Cardiac Microstructure and Heart Failure Risk in the Community
Cardiac Microstructure and Heart Failure Risk in the Community
批准号:
9229570
负责人:
Susan Cheng
金额:
$63.79万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-04-01 至 2021-01-31
关键词:
AdultAgeAgingAlgorithmic AnalysisAlgorithmsAnimalsBiological MarkersBlood PressureCardiacCardiovascular DiseasesCause of DeathCell SizeCessation of lifeChronicChronic stressClinicalCommunitiesCongestive Heart FailureCoronary heart diseaseDataDevelopmentDiagnosisDiseaseEFRACElderlyEvaluationEventExposure toFibrosisFramingham Heart StudyGoalsHeart AbnormalitiesHeart failureHeterogeneityHospitalizationHumanImageImage AnalysisImaging TechniquesIndividualInflammationInjuryInterventionLeadLeftLeft Ventricular MassLeft Ventricular RemodelingLeft ventricular structureLife Cycle StagesMeasuresMenopausal StatusMethodsMorbidity - disease rateMorphologyMuscle CellsMyocardialMyocardial tissueMyocardiumNatural HistoryObesityOutcomeParticipantPathologicPathway interactionsPatientsPatternPericardial body locationPersonsPopulationPrognostic MarkerPropertyReportingResearchResistanceRiskRisk FactorsRisk MarkerRoleSamplingSignal TransductionStressStructureTechniquesTherapeutic InterventionThickTimeTissuesUltrasonicsUltrasonographyUnited StatesVentricularWomanWorkadverse outcomeaging populationbasecardiogenesiscardiovascular disorder riskclinical imagingclinical practicecohortcoronary fibrosiscost effectivedensitydisabilityextracellularfollow-uphemodynamicsimaging biomarkerimaging modalityinterstitialmortalitynew therapeutic targetnovelnovel markernovel strategiesnovel therapeuticspredictive toolsprospectivepublic health relevanceresponse
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Heart failure (HF) remains a leading cause of morbidity and mortality in the United States. With the majority of new HF diagnoses occurring in adults over age 75 years, HF is now recognized as a life course disease. It logically follows that a person's increasing risk for HF should manifest with progressive cardiac abnormalities that can be tracked over time, in relation to advancing age and cumulative risk exposures. However, conventional imaging methods have limited ability to discriminate between individuals more or less likely to develop clinical HF. We and others have shown that advanced ultrasonic measures of cardiac microstructure can reliably quantify tissue-level alterations in the cellular and extracellular composition of the myocardium, including fibrosis. Based on our prior work and preliminary data, we hypothesize that changes in cardiac microstructure over time are influenced by cumulative exposure to risk factors and that distinct patterns of change in cardiac microstructure can differentiate individuals at greater or lesser risk for HF. Therefore, we propose to use a novel ultrasonic method to study the changes in cardiac microstructure that occur over the life course and leading up to the development of HF and related adverse outcomes. Specifically, we will investigate: (1) the natural history and correlates of change in cardiac microstructure with aging, (2) the extent to which progressive alterations in cardiac microstructure predispose specifically to HF, and (3) the potential utility of cardiac microstructure to serve as a prognostic marker of risk for adverse outcomes across the spectrum of HF among persons living in the community. The overall contribution of the proposed research is expected to include: a comprehensive understanding of how cardiac microstructure is altered during the progression from risk factors to the onset of HF outcomes; and evaluation of a novel imaging-based measure of cardiac microstructure that could serve as a widely-accessible and cost-effective tool for predicting HF in individuals at risk. These contributions will be significant because they will lay groundwork for developing targeted interventions to reduce HF related morbidity and mortality in the population at large.
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