Awardee OrganizationVANDERBILT UNIVERSITY MEDICAL CENTER
Description
Abstract Text
Project Summary
Of people admitted emergently to the Intensive Care Unit (ICU) in respiratory failure or shock, 50% to 70%
develop delirium (by far the highest in any healthcare setting). The duration of this delirium independently
predicts earlier death, longer hospital stay, and higher healthcare expenses annually. Delirium in ICU patients
has been shown to be the strongest potentially modifiable risk factor for development of a long-term cognitive
impairment, which resembles moderate to severe Alzheimer’s Disease and Related Dementias (ADRDs).
Thus, medical and surgical ICU patients on ventilators or in shock are a prime population in whom to study the
relationship between delirium and dementia. Our NIA-funded, NEJM published, and PAR-18-029 cited BRAIN-
ICU-1 study [Bringing to light the Risk factors And Incidence of Neuropsychological dysfunction in ICU
Survivors, 1st Study] showed over that one-third of ICU survivors (without preexisting dementia) emerged with
new cognitive impairments or ADRD at 1 year. Some BRAIN-ICU-1 patients had cognitive resilience against
ADRD, but others developed a persistent or progressive dementia-like illness. We are eager to develop
interventions against this ICU-related dementia, but without knowing more about this form of brain injury, we
are very limited. Now, we have pilot neuroimaging (MRI) data show that acute ICU delirium is associated with
atrophy of the whole brain, frontal lobe, and hippocampus, but this problem requires an in-depth investigation.
We know abnormal brain proteins (amyloid, tau) relate to Alzheimer’s disease, however, we know nearly
nothing about protein pathology or other causes of this ICU-related dementia. It is critical to understand why
ICU survivors are losing their jobs, and the leadership as matriarchs and patriarchs of their families. This
BRAIN-ICU-2 study [Bringing to light the Risk factors And Incidence of Neuropsychological dysfunction
(dementia) in ICU Survivors, 2nd Study] is in direct response to PAR-18-029 and will determine ICU patients’
main paths to decline, maintenance, or recovery of brain function. We will answer gaps in knowledge about
long-term outcome of post-ICU brain disease by following the remaining ICU survivors from the original
BRAIN-ICU-1 study with complete cognitive testing for the first time ever to 14 years (AIM 1). We will consent
and enroll 567 new ICU patients at Vanderbilt and Rush Universities (i.e., new ICU cohort) and determine how
detailed neuroimaging and cerebrospinal fluid samples can help reveal locations and mechanisms of injury
beyond what we learned from the clinical information collected in our original study (AIM 2). Importantly, we
are partnering with the world-renowned Rush Alzheimer's Disease Research Center brain bank program so
that all patients enrolled in Aims 1 and 2 will able to donate their brains to science for the first-ever in-depth
pathological study of those who do and do not get post-ICU dementia to define this disease formally (AIM 3).
Public Health Relevance Statement
Project Narrative
PUBLIC HEALTH RELEVANCE:
Annually around the world, millions of old (and even young) people cared for in Intensive Care Units (ICUs)
suffer through a period of confusion or delirium. These ICU survivors have new life-altering, long-lasting, and
often permanent cognitive impairment, which looks like Alzheimer’s disease and/or related dementias. This
BRAIN-ICU-2 Study [Bringing to light the Risk factors And Incidence of Neuropsychological dysfunction
(dementia) in ICU Survivors, 2nd Study] will define the relationship between ICU delirium and dementia, will
explain this unfortunate and life-changing brain damage in ICU survivors, and will pave the way for preventive
programs, strategic rehabilitation, and targeted future interventions.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AcuteAddressAdmission activityAffectAlzheimer's DiseaseAlzheimer's disease related dementiaAlzheimer's disease riskAmyloidApolipoprotein EAtrophicAutopsyAxonBiological MarkersBrainBrain DiseasesBrain InjuriesCaringCerebrospinal FluidCerebrovascular DisordersCessation of lifeClimactericClinicalCognitiveConfusionConsensusConsentDataDeliriumDementiaDevelopmentDiagnosisDiagnosticDiseaseDrug ExposureEducationEndotheliumEnrollmentFamilyFunctional disorderFundingFutureHMGB1 geneHealthcareHippocampusHistopathologyHospitalsImmobilizationImpaired cognitionIncidenceInfarctionInflammationInjuryIntensive Care UnitsInterventionInvestigationKnowledgeLeadershipLearningLength of StayLifeLinkLocationMagnetic Resonance ImagingMaintenanceMeasuresMediatingMedicalMemoryNerve DegenerationNeurofibrillary TanglesNeuropsychologyOccupationsOutcomePathologicPathologyPathway interactionsPatientsPerfusionPersonsPhenotypePlasmaPlasminogen Activator Inhibitor 1PopulationPreventiveProteinsPublishingQuality of lifeRecoveryRehabilitation therapyResearchRespiratory FailureRiskRisk FactorsSamplingScienceSepsisShockStructureSurgical Intensive CareSurvivorsSynapsesTestingTimeUniversitiesVentilatorWhite Matter DiseaseWorkbrain abnormalitiescerebral atrophyclinical riskcognitive recoverycognitive rehabilitationcognitive reservecognitive testingcohortcomorbidityconfusion assessment methodcostdiagnostic toolexecutive functionfollow-upfrailtyfrontal lobefunctional outcomeshealth care settingsimaging biomarkermicrovascular pathologymodifiable riskmortalityneuroimagingneuroinflammationneuropathologyparticipant enrollmentprogramsprotein TDP-43public health relevancerepositoryresilienceresponsesecondary analysissurvivorshiptau Proteinsvascular injurywhite matter
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