Epidemiology and Mechanisms of ECG Abnormalities: Young Adulthood to Middle Age
Epidemiology and Mechanisms of ECG Abnormalities: Young Adulthood to Middle Age
批准号:
7479119
负责人:
DONALD M LLOYD-JONES
金额:
$38.01万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-15 至 2010-04-30
关键词:
AdultAfrican AmericanAgeArtsAtherosclerosisAutonomic DysfunctionBlood PressureC-reactive proteinCardiovascular DiseasesCodeCohort AnalysisCohort StudiesCoronary arteryCoronary heart diseaseDataDevelopmentDiabetes MellitusDiseaseElderlyElectrocardiogramEnrollmentEpidemiologyEthnic OriginEtiologyEventFutureHeart DiseasesHeart RateHigh PrevalenceHypertensionHypertrophyIncidenceIndividualInvasiveKnowledgeLeadLeftLeft Ventricular MassLipidsLiteratureMeasuresMediatingMethodsMinnesotaMinorMorbidity - disease rateMorphologyMyocardial InfarctionNatural HistoryNumbersObesityParticipantPathologicPatternPrevalencePrevention strategyPrimary PreventionRaceRateResearchResearch PersonnelResourcesRestRiskRisk FactorsRoleSmokingTechnologyTimeUrsidae FamilyVariantVentricularWomanagedblood glucose regulationcardiovascular disorder riskcohortcoronary artery calcificationcostfollow-upinsightinterestmenmiddle agemortalitynovelprognosticprogramsprospectiveresearch clinical testingsexyoung adult
中文摘要
描述(由申请方提供):拟议研究的总体目标是对现有的连续12导联心电图(EGG)描记进行编码,以便:1)评估不同种族年轻成人中ECG异常的发生率; 2)检查ECG异常发生和进展的潜在风险因素; 3)研究ECG异常与亚临床心脏病的其他指标之间的相关性(亚临床动脉粥样硬化、左心室质量/肥大和自主神经功能障碍);和4)评估黑人和白人中ECG异常的发生率和关联模式的差异。最终,研究结果可能有助于确定静息心电图(一种低成本,无创,广泛可用且易于解释的临床测试)在CVD一级预防中的潜在作用。我们将在1985-1986年入组的年轻人冠状动脉风险发展(CARDIA)研究的男性和女性参与者的大型birthday队列中进行这项研究。我们计划使用最先进的技术和标准化的Minnesota Code和Novacode方法,对从0年级、7年级和20年级的CARDIA参与者中获得的静息12导联ECG进行编码。该项目将首次分析年轻黑人和白色成年人在出现这些异常的关键年龄段的长期心电图变化。这项研究是独特的,及时的,极具成本效益的,因为它利用了一项大型的,预先存在的,birthorm流行病学队列研究,具有高质量的连续12导联ECG描记(以前收集,但从未编码)和其他以前收集的CVD风险因素,亚临床动脉粥样硬化和左心室形态的措施。在可预见的未来,其他队列研究不太可能提供类似的数据。CARDIA的静息12导联ECG是研究的宝贵资源,可以为ECG异常和CVD之间的流行病学关联提供重要见解。这项研究将填补我们对年轻人心电图异常的流行病学、病因学和自然史知识的重要空白。此外,它还将提供重要的见解,了解ECG异常与CVD风险增加相关的潜在机制,以及这些机制在黑人和白人之间的差异,这可能最终导致年轻人预防策略的改善。
英文摘要
DESCRIPTION (provided by applicant): The overall objective of the proposed research is to code existing serial 12-lead electrocardiographic (EGG) tracings in order to: 1) assess the incidence of ECG abnormalities in young adults of different races; 2) examine potential risk factors for development and progression of ECG abnormalities; 3) investigate associations between ECG abnormalities and other measures of subclinical cardiac disease (subclinical atherosclerosis, left ventricular mass/hypertrophy, and autonomic dysfunction); and 4) assess differences in incidence and patterns of associations of ECG abnormalities in blacks and whites. Ultimately, the results of the study may help to define a potential role for the resting ECG (a low-cost, non-invasive, widely available and easily interpretable clinical test) in primary prevention of CVD. We will perform this study in the large biracial cohort of men and women participants of the Coronary Artery Risk Development in Young Adults (CARDIA) Study, who were aged 18 to 30 years at enrollment in 1985-1986. We plan to code resting 12-lead ECGs obtained from CARDIA participants at the Year 0, Year 7, and Year 20 examinations, using state-of- the-art technology and standardized Minnesota Code and Novacode methods. This project will provide the first analyses of long-term ECG changes in young black and white adults, during a critical age period when these abnormalities appear to develop. The proposed study is unique, timely and extremely cost-effective in that it takes advantage of a large, pre-existing, biracial epidemiologic cohort study with high-quality serial 12- lead ECG tracings (previously collected but never coded) and with other previously collected measures of CVD risk factors, subclinical atherosclerosis and left ventricular morphology. It is unlikely that other cohort studies will be able to provide similar data for the foreseeable future. The resting 12-lead ECGs from CARDIA represent a precious resource for research that can offer important insights into the epidemiologic associations between ECG abnormalities and CVD. The proposed research will fill critical gaps in our knowledge of the epidemiology, etiology and natural history of ECG abnormalities in young adults. Furthermore, it will provide important insights into the potential mechanisms by which ECG abnormalities are associated with increased risk for CVD, and how these mechanisms may differ between blacks and whites, which may ultimately lead to improvements in preventive strategies for young adults.
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