Social Context and Inflammatory Risk for Stroke in African American Women

描述(申请人提供)：尽管年龄调整后的心血管疾病(CVD)死亡率有所下降，但非裔美国人(AA)女性的冠心病(CHD)/中风发病率几乎是非西班牙裔白人(NHW)女性的两倍。再生障碍性贫血妇女承担的冠心病/中风疾病的额外负担归因于社会经济地位、心理社会压力和更多的风险因素。经济上处于不利地位的AA妇女比NHW妇女经历更高水平的慢性压力。然而，很少有人知道以前的生活逆境，如童年虐待、慢性/感知到的压力、感知到的歧视、主观社会经济地位(SSS)和社会经济地位(SES)如何导致再生障碍性心脏病和非高龄女性之间的冠心病/中风疾病的差异。此外，已知促炎过程有助于冠心病/卒中，令人信服的证据表明，不良的既往生活经历会导致表观遗传改变(即DNA甲基化的改变)，这反过来又会增加应激反应和促炎细胞因子的产生。这项为期三年的有指导的研究开发申请的目的是提供必要的培训和经验，以便能够在独立的职业生涯中确定导致冠心病/中风疾病差异的心理社会和促炎机制。培训目标是：(1)扩大关于既往生活逆境、促炎应激反应和全球DNA甲基化状况与冠心病/中风疾病差异之间的关系的知识；(2)在研究设计、招募、数据收集和数据解释方面获得新的知识和研究技能，因为它与先天生活逆境、促炎应激反应和全球DNA甲基化有关；(3)获得动手培训并获得实验室分析和解释唾液皮质醇、促炎细胞因子和全球DNA甲基化的知识；以及(4)发展建模方面的高级统计专业知识。为了实现这些目标并为持续的研究生涯提供基础，候选人将进行一项研究，比较46名AA和46名NHW患CHD/中风的风险，以(1)确定AA和NHW女性中有冠心病/中风风险的既往生活逆境对急性应激的促炎反应(IL-6)的程度，(2)确定在AA和NHW面临CHD/中风风险的AA和NHW女性中，既往生活逆境预测全球DNA甲基化状态的程度。以及(3)评估全球DNA甲基化状态作为预测AA和NHW女性冠心病/中风风险的急性应激反应(IL-6)的指标。这项研究的意义在于它有可能阐明冠心病/中风疾病的易感性机制，并确定弱势少数族裔妇女健康差异的可能基础。这些发现将有助于开发新的风险概况，以确定那些冠心病/中风负担风险最高的人。

DESCRIPTION (provided by applicant): Despite declines in age-adjusted cardiovascular (CVD) mortality, the incidence of coronary heart disease (CHD)/ stroke is almost twice as high in African American (AA) women compared to non-Hispanic White (NHW) women. The additional burden of CHD/stroke disease borne by AA women is attributed to factors such as socioeconomic status, psychosocial stress, and greater number of risk factors. Economically disadvantaged AA women experience higher levels of chronic stress than NHW women. Yet, little is known about how prior life adversity, such as childhood maltreatment, chronic/perceived stress, perceived discrimination, subjective socio-economic status (SSS), and socioeconomic status (SES) contribute to the disparity in CHD/stroke disease between AA and NHW women. Further, proinflammatory processes are known to contribute to CHD/stroke and compelling evidence demonstrates that adverse prior life experiences result in epigenetic alterations (i.e., changes in DNA methylation), which, in turn, increase stress reactivity and proinflammatory cytokine production. The purpose of this three-year mentored research development application is to provide the necessary training and experience to allow for an independent career in which the psychosocial and proinflammatory mechanisms that underlie CHD/stroke disease disparities can be identified. The training objectives are to: (1) Expand knowledge of the relationships among prior life adversity, proinflammatory stress response, and global DNA methylation status in relation to CHD/stroke disease disparities; (2) Acquire new knowledge and research skills in study design, recruitment, data collection, and interpretation of data as it relates to prior life adversity, proinflammatory stress response, and global DNA methylation in minority women at risk for CHD/stroke; (3) Obtain hands-on training and gain knowledge in the laboratory analysis and interpretation of salivary cortisol, proinflammatory cytokines, and global DNA methylation; and (4) Develop advanced statistical expertise in modeling. To accomplish these objectives and provide a foundation for a sustained research career, the candidate will conduct a study comparing 46 AA and 46 NHW at risk for CHD/stroke in order to (1) Determine the extent to which prior life adversity contributes to CHD/stroke risk and the proinflammatory response (IL-6) to acute stress in AA compared to NHW women at risk for CHD/stroke, (2) Determine the degree to which prior life adversity predicts global DNA methylation status in AA and NHW women at risk for CHD/stroke, and (3) Evaluate global DNA methylation status as a predictor of the proinflammatory response (IL-6) to acute stress in AA and NHW women at risk for CHD/stroke. The significance of this study lies in its potential to clarify mechanisms of CHD/stroke disease susceptibility and to determine the possible basis for the health disparity exhibited by disadvantaged, minority women. Findings will inform the development of novel risk profiles to identify those at most risk for CHD/stroke burden.