课题基金 / 基金详情

Macronutrients, Mitochondria and Blood Metabolome/Proteome Disease Risk Profiles

Macronutrients, Mitochondria and Blood Metabolome/Proteome Disease Risk Profiles
常量营养素、线粒体和血液代谢组/蛋白质组疾病风险概况
批准号:
7337718
负责人:
BRUCE S KRISTAL
金额:
$45.76万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-15 至 2011-05-31
关键词:
AdherenceAffectAgeAlgorithmsAnimal FeedAnimalsAppendixArchivesAssesBindingBiochemicalBiochemistryBioinformaticsBiologicalBiological MarkersBiomarker of Dietary IntakeBloodBody TemperatureCalciumCaloric RestrictionCarbohydratesCatabolismCell DeathCholecystokininClassificationCluster AnalysisColorComputersConditionCorticosteroneCoupledDataDatabasesDehydroepiandrosterone SulfateDetectionDevelopmentDiabetes MellitusDietDiet RecordsDiseaseDropsDrug Metabolic DetoxicationEarly InterventionEatingElectrodesElectronicsElectrophoresisEnergy IntakeEnvironmentEpidemiologic StudiesEquilibriumExpert SystemsFatty AcidsFatty acid glycerol estersFemaleFoodFractionationFree RadicalsFunctional disorderFundingFutureGene ChipsGeneral PopulationGenerationsGenesGlucoseGlutathione DisulfideGlycemic IndexGoalsGoldGrantGrowthGuineaHealthHigh Pressure Liquid ChromatographyHormonalHormonesHumanIncidenceIndividualInsulinIntakeInterventionIonsKnowledgeLaboratoriesLeadLearningLeftLifeLinkLiver MitochondriaLogicLongevityMacronutrients NutritionMalignant NeoplasmsMammalsMass Spectrum AnalysisMeasurableMeasurementMeasuresMessenger RNAMetabolicMetabolic PathwayMetabolismMethodologyMethodsMineralsMiningMitochondriaModelingMolecular ProfilingMolecular WeightMorbidity - disease rateMusNatureNerve DegenerationNested Case-Control StudyNon-Insulin-Dependent Diabetes MellitusNormal Horse SerumNurses&apos Health StudyNutrientObesityOxidation-ReductionParticipantPatternPattern RecognitionPhysiologicalPhysiological ProcessesPhysiologyPlaguePlasmaPopulationPrincipal Component AnalysisPrincipal InvestigatorProductionPropertyProtein MicrochipsProteinsProteomeProteomicsProtocols documentationPubMedPurinesRangeRattusReactive Oxygen SpeciesReadingRelative (related person)Relative RisksResearch PersonnelResistanceResolutionResourcesRespirationRiskRodentRoleRotationSamplingSchemeSerotypingSerumSerum ProteinsSignal TransductionSocietiesStagingStandards of Weights and MeasuresState InterestsStatistically SignificantSystemTechniquesTechnologyTestingTextbooksThioctic AcidTimeTocopherolsTrainingTreatment ProtocolsTryptophan Metabolism PathwayTyrosineUnited States National Institutes of HealthValidationVariantVitaminsWaterWorkage relatedascorbatebasecancer typecase controlcohortcompound 20conceptcostdaydetectordietary constituentdihydrolipoic aciddisorder riskenvironmental stressorfeedinggene environment interactionglucose metabolismhigh schoolhuman diseasehuman studyinnovationinterestmalemalignant breast neoplasmmetabolomicsmortalitynanonew technologynonhuman primateoxidationpreventprogramsprotein metabolitepurinereproductive hormoneresponsescale upsensorsizesmall moleculesuccesstool

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DESCRIPTION (provided by applicant): Links between diet and human disease, and between reactive species and disease, are so commonly considered as to lie in the realm of textbooks and the popular press. Links between mitochondria and energy production are generally appreciated by junior high school. Links between mitochondria and calcium (including signaling), free radicals, or cell death may be less known to the general public, but each has in excess of 10,000 PubMed citations. However, despite broad and strong theoretical considerations supporting casual connections between diet effects on mitochondria and diet effects on disease - and some specific experimental support - there are, to our knowledge, no systematic studies that bridge this fundamental gap. Bridging this gap is central to understanding environment-gene interactions, as suboptimal dietary macronutrient choices are arguably the major environmental stressor in individuals living in Western societies. We therefore propose to bridge this gap using an interdisciplinary, product-development approach to discover and confirm innovative plasma metabolomic and proteomic biomarkers for dietary intake of subclasses of fats and carbohydrates, and for their effects on mitochondrial (dys)function. We will then validate these markers by using them to test the hypothesis that diet-associated effects on mitochondria are linked to diet-associated changes in disease risk. Five Aims are proposed. Aim 1 To determine the effects of dietary changes in fatty acid and carbohydrate composition on mitochondrial physiology Aim 2 To determine the effects of dietary changes in fatty acid and carbohydrate composition on the plasma metabolome and proteome Aims 3 and 4: To determine the extent to which adherence to/presence of each diet, dietary constituent, and mitochondrial property predict type II diabetes (Aim 3) and breast cancer (Aim 4) in previously profiled case control studies nested within the Nurses' Health Study Aim 5: To provide an electronic archive of the metabolomic and proteomic constituents of the blood of participants that could be repeatedly mined for future testing of new hypotheses. The proposed studies are directly responsive to the RFA and further general NIH goals of focusing on health and early interventions rather than late stage disease.
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Lipidomics Biomarkers Link Sleep Restriction to Adiposity Phenotype, Diabetes, and Cardiovascular Risk
  • 批准号:
    10212442
  • 项目类别:
  • 资助金额:
    $85.07万
  • 财政年份:
    2018
  • 负责人:
    BRUCE S KRISTAL
  • 依托单位:
Lipidomics Biomarkers Link Sleep Restriction to Adiposity Phenotype, Diabetes, and Cardiovascular Risk
  • 批准号:
    9981539
  • 项目类别:
  • 资助金额:
    $85.65万
  • 财政年份:
    2018
  • 负责人:
    BRUCE S KRISTAL
  • 依托单位:
Circadian Lipidomics in Constant Routine, Forced Desynchrony, and Non-lab Setting
  • 批准号:
    9083622
  • 项目类别:
  • 资助金额:
    $84.9万
  • 财政年份:
    2016
  • 负责人:
    BRUCE S KRISTAL
  • 依托单位:
Circadian Lipidomics in Constant Routine, Forced Desynchrony, and Non-lab Setting
  • 批准号:
    9264015
  • 项目类别:
  • 资助金额:
    $87.73万
  • 财政年份:
    2016
  • 负责人:
    BRUCE S KRISTAL
  • 依托单位:
海外基金