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Arrhythmia Risk Predictors in Populations with High versus Low Risk for Sudden Death.

机译:高或低猝死风险人群中的心律失常风险预测指标。

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摘要

Characteristics of clinical, electrocardiographic (ECG), and imaging risk markers for prediction of sudden death in high versus relatively low risk populations are examined in this thesis. The high-risk population, myotonic muscular dystrophy, is an inherited multi-system disorder associated with myotonia, progressive skeletal muscle weakness, and sudden cardiac death. 1, 2 Cytosine-thymine-guanine (CTG) repeats on chromosome 19 in the 3' untranslated region of a serine-threonine protein kinase gene underlie type I myotonic muscular dystrophy (MMD-I), the more common form of the disease. 3 Type II MMD is associated with CCTG tetra-nucleotide repeats in intron 1 of the zinc finger protein 9 gene (ZNF9). 4 The presence of severe baseline ECG abnormalities is associated with sudden death in adults with MMD-I,2 and points to progression of atrioventricular (AV) block or ventricular arrhythmia as the predominant mode of cardiac mortality in this population. Additionally, patients with MMD and atrial fibrillation (AF) appear to have an elevated risk for development of AV block.2, 5 However, these abnormalities are commonly observed in patients with MMD, and provide a low positive predictive value for identification of risk for sudden death. We have previously shown that myocardial scar imaging can identify the substrate for inducible ventricular tachycardia (VT) in patients with non-ischemic cardiomyopathy.6 This technique has since been validated by other groups, and was later shown to identify non-ischemic cardiomyopathy patients at high risk of sudden death. 7, 8 This thesis describes a) the trends and clinical predictors of time dependent ECG variations in MMD, b) magnetic resonance imaging findings regarding cardiac function and diffuse fibrotic changes in MMD, and c) the association between elevation at various ST points and sudden death, and the heterogeneity of this association in the biracial population of the Atherosclerosis Risk in Communities (ARIC) study. The topics are broad and encompass two different populations; however, an underlying common theme is the characterization of risk factors for sudden death. The strengths and weaknesses of each population under study, the study designs, and implications upon results and future utility of findings will be discussed.
机译:本文探讨了临床,心电图和影像学风险标志物的特征,用于预测高危人群和相对低危人群的猝死。高危人群,肌强直性肌营养不良症,是一种与肌强直,骨骼肌进行性肌无力和心源性猝死有关的遗传性多系统疾病。 1,2型胞嘧啶-胸腺嘧啶-鸟嘌呤(CTG)在19型染色体上的丝氨酸-苏氨酸蛋白激酶基因3'非翻译区重复,是I型肌强直性肌营养不良症(MMD-1)的基础,是该病的最常见形式。 3型II MMD与锌指蛋白9基因(ZNF9)内含子1中的CCTG四核苷酸重复序列相关。 4严重的基线ECG异常的存在与MMD-I,2成年人的猝死有关,并指出房室(AV)阻滞或室性心律失常的进展是该人群心源性死亡的主要方式。此外,MMD和心房纤颤(AF)的患者出现房室传导阻滞的风险较高[2,5]。但是,这些异常通常在MMD患者中观察到,因此对于确定罹患房颤的风险提供较低的阳性预测价值猝死。先前我们已经表明,心肌瘢痕显像可以识别非缺血性心肌病患者的诱导性室性心动过速(VT)的底物。6此技术已得到其他研究小组的验证,后来被证明可用于识别非缺血性心肌病的患者。猝死的高风险。 7,8本文介绍了a)MMD中随时间变化的心电图变化的趋势和临床预测指标,b)关于MMD的心脏功能和弥漫性纤维化变化的磁共振成像结果,以及c)不同ST点抬高与突然发作之间的关联死亡,以及在动脉粥样硬化风险社区中的两种种族的人群中这种关联的异质性(ARIC)研究。主题很广泛,涵盖了两个不同的人群。然而,一个潜在的共同主题是猝死危险因素的表征。将讨论每个研究对象,研究设计的优缺点,以及对结果的影响以及研究结果的未来用途。

著录项

  • 作者

    Nazarian, Saman.;

  • 作者单位

    The Johns Hopkins University.;

  • 授予单位 The Johns Hopkins University.;
  • 学科 Health Sciences Radiology.;Health Sciences Epidemiology.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 135 p.
  • 总页数 135
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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