortisol biomarkers from adolescents and among those that have, significant methodological challenges ultimately hampered data quality. Therefore, the purpose of this R21 proposal is to field test the collection of non-invasive longitudinal cortisol samples from adolescents to explore the validity and reliability of nightly measures of salivary cortisol for 6 nights and one hair sample for cortisol. The findings will determine if the collection of these measures is feasible and informative in a population of adolescents across a spectrum of social risk for impaired health. This R21 proposal is unique in that we will leverage a subsample of adolescents participating in the first wave of a recently funded prospective cohort study - the Adolescent Health and Development in Context (AHDC) study (PI Browning; NIH 1R01DA032371-01 and the William T. Grant Foundation). The AHDC study will examine the impact of spatial and social exposures on the risk behavior, victimization and mental health outcomes of 4,000 adolescents aged 11-17 years in Franklin County, Ohio. The specific aims of this R21 proposal are: Aim 1: To field test the collection of non-invasive biomarkers of cortisol in adolescents via nightly salivary samples for 6 nights and one hair sample and Aim 2: To examine the relationships between the (a) cortisol biomarkers; (b) immune function biomarkers (EBV DNA) and (c) linked secondary data from the AHDC study of adolescent risk behavior, psychosocial stressors, and environmental stressors. Our analytic strategy will employ advanced multilevel modeling techniques designed to estimate the variability in cortisol levels between and within individuals and the behavioral, psychosocial and environmental stressors associated with this variability. The findings of this R21 proposal will inform the selection of a high-quality, feasible and cost-effective biomarker data collection protocol to determine the biological impact of social risk on adolescent health and behavior in the second wave of the AHDC study. In addition, these data will inform the design of future population research studies to reduce adolescent health risk and disparities, with potential health benefits over the life course.

描述（由申请人提供）：将生物学和社会途径与青少年健康和跨学科的福利研究联系起来提供了有力的证据，表明暴露于慢性压力会导致整个生活过程中的身体和心理健康状况不佳。因此，大规模的人群研究越来越多地整合了下丘脑 - 垂体 - 肾上腺肾上腺（HPA）活性（例如皮质醇）的生物标志物，以研究神经内分泌途径在多大程度上阐明了慢性应激在塑造较差的健康/种族/种族/种族/种族/种族和社会经济学方面的慢性应激的作用。但是，很少有人口研究从青少年收集皮质醇生物标志物，而在具有重大方法论挑战最终会阻碍数据质量的那些人群中。因此，该R21提案的目的是现场测试青少年的非侵入性纵向皮质醇样品的收集，以探索6晚唾液皮质醇的夜间唾液性皮质醇的有效性和可靠性，并为皮质醇提供一个毛发样本。这些发现将确定这些措施的收集是否是可行的，并且在各种各样的社会风险中对健康受损的青少年人群中的收集是可行的和有益的。该R21提案的独特之处在于，我们将利用参与最近资助的前瞻性队列研究的第一波浪潮的青少年子样本 - 上下文中的青少年健康与发展（PI Browning; NIH 1R01DA03232371-01）和威廉·T·格兰特基金会（William T. Grant Foundation）。 AHDC研究将研究空间和社会暴露对4,000名在俄亥俄州富兰克林县的11-17岁青少年的风险行为，受害和心理健康成果的影响。该R21提案的具体目的是：目标1：通过夜间唾液样本进行6晚和一个头发样本2：检查（a）皮质醇生物标志物之间的关系； （b）免疫功能生物标志物（EBV DNA）和（c）来自AHDC研究的二级数据，对青少年风险行为，社会心理压力源和环境压力源。我们的分析策略将采用高级多级建模技术，旨在估计个体之间和内部皮质醇水平的可变性以及与此变异性相关的行为，社会心理和环境压力源。该R21提案的发现将为选择高质量，可行且具有成本效益的生物标志物数据收集方案提供信息，以确定社会风险对AHDC研究的第二波对青少年健康和行为的生物学影响。此外，这些数据将为未来的人口研究的设计提供介绍，以减少青少年健康风险和差异，并在整个生命过程中潜在的健康益处。