grant

Pre-diagnosis Biomarker Discovery for Age-Related Macular Degeneration

Organization ICAHN SCHOOL OF MEDICINE AT MOUNT SINAILocation NEW YORK, UNITED STATESPosted 1 Jan 2024Deadline 31 Dec 2026
NIHUS FederalResearch GrantFY2025AffectAgeAge related macular degenerationAge-Related MaculopathyAreaAtrophic AMDAtrophic age-related macular degenerationAwardBiological MarkersBloodBlood DonationsBlood PlasmaBlood Reticuloendothelial SystemBlood SampleBlood specimenClinicalClinical EvaluationClinical TestingColor VisionsDNADeoxyribonucleic AcidDeveloped CountriesDevelopmentDiagnosisDiagnosticDiminished VisionDisciform macular degenerationDisciform senile macular retinal degenerationDiseaseDisorderDry AMDDrynessElderlyElectronic Health RecordEnvironmental FactorEnvironmental Risk FactorExclusionExudative AMDExudative age-related macular degenerationFTIRFTIR spectroscopyFingerprintFundingGeneticGenetic predisposing factorGenetic studyGenotypeGoalsIncidenceIndividualIndustrialized CountriesIndustrialized NationsIntelligenceInterventionInvestigatorsLaboratoriesLife StyleLifestyleLinkLongitudinal StudiesLow VisionMeasuresMethodsNational Institutes of HealthNeovascular AMDNeovascular age-related macular degenerationNon-exudative age-related macular degenerationNonexudative age-related macular degenerationPOAGPartial SightPatientsPersonsPhasePlasmaPlasma ProteinsPlasma SerumPredisposing FactorPrevalencePreventative strategyPreventative therapyPreventionPrevention strategyPreventive strategyPreventive therapyPrimary Open Angle GlaucomaProteinsProteomicsPublishingReduced VisionReportingResearch DesignResearch PersonnelResearchersReticuloendothelial System, Serum, PlasmaRetinal DegenerationSamplingSpectroscopy, Fourier Transform InfraredStudy TypeSubjects SelectionsSubnormal VisionUnited StatesUnited States National Institutes of HealthVEGFVEGFsVascular Endothelial Growth FactorsVisual AcuityVisual impairmentWet AMDadvanced ageage associated biomarkersage associated markerage dependent macular degenerationage induced macular degenerationage markerage related biomarkersage related macular diseaseage related macular dystrophyage related markersagesaging preventionanti aginganti geronicantiagingaptamerbio-markersbiobankbiologic markerbiological markers of agebiomarkerbiomarker discoverybiomarkers of agebiorepositorychemical bondclinical testcostdata acquisitiondata acquisitionsdegenerative retina diseasesdepositorydeveloped countrydeveloped nationdeveloped nationsdevelopmentaldiagnostic biomarkerdiagnostic markerdiet supplementdietary supplementsdisease preventiondisorder preventiondry age-related macular degenerationeffective interventionelectronic health care recordelectronic health medical recordelectronic health plan recordelectronic health registryelectronic medical health recordemission spectraemission spectrumenvironmental riskgenetic informationgenetic risk factorgeographic atrophygeriatrichigh rewardhigh riskinherited factorinnovateinnovationinnovativelong-term studylongitudinal outcome studiesmaculamacularmedical collegemedical schoolsmultiplex assaynutritional supplementoptical spectraoptical spectrumpredictive biological markerpredictive biomarkerspredictive markerpredictive molecular biomarkerprevent age relatedprevent agingrepositoryresearch clinical testingretina degenerationretinal degenerativeretinal degenerative diseasesschool of medicinesenile macular diseasesenior citizenstudy designsuccesssuppress agingvision impairmentvisually impairedwet form of AMD
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Full Description

The goal of the project is to identify pre-diagnosis plasma biomarkers for AMD, i.e., markers that can be
measured in plasma samples from healthy donors and may predict which donors will get AMD in the following

years. We will use approx.150 plasma samples collected and stored at the Biome MSSM Biorepository, from

healthy, non-AMD donors, which eventually became diagnosed with AMD 2-8 years after the blood donation.

These samples will be compared to samples from donors that did not develop AMD after a similar number of

years. We will use two strategies. The first strategy (Aim 1) consists of analyzing the protein composition of

plasma samples using the SOMAscan platform, which allows quantitation of approx. 7000 proteins. In addition,

we will investigate whether pre-diagnostic differences exist in the optical spectra generated by Fourier Transform

Infrared (FTIR) spectroscopy. Aim 2 is based on the hypothesis that some post-diagnostic biomarkers, shown

by published studies to robustly differentiate healthy donors from AMD patients, reflect differences that pre-exist

years before the donors are diagnosed. We will investigate, using the BioMe plasma samples, whether the

differences exist years before the disease develops. As most BioMe donors have been fully genotyped, genetic

information will be also included in the effort to find pre-diagnostic biomarkers. Regarding the potential impact of

the study, a large-scale effort is underway for years to find dietary supplements and other agents that could

prevent AMD. Such studies involve administration for years of supplements to relatively large numbers of

subjects that do not have yet AMD and waiting for years to determine if the proportion of persons that develop

the disease is reduced. Development of predictive biomarkers could enormously simplify such efforts, by

assessing the immediate effect of the supplements on the biomarkers. At the level of individual subjects, if

protective interventions are found, the pre-diagnostic markers will help detect the persons for which the

interventions are necessary.

Grant Number: 5R21EY035793-02
NIH Institute/Center: NIH

Principal Investigator: Timothy Blenkinsop

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