ArticleAnnals of epidemiology2026
GLP-1 receptor agonist medications for weight loss: Sociodemographic patterns of awareness, use, and access in a U.S. national cohort.
Article in Annals of epidemiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Disparities in GLP-1RA and SGLT2i Uptake: a Systematic Review and an Equity-First Framework for Cardiovascular-Kidney-Metabolic Care.Current cardiology reports · 2026Pooled it
- Sociodemographic disparities in semaglutide and tirzepatide prescription for obesity treatment.Health affairs scholar · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
purposeTo describe patterns of glucagon-like peptide-1 receptor agonist (GLP1-RA) medication awareness, use, and access in a US adult cohort.
methodsUsing self-reported December 2023 data from a nationwide cohort (N = 4555), we examined predictors of awareness, use (≤3 years), and inability to access GLP1-RA medications. Poisson regression with robust standard errors estimated age/sex-adjusted prevalence ratios. Analyses were conducted overall and among participants meeting FDA clinical-eligibility criteria (BMI ≥30 kg/m² or ≥27 kg/m² + ≥1 comorbidity; N = 1883).
resultsAwareness was 81.6%; use was 8.3% overall, 13.4% among clinically-eligible participants, and 4.0% among ineligible participants. Overall, use was highest at ages 30-39 and 50-64 and among Hispanic and Black adults, parents, smokers, and those with healthcare barriers. Among clinically-eligible participants, use was lower among men (aPR=0.76, 95% CI: 0.60-0.96) and those with healthcare access barriers (aPR=0.47 [0.35-0.63]), and higher among those with income ≥ $100,000 versus < $49,000 (aPR=1.49 [1.12-1.98]). Among those who attempted treatment, 49.9% were unsuccessful; inability was more common for those with healthcare barriers (aPR=1.42 [1.14-1.77]).
conclusionsGLP1-RA awareness is high, but predictors of uptake and access differ by eligibility. Sociodemographic factors predicted uptake in the full cohort; income, sex, and healthcare barriers were significant predictors among clinically-eligible adults.
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