MicroRNA Profile in Peripheral Artery Disease

外周动脉疾病中的 MicroRNA 谱

• 批准号: 8301065
• 负责人: Naomi Miriam Hamburg
• 金额: $ 22.09万
• 依托单位: BOSTON UNIVERSITY MEDICAL CAMPUS
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-04-01 至 2014-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8301065
• 关键词: Activities of Daily Living; Affect; Age; American; Amputation; Angiogenesis Modulating Agents; Angiography; Animal Model; Arteries; Automobile Driving; Biological Markers; Biology; Biopsy; Blood; Blood Vessels; Cardiac Death; Cardiovascular Diseases; Cardiovascular system; Cell Separation; Clinical; Complication; Congestive Heart Failure; Coronary; Coronary artery; Cross-Sectional Studies; Data; Disease; Endocrine; Endothelial Cells; Enrollment; Epidemiologic Studies; Evaluation; Event; Experimental Models; Funding; Gene Expression; Inflammation; Inflammatory; Injury; Intervention; Ischemia; Isolated limb perfusion; Limb structure; Link; Lower Extremity; Measurement; Measures; Medicine; Methodology; Methods; MicroRNAs; Molecular Profiling; Myocardial Infarction; National Heart, Lung, and Blood Institute; Outcome; Patients; Pattern; Peripheral; Peripheral arterial disease; Pharmaceutical Preparations; Phenotype; Plasma; Prevalence; Prevention strategy; Procedures; Process; Research; Research Personnel; Reverse Transcriptase Polymerase Chain Reaction; Sampling; Severity of illness; Signal Transduction; Source; Specialist; Stroke; Symptoms; Techniques; Testing; Time; Tissues; Translational Research; United States; Unstable angina; Vascular Diseases; Work; aging population; angiogenesis; base; cardiovascular disorder epidemiology; cardiovascular risk factor; cohort; cytokine; disability; experience; follow-up; functional disability; human subject; improved; innovation; insight; longitudinal design; novel; novel therapeutic intervention; outcome forecast; prospective; research study; response; response to injury; restenosis; therapeutic target; treatment strategy

DESCRIPTION (provided by applicant): Peripheral artery disease (PAD) is increasingly prevalent and leads to disability and high cardiovascular risk. The determinants of clinical status and prognosis in PAD are not well understood. Emerging evidence from experimental models identifies microRNAs (miRNAs) as regulators of cellular responses to limb ischemia and as potential therapeutic targets. Altered miRNA expression may contribute to PAD by modulating angiogenesis, inflammation and endothelial injury response, but little is known about these mechanisms in patients. MiRNAs circulate in the blood, hold potential as biomarkers, and may function as endocrine signaling factors. Endothelial cells are a potential source for circulating miRNA. We have developed methods to perform comprehensive quantitative RT-PCR based miRNA profiling in plasma. In addition, we have established the ability to characterize miRNA expression in freshly isolated endothelial cells. The proposed research aims to define circulating and arterial endothelial miRNAs in PAD to provide insight into the mechanisms driving clinical disease in PAD. We will accomplish Aims 1 and 2 by studying our well-characterized, National Heart Lung and Blood Institute-funded PAD cohort and controls (306 PAD patients, 50 CAD patients and 50 controls) with longitudinal outcome evaluation and Aim 3 by enrolling 90 patients (30 each PAD, CAD alone and control) for endothelial cell isolation. In Aim 1, we will test the hypothesis that PAD alters circulating miRNA expression by comparing PAD patients to CAD and healthy controls. In Aim 2, we will relate circulating miRNAs to disease severity, inflammatory cytokines, and circulating angiogenesis modulators in PAD. Further, we will use previously collected 2-year follow-up data to test the hypothesis that circulating miRNAs are associated with coronary and peripheral disease events in PAD. In Aim 3, we will collect arterial endothelial cells at the time of angiography by J-wire biopsy from the iliofemoral arteries. We relate endothelial cell miRNA expression to circulating miRNAs and PAD status. These studies will provide new information regarding circulating and endothelial miRNAs in PAD and may stimulate innovative treatment strategies. PUBLIC HEALTH RELEVANCE: Peripheral arterial disease (PAD) affects over 8 million Americans and leads to physical disability, limb amputation, heart attack and stroke. The determinants of the clinical status and prognosis in PAD are not well understood. This application focuses on microRNAs to understand the mechanisms of cardiovascular risk in PAD and may generate novel therapeutic approaches for PAD.

描述（由申请人提供）：外周动脉疾病（PAD）越来越普遍，并导致残疾和高心血管风险。临床状态的决定因素 PAD的预后尚不清楚。来自实验模型的新证据将microRNAs（miRNAs）鉴定为肢体缺血细胞反应的调节因子和潜在的治疗靶点。miRNA表达的改变可能通过调节血管生成、炎症和内皮损伤反应而导致PAD的发生，但对患者的这些机制知之甚少。MiRNA在血液中循环，具有作为生物标志物的潜力，并可能充当内分泌信号传导因子。内皮细胞是循环miRNA的潜在来源。我们已经开发了在血浆中进行基于全面定量RT-PCR的miRNA谱分析的方法。此外，我们已经建立了在新鲜分离的内皮细胞中表征miRNA表达的能力。该研究旨在确定PAD中的循环和动脉内皮miRNAs，以深入了解PAD临床疾病的驱动机制。我们将通过研究我们充分表征的、由国家心肺和血液研究所资助的PAD队列和对照组（306例PAD患者、50例CAD患者和50例对照组）并进行纵向结局评价来实现目标1和目标2，并通过招募90例患者（PAD、单独CAD和对照组各30例）进行内皮细胞分离来实现目标3。在目标1中，我们将通过比较PAD患者与CAD和健康对照来检验PAD改变循环miRNA表达的假设。在目标2中，我们将循环miRNA与PAD中疾病严重程度、炎性细胞因子和循环血管生成调节因子相关。此外，我们将使用先前收集的2年随访数据来检验循环miRNA与PAD中的冠状动脉和外周疾病事件相关的假设。在目标3中，我们将在血管造影术时通过J-线活检从髂股动脉收集动脉内皮细胞。我们将内皮细胞miRNA表达与循环miRNA和PAD状态联系起来。这些研究将提供关于PAD中循环和内皮miRNAs的新信息，并可能刺激创新的治疗策略。 公共卫生相关性：外周动脉疾病（PAD）影响了超过800万美国人，并导致身体残疾，截肢，心脏病发作和中风。PAD的临床状态和预后的决定因素还不清楚。该应用程序侧重于microRNA，以了解PAD中心血管风险的机制，并可能产生PAD的新治疗方法。