NFkb Related Genetic Influences on Inflammation and Poor Health in Older Adults
NFkb Related Genetic Influences on Inflammation and Poor Health in Older Adults
批准号:
7672250
负责人:
Jeremy D Walston
金额:
$42.66万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-01 至 2011-08-31
关键词:
AdherenceAgeAgingAmericanBiologyCandidate Disease GeneCardiovascular systemCase-Control StudiesClinicalCodeCohort StudiesComplement 4bDataData SetDevelopmentElderlyExhibitsFundingGenesGeneticGenetic PolymorphismGenetic VariationGenotypeGoalsHaplotypesHealthHealthcareIndividualInflammationInflammation MediatorsInflammatoryInfluentialsInterventionKnowledgeLabelMeasurementMeasuresMediator of activation proteinModelingNF-kappa BOutcomeParticipantPathway interactionsPhenotypePopulationPopulation StudyProcessProteinsRegulationResearch PersonnelRiskSerumSignal TransductionSignal Transduction PathwaySpecificitySumTestingUniversitiesValidationVariantage relatedcytokinedisabilityfrailtyfunctional declinegenetic analysisgenetic associationindexingmortalitymultidisciplinaryprogramstheories
中文摘要
描述(申请人提供):这项研究的长期目标是确定与炎症相关的基因和生物途径,这些基因和生物途径影响老年人功能的迅速下降,并影响虚弱和死亡率。促炎蛋白NFkB的不适当激活在这一过程中起着重要的门户作用。我们已经确定了一组与NFkB相关的炎性介质,它们预测了不良的健康结果。我们假设这一组细胞因子代表一种促炎表型,并且触发或传播NFkB活性的基因变异有助于促炎状态,从而在一些老年人中观察到较差的健康状况。我们建议在这里进一步提炼基安蒂红酒老年人群中的炎症表型,随后进行验证步骤,在此步骤中,我们将测量心血管健康研究存储的血清中导致此表型的最重要因素,并确定这些标记物是否与同样糟糕的健康结果相关。然后,我们将在CHS参与者的病例对照研究中确定NFkB相关候选基因中潜在有意义的基因变异,并确定这些多态中的任何一个或这些多态的组合是否会影响炎症和不良的健康结局。最后,我们将挑选在CHS研究中确定的最有影响力的候选基因,并在整个CHS人群和基安蒂红酒中测试它们,并确定这些基因是否可以预测同样糟糕的医疗结果。具有临床意义的基因分型将突出潜在的生物途径,用于干预一系列老年人的不良健康结果。
英文摘要
DESCRIPTION (provided by applicant): The long-term goal of this study is to identify genes and biologic pathways related to inflammation that influence the rapid decline in function and influence frailty and mortality in a subset of older adults. Inappropriate activation of the pro-inflammatory protein NFkB acts as an important gateway in this process. We have identified a cluster of inflammatory mediators that are related to NFkB and that predict poor health outcomes. We hypothesize that this cluster of cytokines represents a pro-inflammatory phenotype, and that variation in genes that trigger or propagate NFkB activity contributes to the pro-inflammatory state and hence to the poor health comes observed in some older adults. We propose here to further refine the inflammatory phenotype in the In Chianti population of older adults, followed by a validation step in which we will measure the most important contributors to this phenotype in stored serum from the Cardiovascular Health Study and determine if these markers are related to the same poor health outcomes. We will then identify potentially meaningful gene variants within NFkB related candidate genes in a case control study of CHS participants, and determine if any of these polymorphisms, or combination of these polymorphisms influence inflammation and poor health outcomes. Finally, we will pick the most influential candidate genes determined in the CHS study, and test them in the entire CHS population and in In CHIANTI and determine if these genes are predictive of the same poor health care outcomes. Clinically meaningful genotypes will highlight potential biologic pathways for interventions into a range of poor health outcomes in older adults.
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Development of a Mouse Model for Frailty
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NFkb Related Genetic Influences on Inflammation and Poor Health in Older Adults
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NFkb Related Genetic Influences on Inflammation and Poor Health in Older Adults
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依托单位:
NFkb Related Genetic Influences Inflammation Poor Health
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项目类别:
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依托单位:
NFkb Related Genetic Influences on Inflammation and Poor Health in Older Adults
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