Retrospective Single Image Multi-endPoint anaLysis (SIMPL) to define pathophysiologic mechanisms of heart failure with preserved ejection fraction.
Retrospective Single Image Multi-endPoint anaLysis (SIMPL) to define pathophysiologic mechanisms of heart failure with preserved ejection fraction.
批准号:
10580172
负责人:
Michael Douglas Nelson
金额:
$12.56万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-09-01 至 2025-08-31
关键词:
Activities of Daily LivingAgeAortaAreaAutomobile DrivingClinicalCommunitiesDataData SetDatabasesDiabetes MellitusDiagnosisDiseaseEFRACEvaluationExercise ToleranceFatty acid glycerol estersFunctional disorderFundingFutureGroup MeetingsHeart failureHypertensionImageImage AnalysisIndividualInvestigationLeft atrial structureLeft ventricular structureMalignant NeoplasmsMethodsModelingMolecularMonitorMorbidity - disease rateMultivariate AnalysisMyocardiumNational Heart, Lung, and Blood InstituteNatureObesity EpidemicOrganPatient Outcomes AssessmentsPatientsPericardial body locationPhenotypePositioning AttributePrevalencePrognosisPublic HealthQuality of lifeResearchResearch MethodologyResearch PriorityResolutionRight atrial structureRight ventricular structureStudy SectionSurvival RateTherapeuticTissuesUnited StatesValidationaging populationbiobehaviorcardiac magnetic resonance imagingcohorteffective therapyexercise intoleranceexperimental studyheart functionhuman datainnovationmortalitynovelpreservationpreventsecondary analysissextoolworking group
中文摘要
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英文摘要
Project Summary
Heart Failure with Preserved Ejection Fraction (HFpEF) is the most common form of heart failure, is associated
with high morbidity and mortality, with increasing prevalence and worsening prognosis. Quality-of-life in HFpEF
is as poor or worse than heart failure with reduced ejection fraction, in large part because of severe exercise
intolerance; the primary manifestation of this bourgeoning condition. Per funding announcement PAR-20-078
which supports the use of existing human datasets for well-focused secondary analyses to investigate new
methods that have the potential for significant impact on NHLBI relevant biomedical or biobehavioral research,
we will leverage an existing database of cardiac magnetic resonance images in a cohort of well-phenotyped
patients with HFpEF and age- and sex-matched healthy controls to comprehensively identify and characterize
pathophysiologic mechanisms driving HFpEF. We will use a novel Single Image Multi-endPoint anaLysis
(SIMPL) approach to compare four chamber cardiac function (right atrium, right ventricle, left atrium, left
ventricle), aortic distensibility, and pericardial fat burden between HFpEF and healthy controls, and to determine
their independent and combined association with exercise tolerance and quality of life.
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