LIFE COURSE SES, SOCIAL CONTEXT & CARDIOVASCULAR DISEASE
生命历程、社会背景
基本信息
- 批准号:6287955
- 负责人:
- 金额:$ 55.93万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-03-01 至 2005-02-28
- 项目状态:已结题
- 来源:
- 关键词:African American atherosclerosis autonomic disorder behavioral /social science research tag cardiovascular disorder epidemiology caucasian American chronic disease /disorder clinical research disease /disorder proneness /risk gender difference health behavior human data human middle age (35-64) human subject life cycle lifestyle longitudinal human study marriage /marital status metabolism disorder psychological stressor questionnaires racial /ethnic difference social status social support network socioeconomics
项目摘要
In this revision to application 1 R01 HL-64141-01 submitted in
response to Program Announcement number 98-098, we propose to identify
mechanisms explanatory of the strong inverse association between socioeconomic
status (SES) over the life course and cardiovascular disease morbidity and
mortality, in a bi-ethnic population-based sample of four U.S. communities.
Cumulative and contemporaneous effects of diverse SES measures will be tested
for their predictive validity on health outcomes, with consideration of
differences by gender and ethnicity in their (additive or interactive) effects.
Health outcomes will include non-invasively measured subclinical cardiovascular
disease, as well as fatal and non-fatal clinical disease manifestations
ascertained over the course of 10 years of follow-up. Earlier life course
socioeconomic status and measurements of current socioeconomic status and
biomedical cardiovascular risk factors will be integrated with geocoded
contemporary social environmental exposures to assess their impact on
cardiovascular function, metabolic impairments, allostatic load, and
subclinical and clinical disease. Multilevel analyses will be performed with
the goal of identifying pathways by which socioeconomic status is related to
cardiovascular disease, considering relevant health behavior, life styles,
psychosocial stressors/support mechanisms, chronic infection/chronic
inflammatory burden, autonomic nervous system dysfunction, and sustained
metabolic impairments. The potential modification of the above associations by
the social environment will be addressed by these analyses, as well as putative
differences by gender and ethnicity.
These staged analytic goals are made possible by linking Census-based
indicators of the social environment to the rich data resources of the
Atherosclerosis Risk in Communities (ARIC) Study, a bi-ethnic, community-based
sample of men and women aged 45-64 years at the time of their baseline
examination in 1987-1989. This cohort was re-examined every three years through
January, 1999 with ascertainment of SES during childhood, early adulthood and
in mid-life, health-relevant behaviors, numerous measurements of risk factors,
and measures of subclinical cardiovascular disease such as carotid artery wall
thickness, arterial distensibility, retinopathy, and lower extremity arterial
disease. These data, as well as validated information on hospital discharge
diagnoses and on cause-specific mortality accrued over 10 years of follow-up
will be made available to the study proposed in this application. Additional
life course information on the members of the ARIC cohort will be collected
during Year 1 of the study.
Our goal is to explicate the associations and interactive effects of individual
SES attributes and their social context on pathways of development of
cardiovascular disease in individuals and populations. Increased insight into
the mechanisms responsible for these associations should strengthen the basis
for public health preventive measures.
在本次修订中提交的申请 1 R01 HL-64141-01
响应计划公告编号 98-098,我们建议确定
社会经济之间强逆相关的机制解释
生命历程中的状态(SES)和心血管疾病发病率
死亡率,在美国四个社区的双种族人口样本中。
将测试各种社会经济地位措施的累积和同期效果
其对健康结果的预测有效性,并考虑到
性别和种族的差异(相加或交互)影响。
健康结果将包括非侵入性测量的亚临床心血管疾病
疾病,以及致命和非致命的临床疾病表现
经过10年的跟踪调查才得以确定。早年人生历程
社会经济状况以及当前社会经济状况的衡量标准和
生物医学心血管危险因素将与地理编码相结合
当代社会环境暴露,以评估其对
心血管功能、代谢障碍、稳态负荷和
亚临床和临床疾病。将执行多级分析
确定与社会经济地位相关的途径的目标
心血管疾病,考虑相关的健康行为、生活方式,
社会心理压力源/支持机制、慢性感染/慢性
炎症负担、自主神经系统功能障碍和持续的
代谢障碍。上述关联的潜在修改
这些分析将涉及社会环境以及假定的
性别和种族的差异。
这些分阶段的分析目标是通过将基于人口普查的
社会环境指标丰富的数据资源
社区动脉粥样硬化风险 (ARIC) 研究,一项基于社区的双种族研究
基线时年龄为 45-64 岁的男性和女性样本
1987-1989年考试。该队列每三年重新检查一次
1999 年 1 月,确定儿童期、成年早期和成年期的 SES
在中年,与健康相关的行为,对危险因素的大量测量,
颈动脉壁等亚临床心血管疾病及措施
厚度、动脉扩张性、视网膜病变和下肢动脉
疾病。这些数据以及经过验证的出院信息
诊断和 10 年随访期间累积的特定原因死亡率
将可供本申请中提议的研究使用。额外的
ARIC队列成员的生命历程信息将被收集
在研究的第一年。
我们的目标是阐明个体之间的关联和互动效果
SES属性及其社会背景对发展路径的影响
个人和人群的心血管疾病。增加洞察力
负责这些协会的机制应加强基础
用于公共卫生预防措施。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Gerardo Heiss其他文献
Gerardo Heiss的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Gerardo Heiss', 18)}}的其他基金
Changes in arterial stiffness, cognition and dementia risk in a diverse cohort
不同人群中动脉硬度、认知和痴呆风险的变化
- 批准号:
9532012 - 财政年份:2016
- 资助金额:
$ 55.93万 - 项目类别:
IGF::OT::IGF ATHEROSCLEROSIS IN RISK COMMUNITIES - FIELD CENTER - CORE STUDY OPERATIONS
IGF::OT::IGF 动脉粥样硬化风险社区 - 现场中心 - 核心研究操作
- 批准号:
9915754 - 财政年份:2016
- 资助金额:
$ 55.93万 - 项目类别:
IGF::OT::IGF ATHEROSCLEROSIS IN RISK COMMUNITIES - FIELD CENTER - CORE STUDY OPERATIONS
IGF::OT::IGF 动脉粥样硬化风险社区 - 现场中心 - 核心研究操作
- 批准号:
10329838 - 财政年份:2016
- 资助金额:
$ 55.93万 - 项目类别:
IGF::OT::IGF ATHEROSCLEROSIS IN RISK COMMUNITIES - FIELD CENTER - CORE STUDY OPERATIONS
IGF::OT::IGF 动脉粥样硬化风险社区 - 现场中心 - 核心研究操作
- 批准号:
10074453 - 财政年份:2016
- 资助金额:
$ 55.93万 - 项目类别:
TAS::75 0872::TAS ARIC CLINICAL EXAMINATION CENTER
塔斯马尼亚州::75 0872::塔斯马尼亚州阿里克临床检查中心
- 批准号:
8354875 - 财政年份:2010
- 资助金额:
$ 55.93万 - 项目类别:
相似海外基金
Targeted ablation of cerebral atherosclerosis using supramolecular self-assembly
利用超分子自组装靶向消融脑动脉粥样硬化
- 批准号:
24K21101 - 财政年份:2024
- 资助金额:
$ 55.93万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
Body composition and atherosclerosis-related biomarkers in women with endometriosis
子宫内膜异位症女性的身体成分和动脉粥样硬化相关生物标志物
- 批准号:
23K15842 - 财政年份:2023
- 资助金额:
$ 55.93万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
Targeted multimodal stimuli-responsive nanogels for atherosclerosis imaging and therapy
用于动脉粥样硬化成像和治疗的靶向多模式刺激响应纳米凝胶
- 批准号:
2880683 - 财政年份:2023
- 资助金额:
$ 55.93万 - 项目类别:
Studentship
The Epigenetic Regulator Prdm16 Controls Smooth Muscle Phenotypic Modulation and Atherosclerosis Risk
表观遗传调节因子 Prdm16 控制平滑肌表型调节和动脉粥样硬化风险
- 批准号:
10537602 - 财政年份:2023
- 资助金额:
$ 55.93万 - 项目类别:
Role of IL-6 trans signaling in atherosclerosis development and late-stage pathogenesis
IL-6反式信号传导在动脉粥样硬化发展和晚期发病机制中的作用
- 批准号:
10652788 - 财政年份:2023
- 资助金额:
$ 55.93万 - 项目类别:
Novel Mechanisms Underlying the Development of Atherosclerosis
动脉粥样硬化发展的新机制
- 批准号:
10589484 - 财政年份:2023
- 资助金额:
$ 55.93万 - 项目类别:
Alcohol Regulation of Endothelial Plasticity in Atherosclerosis
酒精对动脉粥样硬化内皮可塑性的调节
- 批准号:
10585070 - 财政年份:2023
- 资助金额:
$ 55.93万 - 项目类别:
From genotype to phenotype in a GWAS locus: the role of REST in atherosclerosis
GWAS 位点从基因型到表型:REST 在动脉粥样硬化中的作用
- 批准号:
10570469 - 财政年份:2023
- 资助金额:
$ 55.93万 - 项目类别:
The role of extracellular vesicle-associated MicroRNAs in HIV-associated atherosclerosis
细胞外囊泡相关 MicroRNA 在 HIV 相关动脉粥样硬化中的作用
- 批准号:
10619831 - 财政年份:2023
- 资助金额:
$ 55.93万 - 项目类别: