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Improved Renal Denervation Mitigated Hypertension Induced by Angiotensin II Infusion
Published on: May 26, 2022
Renal denervation in 2025: long-term evidence supporting sympathetic modulation as a durable strategy for
Dominique Stephan1, Emma Morisot1, François Bronner2
1Service d'HTA et Maladies Vasculaires, Hôpitaux Universitaires de Strasbourg, France.
Insights
Renal denervation (RDN) offers sustained blood pressure reduction for uncontrolled hypertension over 3 years. This safe therapy shows promise for high-risk patients, with no observed renal artery issues.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Hypertension Management
Background:
- Renal denervation (RDN) is an emerging device-based therapy for resistant hypertension.
- Recent major cardiovascular conferences presented 3-year follow-up data on RDN's efficacy and safety.
- Uncontrolled hypertension remains a significant global health challenge requiring innovative treatment strategies.
Purpose of the Study:
- To synthesize 3-year follow-up data on renal denervation (RDN) for uncontrolled hypertension.
- To evaluate the sustained efficacy and safety of RDN based on randomized trials and real-world registry data.
- To assess the impact of RDN on blood pressure control and acute hypertensive events.
Main Methods:
- Synthesis of data from SPYRAL HTN-ON MED, GSR-DEFINE registry, SPYRAL AFFIRM, and pooled analyses.
- Comparison of randomized sham-controlled trials with observational registry data.
- Analysis of office systolic blood pressure (SBP) reduction and acute hypertensive events at 3-year follow-up.
Main Results:
- Sustained office SBP reduction of -18.5 mmHg with RDN vs. -11.7 mmHg with sham at 3 years (SPYRAL HTN-ON MED).
- Global Symplicity Registry DEFINE showed -20.5 mmHg office SBP reduction at 3 years, with effects increasing over time.
- Pooled analysis indicated a 43% reduction in acute hypertensive events; no renal artery stenosis or reintervention needed.
Conclusions:
- RDN demonstrates durable and safe adjunctive therapy for selected patients with uncontrolled hypertension.
- Benefits of RDN extend to high-risk populations, including those with diabetes, CKD, and prior stroke.
- Long-term cardiovascular outcome data are still pending but initial results are promising.
Background:
Renal denervation (RDN) has emerged as a promising device-based therapy for uncontrolled hypertension. Recent data from major cardiovascular conferences (EuroPCR, ESH, TCT 2025) provide unprecedented 3-year follow-up evidence on efficacy, safety, and clinical outcomes.
Methods:
We synthesize key findings from the SPYRAL HTN-ON MED 3-year final report, the Global Symplicity Registry DEFINE (GSR-DEFINE) real-world data, SPYRAL AFFIRM post-approval study, and pooled analyses on acute hypertensive events. Data sources are distiguisehed by level of evidence: randomized sham-controlled trials versus observational registry data.
Results:
At 3 years, SPYRAL HTN-ON MED demonstrated sustained office systolic blood pressure (SBP) reductions of -18.5 mmHg (RDN) versus -11.7 mmHg (sham), with treatment difference of -6.8 mmHg (p = 0.0002). The GSR-DEFINE registry (n = 3109) showed -20.5 mmHg office SBP reduction at 3 years with progressively increasing effect over time. Pooled analysis revealed a 43% reduction in acute hypertensive events with RDN. No renal artery stenosis or need for reintervention was observed through 3 years.
Conclusion:
These data support RDN as a potentially durable and safe adjunctive therapy for uncontrolled hypertension in appropriately selected patients. Benefits appear to extend to high-risk populations including patients with diabetes, chronic kidney disease, and prior stroke, though long-term cardiovascular outcome data remain awaited.
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