Efficacy and Safety of Catheter-Based Radiofrequency Renal Denervation in Chinese Patients With Uncontrolled Hypertension: The Randomized, Sham-Controlled, Multi-Center Iberis-HTN Trial
机构:[1]Fuwai Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences[2]Department of Cardiology and Cardiovascular Research Institute Basel, University Heart Center, University Hospital Basel, Switzerland[3]Medical Research & Biometrics Center, National Center for Cardiovascular Diseases, The Chinese Academy of Medical Sciences[4]Lanzhou University Second Hospital, China[5]Zhengzhou Central Hospital Affiliated to Zhengzhou University, China[6]West China Hospital, Sichuan University, China四川大学华西医院[7]The First Affiliated Hospital of Chengdu Medical Collage, China[8]Affiliated Hospital of Hebei University河北大学附属医院[9]Xinxiang Central Hospital, China[10]Tangshan Workers' Hospital[11]The Second Affiliated Hospital of Nanchang University[12]Xuzhou Central Hospital[13]Daping Hospital, The Third Military Medical University[14]The Affiliated Hospital of Hangzhou Normal University[15]Ruijin Hospital, Shanghai Jiaotong University School of Medicine[16]Inner Mongolia Autonomous Region People's Hospital[17]Henan Provincial Chest Hospital[18]Hospital of Chengdu University of Traditional Chinese Medicine[19]EastPoint Innovation Center, Hangzhou, China[20]Shanghai Angiocare Medical Technology, China[21]Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical University School of Medicine, Tochigi Japan
Renal denervation (RDN) can lower blood pressure (BP) in patients with hypertension in both the presence and absence of medication. This is the first sham-controlled trial investigating the safety and efficacy of RDN in China.This prospective, multicenter, randomized, patient- and outcome-assessor-blinded, sham-controlled trial investigated radiofrequency RDN in patients with hypertension on standardized triple antihypertensive therapy. Eligible patients were randomized 1:1 to undergo RDN using a multi-electrode radiofrequency catheter (Iberis; AngioCare, Shanghai, China) or a sham procedure. The primary efficacy outcome was the between-group difference in baseline-adjusted change in mean 24-hour ambulatory systolic BP from randomization to 6 months.Of 217 randomized patients (mean age, 45.3±10.2 years; 21% female), 107 were randomized to RDN and 110 were randomized to sham control. At 6 months, there was a greater reduction in 24-hour systolic BP in the RDN (-13.0±12.1 mm Hg) compared with the sham control group (-3.0±13.0 mm Hg; baseline-adjusted between-group difference, -9.4 mm Hg [95% CI, -12.8 to -5.9]; P<0.001). Compared with sham, 24-hour diastolic BP was lowered by -5.0 mm Hg ([95% CI, -7.5 to -2.4]; P<0.001) 6 months after RDN, and office systolic and diastolic BP was lowered by -6.4 mm Hg ([95% CI, -10.5 to -2.3]; P=0.003) and -5.1 mm Hg ([95% CI, -8.2 to -2.0]; P=0.001), respectively. One patient in the RDN group experienced an access site complication (hematoma), which resolved without sequelae. No other major device- or procedure-related safety events occurred through follow-up.In this trial of Chinese patients with uncontrolled hypertension on a standardized triple pharmacotherapy, RDN was safe and reduced ambulatory and office BP at 6 months compared with sham.URL: https://clinicaltrials.gov; Unique identifier: NCT02901704.
基金:
X. Jiang is supported by Iberis-HTN trial fund from Shanghai Angiocare Medical
Technology, CAMS Innovation Fund for Medical Sciences (grant Nos. 2021-I2MC&
T-B-026 and 2021-I2M-C&T-B-027). He has received speaker honoraria
fees from Medtronic and Terumo. Felix Mahfoud is supported by Deutsche Gesellschaft
für Kardiologie, Deutsche Forschungsgemeinschaft (SFB TRR219, Project
ID 322900939), and Deutsche Herzstiftung. He has received scientific support
from Ablative Solutions, Medtronic, and ReCor Medical, and speaker honoraria/
consulting fees from Ablative Solutions, Amgen, Astra-Zeneca, Bayer, Boehringer
Ingelheim, Inari, Medtronic, Merck, ReCor Medical, Servier, and Terumo. L. Lauder
received speaker honoraria/consulting fees from AstraZeneca, Medtronic, Pfizer,
and ReCor. Brad Hubbard is an employee of EastPoint Innovation Center. X. Hu
is an employee of Shanghai Angiocare Medical Technology. R. Gao received institutional
research grants from Shanghai Angiocare Medical Technology (Shanghai,
China) and Biotyx Medical (Shenzhen, China).
第一作者机构:[1]Fuwai Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences
共同第一作者:
通讯作者:
推荐引用方式(GB/T 7714):
Jiang Xiongjing,Mahfoud Felix,Li Wei,et al.Efficacy and Safety of Catheter-Based Radiofrequency Renal Denervation in Chinese Patients With Uncontrolled Hypertension: The Randomized, Sham-Controlled, Multi-Center Iberis-HTN Trial[J].Circulation.2024,150(20):1588-1598.doi:10.1161/CIRCULATIONAHA.124.069215.
APA:
Jiang Xiongjing,Mahfoud Felix,Li Wei,Dong Hui,Yu Jing...&Gao Runlin.(2024).Efficacy and Safety of Catheter-Based Radiofrequency Renal Denervation in Chinese Patients With Uncontrolled Hypertension: The Randomized, Sham-Controlled, Multi-Center Iberis-HTN Trial.Circulation,150,(20)
MLA:
Jiang Xiongjing,et al."Efficacy and Safety of Catheter-Based Radiofrequency Renal Denervation in Chinese Patients With Uncontrolled Hypertension: The Randomized, Sham-Controlled, Multi-Center Iberis-HTN Trial".Circulation 150..20(2024):1588-1598