grant

Intradialytic Myocardial Stunning in Hemodialysis Patients - a Novel Cardiovascular Risk Factor

Organization NEW YORK UNIVERSITY SCHOOL OF MEDICINELocation NEW YORK, UNITED STATESPosted 24 Dec 2021Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY2025AcuteAddressAmericanArrhythmiaAttentionAutonomic DysfunctionAutonomic nervous systemBaroreceptor ReflexBaroreflexBiological MarkersBlack PopulationsBlack groupBlack individualBlack peopleBlacksBlood PlasmaBlood PressureCardiacCardiac ArrhythmiaCardiovascularCardiovascular Body SystemCardiovascular Organ SystemCardiovascular systemCaringCatecholaminesCessation of lifeCitiesCollaborationsComplicationDataDeathDeath RateDedicationsDevelopmentDialysisDialysis patientsDialysis procedureDysfunctionESKDESRDEchocardiogramEchocardiographyEnd stage renal failureEnd-Stage Kidney DiseaseEnd-Stage Renal DiseaseEndocrine Gland SecretionEpidemiologyEventExpenditureFunctional disorderFundingHealth Insurance for Aged and Disabled, Title 18Health Insurance for Disabled Title 18HeartHeart ArrhythmiasHeart VascularHeart failureHemodialysesHemodialysisHispanicHispanic PopulationsHispanic groupHispanic individualHispanic peopleHispanicsHormonesImpairmentIncidenceIntervention TrialInterventional trialInvestigationIschemic HeartIschemic Heart DiseaseIschemic myocardiumKnowledgeLeadLeftLeft Ventricular HypertrophyLevarterenolLevonorepinephrineLifeLinkMaintenanceMeasurementMeasuresMedicareModalityMonitorMorbidityMorbidity - disease rateMotionMulti-center studiesMulticenter StudiesMyocardialMyocardial IschemiaMyocardial StunningMyocardial depressionMyocardial dysfunctionNational Institutes of HealthNecrosisNecroticNerve CellsNerve UnitNervous System controlNeural CellNeurocyteNeuronsNoradrenalineNorepinephrineOsmolar ConcentrationOsmolarityPETPET ScanPET imagingPETSCANPETTPathogenesisPathologicPatientsPatternPb elementPhenotypePhysiologyPhysiopathologyPlasmaPlasma SerumPopulationPositron Emission Tomography Medical ImagingPositron Emission Tomography ScanPositron-Emission TomographyPredispositionPrevalenceProceduresPublishingRad.-PETRecurrenceRecurrentReflexReflex actionResearch DesignReticuloendothelial System, Serum, PlasmaRisk FactorsRoleSamplingStressStress cardiomyopathyStudy TypeStunned MyocardiumSubgroupSusceptibilitySympathetic Nervous SystemSympathinsSyndromeTakotsuboTestingTherapeutic HormoneTimeTitle 18Toxic effectToxicitiesTransthoracic EchocardiographyUltrafiltrationUnited StatesUnited States National Institutes of HealthVariantVariationVentricularWomanattributable deathattributable mortalityautonomic reflexbio-markersbiologic markerbiomarkerblack patientcardiac damagecardiac dysfunctioncardiac failurecardiac ischemiacardiovascular riskcardiovascular risk factorcirculatory systemcohortcoronary ischemiadesigndesigningdevelopmentaldialysis therapyepidemiologicepidemiologicalhealth insurance for disabledheart damageheart dysfunctionheart ischemiaheart sonographyheavy metal Pbheavy metal leadhemodynamicshigh riskhigh risk grouphigh risk individualhigh risk peoplehigh risk populationimprovedinnovateinnovationinnovativeinsightmortalitymortality ratemortality ratiomyocardial damagemyocardial ischemia/hypoxiamyocardium ischemianeural imagingneuro-imagingneuroimagingneurological imagingneuronalneurophysiologicalneurophysiologynew drug targetnew drug treatmentsnew druggable targetnew drugsnew pharmacological therapeuticnew pharmacotherapy targetnew therapeutic targetnew therapeuticsnew therapynew therapy targetnext generation therapeuticsnovelnovel drug targetnovel drug treatmentsnovel druggable targetnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel pharmacotherapy targetnovel therapeutic targetnovel therapeuticsnovel therapynovel therapy targetpathophysiologypatient subclasspatient subclusterpatient subgroupspatient subpopulationspatient subsetspatient subtypespositron emission tomographic (PET) imagingpositron emission tomographic imagingpositron emitting tomographypreventpreventingresponsesocial rolestress-induced cardiomyopathystudy designsudden cardiac deathtargeted drug therapytargeted drug treatmentstargeted therapeutictargeted therapeutic agentstargeted therapytargeted treatmenttrial design
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Full Description

Despite rigorous investigations and the expenditure of nearly 6% of Medicare funds on their care, annual
mortality among the 511,000 dialysis patients in the United States is extraordinarily high. Approximately, 17%

of patients die annually with half of deaths attributable to cardiovascular (CV) causes, particularly sudden

cardiac death. Current therapies do not effectively lower CV mortality in hemodialysis (HD) patients thus

highlighting the importance of addressing existing gaps in understanding of the mechanisms underlying CV

complications in HD patients and identifying novel therapeutic targets. Transient intra-dialytic myocardial

stunning (IdMS) during HD—the dominant dialysis modality in the US—has been increasingly implicated as

one such mechanism potentially responsible for progressive myocardial damage and subsequent development

of heart failure, arrhythmia, and CV death. However, current understanding of this novel risk factor is woefully

incomplete. Prior studies were small, included few women, non-white, or incident patients—those with the

highest risk of CV death—and variation in estimated prevalence was extreme (20-100%). In addition, studies of

IdMS risk factors were underpowered and conflicting, and it is remains unknown whether IdMS occurs

intermittently or repetitively. Finally, although our both our own preliminary data and studies by other groups

implicate a potential role for autonomic dysfunction in IdMS pathophysiology, there have been few mechanistic

investigations and understanding of the underlying pathophysiology is incomplete.

In short, IdMS is a potentially important and treatable contributor to CV death in the HD population, but there

are major gaps in understanding its epidemiology, risk factors, and mechanisms. We propose studies designed

to address these critical knowledge gaps and provide the necessary information to determine whether and how

IdMS should be targeted to reduce CV mortality in HD: In Aim 1, we propose performing intradialytic

echocardiography on a large, diverse cohort of 400 incident HD patients to facilitate stable, generalizable

estimates of IdMS prevalence, the analysis of important subgroups, and the study of associations with key risk

factors. In Aim 2, we propose a comprehensive investigation of the hypothesis that unopposed surges in

sympathetic tone underlie susceptibility to IdMS. Myocardial 11C-hydroxephderine PET scanning and dedicated

studies in an autonomic function lab will be utilized to assess systematic and myocardial-specific autonomic

function. Conversely, intradialytic autonomic tone and circulating hormones will be measured during dialysis to

systematically define the patterns of change in autonomic tone preceding and predisposing to episodes of

IdMS. These studies will improve understanding of the epidemiology and physiology of a potentially critical

contributor to cardiovascular morbidity and mortality in the dialysis population, improve basic understanding of

the pathophysiologic impact of HD on the heart, and provide the necessary data to design targeted

therapeutics to reduce CV death for high-risk patients.

Grant Number: 5R01HL157220-04
NIH Institute/Center: NIH

Principal Investigator: David Charytan

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