Angiotensin-Neprilysin Inhibition and Renal Outcomes in Heart Failure With Preserved Ejection Fraction

Background: In patients with heart failure, chronic kidney disease is common and associated with a higher risk of renal events than in patients without chronic kidney disease. We assessed the renal effects of angiotensin/neprilysin inhibition in patients who have heart failure with preserved ejectio...

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Veröffentlicht in:Circulation (New York, N.Y.) N.Y.), 2020-09, Vol.142 (13), p.1236-1245
Hauptverfasser: Mc Causland, Finnian R., Lefkowitz, Martin P., Claggett, Brian, Anavekar, Nagesh S., Senni, Michele, Gori, Mauro, Jhund, Pardeep S., McGrath, Martina M., Packer, Milton, Shi, Victor, Van Veldhuisen, Dirk J., Zannad, Faiez, Comin-Colet, Josep, Pfeffer, Marc A., McMurray, John J.V., Solomon, Scott D.
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container_end_page 1245
container_issue 13
container_start_page 1236
container_title Circulation (New York, N.Y.)
container_volume 142
creator Mc Causland, Finnian R.
Lefkowitz, Martin P.
Claggett, Brian
Anavekar, Nagesh S.
Senni, Michele
Gori, Mauro
Jhund, Pardeep S.
McGrath, Martina M.
Packer, Milton
Shi, Victor
Van Veldhuisen, Dirk J.
Zannad, Faiez
Comin-Colet, Josep
Pfeffer, Marc A.
McMurray, John J.V.
Solomon, Scott D.
description Background: In patients with heart failure, chronic kidney disease is common and associated with a higher risk of renal events than in patients without chronic kidney disease. We assessed the renal effects of angiotensin/neprilysin inhibition in patients who have heart failure with preserved ejection fraction enrolled in the PARAGON-HF trial (Prospective Comparison of ARNI With ARB Global Outcomes in HF With Preserved Ejection Fraction). Methods: In this randomized, double-blind, event-driven trial, we assigned 4822 patients who had heart failure with preserved ejection fraction to receive sacubitril/valsartan (n=2419) or valsartan (n=2403). Herein, we present the results of the prespecified renal composite outcome (time to first occurrence of either: >= 50% reduction in estimated glomerular filtration rate (eGFR), end-stage renal disease, or death from renal causes), the individual components of this composite, and the influence of therapy on eGFR slope. Results: At randomization, eGFR was 63 +/- 19 mL.min(-1).1.73 m(-2). At study closure, the composite renal outcome occurred in 33 patients (1.4%) assigned to sacubitril/valsartan and 64 patients (2.7%) assigned to valsartan (hazard ratio, 0.50 [95% CI, 0.33-0.77];P=0.001). The treatment effect on the composite renal end point did not differ according to the baseline eGFR (= 60 mL.min(-1).1.73 m(-2) (P-interaction=0.92). The decline in eGFR was less for sacubitril/valsartan than for valsartan (-2.0 [95% CI, -2.2 to -1.9] versus -2.7 [95% CI, -2.8 to -2.5] mL.min(-1).1.73 m(-2) per year). Conclusions: In patients with heart failure with preserved ejection fraction, sacubitril/valsartan reduced the risk of renal events, and slowed decline in eGFR, in comparison with valsartan. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01920711.
doi_str_mv 10.1161/CIRCULATIONAHA.120.047643
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We assessed the renal effects of angiotensin/neprilysin inhibition in patients who have heart failure with preserved ejection fraction enrolled in the PARAGON-HF trial (Prospective Comparison of ARNI With ARB Global Outcomes in HF With Preserved Ejection Fraction). Methods: In this randomized, double-blind, event-driven trial, we assigned 4822 patients who had heart failure with preserved ejection fraction to receive sacubitril/valsartan (n=2419) or valsartan (n=2403). Herein, we present the results of the prespecified renal composite outcome (time to first occurrence of either: &gt;= 50% reduction in estimated glomerular filtration rate (eGFR), end-stage renal disease, or death from renal causes), the individual components of this composite, and the influence of therapy on eGFR slope. Results: At randomization, eGFR was 63 +/- 19 mL.min(-1).1.73 m(-2). At study closure, the composite renal outcome occurred in 33 patients (1.4%) assigned to sacubitril/valsartan and 64 patients (2.7%) assigned to valsartan (hazard ratio, 0.50 [95% CI, 0.33-0.77];P=0.001). The treatment effect on the composite renal end point did not differ according to the baseline eGFR (&lt;60 versus &gt;= 60 mL.min(-1).1.73 m(-2) (P-interaction=0.92). The decline in eGFR was less for sacubitril/valsartan than for valsartan (-2.0 [95% CI, -2.2 to -1.9] versus -2.7 [95% CI, -2.8 to -2.5] mL.min(-1).1.73 m(-2) per year). Conclusions: In patients with heart failure with preserved ejection fraction, sacubitril/valsartan reduced the risk of renal events, and slowed decline in eGFR, in comparison with valsartan. 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We assessed the renal effects of angiotensin/neprilysin inhibition in patients who have heart failure with preserved ejection fraction enrolled in the PARAGON-HF trial (Prospective Comparison of ARNI With ARB Global Outcomes in HF With Preserved Ejection Fraction). Methods: In this randomized, double-blind, event-driven trial, we assigned 4822 patients who had heart failure with preserved ejection fraction to receive sacubitril/valsartan (n=2419) or valsartan (n=2403). Herein, we present the results of the prespecified renal composite outcome (time to first occurrence of either: &gt;= 50% reduction in estimated glomerular filtration rate (eGFR), end-stage renal disease, or death from renal causes), the individual components of this composite, and the influence of therapy on eGFR slope. Results: At randomization, eGFR was 63 +/- 19 mL.min(-1).1.73 m(-2). At study closure, the composite renal outcome occurred in 33 patients (1.4%) assigned to sacubitril/valsartan and 64 patients (2.7%) assigned to valsartan (hazard ratio, 0.50 [95% CI, 0.33-0.77];P=0.001). The treatment effect on the composite renal end point did not differ according to the baseline eGFR (&lt;60 versus &gt;= 60 mL.min(-1).1.73 m(-2) (P-interaction=0.92). The decline in eGFR was less for sacubitril/valsartan than for valsartan (-2.0 [95% CI, -2.2 to -1.9] versus -2.7 [95% CI, -2.8 to -2.5] mL.min(-1).1.73 m(-2) per year). Conclusions: In patients with heart failure with preserved ejection fraction, sacubitril/valsartan reduced the risk of renal events, and slowed decline in eGFR, in comparison with valsartan. 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We assessed the renal effects of angiotensin/neprilysin inhibition in patients who have heart failure with preserved ejection fraction enrolled in the PARAGON-HF trial (Prospective Comparison of ARNI With ARB Global Outcomes in HF With Preserved Ejection Fraction). Methods: In this randomized, double-blind, event-driven trial, we assigned 4822 patients who had heart failure with preserved ejection fraction to receive sacubitril/valsartan (n=2419) or valsartan (n=2403). Herein, we present the results of the prespecified renal composite outcome (time to first occurrence of either: &gt;= 50% reduction in estimated glomerular filtration rate (eGFR), end-stage renal disease, or death from renal causes), the individual components of this composite, and the influence of therapy on eGFR slope. Results: At randomization, eGFR was 63 +/- 19 mL.min(-1).1.73 m(-2). At study closure, the composite renal outcome occurred in 33 patients (1.4%) assigned to sacubitril/valsartan and 64 patients (2.7%) assigned to valsartan (hazard ratio, 0.50 [95% CI, 0.33-0.77];P=0.001). The treatment effect on the composite renal end point did not differ according to the baseline eGFR (&lt;60 versus &gt;= 60 mL.min(-1).1.73 m(-2) (P-interaction=0.92). The decline in eGFR was less for sacubitril/valsartan than for valsartan (-2.0 [95% CI, -2.2 to -1.9] versus -2.7 [95% CI, -2.8 to -2.5] mL.min(-1).1.73 m(-2) per year). Conclusions: In patients with heart failure with preserved ejection fraction, sacubitril/valsartan reduced the risk of renal events, and slowed decline in eGFR, in comparison with valsartan. 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subjects Cardiac & Cardiovascular Systems
Cardiology and cardiovascular system
Cardiovascular System & Cardiology
Human health and pathology
Life Sciences
Life Sciences & Biomedicine
Peripheral Vascular Disease
Science & Technology
title Angiotensin-Neprilysin Inhibition and Renal Outcomes in Heart Failure With Preserved Ejection Fraction
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