CTN - Effects of semaglutide (Ozempic, Wegovy) and tirzepatide (Mounjaro and Zepbound) on incidence and outcomes of stimulant use disorders and opioid use disorder in real-world populations: target tr
Project Number3UG1DA013732-25S2
Former Number5UG1DA013732-25
Contact PI/Project LeaderWINHUSEN, T JOHN
Awardee OrganizationUNIVERSITY OF CINCINNATI
Description
Abstract Text
Effects of semaglutide (Ozempic, Wegovy) and tirzepatide (Mounjaro and Zepbound) on incidence and
outcomes of stimulant use disorders and opioid use disorder in real-world populations: target trial
emulation using patient electronic health records
ABSTRACT/PROJECT SUMMARY
There is a steady rise in the incidence and associated death of StUDs including methamphetamine use
disorder (MUD) and cocaine use disorder (CUD). Among people aged 12 or older in 2022, 0.6 percent (or
1.8 million people) had MUD and 0.5 percent (or 1.4 million people) had CUD in the past year. Currently,
there are no treatments approved by the U.S. Food and Drug Administration for StUDs and there is a
critical unmet need. Clinical anecdotes that patients treated with semaglutide, a glucagon-like peptide-1
receptor agonist (GLP-1RA) approved for treating type 2 diabetes (T2DM) in 2017 and for weight
management in 2021 reported reduced desire to drink and smoke have attracted attention regarding its
potential to treat addiction. Currently, several registered clinical trials are ongoing to evaluate the effect
of semaglutide on alcohol consumption and smoking cessation. Preclinical studies have investigated the
effects of semaglutide or other GLP1R agonists on nicotine, alcohol, or opioids. However, little attention
has been placed on the effects of semaglutide on StUDs; the present project will help address this gap.
The proposed study would utilize TriNetX Analytics, a nationwide electronic health records (EHR)
database, to evaluate semaglutide’s association with changes in both the incidence of StUDs (MUD, CUD)
and clinical outcomes associated with StUDs. Outcomes will be separately assessed by age groups, sex,
and race and in patients with co-occurring mental disorders or other substance use disorders (SUDs)
including alcohol, nicotine, opioid, and cannabis use disorders, whenever sample sizes permit. Our
methodology is based on our successful use of TriNetX Analytics to evaluate semaglutide’s association
with reduced incidence and relapse of cannabis use disorder.
Public Health Relevance Statement
Effects of semaglutide (Ozempic, Wegovy) and tirzepatide (Mounjaro and Zepbound) on incidence and
outcomes of stimulant use disorders and opioid use disorder in real-world populations: target trial
emulation using patient electronic health records
PROJECT NARRATIVE
The proposed study would utilize TriNetX Analytics, a nationwide electronic health records
(EHR) database, to evaluate semaglutide’s association with changes in both the incidence of
StUDs (MUD, CUD) and clinical outcomes associated with StUDs. Outcomes will be separately
assessed by age groups, sex, and race and in patients with co-occurring mental disorders or
other substance use disorders (SUDs) including alcohol, nicotine, opioid, and cannabis use
disorders, whenever sample sizes permit. Our methodology is based on our successful use of
TriNetX Analytics to evaluate semaglutide’s association with reduced incidence and relapse of
cannabis use disorder.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AddressAdverse effectsAgonistAlcohol consumptionAlcoholsAnecdotesAttentionCessation of lifeClinicalClinical TrialsCocaine use disorderDataDatabasesElectronic Health RecordEthnic OriginGLP-I receptorGeneral PopulationIncidenceMental disordersMethamphetamine use disorderMethodologyNicotineNicotine Use DisorderNon-Insulin-Dependent Diabetes MellitusOpioidOutcomePatientsPersonsPopulationRaceRecording of previous eventsRelapseReportingSample SizeSmokeSubstance Use DisorderUnited States Food and Drug AdministrationWeight maintenance regimenaddictionage groupage stratificationagedalcohol use disordermarijuana use disorderopioid use disorderpreclinical studysexsmoking cessationstimulant usestimulant use disorder
No Sub Projects information available for 3UG1DA013732-25S2
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