Early Noninvasive Detection of Myocardial Microbascular Dysfunction in Diabetes

糖尿病心肌微血管功能障碍的早期无创检测

基本信息

  • 批准号:
    8269141
  • 负责人:
  • 金额:
    $ 12.69万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2009
  • 资助国家:
    美国
  • 起止时间:
    2009-09-01 至 2014-05-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): The purpose of this proposal is to foster the scientific development of Angela Taylor, M.D. as she develops an independent clinical research career. The University of Virginia will provide Dr. Taylor with the ideal setting under the mentorship of Dr. Christopher Kramer in which to investigate the imaging and treatment of early coronary artery disease in diabetes. Type II diabetes has become an epidemic in the United States. Death from cardiovascular disease is 2 to 4 fold the general population. Recent trials have demonstrated that traditional risk factors alone are not completely predictive of disease burden as measured with current noninvasive imaging technology particularly early in the disease process. Overt coronary artery disease is preceded by abnormalities in myocardial microvascular function and nonocclusive plaque accumulation in the artery wall both of which can be measured invasively. It has been shown that risl< factors associated with diabetes and the metabolic syndrome predict invasive measurements. However, current noninvasive technology does not have the ability to reliably measure these early abnormalities. Cardiac Magnetic Resonance (CMR) provides a noninvasive technology capable of directly assessing microvascular function within the heart. Our preliminary data shows a reduction of microvascular function in diabetes prior to overt coronary stenoses as compared to controls. The purpose of this study will be to demonstrate that CMR can reliably diagnose early nonocclusive coronary artery disease. Subject will undergo risk factor measurement, direct imaging of the artery wall with intravascular ultrasound, and noninvasive measurement of microvascular function with CMR. Specific aims include demonstrating that risk factors for coronary artery disease predict invasive and noninvasive measurements, that improvements in risk factors result in improvements in invasive and noninvasive measurements, and that CMR predicts invasive findings. RELEVANCE (See instructions): An eariier noninvasive mechanism of detection of cardiovascular disease will provide the potential to determine which risk factors have the greatest effect early in the disease process thus tailoring therapy and reducing costs, to offer a safer diagnostic mechanism, and to treat coronary disease eariier preventing future events thus contributing to significant improvements in public health. (End of Abstract)
描述(由申请人提供):本提案的目的是促进安吉拉·泰勒医学博士的科学发展。因为她发展了独立的临床研究事业。弗吉尼亚大学将在克里斯托弗克雷默博士的指导下为泰勒博士提供理想的环境,以研究糖尿病早期冠状动脉疾病的成像和治疗。2型糖尿病在美国已经成为一种流行病。死于心血管疾病的人数是一般人口的2至4倍。最近的试验表明,传统的风险因素本身并不能完全预测疾病负担,特别是在疾病过程的早期,用目前的无创成像技术测量。显性冠状动脉疾病发生之前,心肌微血管功能异常和动脉壁非闭塞性斑块积聚,这两者都可以有创测量。已经表明,与糖尿病和代谢综合征相关的risl因子预测侵入性测量。然而,目前的非侵入性技术没有能力可靠地测量这些早期异常。心脏磁共振(CMR)提供了一种能够直接评估心脏内微血管功能的无创技术。我们的初步数据显示,与对照组相比,糖尿病患者在冠状动脉明显狭窄之前微血管功能降低。本研究的目的是证明CMR可以可靠地诊断早期非闭塞性冠状动脉疾病。受试者将接受风险因素测量、血管内超声直接成像动脉壁和CMR无创测量微血管功能。具体目标包括证明冠状动脉疾病的风险因素可预测有创和无创测量,风险因素的改善可导致有创和无创测量的改善,CMR可预测有创结果。相关性(参见说明):心血管疾病的早期非侵入性检测机制将提供确定哪些风险因素在疾病过程早期具有最大影响的潜力,从而定制治疗并降低成本,提供更安全的诊断机制,并更早地治疗冠状动脉疾病,预防未来事件,从而有助于显著改善公共健康。 (End摘要)

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)

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Angela M Taylor其他文献

IgE to the Mammalian Oligosaccharide Galactose-α-1,3-Galactose Is Associated With Increased Atheroma Volume and Plaques With Unstable Characteristics—Brief Report
哺乳动物寡糖半乳糖-α-1,3-半乳糖的 IgE 与动脉粥样硬化体积增加和特性不稳定斑块相关 - 简要报告
High resolution CMR perfusion imaging demonstrates reduced flow reserve and endo/epi ratio in microvascular coronary disease
  • DOI:
    10.1186/1532-429x-17-s1-p148
  • 发表时间:
    2015-02-03
  • 期刊:
  • 影响因子:
  • 作者:
    Peter Shaw;Yang Yang;Yan Li;Jorge A Gonzalez;Angela M Taylor;Craig H Meyer;Frederick H Epstein;Michael Salerno;Christopher M Kramer
  • 通讯作者:
    Christopher M Kramer
Correction: A Functionally Significant Polymorphism in ID3 Is Associated with Human Coronary Pathology
更正:ID3 中具有功能意义的多态性与人类冠状动脉病理学相关
  • DOI:
  • 发表时间:
    2014
  • 期刊:
  • 影响因子:
    3.7
  • 作者:
    A. Manichaikul;S. Rich;H. Perry;J. Yeboah;M. Law;M. Davis;Matthew Parker;M. Ragosta;J. Connelly;C. McNamara;Angela M Taylor;A. Abbate
  • 通讯作者:
    A. Abbate
2141 A novel approach for screening atherosclerosis in diabetes: MRI of the superficial femoral artery
第2141章 一种筛查糖尿病动脉粥样硬化的新方法:股浅动脉MRI
  • DOI:
  • 发表时间:
    2008
  • 期刊:
  • 影响因子:
    0
  • 作者:
    J. Bourque;Brian J. Schietinger;J. Kennedy;J. Christopher;Angela M Taylor;Colleen Mcnamara;C. Kramer
  • 通讯作者:
    C. Kramer
Adenosine stress CMR with variable density spiral pulse sequences accurately detects CAD with minimal dark-rim artifacts
  • DOI:
    10.1186/1532-429x-16-s1-o58
  • 发表时间:
    2014-01-16
  • 期刊:
  • 影响因子:
  • 作者:
    Michael Salerno;Angela M Taylor;Yang Yang;Sujith Kuruvilla;Craig H Meyer;Christopher M Kramer
  • 通讯作者:
    Christopher M Kramer

Angela M Taylor的其他文献

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{{ truncateString('Angela M Taylor', 18)}}的其他基金

Core C: UVA Cardiovascular Cohort
核心 C:UVA 心血管队列
  • 批准号:
    10188602
  • 财政年份:
    2017
  • 资助金额:
    $ 12.69万
  • 项目类别:
Core C: Human Clinical Cardiovascular and Biostatistics Core
核心 C:人类临床心血管和生物统计学核心
  • 批准号:
    10334093
  • 财政年份:
    2017
  • 资助金额:
    $ 12.69万
  • 项目类别:
Early Noninvasive Detection of Myocardial Microbascular Dysfunction in Diabetes
糖尿病心肌微血管功能障碍的早期无创检测
  • 批准号:
    7738585
  • 财政年份:
    2009
  • 资助金额:
    $ 12.69万
  • 项目类别:
Early Noninvasive Detection of Myocardial Microbascular Dysfunction in Diabetes
糖尿病心肌微血管功能障碍的早期无创检测
  • 批准号:
    8473907
  • 财政年份:
    2009
  • 资助金额:
    $ 12.69万
  • 项目类别:
Early Noninvasive Detection of Myocardial Microbascular Dysfunction in Diabetes
糖尿病心肌微血管功能障碍的早期无创检测
  • 批准号:
    8125085
  • 财政年份:
    2009
  • 资助金额:
    $ 12.69万
  • 项目类别:
Early Noninvasive Detection of Myocardial Microbascular Dysfunction in Diabetes
糖尿病心肌微血管功能障碍的早期无创检测
  • 批准号:
    7924722
  • 财政年份:
    2009
  • 资助金额:
    $ 12.69万
  • 项目类别:
Human Phenotyping and Immune Cell
人类表型和免疫细胞
  • 批准号:
    8396707
  • 财政年份:
  • 资助金额:
    $ 12.69万
  • 项目类别:
Core C: UVA Cardiovascular Cohort
核心 C:UVA 心血管队列
  • 批准号:
    9280664
  • 财政年份:
  • 资助金额:
    $ 12.69万
  • 项目类别:
Human Phenotyping and Immune Cell
人类表型和免疫细胞
  • 批准号:
    8707528
  • 财政年份:
  • 资助金额:
    $ 12.69万
  • 项目类别:
Core C: UVA Cardiovascular Cohort
核心 C:UVA 心血管队列
  • 批准号:
    9514254
  • 财政年份:
  • 资助金额:
    $ 12.69万
  • 项目类别:

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