In matched patients with heart failure with preserved ejection fraction, obesity and type 2 diabetes, a primary outcome event (KCCQ difference of 5 points or more) occurred in 60.6% on once-weekly semaglutide versus 17.7% of controls.
In plain wordsIn patients with heart failure, obesity and type 2 diabetes, more semaglutide users than controls had a clear gain in heart failure symptom score.
- Peptide
- Semaglutide
- Outcome
- IncreaseHeart failure status (KCCQ total symptom score difference of 5 points or more)
- Study
n = 406
- Comparator
- Patients not treated with GLP-1 receptor agonists (propensity-matched)
- Analysis
- Primary
- Outcome group
- Heart function · Cardiovascular
- Studied dose
- 1.00 mg once weeklyAs given in this study (human).
Measurements
- Primary outcome event
- 60.6%
- semaglutide
- Primary outcome event
- 17.7%
- control
- Odds ratio
- 3.99 ratio
- semaglutide versus control
Source sentences
A primary outcome event occurred in 123 patients (60.6%) in the Sema-Preserved Group and 36 (17.7%) in the Control-Preserved Group (odds ratio: 3.99; 95% confidence interval: 1.69-6.28; p<0.01)
2 context sentences(design, population, supporting numbers)
This prospective, real-world study included patients with heart heart failure with preserved ejection fraction, obesity and type 2 diabetes treated with once-weekly 1.00mg semaglutide (Sema-Preserved Group) and patients not treated with glucagon-like peptide-1 receptor agonists (Control-Preserved Group).
After matching, 203 patients were included in each group.