Emulated Effects of Glucagon-Like Peptide 1 Receptor Agonist Therapy in the General Population
Authors' conclusion
In appropriately selected individuals at high CVD risk, GLP-1RA therapy may complement existing primary prevention strategies
Study context
- Population
- Cardiovascular disease (CVD)-free individuals with body mass index (BMI) ≥27 kg/m² and SCORE2-derived baseline risk ≥7.5%, 2 contemporary health examination surveys21,720 in primary analysis
- Participants
- 200,012 individuals
- Comparison
- Emulated GLP-1RA therapy vs observed
- Outcome
- 10-year CVD incidence
- Follow-up
- 10 years
Methodological detailsemulation of GLP-1RA therapy in population cohorts, risk-factor changes from SELECT trial applied, prespecified risk factors, sex-stratified, placebo-adjusted, Model fitted in 610,789 CVD-free individuals from European and North American Global Cardiovascular Risk Consortium cohorts
- Emulation of GLP-1RA therapy in population cohorts
- Risk-factor changes from SELECT trial applied
- Prespecified risk factors
- Sex-stratified, placebo-adjusted
- Model fitted in 610,789 CVD-free individuals from European and North American Global Cardiovascular Risk Consortium cohorts
Main finding
As reported in the abstract
Absolute reduction
2.99%
95% CI 2.67%–3.31%
By group
Further findings
Absolute reduction in projected 10-year CVD incidence, by sex (subgroup)
- Absolute reduction, men
- 3.14% (95% CI: 2.82%-3.47%)
- Absolute reduction, women
- 2.7% (95% CI: 2.23%-3.16%)
- Relative reduction, men vs women
- 21% vs 23%
Nonobese and lower SCORE2 groups; reduced compliance
- Modeled risk reductions attenuated in nonobese and lower SCORE2 groups and diminished further with lower compliance assumptions
Parts of this Brief are withheld: the automatic checks could not confirm them against the abstract.
Original publication
Emulated Effects of Glucagon-Like Peptide 1 Receptor Agonist Therapy in the General Population. J Am Coll Cardiol. Published 11 March 2026. doi:10. 1016/ j. jacc. 2026. 01. 055
Summarised from the published abstract; every number is checked against it