Sex-Specific Genetic Drivers of Alzheimer's Disease Neuropathology
Sex-Specific Genetic Drivers of Alzheimer's Disease Neuropathology
批准号:
9766995
负责人:
Timothy J Hohman
金额:
$19.75万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-09-01 至 2021-05-31
关键词:
AffectAgeAlzheimer&aposs DiseaseAlzheimer’s disease biomarkerAmyloidAmyloidosisAutopsyBiological MarkersBrainCandidate Disease GeneCase-Control StudiesCessation of lifeClinicalCognitionCouplingDataData SetDevelopmentDiseaseFemaleFoundationsFutureGene ExpressionGenesGeneticGenetic DiseasesGenetic MarkersGenetic VariationGenomicsGoalsImpaired cognitionIndividualInflammatoryInjuryInternationalLate Onset Alzheimer DiseaseMeasuresMemoryModelingNerve DegenerationNeurobehavioral ManifestationsNeurofibrillary TanglesNeurologyOutcomePathologyPathway interactionsPerformancePhenotypePopulationProcessProteomicsPublic HealthResearchRiskSeveritiesSex DifferencesSymptomsTREM2 geneUnited StatesWidthWomanX Chromosomebasecase controlcognitive performancecohorteffective interventionendophenotypegenetic architecturegenetic associationgenome wide association studyhippocampal atrophyin vivoinnovationmalemenmental statemetabolomicsneuropathologynovelpersonalized interventionrare variantsecondary analysissextau Proteinstherapeutic target
中文摘要
点击翻译按钮获取中文摘要
英文摘要
As the population ages, late-onset Alzheimer's disease (AD) is becoming an increasingly important public
health issue. AD disproportionately affects women. Of the more than 5 million people in the United States
afflicted with this disease, two-thirds are women. Women with AD have more neuropathology than men with
AD, have more severe cognitive symptoms, and more severe neurodegeneration, suggesting that the disease
affects male and female brains in different ways. Thus, a focus on sex differences in AD is essential to move
the field towards effective interventions. The identification of sex-specific genetic drivers of AD neuropathology
and cognitive decline could transform the way treatments are administered, and be a critical step towards
personalized interventions for AD. Research from both our group and others has begun to uncover genetic
factors that explain some of the observed discrepancies between males and females, specifically in terms of
neuropathology and cognitive decline. To advance the field, additional genetic effects must be discovered and
the underlying mechanisms of sex-specific pathways of injury must be examined. The objective of this project
is to identify and replicate genetic effects that act in a sex-specific manner to drive the neuropathological
presentation and clinical progression of AD. The present proposal will advance our understanding of sex-
specific genetic contributors to AD by leveraging 8 existing in vivo biomarker cohorts (n=3,433) and 6 existing
autopsy cohorts (n=4,821) to assess genetic associations with AD neuropathology and cognitive decline. The
outcome of this project will highlight new candidate pathways, and begin the process of characterizing the
mechanisms by which genetic variation among males and females affects the risk and clinical symptoms of
AD. The sex-specific pathways identified will offer therapeutic targets and help move the field towards
personalized interventions that consider an individual's sex and neuropathological presentation.
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Biomarker Core
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Neuroprotective Effects of Vascular Endothelial Growth Factor in Alzheimer's Disease
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Neuroprotective Effects of Vascular Endothelial Growth Factor in Alzheimer's Disease
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资助金额:$80.8万
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财政年份:2019
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Neuroprotective Effects of Vascular Endothelial Growth Factor in Alzheimer's Disease
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批准号:9883697
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财政年份:2019
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批准号:10431862
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Genetic Drivers of Resilience to Alzheimer's Disease
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批准号:9577410
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资助金额:$84.69万
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项目类别:
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财政年份:2016
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依托单位:
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