CagriSema Reduces Blood Pressure in Adults With Overweight or Obesity: REDEFINE 1.
Summary
In REDEFINE 1, 68 weeks of CagriSema yielded a −10.9/−5.4 mmHg reduction in systolic/diastolic BP versus placebo, doubled the proportion achieving BP targets, and allowed de-escalation of antihypertensives in ~40% of users. Benefits were observed across subgroups, including resistant hypertension.
Key Findings
- BP change at 68 weeks: −10.9/−5.4 mmHg (systolic/diastolic) with CagriSema vs −2.8/−1.7 mmHg with placebo.
- BP target attainment: 63.0% with CagriSema vs 32.0% with placebo.
- Among resistant hypertension at baseline (n=167), BP target attainment 42.0% vs 29.3% (CagriSema vs placebo).
- 39.6% of antihypertensive users on CagriSema decreased or stopped therapy vs 18.8% with placebo.
Clinical Implications
For adults with obesity and elevated BP, CagriSema may provide dual benefits (weight loss and BP lowering), enabling BP target attainment and medication de-escalation. Clinicians should monitor for hypotension and individualize antihypertensive adjustments.
Why It Matters
Large, randomized phase 3 data show a weight-loss agent combination yields clinically meaningful BP reductions, potentially reframing hypertension management in obesity.
Limitations
- Diabetes excluded; generalizability to patients with diabetes is uncertain.
- Cardiovascular outcomes were not assessed; BP was a secondary endpoint in a weight-loss trial.
- Details on antihypertensive titration protocols are limited.
Future Directions
Evaluate hard cardiovascular outcomes and renal endpoints, assess efficacy in patients with diabetes, and define standardized antihypertensive de-escalation pathways with CagriSema.
Study Information
- Study Type
- RCT
- Research Domain
- Treatment
- Evidence Level
- I - Phase 3 randomized controlled trial with large sample size.
- Study Design
- OTHER