Genomics of myocardial transcription factors in cardiac remodeling

描述（由申请人提供）：心脏重构是人类心力衰竭的核心特征，在人类受试者中表现出实质性的差异。首席研究员在小鼠模型和人类研究中进行的十年研究表明，一组谨慎的心脏转录因子整合应激信号导致心脏重塑。我们的中心假设是，一组核心心脏转录因子（MEF2， NKX， NFAT， GATA， FOX）的共同遗传变异在很大程度上负责人类心脏重塑的可变过程。我们将通过在两个现有的队列研究中对候选转录因子进行基于SNP和单倍型的关联研究来解决这一假设，这些研究捕获了临床实践中遇到的重塑的常见表型。在Aim 1中，我们将在慢性肾功能不全队列研究（CRIC）中验证候选转录因子的变异与同心重构相关的假设，这是一个具有高患病率同心重构的大型队列研究。在Aim 2中，我们将在宾夕法尼亚大学心力衰竭研究中进行类似的分析，该研究是由申请人发起的一项大型单中心队列研究，具有较高的偏心重构患病率。在目标3中，我们将与宾夕法尼亚大学的专家分子生物学家Edward Morrisey博士合作，利用体外技术确定观察到的风险变异改变转录因子功能的机制。该应用程序使用基因组方法直接在患有常见心脏病的人类受试者中研究心脏转录因子。使用两个已建立的大样本量队列和定量超声心动图将提供必要的表型数据，以明确地解决我们的假设，并将利用已经建立的大型，良好表型队列的投资。通过关注动物模型中尚未在人类中充分研究的重要因素，我们的发现将把多年的基础研究转化为对人类心脏重塑的机制理解。最重要的是，我们希望确定和验证心脏重塑的基因组预测因子，这些预测因子可能具有临床应用价值，作为预测预后和选择高风险患者进行积极治疗的工具。

DESCRIPTION (provided by applicant): Cardiac remodeling is a central feature of human heart failure and shows substantial variation in human subjects. A decade of research in murine models and research in humans performed by the Principal Investigator show that a discreet set of cardiac transcription factors integrate stress signals to cause cardiac remodeling. Our central hypothesis is that common genetic variation in a core set of cardiac transcription factors (MEF2, NKX, NFAT, GATA, FOX) is in large part responsible for the variable course of cardiac remodeling in humans. We will address this hypothesis by performing SNP- and haplotype-based association studies of candidate transcription factors in two existing cohort studies that capture the common phenotypes of remodeling encountered in clinical practice. In Aim 1 we will test the hypothesis that variation in candidate transcription factors is associated with concentric cardiac remodeling in the Chronic Renal Insufficiency Cohort study (CRIC), a large cohort with a high prevalence of concentric remodeling. In Aim 2 we will perform similar analyses in the Penn Heart Failure Study, a large single-center cohort initiated by the applicant with a high prevalence of eccentric remodeling. In aim 3 we will collaborate with an expert molecular biologist at Penn, Dr. Edward Morrisey, to determine the mechanisms by which the observed risk variants alter transcription factor function using in vitro techniques. This application uses genomic approaches to study cardiac transcription factors directly in human subjects with common forms of heart disease. The use of two established cohorts with large sample sizes and quantitative echocardiography will provide the phenotypic data necessary to address our hypotheses definitively, and will capitalize on investments already made in establishing large, well-phenotyped cohorts. By focusing on factors of central importance in animal models that have not been adequately studied in humans, our findings will translate years of basic research into a mechanistic understanding of human cardiac remodeling. Most importantly, we expect to determine and validate genomic predictors of cardiac remodeling that may have clinical applications as tools to predict prognosis and to select high-risk patients for aggressive therapy.