Ambulatory Blood Pressure Monitoring to Predict Response to Renal Denervation

Author:

Gosse Philippe1,Cremer Antoine1,Kirtane Ajay J.2ORCID,Lobo Melvin D.3,Saxena Manish3ORCID,Daemen Joost4,Wang Yale5,Stegbauer Johannes6,Weber Michael A.7,Abraham Josephine8,Kario Kazuomi9,Bangalore Sripal10ORCID,Claude Lisa11ORCID,Liu Yuyin12ORCID,Azizi Michel131415

Affiliation:

1. From the Hôpital Saint-André–CHU, Bordeaux, France (P.G., A.C.)

2. Columbia University Medical Center/New York-Presbyterian Hospital and the Cardiovascular Research Foundation (A.J.K.)

3. Barts NIHR Biomedical Research Centre, William Harvey Research Institute, Queen Mary University of London, United Kingdom (M.D.L., M.S.)

4. Department of Cardiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, NL, the Netherlands (J.D.)

5. Minneapolis Heart Institute, Abbott Northwestern Hospital, MN (Y.W.)

6. Department of Nephrology, Medical Faculty, University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Germany (J.S.)

7. Division of Cardiovascular Medicine, State University of New York, Downstate Medical Center (M.A.W.)

8. Division of Nephrology and Hypertension, University of Utah, Salt lake city (J.A.)

9. Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical University School of Medicine, Tochigi, Japan (K.K.)

10. NYU School of Medicine, New York (S.B.)

11. ReCor Medical, Inc, Palo Alto, CA (L.C.)

12. Baim Institute for Clinical Research, Boston, MA (Y.L.)

13. Université de Paris, F-75006 Paris, France (M.A.)

14. AP-HP, Hôpital Européen Georges-Pompidou, Hypertension Department and DMU CARTE, F-75015 Paris, France (M.A.)

15. INSERM, CIC1418, F-75015 Paris, France (M.A.).

Abstract

Renal denervation (RDN) is effective in lowering blood pressure (BP) in patients with hypertension. The issue remains how to best identify potential responders. Ambulatory BP monitoring may be useful. Baseline nighttime systolic BP (SBP) ≥136 mm Hg and its variability (SD) ≥12 mm Hg in DENER-HTN trial or 24-hour heart rate ≥73.5 bpm in SPYRAL HTN-OFF MED Trial were shown to predict the BP response to RDN. We applied these criteria to the patients with hypertension in the sham-controlled RADIANCE-HTN SOLO trial to predict the BP response to ultrasound RDN at 2 months while patients were maintained off medications. BP responders were defined as: clinical with 24-hour SBP <130 mm Hg (RDN: 22/64 versus sham: 7/58); meaningful with 24-hour SBP reduction ≥10 mm Hg (RDN: 24/64, sham: 7/58); and extreme with 24-hour SBP reduction above mean+2 SD of the SBP decrease in the sham group, that is, ≥16.5 mm Hg (RDN: 10/64 versus sham: 2/58). The predictive criteria reported above were tested for sensitivity, specificity, and positive and negative predictive values. The predictive value varied according to the definition of response, with the clinical definition being strongly influenced by regression to the mean. Baseline nighttime SBP and its variability, especially when combined, offered good specificity (>90% irrespective of definition) but low sensitivity (from 9.1% to 30% depending on the definition) to predict responders; the heart rate criterion had insufficient predictive value. This analysis suggests the potential role of nighttime SBP and its variability to predict BP response to RDN in patients with hypertension. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT02649426.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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