GLP-1 Evidence

Not medical advice. A record of published research and our assessments of it. The limits

GLP-1/GIP Uptake, Indication, and Access Pathways Among US Adults in the Understanding America Study

Design
Prospective cohort · 9150 participants · Unknown outcome
Match to healthy normal-weight adults aged 55–75
Different population[Auto] Participants had obesity/overweight (mean age 53).
Could weight loss explain it?
Unknown[Auto] Harm signal; weight-loss mediation not the relevant question, but consider whether harms relate to rapid weight loss or reduced intake.
Study tier
Preliminary[Auto] Not peer reviewed (preprint, abstract or registration). Early-warning only.
Assessment
Version 1 · automatic, not yet reviewed by a person · Sep 13, 2026

Study facts come from the paper. Population match, weight-loss explanation and study tier are our judgments, made against the reference group of healthy normal-weight adults aged 55–75. This item has not been peer reviewed.

[Auto, unreviewed; last sentences of abstract] Overall, 1 in 3 users obtained treatment outside conventional prescribing and dispensing channels. MeaningA large and growing share of GLP-1/GIP exposure occurs outside the channels visible to claims-based surveillance.

01Findings

What the study reported

Drugs
Class unspecified
Comparator
any use
Primary outcome
Not extracted
Effect
Not extracted
95% confidence interval
Not extracted
Follow-up
53 years
Adverse events
Not extracted
Limitations
Auto-classified from abstract only; effect estimates, adverse events and limitations not extracted. Requires manual review.

Who was studied

Mean age
53
Age min
18
Sex distribution
60.9% female
Obesity status
obesity/overweight present (all or most)
Diabetes status
diabetes mentioned
Sample size
9150

Study quality details

Study design
Prospective cohort
Sample size
9150
Randomization
no
Blinding
not stated
Comparator
not stated
Follow up duration
53 years
Outcome type
unknown
Replication
not assessed (auto)
Consistency with other evidence
not assessed (auto)
Population applicability
INDIRECT
Statistical precision
not extracted
Risk of bias
not assessed (auto)
Funding conflicts
unclear
Peer review status
no
02Funding

Funding and conflicts

Funding
not reported in abstract
Industry funded
Unclear
Manufacturer
None identified
Sponsor role
not reported in abstract
Author conflicts
not available in metadata
Independent replication
unknown

Funding is shown on every study and never used to score it.

04Source

The source, as retrieved

Abstract

ImportanceEvidence on GLP-1/GIP therapies is largely derived from trials enrolling selected populations or medical records that miss utilization outside healthcare channels. No nationally representative cohort has characterized real-world uptake, indications, and access. ObjectiveTo characterize GLP-1/GIP prevalence, indication, clinical profile, and access. DesignProspective cohort study with three GLP-1/GIP surveillance waves (March 2024, December 2024, October 2025). SettingThe Understanding America Study, an address-based, nationally representative panel of approximately 15,000 US adults aged 18+ years initiated in 2014. ParticipantsUAS participants responding to at least one surveillance wave (n=9150). ExposuresGLP-1/GIP use status (never vs any use, comprising current and former use), self-reported primary indication (diabetes, weight loss, or other), and access pathway (traditional vs non-traditional). Main Outcomes and MeasuresSurvey-weighted prevalence of GLP-1/GIP use, overall and by indication and access pathway; sociodemographic, cardiometabolic, treatment, and access characteristics; and smartwatch-derived resting heart rate, heart rate variability, maximum activity heart rate, step count, and sleep duration and variability. ResultsAmong n=9150 adults (1274 with any use; 60.9% female; median age 53 years), weighted prevalence increased 46%, from 8.2% (March 2024) to 12.0% (October 2025) representing 32 million. Weight-loss indications grew, reaching nearly half of use (4.1% to 5.6%); diabetes-indicated use was stable (5.3% to 5.4%). Users carried high cardiometabolic burden (obesity, 68.2%; diabetes, 53.6%) but diverged by indication: diabetes-indicated users were older (median, 59 vs 49 years), whereas weight-loss-indicated users were more often female (69.9% vs 51.3%) and healthier. One in three users (~9 million) had non-traditional access, especially in weight-loss-indicated users, of whom 33% had no conventional prescription; 41% used compounding, online, or foreign pharmacies; and, 43% lacked coverage. Non-traditional users were five times as likely to report an unlisted, likely compounded formulation (19.8% vs 4.1%). All p<0.05. Conclusions and RelevanceReal-world GLP-1/GIP use has grown rapidly and diversified substantially in indication, access, and population profile. One in 3 users obtained treatment through nontraditional channels largely invisible to claims data, raising long-term safety, efficacy, and coverage questions. GLIMMER provides a public, nationally representative longitudinal evidence base for future payer and provider decisions. KEY POINTSO_ST_ABSQuestionC_ST_ABSWho is using glucagon-like peptide-1 receptor agonists or glucose-dependent insulinotropic polypeptides (GLP-1/GIP) therapies in the US, how has use changed since 2024, and how are these medications obtained? FindingsIn this cohort study of 9150 US adults, GLP-1/GIP use rose significantly from 8.2% to 12.0% (March 2024-October 2025), driven by weight loss; those treated for diabetes were a decade older, lower-income, and in poorer health than those treated for weight loss. Overall, 1 in 3 users obtained treatment outside conventional prescribing and dispensing channels. MeaningA large and growing share of GLP-1/GIP exposure occurs outside the channels visible to claims-based surveillance.

Where this record came from

SourceRetrievedIdentifier
medrxiv:medrxivSep 13, 202610.64898/2026.08.28.26361368
first ingestion