grant

Preventing Obesity in Preterm Infants

Organization YALE UNIVERSITYLocation NEW HAVEN, UNITED STATESPosted 1 Aug 2022Deadline 31 Jul 2027
NIHUS FederalResearch GrantFY20250-11 years old0-4 weeks old12-20 years old2 year old2 years of age21+ years oldACRP30 proteinAccelerationAdipose tissueAdolescenceAdultAdult HumanAffectAgeBMIBMI percentileBMI z-scoreBig BabyBiological MarkersBiometricsBiometryBiostatistical MethodsBiostatisticsBirthBirthweight HighBlood PressureBody CompositionBody TissuesBody fatBody mass indexCardiometabolic DiseaseCardiometabolic DisorderChildChild YouthChildhoodChildren (0-21)Chronologic Fetal MaturityClinical ResearchClinical StudyClinical TrialsDataDevelopmentDevelopment PlansDiabetes MellitusDietary InterventionDrug TherapyEndocrinologyEnergy ExpenditureEnergy MetabolismEpidemiologic ResearchEpidemiologic StudiesEpidemiological StudiesEpidemiology ResearchExposure toFatsFatty TissueFatty acid glycerol estersFetal AgeFutureGeneralized GrowthGestationGestational AgeGestational DiabetesGestational Diabetes MellitusGoalsGrowthGrowth and DevelopmentGrowth and Development functionHeavy babyHigh birth weight babyHigh birth weight infantHigh birthweight babyHospital AdmissionHospitalizationHospitalsInfantIntermediary MetabolismInterventionInvestigatorsLarge babyLarge baby for gestational ageLarge birth weightLeadLeptinLifeMR ImagingMR TomographyMRIMRIsMagnetic Resonance ImagingMedical Imaging, Magnetic Resonance / Nuclear Magnetic ResonanceMentorsMetabolic ProcessesMetabolic syndromeMetabolismMetabolism and EndocrinologyMonitorMothersNMR ImagingNMR TomographyNewborn InfantNewbornsNuclear Magnetic Resonance ImagingNutrition InterventionsNutritionalNutritional InterventionsOb Gene ProductOb ProteinObese Gene ProductObese ProteinObesityParturitionPatternPb elementPerinatalPerinatal EpidemiologyPerinatal ExposurePeripartumPharmacological TreatmentPharmacotherapyPhenotypePregnancyPregnancy-Induced DiabetesPremature BirthPremature InfantPrematurely deliveringPreterm BirthProspective cohortQuetelet indexR-Series Research ProjectsR01 MechanismR01 ProgramRaceRacesResearchResearch GrantsResearch MethodologyResearch MethodsResearch PersonnelResearch Project GrantsResearch ProjectsResearchersRiskRoleSkinfold ThicknessTissue GrowthTissuesTrainingUnited StatesVisceralVulnerable PopulationsWeightWeight GainWeight IncreaseWomanZeugmatographyadipocyte complement-related protein 30-kDaadipocyte, C1q and collagen domain containing proteinadiponectinadiposeadiposityadolescence (12-20)adulthoodage 2 yearsaged 2 yearsaged two yearsagesapM-1 proteinapM1 (adipose-specific) proteinbio-markersbiologic markerbiomarkerbody weight gainbody weight increasecandidate biomarkercandidate markercardiometaboliccardiometabolismcareer developmentchild adipositychild obesitychildhood adipositychildhood obesitycorpulencecost estimatecost estimationcritical perioddevelop therapydevelopmentaldiabetesdiet interventiondrug interventiondrug treatmentearly biomarkersearly childhoodearly detection biomarkersearly detection markersepidemiologic investigationepidemiology studyheavy metal Pbheavy metal leadhigh risk grouphigh risk individualhigh risk peoplehigh risk populationhormone metabolisminfant nutritioninfants born prematureinfants born prematurelyinsulin sensitivityintervention developmentkidslongitudinal designlongitudinal experimental designlongitudinal research designlongitudinal study designmaternal adipositymaternal diabetesmaternal obesityneonatal adipositynewborn adipositynewborn childnewborn childrennewborn obesitynon-diabeticnondiabeticnutritiousobese childrenobesity developmentobesity during childhoodobesity in childrenobesity preventionobesity riskoffspringontogenypediatricpediatric obesityperinatal environmentperinatal periodperinatal phasepharmaceutical interventionpharmacological interventionpharmacological therapypharmacology interventionpharmacology treatmentpharmacotherapeuticspostnatalpregnancy diabetespremature babypremature childbirthpremature deliverypremature infant humanprepregnancypreterm babypreterm deliverypreterm infantpreterm infant humanpreventprevent obesitypreventingprospectivepublic health relevanceracialracial backgroundracial originresearch and methodsrisk for obesityrisk of obesityrisk stratificationsexskin fold measurementskin fold thicknessskinfold measurementsocial rolesocio-demographic factorssociodemographic factorsstratify risksubcutaneoussubdermaltherapy developmenttreatment developmenttwo year oldtwo years of agevulnerable groupvulnerable individualvulnerable peopleweightswhite adipose tissuewt gainyellow adipose tissueyoungster
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Full Description

PROJECT SUMMARY
The objective of this research project is to determine if indicators of adipose tissue development and

metabolism are candidate biomarkers to identify preterm infants at risk of childhood obesity and

cardiometabolic abnormalities. Infants born moderately preterm, between 32- and 36-weeks of gestational age,

have 20% higher odds of obesity and cardiometabolic disease in adulthood compared with those born at term.

Moderate preterm birth accounts for 8% of all births, or approximately 300,000 children born in the United

States each year. Factors that may contribute to obesity risk among preterm infants include developmental re-

programming due to perinatal exposure to maternal obesity and diabetes. Preliminary data shows that

moderate preterm infants of mothers with diabetes have greater in-hospital growth over an average of 9 days

compared with infants of non-diabetic mothers, after adjustment for gestational age, sex, and race. Accelerated

growth in these infants may be due to alterations in the development, metabolism, and localization of adipose

tissue. In a prospective cohort of moderately preterm infants, the aims of this project are: To determine the

effect of maternal obesity and gestational diabetes on the development of adiposity at term corrected age and

its association with adipose tissue metabolism biomarkers at birth (Aim 1) and to identify the role of early body

composition assessments by magnetic resonance imaging and adipose tissue metabolism biomarkers at birth

in predicting early childhood growth and development of adiposity and cardiometabolic abnormalities at age 2

years (Aim 2). Identification of these perinatal biomarkers is critical in the ability to risk-stratify infants at

heightened risk of obesity and cardiometabolic abnormalities, and for the future development of interventions

to optimize healthy growth and reduce obesity among preterm infants.

Dr. Buck is a neonatologist whose long-term goal is to lead independent research examining perinatal risks

that influence growth and development among preterm infants. The career development plan for this proposal

builds upon Dr. Buck's prior training in epidemiology and clinical research methods through graduate-level

coursework and mentored training in longitudinal study design, advanced biostatistical methods, biomarker and

body composition assessment, and clinical trial study conduction. Dr. Buck has assembled a strong, committed

team of mentors and advisors with expertise in infant nutrition, pediatric endocrinology, perinatal epidemiology,

and biostatistics to help guide her successful transition to becoming an independent investigator, optimizing

healthy growth and development of preterm infants and minimizing the development of obesity and

cardiometabolic abnormalities in this vulnerable population.

Grant Number: 5K23HD104907-04
NIH Institute/Center: NIH

Principal Investigator: Catherine Buck

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