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:
8121771
负责人:
BRUCE S KRISTAL
金额:
$16.18万
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 2012-05-31
关键词:
AdherenceAffectAntioxidantsArchivesAreaBindingBiochemicalBioinformaticsBiological MarkersBiomarker of Dietary IntakeBloodBody TemperatureCalciumCalcium SignalingCaloric RestrictionCarbohydratesCardiovascular systemCell DeathCerebrovascular DisordersChronicChronic DiseaseComputational algorithmConsumptionCoupledDataDegenerative DisorderDehydroepiandrosterone SulfateDetectionDiabetes MellitusDietDiet RecordsDiseaseEarly treatmentElectrodesElectron TransportElectronicsEpidemiologic StudiesEpidemiologyExpert SystemsFatty AcidsFatty acid glycerol estersFree RadicalsFundingFutureGeneral PopulationGenerationsGlycemic IndexGoalsGrantGrowthHealthHigh Pressure Liquid ChromatographyHumanIndividualInflammationInsulinInterventionIonsKnowledgeLeadLifeLinkLipidsLiteratureLiver MitochondriaLongevityMacronutrients NutritionMeasuresMetabolicMetabolic syndromeMetabolismMethodologyMethodsMiningMitochondriaNeoplasmsNested Case-Control StudyNon-Insulin-Dependent Diabetes MellitusNurses&apos Health StudyNutrientOxidantsOxidation-ReductionParticipantPathogenesisPattern RecognitionPhysiologicalPhysiologyPlasmaPopulationPopulation StudyPrincipal Component AnalysisProductionPropertyProteomeProteomicsPubMedRattusRecyclingRelative RisksRespirationRespiratory ChainRodentRoleSamplingSerotypingSerumSignal TransductionSocietiesStagingTestingTextbooksTrainingUnited States National Institutes of HealthVariantWorkbasecase controlcostdetectordietary constituentdisorder riskenvironmental stressorgene environment interactionhuman diseaseinnovationjunior high schoolmalemalignant breast neoplasmmetabolomicsmitochondrial dysfunctionproduct developmentsaturated fatsmall moleculetheoriestooltranscription factor

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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.
期刊论文(9)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1021/ac201195d
发表时间: 2011-09-01
期刊: ANALYTICAL CHEMISTRY
影响因子: 7.4
作者: [Bird, Susan S., Marur, Vasant R., Sniatynski, Matthew J., Greenberg, Heather K., Kristal, Bruce S.]
通讯作者: Kristal, Bruce S.
DOI: 10.1021/ac102598u
发表时间: 2011-02-01
期刊: ANALYTICAL CHEMISTRY
影响因子: 7.4
作者: [Bird, Susan S., Marur, Vasant R., Sniatynski, Matthew J., Greenberg, Heather K., Kristal, Bruce S.]
通讯作者: Kristal, Bruce S.
DOI: 10.1021/ac303011k
发表时间: 2013-01-15
期刊: Analytical chemistry
影响因子: 7.4
作者: [Gregory KE, Bird SS, Gross VS, Marur VR, Lazarev AV, Walker WA, Kristal BS]
通讯作者: Kristal BS
DOI: 10.1016/j.ab.2011.07.017
发表时间: 2011-11-15
期刊: Analytical biochemistry
影响因子: 2.9
作者: [Gross VS, Greenberg HK, Baranov SV, Carlson GM, Stavrovskaya IG, Lazarev AV, Kristal BS]
通讯作者: Kristal BS
6
    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