Influence of neprilysin inhibition on the efficacy and safety of empagliflozin in patients with chronic heart failure and a reduced ejection fraction: the EMPEROR-Reduced trial

Author:

Packer Milton12ORCID,Anker Stefan D3ORCID,Butler Javed4,Filippatos Gerasimos5,Ferreira Joao Pedro6,Pocock Stuart J7ORCID,Rocca Hans-Peter Brunner-La8,Janssens Stefan9,Tsutsui Hiroyuki10,Zhang Jian11,Brueckmann Martina12,Jamal Waheed13ORCID,Cotton Daniel14ORCID,Iwata Tomoko15,Schnee Janet14ORCID,Zannad Faiez6ORCID,

Affiliation:

1. Baylor Heart and Vascular Institute, Baylor University Medical Center, 621 N. Hall Street, Dallas, TX, USA

2. Imperial College, London, UK

3. Department of Cardiology (CVK), and Berlin Institute of Health Center for Regenerative Therapies, German Centre for Cardiovascular Research Partner Site Berlin, Charité Universitätsmedizin, Berlin, Germany

4. Department of Medicine, University of Mississippi School of Medicine, Jackson, MS, USA

5. National and Kapodistrian, University of Athens School of Medicine, Athens University Hospital Attikon, Athens, Greece

6. Université de Lorraine, Inserm INI-CRCT, CHRU, Nancy, France

7. Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, UK

8. Department of Cardiology, Maastricht University Medical Center, Maastricht, The Netherlands

9. Department of Cardiology, University Hospital Gasthuisberg of Leuven, Leuven, Belgium

10. Department of Cardiovascular Medicine, Kyushu University, Higashi-ku, Fukuoka, Japan

11. Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People’s Republic of China

12. Boehringer Ingelheim International GmbH and Faculty of Medicine Mannheim, University of Heidelberg, Mannheim, Germany

13. Boehringer Ingelheim International GmbH, Ingelheim, Germany

14. Boehringer Ingelheim Pharmaceuticals, Inc, Ridgefield, CT, USA

15. Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany

Abstract

Abstract Aims We evaluated the influence of sacubitril/valsartan on the effects of sodium-glucose cotransporter 2 (SGLT2) inhibition with empagliflozin in patients with heart failure and a reduced ejection fraction. Methods and results The EMPEROR-Reduced trial randomized 3730 patients with heart failure and an ejection fraction ≤40% to placebo or empagliflozin (10 mg/day), in addition to recommended treatment for heart failure, for a median of 16 months. A total of 727 patients (19.5%) received sacubitril/valsartan at baseline. Analysis of the effect of neprilysin inhibition was 1 of 12 pre-specified subgroups. Patients receiving a neprilysin inhibitor were particularly well-treated, as evidenced by lower systolic pressures, heart rates, N-terminal prohormone B-type natriuretic peptide, and greater use of cardiac devices (all P < 0.001) when compared with those not receiving sacubitril/valsartan. Nevertheless, when compared with placebo, empagliflozin reduced the risk of cardiovascular death or hospitalization for heart failure in patients receiving or not receiving sacubitril/valsartan [hazard ratio 0.64 (95% CI 0.45–0.89), P = 0.009 and hazard ratio 0.77 (95% CI 0.66–0.90), P = 0.0008, respectively, interaction P = 0.31]. Empagliflozin slowed the rate of decline in estimated glomerular filtration rate by 1.92 ± 0.80 mL/min/1.73 m2/year in patients taking a neprilysin inhibitor (P = 0.016) and by 1.71 ± 0.35 mL/min/1.73 m2/year in patients not taking a neprilysin inhibitor (P < 0.0001), interaction P = 0.81. Combined inhibition of SGLT2 and neprilysin was well-tolerated. Conclusion The effects on empagliflozin to reduce the risk of heart failure and renal events are not diminished in intensively treated patients who are receiving sacubitril/valsartan. Combined treatment with both SGLT2 and neprilysin inhibitors can be expected to yield substantial additional benefits.

Funder

Boehringer Ingelheim

Eli Lilly and Company

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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