grant

Disparities in the burden and progression of multi-morbidity across adulthood

Organization EMORY UNIVERSITYLocation ATLANTA, UNITED STATESPosted 1 May 2022Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY202521+ years oldActive Follow-upAdd HealthAddressAdultAdult HumanAffectAfrican American groupAfrican American individualAfrican American peopleAfrican American populationAfrican AmericansAgeAge of OnsetAmentiaApoplexyArthritisAsthmaBirthBrain Vascular AccidentBronchial AsthmaCancersCardiac DiseasesCardiac DisordersCardiac infarctionCardiometabolic DiseaseCardiometabolic DisorderCardiovascular DiseasesCaringCerebral StrokeCerebrovascular ApoplexyCerebrovascular StrokeChronicChronic DiseaseChronic IllnessClinical Practice GuidelineCohort StudiesCommunitiesConcurrent StudiesDataData SetDecrease disparityDementiaDiabetes MellitusDifferential MortalityDiseaseDisease ClusteringsDisease ProgressionDisorderDisparitiesDisparityEconomicsElderlyEnrollmentEpidemiologic ResearchEpidemiologic StudiesEpidemiological StudiesEpidemiology ResearchEthnic OriginEthnicityEuropeGenderGeographyGoalsGuidelinesHealthHealth CareHealth and Retirement StudyHeart DiseasesHepatic DisorderHispanicHispanic PopulationsHispanic groupHispanic individualHispanic peopleHispanicsHypertensionIncidenceIndividualInstitutionalizationInterruptionInterventionKidney DiseasesLifeLife CycleLife Cycle StagesLife ExpectancyLiver diseasesLongitudinal StudiesLower disparityLung DiseasesMalignant NeoplasmsMalignant TumorMeasuresMedical Care CostsMental DepressionModelingMorbidityMorbidity - disease rateMyocardial InfarctMyocardial InfarctionNational Longitudinal Study of Adolescent HealthNational Longitudinal Survey of Adolescent to Adult HealthNational Longitudinal Survey of YouthNatureNephropathyObesityOsteoporosisParturitionPatternPersonsPoliciesPopulationPopulation GroupPremature MortalityProbabilityProceduresPulmonary DiseasesPulmonary DisorderQOLQuality of lifeRaceRacesReasons for Geographic And Racial Differences in StrokeRenal DiseaseResearchRiskSentinelStrokeTimeVascular Hypertensive DiseaseVascular Hypertensive DisorderWorkactive followupadiposityadulthoodadvanced ageage associatedage correlatedage dependentage linkedage relatedage specificagesaging associatedaging relatedarthriticbrain attackcardiac infarctcardiovascular disordercerebral vascular accidentcerebrovascular accidentchronic disorderclinical practiceclinical practice and guidelinescohortcoronary attackcoronary infarctcoronary infarctioncorpulencedata infrastructuredeath riskdepressiondiabetesdisabilitydisability riskdisease of the lungdisorder of the lungdisparity in healthdisparity reductioneconomicenrollepidemiologic investigationepidemiology studyethnic minorityexperiencefollow upfollow-upfollowed upfollowupgeriatrichealth disparityheart attackheart disorderheart infarctheart infarctionhepatic diseasehepatopathyhigh blood pressurehigh riskhyperpiesiahyperpiesishypertensive diseasehypertensive disorderinnovateinnovationinnovativekidney disorderlife courselife-time risklifetime riskliver disorderlong-term studylongitudinal outcome studieslung disordermalignancymedical costsmedical expensesmitigate disparitymortality riskmultimorbiditymultiple chronic conditionsneoplasm/cancerolder adultolder adulthoodpanel study of income dynamicspreventpreventingprogression riskracialracial backgroundracial minorityracial originreduce disparityreduction in disparityrenal disordersenior citizensexstrokedstrokesworking class
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Full Description

PROJECT SUMMARY
RELEVANCE: Approximately 1 in 4 U.S. adults suffers from multimorbidity, or two or more concurrent

chronic diseases. People with multimorbidity experience more disability and higher mortality risk and have

higher medical costs than people with 1 chronic condition. Our understanding of the onset and progression of

multimorbidity is limited. OBJECTIVES: To develop clinical practice guidelines and interventions, it is

necessary to have accurate information about the progression of multimorbidity, the age and timing of onset,

and differences in these across population groups. AIMS: 1) Harmonize and bridge national longitudinal data

to track the incidence of chronic diseases and multimorbidity in the U.S. starting at age 30. We will combine 7

premier national cohort datasets of adult health (Add Health, NLSY79, NLSY97, PSID, REGARDS, H-EPESE,

HRS) to create a synthetic nationally representative cohort of adults starting at age 30 years, compiling over 1.7

million person-years of follow-up and include sizeable number of racial/ethnic minorities. 2) Estimate the

progression to multimorbidity starting at age 30 years. We will identify the age-specific progression rate of

common chronic disease clusters and the sentinel conditions associated with higher risks of progression to

additional diseases. 3) Develop measures of age-specific risk of multimorbidity for the US adult population and

calculate the lifetime risk of developing multimorbidity and years spent with multimorbidity. 4) For major

race-ethnic, sex, economic, and geographic groups, identify the sentinel conditions, age-specific progression,

and lifetime risk of multimorbidity. We will estimate differences across groups and quantify the implications of

reducing these disparities on disease-free life expectancy, with the additional innovation of adjusting for biases

due to differential mortality and institutionalization. DESIGN: Bridging and reweighting procedures will be

applied to develop a new data infrastructure with nationally representative longitudinal birth cohorts and

synthetic cohorts. We will use Poisson regression to model the ages at which disparities in multi-morbidity

emerge. To capture the sequencing and pacing of multimorbidity, we will estimate the probability of

experiencing an additional (k+1th) condition for those with k prior chronic conditions. We will estimate

cumulative probabilities based on Kaplan-Meier survival probabilities. Disparities will be quantified using

Greenwood’s estimator. IMPACT: This project will advance understanding of the nature, onset, and

progression of multimorbidity. To inform clinical practice and healthcare guidelines, we will identify

conditional risks of transitioning to additional diseases given age of onset and sentinel disease. With particular

relevance to policy, we will model the years of disease-free life expectancy that would be gained by

interventions that delay or avert the onset of sentinel diseases. The data infrastructure generated from this

project will be made available to the research community and will be useful for a variety of aging-related

research questions.

Grant Number: 5R01AG074019-04
NIH Institute/Center: NIH

Principal Investigator: Solveig Argeseanu Cunningham

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Disparities in the burden and progression of multi-morbidity across adulthood — EMORY UNIVERSITY | UNITED STATES | May 2 | Dev Procure