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CagriSema Reduces Blood Pressure in Adults With Overweight or Obesity: REDEFINE 1.

Hypertension (Dallas, Tex. : 1979)2025-12-02PubMed
Total: 82.5Innovation: 7Impact: 9Rigor: 9Citation: 8

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