Epidemiology & epigenetics: Maternal diet, DNA methylation, & offspring adiposity
Epidemiology & epigenetics: Maternal diet, DNA methylation, & offspring adiposity
批准号:
7942062
负责人:
MATTHEW W GILLMAN
金额:
$49.85万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2012-08-31
关键词:
7 year oldAddressAdultAffectAgeAnimal ExperimentsAnimalsAreaBehaviorBetaineBirthBloodBlood CellsBlood PressureBlood specimenBody mass indexCardiovascular DiseasesChildCholineChronicCohort StudiesConceptionsDNADNA MethylationDataDevelopmentDiabetes MellitusDietEnvironmentEpidemiologic StudiesEpidemiologyEpigenetic ProcessFatty acid glycerol estersFolateFundingGeneticGenomicsGlucose IntoleranceGoalsGrantHealthHumanIndividualInsulin ResistanceIntakeKnowledgeKnowledge acquisitionLeptinLong Interspersed Nucleotide ElementsLongevityMalignant NeoplasmsMeasuresMetabolicMetabolic DiseasesMethodologyMethylationMorbidity - disease rateObesityOutcomePathway interactionsPhenotypePhysical environmentPhysiologyPlasmaPlasticsPopulationPregnancyPreventive InterventionPublic HealthResearchResearch PersonnelSkinfold ThicknessSocial BehaviorSpecies SpecificitySumTechnologyTimeTissuesTranslatingTriceps Brachii MuscleUmbilical Cord BloodVariantVitamin B 12Workadiponectinbasecardiovascular risk factorclinically relevantcostcritical developmental periodcritical perioddesigndiabeticfetalhuman population studyimprovedindexingmortalitymouse modelnext generationoffspringprenatalpreventprogramspublic health relevanceresearch study
中文摘要
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英文摘要
DESCRIPTION (provided by investigator): This application addresses Challenge Area 08, "Genomics," and Challenge Topic 08-AG-105 (also OD [OBSSR] - 102), "Approaches to study the interactions among individual behaviors, social and physical environments, and genetic/epigenetic processes during critical developmental periods." Decades of animal physiology experiments unequivocally show that perturbations during early, plastic, critical periods of development can have lifelong, sometimes irreversible adverse impact on markers of chronic cardio- metabolic disease like adiposity, blood pressure and glucose intolerance, and on lifespan itself. The field of epigenetics has recently revealed some of the mechanisms underlying these observations. For example, in the yellow agouti mouse model, a maternal diet rich in methyl donors around conception causes DNA methylation of a metastable epiallele, preventing offspring from becoming fat, diabetic, and cancer-prone. No study in human populations, however, has examined pathways from maternal diet in early pregnancy through epigenetic changes to offspring phenotype. The goals of this study are to examine relationships among maternal diet in early pregnancy, particularly variation in intake of methyl donors, global DNA methylation in maternal blood in early and late pregnancy and in umbilical cord blood, and adiposity-related outcomes in 3- and 7-year-old children. We will carry out this project within the well-characterized pre-birth cohort study Project Viva, which is perhaps the only US-based epidemiologic study with the design features to address these aims: prospectively collected, validated, early pregnancy diet information, maternal and cord blood specimens, and research- quality offspring cardio-metabolic phenotype data. Obesity, cardiovascular disease, diabetes, and related conditions are leading causes of morbidity and mortality in the U.S., and their earliest origins exist in behavior and environment during the prenatal period. Adding epigenetic data to existing epidemiologic studies offers the potential to translate knowledge from animal experiments to the human condition as well as to mount preventive interventions. Given the potential scientific and public health impact, the time has come for an influx of funds to advance this area in significant ways quickly, and the Challenge Grants program provides the right vehicle to do so.
PUBLIC HEALTH RELEVANCE: The goals of this study are to examine the extent to which maternal diet in early pregnancy affects methylation of maternal and fetal DNA, an epigenetic process; and the extent to which DNA methylation predicts obesity and cardiovascular risk factors in 3- and 7-year-old children. The importance of this research is two-fold. First is knowledge acquisition--the potential to translate findings from animal experiments to the human condition. Second is public health importance-- optimizing maternal diet in early pregnancy could improve the health of the next generation.
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批准号:8850265
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依托单位:
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Weight and weight-related behaviors in youth: Influence of the family context
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资助金额:$43.9万
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财政年份:2011
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Weight and weight-related behaviors in youth: Influence of the family context
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批准号:8433479
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依托单位:
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批准号:8316310
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资助金额:$5.44万
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财政年份:2010
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Improving primary care to prevent childhood obesity
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批准号:8128678
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资助金额:$5.56万
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财政年份:2010
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依托单位:
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批准号:7943569
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资助金额:$6.18万
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财政年份:2010
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Pre- and peri-natal predictors of childhood obesity
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资助金额:$9.0万
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项目类别:
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资助金额:$67.75万
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依托单位:
Improving primary care to prevent childhood obesity
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财政年份:2009
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依托单位:
Enhancing the Obesity Prevention Program at Harvard's DACP
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资助金额:$70.12万
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财政年份:2009
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负责人:MATTHEW W GILLMAN
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依托单位:
Epidemiology & epigenetics: Maternal diet, DNA methylation, & offspring adiposity
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依托单位:
Limiting Weight Gain in Overweight Pregnant Women: Effects on Mother and Child
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财政年份:2008
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负责人:MATTHEW W GILLMAN
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依托单位:
Limiting Weight Gain in Overweight Pregnant Women: Effects on Mother and Child
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项目类别:
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资助金额:$31.75万
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财政年份:2008
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负责人:MATTHEW W GILLMAN
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依托单位:
Limiting Weight Gain in Overweight Pregnant Women: Effects on Mother and Child
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负责人:MATTHEW W GILLMAN
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依托单位:
Breastfeeding Promotion RCT and Child Metabolic Syndrome
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项目类别:
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财政年份:2007
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依托单位:
Breastfeeding Promotion RCT and Child Metabolic Syndrome
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依托单位:
海外基金