Is Obstructive Sleep Apnea Important in the Development of Alzheimer's Disease
Is Obstructive Sleep Apnea Important in the Development of Alzheimer's Disease
批准号:
9974144
负责人:
Atul Malhotra
金额:
$72.64万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
未结题
起止时间:
2020-06-01 至 2025-04-30
关键词:
AcetazolamideAdherenceAffectAgingAirAlzheimer&aposs DiseaseAlzheimer&aposs disease patientAlzheimer&aposs disease riskAmyloidAnatomyApneaArousalBrainBrain imagingBreathingCaringClinicalClinical ResearchClinical TrialsCombined Modality TherapyComplexDataDepositionDevelopmentDilatorDiseaseElderlyFrequenciesFunctional disorderFutureGeneticGenetic MarkersGenetic Predisposition to DiseaseHippocampus (Brain)HypoxiaImageImpairmentIndividualInterventionLinkMRI ScansMedialMemoryMemory impairmentMethodsModelingMolecularMultiple AbnormalitiesMuscleNeurocognitiveNeuropsychologyObstructive Sleep ApneaOutcomeOxidative StressOxygenOxygen Therapy CarePathogenesisPatientsPatternPharmaceutical PreparationsPopulationPositron-Emission TomographyPrevalencePrevention trialPublicationsPublishingQuality of lifeRiskRisk FactorsRoleSeveritiesSleepSleep Apnea SyndromesSleep FragmentationsSleep disturbancesStructureSubgroupSuggestionSymptomsTechniquesTherapeuticTimeWorkapolipoprotein E-4basebrain dysfunctioncomparative effectiveness trialdesigndisorder riskepidemiologic dataepidemiology studyexperimental studyhigh riskhippocampal atrophyimprovedindexinginsightmemory consolidationminimally invasiveneuroimagingnovelnovel therapeutic interventionnovel therapeuticsolder patientpre-clinicalpre-clinical therapypredicting responsepressurepreventprimary outcomerandomized trialrecruitrespiratoryresponsetau Proteinstheoriestherapeutic target
中文摘要
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英文摘要
Project Abstract
Aging is a known risk factor for the development of obstructive sleep apnea (OSA), although the underlying
mechanisms are only recently being understood. OSA is associated with Alzheimer’s disease in
epidemiological studies as well as having common genetic links. A number of mechanisms have been
proposed including oxidative stress and amyloid and tau deposition which may contribute to the observed link.
Recent prominent publications have hi-lighted the potential impact of sleep disruption on Alzheimer’s risk. We
have clearly observed impairment in sleep-dependent memory consolidation even with mild OSA and have
developed robust methods to assess these outcomes in a rigorous manner. Recent evidence suggests that
OSA in older individuals may be a somewhat different disease than OSA in younger individuals, based on
relatively unique underlying mechanisms. We have recently published and validated techniques allowing the
assessment of the pathophysiology underlying OSA using minimally invasive methods making disease
endotyping clinically accessible. We have also recently found subgroups of OSA patients who respond well to
oxygen and can be predicted based on the underlying pathophysiology of OSA. We plan to study and further
validate our model by assessing the impact of oxygen therapy in OSA patients who are at risk of developing
Alzheimer’s disease. We have a robust panel of neurocognitive outcomes and have exciting preliminary data
showing reversibility of some of the observed impairment in hippocampal memory. Moreover we are now
working with expert imaging and neuropsychology collaborators who will help us define robust outcome metrics
using MRI and PET scanning (e.g. volumetric analyses, amyloid, tau). Ultimately we hope that this application
will lay the groundwork for a mechanistic comparative effectiveness trial whereby we can compare oxygen with
standard therapy for select OSA patients in an effort to prevent the development of Alzheimer’s disease.
Regardless of the results of the proposed work however we will gain major insights into the mechanisms and
optimal care of elderly people with OSA.
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海外基金