The HIV and Alcohol Research center focused on Polypharmacy (HARP)
Project Number5P01AA029545-02
Contact PI/Project LeaderJUSTICE, AMY CAROLINE
Awardee OrganizationYALE UNIVERSITY
Description
Abstract Text
HARP OVERALL PROJECT SUMMARY
The goal of the HIV and Alcohol Research center focused on Polypharmacy (HARP) is to design and
implement effective personalized interventions for people aging with HIV (PAH) experiencing medical harm
from unhealthy alcohol use (at risk and Alcohol Use Disorder [AUD]) and polypharmacy (5+ medications).
Using large scale, national Veterans Healthcare Administration Electronic Health Record data (EHR data), we
have shown strong independent, dose-response, associations between polypharmacy (medication count and
A-PIMS), alcohol use, and adverse health outcomes. In HARP Project 1, we further explore alcohol and
polypharmacy (AP) risks using a direct alcohol biomarker (Phosphatidylethanol [PEth]), considering genetic
liability, and exploring associations with decompensated liver cirrhosis as a manifestation of alcohol-associated
liver disease (AALD). Polypharmacy and genetic liability also complicate selection of treatment for AUD. In
HARP Project 2, we use genetic liability and real-world data to identify and evaluate candidate medications in
the context of polypharmacy. Further, AP risks, especially genetic liability, are complex and challenging to
summarize. Both summarizing effects of multiple risk factors and using genetic data to identify medications for
repurposing requires large-scale, real-world data, high performance computing and sophisticated analytics.
With support from our Administrative/Data Analytic (ADA) Core, the Department of Energy (DOE), an extended
VA family of EHR cohorts (VACo Family), and an expanded network of experts, we are uniquely poised to
harness “big” data to personalize AP risks for PAH and evaluate medications for AUD. Finally, effective
communication of AP risk messages needs to be integrated into a comprehensive, theory-based behavior
change intervention. We have assembled a Risk Communication Core (RCC) of experts to facilitate risk
communication and motivational interviewing (MI) in our pilot intervention studies. The core includes Dr. Jeffrey
Fisher, co-developer of the Information-Motivation-Behavioral Skills (IMB) model of health behavior change. In
collaboration with Dr. Fisher, this core will guide our application of the IMB-MI model to communicate
personalized risk and other elements required for health behavior change in a linked series of pharmacist-
delivered pilot interventions. Project 1 pilots will compare patient’s responses to AP risk messages (employing
different measures of exposure and outcomes) delivered in the larger context of an IMB-MI intervention for
PAH who are at risk drinkers; Project 2 pilots will incorporate lessons learned in Project 1 and adapt the IMB-
MI intervention to target PAH with AUD, adding a candidate repurposed medication for AUD.
Public Health Relevance Statement
The goal of the HIV and Alcohol Research center focused on Polypharmacy (HARP) is to design and
implement effective personalized treatments for people aging with HIV who are harmed by unhealthy alcohol
use and polypharmacy. We will: 1) develop summary estimates of personal health risk based on alcohol and
medication exposures and on genetics; 2) pilot risk messages as part of a larger behavioral intervention; 3)use
“big data” approaches to identify medications in the context of polypharmacy that might be repurposed to treat
alcohol use disorder or prevent alcohol associated liver disease; and 4) pilot the use of these medications in
people aging with HIV with Alcohol Use Disorder.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AddressAgingAlcohol consumptionAlcoholsAnti-Retroviral AgentsBehavior TherapyBehavioralBig DataBiological MarkersCollaborationsCommunicationComplexConsumptionDataData AnalyticsDepartment of EnergyDoseEffectivenessElectronic Health RecordElementsFamilyFundingGeneticGoalsHIVHealthHealth behavior changeHealthcareHigh Performance ComputingIndividualInterventionIntervention StudiesLaboratoriesLinkLiteratureLiver CirrhosisLiver diseasesMeasuresMedicalMetforminModelingMotivationNational Institute on Alcohol Abuse and AlcoholismOutcomePatient Self-ReportPatientsPersonsPharmaceutical PreparationsPharmacistsPhysiologicalPioglitazonePolypharmacyPrazosinPredispositionProviderRiskRisk AssessmentRisk FactorsSafetySelection for TreatmentsSeriesSystems BiologyToxic effectUnited States Food and Drug AdministrationVariantVerapamilVeteransalcohol abuse therapyalcohol measurementalcohol misusealcohol preventionalcohol researchalcohol responsealcohol riskalcohol use disorderbasebehavior changecohortdesigndrinkingdrug repurposingexperiencefrailtymotivational enhancement therapypatient responsepersonalized interventionpersonalized medicinephosphatidylethanolresponseskillssubstance usetheoriestreatment response
National Institute on Alcohol Abuse and Alcoholism
CFDA Code
273
DUNS Number
043207562
UEI
FL6GV84CKN57
Project Start Date
10-September-2021
Project End Date
31-August-2026
Budget Start Date
01-September-2022
Budget End Date
31-August-2023
Project Funding Information for 2022
Total Funding
$1,203,656
Direct Costs
$1,001,190
Indirect Costs
$202,466
Year
Funding IC
FY Total Cost by IC
2022
National Institute on Alcohol Abuse and Alcoholism
$1,203,656
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5P01AA029545-02
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 5P01AA029545-02
Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
No Outcomes available for 5P01AA029545-02
Clinical Studies
No Clinical Studies information available for 5P01AA029545-02
News and More
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History
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Similar Projects
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