grant

Mineralocorticoid receptor, coronary microvascular function, and cardiac efficiency in hypertension

Organization BRIGHAM AND WOMEN'S HOSPITALLocation BOSTON, UNITED STATESPosted 1 Jan 2023Deadline 31 Dec 2026
NIHUS FederalResearch GrantFY2025ACE InhibitorsAddressAdult-Onset Diabetes MellitusAfter CareAfter-TreatmentAftercareAlbuminuriaAldosteroneAldosterone ReceptorAngiotensin Converting EnzymeAngiotensin I-Converting EnzymeAngiotensin I-Converting Enzyme InhibitorsAngiotensin ReceptorAngiotensin-Converting Enzyme AntagonistsAngiotensin-Converting Enzyme InhibitorsAnti-Hypertensive AgentsAnti-Hypertensive DrugsAnti-HypertensivesBlood PressureBlood Pressure MonitorsBlood VesselsBlood flowBody TissuesCD143 AntigensCarboxycathepsinCardiacCardiac AbnormalitiesCardiac DiseasesCardiac DisordersCardiovascularCardiovascular Body SystemCardiovascular Organ SystemCardiovascular systemChlorphthalidoloneChlorthalidoneChronicClinicalClinical ResearchClinical StudyContinuous SphygmomanometersCoronaryCouplingDipeptidyl Peptidase ADiureticsDysfunctionEchocardiogramEchocardiographyEnacardEnalaprilEnzyme InhibitionFoundationsFunctional disorderGoalsGuidelinesHeartHeart AbnormalitiesHeart DiseasesHeart VascularHumanHypertensionHypotensive AgentHypotensive DrugsImpairmentIndividualK elementKetosis-Resistant Diabetes MellitusKininase AKininase IIKininase II AntagonistsKininase II InhibitorsKnowledgeLeft Ventricular HypertrophyMaturity-Onset Diabetes MellitusMicrovascular DysfunctionMineralocorticoid ReceptorModern ManMorbidityMorbidity - disease rateMyocardialNIDDMNon-Insulin Dependent DiabetesNon-Insulin-Dependent Diabetes MellitusNoninsulin Dependent DiabetesNoninsulin Dependent Diabetes MellitusO elementO2 elementOutcomeOxodolineOxygenOxygen ConsumptionPETPET ScanPET imagingPET/CTPET/CT scanPETSCANPETTParticipantPatientsPeptidyl-Dipeptidase APhthalamudinePhysiopathologyPlacebosPositron Emission Tomography Medical ImagingPositron Emission Tomography ScanPositron-Emission TomographyPotassiumProcessRad.-PETRandomizedReceptor ProteinRecommendationRelaxationRenitecRenitekRestRiskRisk FactorsRoleSham TreatmentSlow-Onset Diabetes MellitusStable Diabetes MellitusStressStructureT2 DMT2DT2DMTestingTissuesTransthoracic EchocardiographyType 2 Diabetes MellitusType 2 diabetesType II Diabetes MellitusType II diabetesVascular Hypertensive DiseaseVascular Hypertensive DisorderVasotecWomanWorkadult onset diabetesantagonismantagonistanti-hypertensioncardiac functioncardiovascular riskcardiovascular risk factorcirculatory systemeplerenoneexperimentexperimental researchexperimental studyexperimentsfunction of the heartheart disorderheart functionheart sonographyhigh blood pressurehyperpiesiahyperpiesishypertension treatmenthypertensivehypertensive diseasehypertensive disorderimprovedketosis resistant diabetesmaturity onset diabetesmechanical energymenmicrovascular complicationsmicrovascular diseasemortalitypathophysiologypositron emission computed tomographypositron emission tomographic (PET) imagingpositron emission tomographic imagingpositron emitting tomographypost treatmentpreventpreventingprimary outcomerandomisationrandomizationrandomly assignedreceptorrecruitsham therapysmall vessel diseasesocial rolethiazidetype 2 DMtype II DMtype two diabetesvascularvascular abnormality
Sign up free to applyApply link · pipeline · email alerts
— or —

Get email alerts for similar roles

Weekly digest · no password needed · unsubscribe any time

Full Description

ABSTRACT
Hypertension is a major risk factor for cardiovascular (CV) morbidity and mortality. Increased CV risk remains

even if blood pressure (BP) is controlled, suggesting there are additional factors associated with hypertension

(influenced by, but independent of, BP per se), which contribute to adverse CV outcomes. This application

focuses on two potentially interrelated CV pathophysiologic processes: 1) impairment in myocardial oxygen

delivery (manifested as coronary microvascular dysfunction, a known predictor of CV morbidity/mortality) and 2)

impairment in cardiac efficiency (manifested as inefficient coupling of myocardial oxygen consumption and

cardiac work). There are no established treatments for coronary microvascular dysfunction or abnormal

cardiac efficiency—a critical knowledge gap. Individuals with hypertension and left ventricular hypertrophy

(LVH) have coronary microvascular dysfunction and excess mineralocorticoid receptor activity. Our overall

hypothesis is that, in individuals with hypertension and LVH, mineralocorticoid receptor blockade will improve

coronary microvascular function and cardiac efficiency, independent of changes in BP; and these improvements

will lead to improved myocardial structure and function and ultimately to improved CV outcomes.

We propose a randomized, controlled, basic experimental study involving humans. Men and women with

hypertension and LVH on enalapril (angiotensin-converting enzyme (ACE) inhibitor) will be randomized to

treatment for 9 months with eplerenone (mineralocorticoid receptor antagonist) or chlorthalidone (thiazide-like

diuretic) + potassium. We will use cardiac PET/CT to quantify changes in coronary microvascular function (i.e.

myocardial flow reserve - ratio of stress/rest myocardial blood flow) and cardiac efficiency (i.e. myocardial

external efficiency - ratio of myocardial work to oxygen consumption); echocardiography to assess changes in

myocardial structure and function; and 24-hr BP monitoring.

This study will test the hypothesis that, in patients with hypertension and LVH on ACE inhibition,

treatment with mineralocorticoid receptor antagonist, as compared with a thiazide-like diuretic,

improves:

• Coronary microvascular function, i.e., myocardial flow reserve (Specific Aim 1)

• Cardiac efficiency, i.e., myocardial external efficiency (Specific Aim 2)

We anticipate that improvements in these outcomes will associate with improvements in myocardial structure

and function (peak global longitudinal strain, tissue Doppler mitral annular early diastolic relaxation velocity [e’],

and ratio of mitral E velocity to e’ [E/e’]).

Grant Number: 5R01HL162960-03
NIH Institute/Center: NIH

Principal Investigator: Gail Adler

Sign up free to get the apply link, save to pipeline, and set email alerts.

Sign up free →

Agency Plan

7-day free trial

Unlock procurement & grants

Upgrade to access active tenders from World Bank, UNDP, ADB and more — with email alerts and pipeline tracking.

$29.99 / month

  • 🔔Email alerts for new matching tenders
  • 🗂️Track tenders in your pipeline
  • 💰Filter by contract value
  • 📥Export results to CSV
  • 📌Save searches with one click
Start 7-day free trial →