In adults with type 2 diabetes and eGFR of 60 or higher, liraglutide did not significantly change the primary composite cardiovascular outcome versus placebo (hazard ratio 0.94).
In plain wordsIn people with type 2 diabetes and eGFR of 60 or higher, liraglutide did not clearly change major heart and stroke events versus placebo.
- Peptide
- Liraglutide
- Outcome
- No significant changePrimary composite cardiovascular outcome, eGFR 60 or higher
- Study
n = 7,182
- Comparator
- Placebo
- Analysis
- Primary
- Outcome group
- Cardiovascular events · Cardiovascular
- Studied dose
- Dose not stated
Measurements
- Hazard ratio
- 0.94
- eGFR >=60
Source sentences
In patients with eGFR 2, risk reduction for the primary composite cardiovascular outcome with liraglutide was greater (hazard ratio [HR], 0.69; 95% CI, 0.57-0.85) versus those with eGFR ≥60 mL/min/1.73 m2 (HR, 0.94; 95% CI, 0.83-1.07; interaction P=0.01).
2 context sentences(design, population, supporting numbers)
Patients were randomized (1:1) to liraglutide or placebo, both in addition to standard of care.
These analyses assessed outcomes stratified by baseline estimated glomerular filtration rate (eGFR; 2) and baseline albuminuria.