In a model of 21,720 survey participants with BMI of 27 or more and high baseline risk, emulated GLP-1 receptor agonist therapy lowered projected 10-year CVD incidence from 13.82% to 10.83%, a relative reduction of 22%.
In plain wordsA computer model projected lower 10-year heart disease risk from GLP-1 drug effects. No drug was given in this study.
- Peptide
- Semaglutide
- Outcome
- DecreaseProjected 10-year CVD incidence, emulated GLP-1RA therapy
- Study
humann = 21,720
Cardiovascular risk model applied to survey cohorts- Outcome group
- Cardiovascular events · Cardiovascular
Measurements
- Projected 10-year CVD incidence
- 10.83%
- emulated GLP-1RA therapy
- Observed 10-year CVD incidence
- 13.82%
- baseline
- Absolute reduction
- 2.99%
- overall
- Relative reduction
- 22%
- overall
Source sentences
Emulated GLP-1RA therapy lowered projected CVD incidence to 10.83% (95% CI: 9.27%-12.39%), an absolute reduction of 2.99% (95% CI: 2.67%-3.31%) and a relative reduction of 22%.
2 context sentences(design, population, supporting numbers)
This study aims to emulate GLP-1RA use for primary prevention by applying risk factor changes observed in the SELECT (Semaglutide and Cardiovascular Outcomes in Obesity without Diabetes) trial to obese individuals at risk of but without established CVD.
This model was applied to 200,012 individuals from 2 contemporary health examination surveys to emulate GLP-1RA therapy by using sex-stratified, placebo-adjusted changes in the 5 risk factors observed with GLP-1RA therapy in SELECT.
In this study, Semaglutide was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Semaglutide.