grant

Assessing the mediating role of kidney function and weight/BMI in the association between INSTI use and blood pressure changes and hypertension in PWH: a secondary analysis of the REPRIEVE study.

Organization BOSTON UNIVERSITY MEDICAL CAMPUSLocation BOSTON, UNITED STATESPosted 1 Dec 2024Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY2026AIDS VirusAcquired Immune Deficiency Syndrome VirusAcquired Immunodeficiency Syndrome VirusActive Follow-upAddressAdherenceAdoptedAffectAlbuminuriaAnti-Hypertensive AgentsAnti-Hypertensive DrugsAnti-HypertensivesBMIBMI percentileBMI z-scoreBP homeostasisBP regulationBechuanalandBlood PressureBlood SerumBlood VesselsBody mass indexBotswanaBrazilCardiovascularCardiovascular Body SystemCardiovascular Organ SystemCardiovascular systemClinicalComplexConfounding Factors (Epidemiology)Confounding VariablesCreatinineDataData SetDiastolic PressureDiastolic blood pressureDrug PrecursorsDrugsEconomic IncomeEconomical IncomeEconomicsEligibilityEligibility DeterminationEnrollmentEnsureEpidemiologic Confounding FactorEpidemiologic MethodologyEpidemiologic MethodsEpidemiologic research methodologyEpidemiologic research methodsEpidemiological MethodsEpidemiological TechniquesEventGeographyGrantGuidelinesHIVHIV individualsHIV infected individualsHIV infected personsHIV interventionHIV peopleHIV positive individualsHIV positive peopleHIV therapeuticHIV therapyHIV treatmentHIV-1 interventionHIV-1 therapeuticHIV-1 therapyHIV-1 treatmentHealthHealth CareHealth PolicyHealth systemHeart VascularHuman Immunodeficiency Virus therapyHuman Immunodeficiency Virus treatmentHuman Immunodeficiency VirusesHypertensionHypotensive AgentHypotensive DrugsIncidenceIncomeInflammatoryIntegraseInternationalInterventionLAV-HTLV-IIILinkLymphadenopathy-Associated VirusMeasurementMeasuresMediatingMediationMediatorMedicationMethodologyMethodsMethods EpidemiologyMethods in epidemiologyModernizationNIH Office of AIDS ResearchNegotiatingNegotiationNucleosidesOutcomePLWHPWHParticipantPathway interactionsPharmaceutical PreparationsPhysiologicPhysiologicalPopulationPopulation HeterogeneityPositionPositioning AttributePro-DrugsProbabilityProdrugsProspective, cohort studyProteinuriaProtocol ScreeningPublic HealthQuetelet indexRandomization trialRandomizedRecommendationRegimenRenal functionReportingResearchResearch PriorityResistanceReverse Transcriptase InhibitorsRiskRisk FactorsRoleSafetySecureSerumSouth AfricaTechniquesTenofovirThailandTherapeuticTimeUnited StatesUpdateVascular Hypertensive DiseaseVascular Hypertensive DisorderVireadVirus-HIVWeightWeight GainWeight Increaseactive followupanti-hypertensionantiretroviral therapyantiretroviral treatmentblood pressure elevationblood pressure homeostasisblood pressure regulationbody weight gainbody weight increasecardiovascular effectscardiovascular healthcardiovascular riskcardiovascular risk factorcirculatory systemclinical practiceco-infectionco-morbidco-morbiditycoinfectioncomorbiditycomparativedata diversitydifferences in healthdisparity in healthdiverse datadiverse populationsdrug/agenteconomicelevated blood pressureenrollfollow upfollow-upfollowed upfollowuphealth care policyhealth differencehealth disparityheterogeneous populationhigh blood pressurehyperpiesiahyperpiesishypertensive diseasehypertensive disorderimprovedincomesincrease in blood pressureincreased blood pressureindividuals infected with HIVindividuals with HIVindividuals with human immunodeficiency virusinhibitorinnovateinnovationinnovativeinsightkidney functionlow income countrynovelpathwaypeople infected with HIVpeople infected with human immunodeficiency viruspeople living with HIVpeople with HIVpeople with human immunodeficiency viruspharmacologicpopulation diversitypreventpreventingrandomisationrandomizationrandomized trialrandomly assignedregulate BPregulate blood pressureresistantresponsesecondary analysissocial rolesoundtreat HIVtreat Human Immunodeficiency Virustreatment riskvascularweightswt gain
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Full Description

Project Summary
Our R03 application critically evaluates cardiovascular risks associated with integrase strand transfer inhibitors (INSTIs),

focusing on blood pressure and hypertension among people living with HIV. Utilizing data from the REPRIEVE

(Randomized Trial to Prevent Vascular Events in HIV) study, our project aims to address significant gaps in the current

understanding of these risks. Aim 1 employs a novel target trial framework to emulate randomized trials using the

REPRIEVE dataset, in which INSTI use was not originally randomized. This innovative approach enables the application of

advanced causal inference techniques, specifically inverse probability of treatment weighting and inverse probability of

censoring weighting, to rigorously assess the effects of INSTIs. These techniques help us adjust for confounding variables,

enabling us to draw robust conclusions about the causal impacts of INSTI use on blood pressure. Through this aim, we

expect to gain clear insights into the direct effects of INSTIs on cardiovascular health. Aim 2 employs causal mediation

methods to dissect the pathways through which INSTIs influence blood pressure. This aim focuses on understanding how

changes in kidney function and body mass index mediate these effects. By exploring both direct and indirect effects of

INSTIs, mediated through physiological changes, we deepen our understanding of how these drugs impact cardiovascular

systems in clinical settings. Our study is distinguished by its global scope, incorporating data from diverse international

settings, including South Africa, Brazil, Botswana, Thailand, and the United States. This wide-reaching approach enhances

the generalizability of our findings and enables comparative analyses across different geographic and economic contexts.

Such comparisons are critical for understanding how systemic health disparities affect the relationship between INSTI use

and cardiovascular outcomes. By including data from both high-income and lower-income countries, our study is uniquely

positioned to highlight differences in health outcomes and healthcare practices. These insights will allow us to identify

specific challenges and opportunities in managing HIV and related comorbid conditions across varied health systems. The

methodological innovations and geographic diversity of our research will significantly contribute to the scientific

understanding of HIV treatment complications. By generating actionable insights, we aim to inform clinical practices and

influence public health policies globally. Ultimately, securing this R03 grant would enable us to make substantial

contributions to international health guidelines, significantly improving the management of HIV and comorbid conditions

such as hypertension through tailored interventions.

Grant Number: 5R03AI189203-02
NIH Institute/Center: NIH

Principal Investigator: Alana Brennan

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