grant

Obesity as a Driver of Inflammation and Brain Volume Loss in Pediatric Multiple Sclerosis

Organization UNIVERSITY OF VIRGINIALocation CHARLOTTESVILLE, UNITED STATESPosted 1 Dec 2020Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY20250-11 years old12-20 years old21+ years oldACRP30 proteinAccelerationAdipocytesAdipose CellAdipose tissueAdolescenceAdultAdult HumanAffectAgeAnimal ModelAnimal Models and Related StudiesAtrophicAtrophyAwardBMIBMI percentileBMI z-scoreBiologicalBiological MarkersBlood SerumBody mass indexBrainBrain Nervous SystemCNS Nervous SystemCNS autoimmune diseaseCategoriesCellular injuryCentral Nervous SystemChildChild YouthChildhoodChildren (0-21)Children's HospitalClinicalClinical ResearchClinical StudyCohort StudiesConcurrent StudiesConduct Clinical TrialsCross Sectional AnalysisCross-Sectional AnalysesCross-Sectional StudiesCross-Sectional SurveyDataData SetDegenerative Neurologic DisordersDemyelinationsDevelopmentDevelopment PlansDiagnosisDiseaseDisease Frequency SurveysDisease ProgressionDisorderDisseminated SclerosisEncephalonEpidemicExhibitsFailureFastingFat CellsFatty TissueFundingFutureGeneral RadiologyGeneralized GrowthGoalsGrowthHealthImageImmuneImmune mediated therapyImmune responseImmune systemImmunesImmunologically Directed TherapyImmunomodulationImmunotherapyInflammationInflammatoryInjuryInternationalIntervention StudiesInvestigatorsIsoformsLeptinLesionLifeLightLinkLipocytesLong-term cohort studyLongitudinal cohort studyMR ImagingMR TomographyMRIMRIsMagnetic Resonance ImagingMature LipocyteMature fat cellMeasuresMediatingMedical Imaging, Magnetic Resonance / Nuclear Magnetic ResonanceMentorsModelingModificationMolecular WeightMulti-center clinical studyMulti-site clinical studyMulticenter clinical studyMultiple SclerosisMultisite clinical studyNMR ImagingNMR TomographyNational Institutes of HealthNerve CellsNerve DegenerationNerve UnitNervous System Degenerative DiseasesNeural CellNeural Degenerative DiseasesNeural degenerative DisordersNeuraxisNeurocognitiveNeurocyteNeurodegenerative DiseasesNeurodegenerative DisordersNeurologic Degenerative ConditionsNeurological disabilityNeurologistNeuron DegenerationNeuronsNon obeseNonobeseNuclear Magnetic Resonance ImagingOb Gene ProductOb ProteinObese Gene ProductObese ProteinObesityOnly ChildOutcomeOver weightOverweightPatientsPediatric HospitalsPersonsPhiladelphiaPhotoradiationProspective StudiesProtein IsoformsPublishingQuetelet indexRadiologyRadiology SpecialtyResearchResearch MethodologyResearch MethodsResearch PersonnelResearchersRiskRisk FactorsRoleSamplingScienceScientistSerologySerumSeveritiesSeverity of illnessTechniquesTherapeuticTimeTissue GrowthTrainingUnited States National Institutes of HealthWeightWorkZeugmatographyadipocyte complement-related protein 30-kDaadipocyte, C1q and collagen domain containing proteinadipocytokinesadipokinesadiponectinadiposeadiposityadolescence (12-20)adult youthadulthoodagesapM-1 proteinapM1 (adipose-specific) proteinbio-markersbiologicbiologic markerbiomarkerbrain atrophybrain volumecareer developmentcell damagecell injurycellular damagecentral nervous system autoimmune diseasecerebral atrophychild adipositychild obesitychild patientschildhood adipositychildhood obesitycohortcorpulencecortical atrophycytokinedamage to cellsdegenerative diseases of motor and sensory neuronsdegenerative neurological diseasesdemyelinatedepositorydesigndesigningdevelopmentaldisabilitydisease severityexperiencefastedfastsgray matterhost responseimagingimmune modulationimmune regulationimmune system responseimmune therapeutic approachimmune therapeutic interventionsimmune therapeutic regimensimmune therapeutic strategyimmune therapyimmune-based therapiesimmune-based treatmentsimmuno therapyimmunologic reactivity controlimmunomodulatoryimmunoregulationimmunoregulatoryimmunoresponseinjuriesinjury to cellsinsular sclerosisintervention researchinterventional researchinterventional studyinterventions researchkidsmalleable riskmodel of animalmodifiable riskneural degenerationneural imagingneuro-imagingneurodegenerationneurodegenerativeneurodegenerative illnessneurofilamentneuroimagingneurological degenerationneurological imagingneuronalneuronal degenerationnovelobese childrenobesity during childhoodobesity in childrenontogenyoverweight childoverweight childhoodpediatricpediatric multiple sclerosispediatric obesitypediatric onset MSpediatric onset multiple sclerosispediatric patientsrecruitrepositoryresearch and methodssexsocial rolesubstantia griseatoolweightswhite adipose tissueyellow adipose tissueyoung adultyoung adult ageyoung adulthoodyounger ageyoungster
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Full Description

PROJECT SUMMARY/ABSTRACT
Dr. Brenton is a pediatric neurologist whose long-term goal is to become an expert in multiple sclerosis

(MS) therapeutics and risk factor modification. The training and mentored research experience proposed will

enable him to develop expertise in: 1) the conduct of multi-centered clinical studies, 2) use of MRI as a

research tool, and 3) obesity science. Dr. Brenton has assembled an expert team of mentors/advisors to help

him. Dr. Karen Johnston (primary mentor) is a highly-successful international expert in clinical trial conduct, Dr.

Myla Goldman (co-mentor) is a nationally-recognized expert in MS clinical research, and Dr. Brenda Banwell

(co-mentor) is a world-expert in pediatric MS clinical research. Dr. Brenton will take courses pertinent to

research methodology, the study of obesity and its relevant biomarkers, and the application of neuroimaging

techniques in clinical research. He will also spend 5 weeks at the Children’s Hospital of Philadelphia to gain

hands-on experience with Dr. Banwell in the use of neuroimaging as a biomarker for pediatric MS outcomes.

Children with MS, the most common autoimmune disease of the central nervous system (CNS),

experience failure of age-expected brain growth followed by progressive brain atrophy during adolescence.

These children often develop physical and neurocognitive disability at a young age. Childhood obesity is an

established risk determinant for pediatric MS, however, the impact of persisting obesity on MS disease course

is unknown. In non-MS children and young adults, obesity (a national health epidemic) associates with

progressive brain volume loss. In adults with MS, greater levels of obesity are associated with significantly

reduced normalized gray matter volumes. This is important, as gray matter atrophy is directly linked with

progressive disability in MS. The impact of obesity in children with MS has not been studied and the

implications of this are particularly important in a pediatric patient – where the negative impact of obesity on the

CNS may exert an even greater detrimental effect on a brain that is still undergoing development.

We will conduct a cross-sectional, multi-center cohort study to determine the relationship between

obesity and biomarkers of 1) inflammation (measured radiologically by T2-hyperintense inflammatory lesion

volumes & serologically by adipocyte-derived cytokines) and 2) neurodegeneration (measured radiologically by

whole brain volumetrics & serologically by neurofilament light chain). This study will help define the role of

obesity in pediatric MS disease and will set the stage for future intervention studies aimed at modifiable risk

factors in MS. Upon completion of this award, Dr. Brenton will be one of the only child neurologists in the world

with formal training in pediatric MS in combination with training in obesity science and MS neuroimaging. His

proposal represents the first and only prospective study evaluating the role of obesity on pediatric MS disease

severity at presentation. This K23 will provide the necessary data and experience to inform future studies, and

he will be well-poised to apply for future R01 funding as an independent, collaborative clinician-scientist.

Grant Number: 5K23NS116225-05
NIH Institute/Center: NIH

Principal Investigator: James Brenton

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