TY - JOUR
T1 - Renal Denervation Effects on Blood Pressure in Resistant and Uncontrolled Hypertension
T2 - A Meta-Analysis of Sham-Controlled Randomized Clinical Trials
AU - Soleimani, Hamidreza
AU - Sattartabar, Babak
AU - Parastooei, Bahar
AU - Eshraghi, Reza
AU - Nazari, Roozbeh
AU - Najdaghi, Soroush
AU - Hobaby, Sara
AU - Etemadi, Ali
AU - Mahalleh, Mehrdad
AU - Taheri, Maryam
AU - Hernandez, Adrian V.
AU - Kuno, Toshiki
AU - Taheri, Homa
AU - Siegel, Robert J.
AU - Rader, Florian
AU - Tehrani, Behnam N.
AU - Mandegar, Mohammad Hossein
AU - Safaee, Ehsan
AU - Ebrahimi, Pouya
AU - Hosseini, Kaveh
N1 - Publisher Copyright:
© 2025 The Author(s). Clinical Cardiology published by Wiley Periodicals LLC.
PY - 2025/3
Y1 - 2025/3
N2 - Background: Although some guidelines recommend Renal denervation (RDN) as an alternative to anti-HTN medications, there are concerns about its efficacy and safety. We aimed to evaluate the benefits and harms of RDN in a systematic review and meta-analysis of sham-controlled randomized clinical trials (RCT). Methods: Databases were searched until September 10th, 2024, to identify RCTs evaluating RDN for treating URH versus sham control. The primary outcomes were the change in office and ambulatory 24-h systolic (SBP) and diastolic blood pressure (DBP). Secondary outcomes were changes in daytime and nighttime SBP and DBP, home BP, number of anti-HTN drugs, and related complications. Mean differences (MD) and relative risks (RR) described the effects of RDN on BP and complications, respectively, using random effects meta-analyses. GRADE methodology was used to assess the certainty of evidence (COE). Results: We found 16 included sham-controlled RCTs [RDN (n = 1594) vs. sham (n = 1225)]. RDN significantly reduced office SBP (MD −4.26 mmHg, 95% CI: −5.68 to −2.84), 24 h ambulatory SBP (MD −2.63 mmHg), office DBP (MD −2.15 mmHg), 24-h ambulatory DBP (MD −1.27 mmHg), and daytime SBP and DBP (MD −3.29 and 2.97 mmHg), compared to the sham. The rate of severe complications was low in both groups (0%–2%). The heterogeneity was high among most indices, and CoE was very low for most outcomes. Conclusion: RDN significantly reduced several SBP and DBP outcomes versus sham without significantly increasing complications. This makes RDN a potentially effective alternative to medications in URH.
AB - Background: Although some guidelines recommend Renal denervation (RDN) as an alternative to anti-HTN medications, there are concerns about its efficacy and safety. We aimed to evaluate the benefits and harms of RDN in a systematic review and meta-analysis of sham-controlled randomized clinical trials (RCT). Methods: Databases were searched until September 10th, 2024, to identify RCTs evaluating RDN for treating URH versus sham control. The primary outcomes were the change in office and ambulatory 24-h systolic (SBP) and diastolic blood pressure (DBP). Secondary outcomes were changes in daytime and nighttime SBP and DBP, home BP, number of anti-HTN drugs, and related complications. Mean differences (MD) and relative risks (RR) described the effects of RDN on BP and complications, respectively, using random effects meta-analyses. GRADE methodology was used to assess the certainty of evidence (COE). Results: We found 16 included sham-controlled RCTs [RDN (n = 1594) vs. sham (n = 1225)]. RDN significantly reduced office SBP (MD −4.26 mmHg, 95% CI: −5.68 to −2.84), 24 h ambulatory SBP (MD −2.63 mmHg), office DBP (MD −2.15 mmHg), 24-h ambulatory DBP (MD −1.27 mmHg), and daytime SBP and DBP (MD −3.29 and 2.97 mmHg), compared to the sham. The rate of severe complications was low in both groups (0%–2%). The heterogeneity was high among most indices, and CoE was very low for most outcomes. Conclusion: RDN significantly reduced several SBP and DBP outcomes versus sham without significantly increasing complications. This makes RDN a potentially effective alternative to medications in URH.
KW - cardiovascular events
KW - meta-analysis
KW - renal denervation
KW - resistant hypertension
KW - sham-controlled
UR - http://www.scopus.com/inward/record.url?scp=85218932156&partnerID=8YFLogxK
U2 - 10.1002/clc.70104
DO - 10.1002/clc.70104
M3 - Artículo de revisión
AN - SCOPUS:85218932156
SN - 0160-9289
VL - 48
JO - Clinical Cardiology
JF - Clinical Cardiology
IS - 3
M1 - e70104
ER -