grant

Kidney Injury in Patients with Acute Decompensated Heart Failure

Organization UNIVERSITY OF WASHINGTONLocation SEATTLE, UNITED STATESPosted 1 Jul 2020Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY202427E10 AntigenAcuteAddressAdmissionAdmission activityAffectAlgorithmsAngiotensinogenBlood SerumBody Weight ChangesCalcium-Binding Myeloid Protein P8,14CalgranulinCalprotectinCardiacCardiac Failure CongestiveClinicalClinical TrialsComplexCongestive Heart FailureCreatinineCritical IllnessCritically IllDataDysfunctionEFRACEchocardiogramEchocardiographyEjection FractionEndotheliumEventFABP1FABP1 geneFABPLFoundationsFunctional disorderFutureGlomerular Filtration RateGoalsGuidelinesHealth StatusHeart DecompensationHeart failureHospital AdmissionHospitalizationHospitalsHypertensinogenIFN-Gamma-Inducing Factor GeneIFN-gamma-Inducing FactorIGFBP-7IGFBP-rP1IGIFIGIF GeneIL-1 GammaIL-1 Gamma GeneIL-18IL-18 GeneIL-1gIL-1g GeneIL18IL18 ProteinIL18 geneIL1F4IL1F4 GeneInflammationInjuryInjury to KidneyInterferon-Gamma-Inducing Factor GeneInterferon-gamma-Inducing FactorInterleukin 18 (Interferon-Gamma-Inducing Factor)Interleukin 18 (Interferon-Gamma-Inducing Factor) GeneInterleukin 18 ProproteinInterleukin 18 Proprotein GeneInterleukin-1 GammaInterleukin-1 Gamma GeneInterleukin-18Interleukin-18 PrecursorInterleukin-18 Precursor GeneInvestigationKidneyKidney Urinary SystemKnowledgeL-FABPL1 AntigenLCN2LCN2 geneLength of StayLeukocyte L1 Antigen ComplexLeukocyte L1 ProteinLevel of HealthLipocalin 2LiteratureMGC12320MGC12320 GeneMeasurementMeasuresMechanicsMigratory Inhibitory Factor-Related Protein MRPMyelomonocytic Antigen L1NGALNeutrophil Gelatinase-Associated LipocalinNumber of Days in HospitalOncogenic Lipocalin 24P3OutcomeOxidative StressPatient AdmissionPatientsPhysiopathologyPopulationProangiotensinPrognosisProspective StudiesPublic HealthRecurrenceRecurrentRenal functionRenin-SubstrateReportingRiskRoleSentinelSerumSeveritiesStandardizationStressSymptomsTestingTitrationsTransthoracic EchocardiographyTreatment FailureTreatment ProtocolsTreatment RegimenTreatment ScheduleTubularTubular formationUniversitiesUterocalinWashingtonWeight ChangeWithdrawalWorkacute carecardiac failurechronic heart failureclinical prognosisevidence basehealth levelheart sonographyhemodynamicshigh riskhospital dayshospital length of stayhospital stayimprovedimproved outcomeinjuriesinjury and repairinsulin like-growth factor binding protein-7insulin-like growth factor binding protein-related protein 1ischemia injuryischemic injurykidney functionkidney injurykidney repairmechanicmechanicalnovelpathophysiologypreservationprognosticpublic health prioritiesrecruitrenalrenal injuryresponsesocial roletherapy failuretreatment strategy
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
Hospitalization for acute decompensated heart failure (ADHF) is a significant public health issue and

represents a sentinel prognostic event, with high risk of poor clinical outcomes during and after the

hospitalization. Investigation to improve the care of ADHF patients is a public health priority. The kidneys

have a central role in the acute management and prognosis of ADHF. Kidney injury is highly prevalent in

ADHF and is the culmination of hemodynamic alterations, neurohormonal dysregulation, and oxidative stress

which cause intra-kidney endothelial damage, inflammation and ischemic injury. Kidney injury is also a key

component in decisions of initiation and withdrawal of standard AHDF therapies, which ultimately affects

clinical prognosis of ADHF. However, systematic measurement and consideration of kidney injury is not

incorporated into algorithms of ADHF therapies, likely due to limitations of current clinically available kidney

injury measures. Serum creatinine has traditionally been used to define kidney injury in ADHF, however rises

late and is slow to change in response to ongoing kidney injury or repair; which limits its use in dynamic

conditions such as ADHF. Studies have shown that serum creatinine is not associated with systemic

decongestion or with short-term prognosis in ADHF. Thus, current ADHF guidelines do not endorse serial

measures of serum creatinine. The goal of this proposal is to identify novel kidney injury markers that can

guide therapy and better determine prognosis in ADHF; thereby improve in-hospital and long-term outcomes.

To address this knowledge gap, we propose to conduct a large, prospective study of ADHF patients to

determine: (1) if systematic, serial measurements of novel kidney injury markers change in response to a

standardized, evidence-based ADHF treatment protocol; (2) and whether these changes are associated with

patient-reported, in-hospital and long-term outcomes. Based on previous literature, we have chosen to study a

panel of novel kidney injury measures of endothelial injury, inflammation, tubular stress/damage which may

better reflect intra-kidney pathophysiology, and may be more dynamic to reflect kidney injury/repair compared

with serum creatinine. These novel kidney injury measures are poised to be clinically available in the near

future, however are not well studied in ADHF. To support our hypothesis, we conducted a pilot prospective

study of 62 patients admitted with ADHF and found that novel kidney injury measures demonstrated greater

relative change in response to standardized ADHF therapies and correlated well with systemic congestion;

while serum creatinine was relatively static and correlated poorly with systemic congestion. This

promising pilot data supports the scientific rationale and feasibility of the proposed work. The data

from this study will be used to identify the most promising kidney injury markers in ADHF patients and may be

the foundation of future mechanistic studies or a clinical trial to test an ADHF treatment strategy guided by

novel kidney injury markers.

Grant Number: 5R01DK121800-05
NIH Institute/Center: NIH

Principal Investigator: Nisha Bansal

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 →