grant

Gut microbiome intervention in preclinical and clinical Alzheimer's disease

Organization UNIVERSITY OF WISCONSIN-MADISONLocation MADISON, UNITED STATESPosted 15 May 2025Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY2026AD and related dementiaAD dementiaAD pathologyAD related dementiaADRDAdherenceAdverse ExperienceAdverse eventAlzheimer Type DementiaAlzheimer disease dementiaAlzheimer sclerosisAlzheimer syndromeAlzheimer'sAlzheimer's DiseaseAlzheimer's Disease and its related dementiasAlzheimer's and related dementiasAlzheimer's dementia and related dementiaAlzheimer's dementia or related dementiaAlzheimer's disease and related dementiaAlzheimer's disease and related disordersAlzheimer's disease and related forms of dementiaAlzheimer's disease or a related dementiaAlzheimer's disease or a related disorderAlzheimer's disease or related dementiaAlzheimer's disease pathologyAlzheimer's disease related dementiaAlzheimer's disease testAlzheimer's pathologyAlzheimer's testAlzheimers DementiaAmentiaAmyloidAmyloid SubstanceAnimalsAstroproteinAβ burdenBacterial GenesBile AcidsBiological MarkersBlood PlasmaBrainBrain Nervous SystemBrain PathologyCapsulesCell Communication and SignalingCell SignalingClinicalClinical TrialsCognitiveCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive function abnormalCustomDataDementiaDisease OutcomeDisturbance in cognitionDouble-blind trialEncephalonFatty Acid Metabolism PathwayFecesFormulationFunctional MetagenomicsFutureGFA-ProteinGFAPGI microbiomeGI microbiotaGastrointestinal microbiotaGlial Fibrillary Acid ProteinGlial Fibrillary Acidic ProteinGlial Intermediate Filament ProteinGut Epithelial PermeabilityGut HyperpermeabilityGut permeabilityHumanImmunologyImpaired cognitionIndividualInfrastructureInterventionIntestinal Epithelial PermeabilityIntestinal HyperpermeabilityIntestinal permeabilityIntracellular Communication and SignalingLightLinkLiquid substanceMeasuresMetagenomicsMicrobiologyModern ManNerve DegenerationNeuron DegenerationOutcomeParticipantPathologyPersonsPhotoradiationPlacebosPlasmaPlasma SerumPrimary Senile Degenerative DementiaProbioticsProceduresProductionProteinsRandomizedResearchReticuloendothelial System, Serum, PlasmaRiskSamplingSham TreatmentShort-Chain Fatty AcidsSignal TransductionSignal Transduction SystemsSignalingTestingTranslatingTranslational ResearchTranslational ScienceVolatile Fatty AcidsWisconsina-beta burdenabeta burdenamyloid burdenbeta amyloid burdenbile acid metabolismbile metabolismbio-markersbiologic markerbiological signal transductionbiomarkerbowel inflammationcapsulecognitive assessmentcognitive dysfunctioncognitive functioncognitive losscognitive testingcustomsdesigndesigningdigestive tract microbiomedouble-blind placebo control trialdouble-blind placebo controlled trialdouble-masked controlled trialenteric microbial communityenteric microbiomeenteric microbiotafatty acid metabolismfecal samplefluidgastrointestinalgastrointestinal microbial floragastrointestinal microbiomeglial activationglial cell activationgut communitygut floragut inflammationgut microbe communitygut microbial communitygut microbial compositiongut microbial consortiagut microbiomegut microbiotagut microbioticgut microfloragut-associated microbiomeindividual heterogeneityindividual variabilityindividual variationinflamed bowelinflamed gutinflamed intestineintestinal biomeintestinal floraintestinal inflammationintestinal microbiomeintestinal microbiotaintestinal microfloraintestinal tract microfloraliquidmicrobial consortiamicrobial floramicrobiome community compositionmicrobiome compositionmicrobiome interventionmicrobiome species compositionmicrobiome structuremicrobiome therapeuticsmicrobiome therapymicrobiome treatmentmicrobiome-based interventionmicrobiome-based therapeuticmicrobiome-based therapymicrobiome-based treatmentmicrobiotamicrofloramultispecies consortianeural degenerationneurodegenerationneurodegenerativeneurofilamentneurological degenerationneuronal degenerationnovelparticipant enrollmentpatient enrollmentpre-clinicalpreclinicalprimary degenerative dementiaprobiotic supplementprobiotic supplementationprogramspublic health relevancerandomisationrandomizationrandomly assignedrecruitsafety and feasibilitysafety testingsecondary outcomesenile dementia of the Alzheimer typesham therapystoolstool samplestool specimensupplementation with probioticstest for Alzheimertranslation researchtranslational investigationβ-amyloid burdenβamyloid burden
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Full Description

ABSTRACT__________________________________________________________________
Evidence from our research group and others suggests that the gut microbiome plays a role in Alzheimer’s

disease (AD), but few studies have tested the impact of gut microbiome modulation in AD. Here we propose to

test the safety and feasibility of a custom probiotic intervention among people with AD dementia and preclinical

AD, test secondary outcomes to prepare for a future clinical trial, and explore potential mechanisms by which

gut microbiome modulation impacts the brain in AD. We will achieve this by enrolling participants from the

Wisconsin Alzheimer’s Disease Research Center to participate in a randomized double-blind trial of a custom

probiotic formulation. Half of the participants will be randomized to probiotic supplementation, and half will be

randomized to placebo. The study will include participants with mild AD dementia and participants with preclinical

AD (cognitively unimpaired and amyloid positive). Participants will undergo the probiotic intervention or placebo

for 24 weeks and be evaluated at baseline, week 12, week 24, week 36, and 1 year. In addition to safety and

feasibility, we will evaluate secondary outcomes to prepare for a future clinical trial. We will assess cognitive

function and plasma biomarkers before, during, and after the intervention, as well as collect stool samples over

the course of the study. We will begin to assess leading mechanisms by which the gut may impact the brain to

prepare for a future trial, including impacts on gut inflammation and intestinal permeability, and modulation of

bile acid metabolism. We hypothesize that the probiotic intervention will be safe and feasible, and will modulate

the composition and activity of gut microbiota, impacting bile acid metabolism, intestinal permeability and AD

outcomes. Very little is yet known about the utility of probiotic interventions in the context of AD, which is critical

for advancing the gut microbiome field toward novel interventions for AD. There is a significant need to ensure

that research on gut microbiome and AD benefits individuals with dementia and those at risk for cognitive decline.

Successful completion of the proposed aims is expected to inform the participant selection, design, and

endpoints of subsequent clinical trials, and inform upon the link between gut and brain in the context of AD.

Grant Number: 5R61AG088913-02
NIH Institute/Center: NIH

Principal Investigator: Barbara Bendlin

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