Renal Denervation in High-Risk Patients With Hypertension

被引:90
|
作者
Mahfoud, Felix [1 ]
Mancia, Giuseppe [2 ,3 ]
Schmieder, Roland [4 ]
Narkiewicz, Krzysztof [5 ]
Ruilope, Luis [6 ,7 ,8 ]
Schlaich, Markus [9 ]
Whitbourn, Robert [10 ]
Zirlik, Andreas [11 ]
Zeller, Thomas [12 ]
Stawowy, Philipp [13 ]
Cohen, Sidney A. [14 ,15 ]
Fahy, Martin [14 ]
Boehm, Michael [1 ]
机构
[1] Saarland Univ Hosp, Dept Internal Med, Homburg, Germany
[2] Univ Milano Bicocca, Monza, Italy
[3] Policlin Monza, Monza, Italy
[4] Univ Hosp Erlangen, Dept Nephrol & Hypertens, Erlangen, Germany
[5] Med Univ Gdansk, Dept Hypertens & Diabetol, Gdansk, Poland
[6] Univ Europea Madrid, Hosp Univ 12 Octubre, Dept Cardiovasc Risk, Madrid, Spain
[7] Univ Europea Madrid, CIBERCV, Madrid, Spain
[8] Univ Europea Madrid, Sch Doctoral Studies & Res, Madrid, Spain
[9] Univ Western Australia, Royal Perth Hosp Unit, Sch Med, Dept Med,Dobney Hypertens Ctr, Perth, WA, Australia
[10] St Vincents Hosp, Dept Cardiol, Melbourne, Vic, Australia
[11] Med Univ Graz, Dept Cardiol, Graz, Austria
[12] Univ Herzzentrum Freiburg, Dept Angiol, Bad Krozingen, Germany
[13] Deutsch Herzzentrum Berlin, Dept Cardiol, Berlin, Germany
[14] Medtron PLC, Coronary & Struct Heart Div, Santa Rosa, CA USA
[15] Univ Penn, Perelman Sch Med, Dept Cardiol, Philadelphia, PA 19104 USA
基金
澳大利亚国家健康与医学研究理事会;
关键词
BLOOD-PRESSURE; SYMPLICITY HTN-3; DESIGN;
D O I
10.1016/j.jacc.2020.04.036
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Renal denervation (RDN) is under investigation for treatment of uncontrolled hypertension and might represent an attractive treatment for patients with high cardiovascular (CV) risk. It is important to determine whether baseline CV risk affects the efficacy of RDN. OBJECTIVES The purpose of this study was to assess blood pressure (BP) reduction and event rates after RDN in patients with various comorbidities, testing the hypothesis that RDN is effective and durable in these high-risk populations. METHODS BP reduction and adverse events over 3 years were evaluated for several high-risk subgroups in the GSR (Global proSpective registrY for syMPathetic renaL denervatIon in seleCted IndicatIons Through 3 Years Registry), an international registry of RDN in patients with uncontrolled hypertension (n = 2,652). Comparisons were made for patients age >= 65 years versus age <65 years, with versus without isolated systolic hypertension, with versus without atrial fibrillation, and with versus without diabetes mellitus. Baseline cardiovascular risk was estimated using the American Heart Association (AHA)/American College of Cardiology (ACC) atherosclerosis cardiovascular disease (ASCVD) risk score. RESULTS Reduction in 24-h systolic BP at 3 years was -8.9 +/- 20.1 mm Hg for the overall cohort, and for high-risk subgroups, BP reduction was -10.4 +/- 21.0 mm Hg for resistant hypertension, -8.7 +/- 17.4 mm Hg in patients age >= 65 years, -10.2 +/- 17.9 mm Hg in patients with diabetes, -8.6 +/- 18.7 mm Hg in isolated systolic hypertension, -10.1 +/- 20.3 mm Hg in chronic kidney disease, and -10.0 +/- 19.1 mm Hg in atrial fibrillation (p < 0.0001 compared with baseline for all). BP reduction in patients with measurements at 6, 12, 24, and 36 months showed similar reductions in office and 24-h BP for patients with varying baseline ASCVD risk scores, which was sustained to 3 years. Adverse event rates at 3 years were higher for patients with higher baseline CV risk. CONCLUSIONS BP reduction after RDN was similar for patients with varying high-risk comorbidities and across the range of ASCVD risk scores. The impact of baseline risk on clinical event reduction by RDN-induced BP changes could be evaluated in further studies. (Global proSpective registrY for syMPathetic renaL denervatIon in seleCted IndicatIons Through 3 Years Registry; NCT01534299) (J Am Coll Cardiol 2020;75:2879-88) (c) 2020 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:2879 / 2888
页数:10
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