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 |
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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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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 versus >= 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.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/CIRCULATIONAHA.120.047643</identifier><identifier>PMID: 32845715</identifier><language>eng</language><publisher>PHILADELPHIA: by the American College of Cardiology Foundation and the American Heart Association, Inc</publisher><subject>Cardiac & Cardiovascular Systems ; Cardiology and cardiovascular system ; Cardiovascular System & Cardiology ; Human health and pathology ; Life Sciences ; Life Sciences & Biomedicine ; Peripheral Vascular Disease ; Science & Technology</subject><ispartof>Circulation (New York, N.Y.), 2020-09, Vol.142 (13), p.1236-1245</ispartof><rights>by the American College of Cardiology Foundation and the American Heart Association, Inc.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>99</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000576528800005</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c4802-90d63920b2ce6c80b3172d0beb7ce9a0be6de1201b4dc4e2b167d1c69bded3d3</citedby><cites>FETCH-LOGICAL-c4802-90d63920b2ce6c80b3172d0beb7ce9a0be6de1201b4dc4e2b167d1c69bded3d3</cites><orcidid>0000-0002-0299-0533 ; 0000-0003-4306-5317 ; 0000-0001-8780-720X ; 0000-0003-1828-2387 ; 0000-0003-3876-7568</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,3688,27929,27930,28253</link.rule.ids><backlink>$$Uhttps://hal.univ-lorraine.fr/hal-03720119$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Mc Causland, Finnian R.</creatorcontrib><creatorcontrib>Lefkowitz, Martin P.</creatorcontrib><creatorcontrib>Claggett, Brian</creatorcontrib><creatorcontrib>Anavekar, Nagesh S.</creatorcontrib><creatorcontrib>Senni, Michele</creatorcontrib><creatorcontrib>Gori, Mauro</creatorcontrib><creatorcontrib>Jhund, Pardeep S.</creatorcontrib><creatorcontrib>McGrath, Martina M.</creatorcontrib><creatorcontrib>Packer, Milton</creatorcontrib><creatorcontrib>Shi, Victor</creatorcontrib><creatorcontrib>Van Veldhuisen, Dirk J.</creatorcontrib><creatorcontrib>Zannad, Faiez</creatorcontrib><creatorcontrib>Comin-Colet, Josep</creatorcontrib><creatorcontrib>Pfeffer, Marc A.</creatorcontrib><creatorcontrib>McMurray, John J.V.</creatorcontrib><creatorcontrib>Solomon, Scott D.</creatorcontrib><title>Angiotensin-Neprilysin Inhibition and Renal Outcomes in Heart Failure With Preserved Ejection Fraction</title><title>Circulation (New York, N.Y.)</title><addtitle>CIRCULATION</addtitle><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 versus >= 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.</description><subject>Cardiac & Cardiovascular Systems</subject><subject>Cardiology and cardiovascular system</subject><subject>Cardiovascular System & Cardiology</subject><subject>Human health and pathology</subject><subject>Life Sciences</subject><subject>Life Sciences & Biomedicine</subject><subject>Peripheral Vascular Disease</subject><subject>Science & Technology</subject><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><recordid>eNqNkl1v0zAUhi0EYmXwH8IdCKX4K3FyGUUrrVStaCri0nLsU-KR2sNONu3f4yzTJO648vHR81g-fo3QR4LXhJTka7u7aX_sm-PucN1smzWheI25KDl7hVakoDznBatfoxXGuM4Fo_QCvYvxNm1LJoq36ILRiheCFCt0atwv60dw0br8Gu6CHR5Tme1cbzs7Wu8y5Ux2A04N2WEatT9DzBKwBRXGbKPsMAXIftqxz74HiBDuwWRXt6Cf3E1QT8V79OakhggfntdLdNxcHdttvj9827XNPte8wjSvsSlZTXFHNZS6wh0jghrcQSc01CoVpYE0Lum40RxoR0phiC7rzoBhhl2iz8uxvRpkmuWswqP0yspts5dzDzORbFLfk8R-Wti74P9MEEd5tlHDMCgHfoqSciaqgiU6ofWC6uBjDHB6OZtgOSci_01EpivKJZHkflncB-j8KWoLTsOLnyIpRFnQqsJzmejq_-nWjmp-3NZPbkwqf1b9MEKIv4fpAYLsQQ1jP6s4zSJyimn6FbTG-dyi7C9Jmq-a</recordid><startdate>20200929</startdate><enddate>20200929</enddate><creator>Mc Causland, Finnian R.</creator><creator>Lefkowitz, Martin P.</creator><creator>Claggett, Brian</creator><creator>Anavekar, Nagesh S.</creator><creator>Senni, Michele</creator><creator>Gori, Mauro</creator><creator>Jhund, Pardeep S.</creator><creator>McGrath, Martina M.</creator><creator>Packer, Milton</creator><creator>Shi, Victor</creator><creator>Van Veldhuisen, Dirk J.</creator><creator>Zannad, Faiez</creator><creator>Comin-Colet, Josep</creator><creator>Pfeffer, Marc A.</creator><creator>McMurray, John J.V.</creator><creator>Solomon, Scott D.</creator><general>by the American College of Cardiology Foundation and the American Heart Association, Inc</general><general>Lippincott Williams & Wilkins</general><general>American Heart Association</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-0299-0533</orcidid><orcidid>https://orcid.org/0000-0003-4306-5317</orcidid><orcidid>https://orcid.org/0000-0001-8780-720X</orcidid><orcidid>https://orcid.org/0000-0003-1828-2387</orcidid><orcidid>https://orcid.org/0000-0003-3876-7568</orcidid></search><sort><creationdate>20200929</creationdate><title>Angiotensin-Neprilysin Inhibition and Renal Outcomes in Heart Failure With Preserved Ejection Fraction</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4802-90d63920b2ce6c80b3172d0beb7ce9a0be6de1201b4dc4e2b167d1c69bded3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cardiac & Cardiovascular Systems</topic><topic>Cardiology and cardiovascular system</topic><topic>Cardiovascular System & Cardiology</topic><topic>Human health and pathology</topic><topic>Life Sciences</topic><topic>Life Sciences & Biomedicine</topic><topic>Peripheral Vascular Disease</topic><topic>Science & Technology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mc Causland, Finnian R.</creatorcontrib><creatorcontrib>Lefkowitz, Martin P.</creatorcontrib><creatorcontrib>Claggett, Brian</creatorcontrib><creatorcontrib>Anavekar, Nagesh S.</creatorcontrib><creatorcontrib>Senni, Michele</creatorcontrib><creatorcontrib>Gori, Mauro</creatorcontrib><creatorcontrib>Jhund, Pardeep S.</creatorcontrib><creatorcontrib>McGrath, Martina M.</creatorcontrib><creatorcontrib>Packer, Milton</creatorcontrib><creatorcontrib>Shi, Victor</creatorcontrib><creatorcontrib>Van Veldhuisen, Dirk J.</creatorcontrib><creatorcontrib>Zannad, Faiez</creatorcontrib><creatorcontrib>Comin-Colet, Josep</creatorcontrib><creatorcontrib>Pfeffer, Marc A.</creatorcontrib><creatorcontrib>McMurray, John J.V.</creatorcontrib><creatorcontrib>Solomon, Scott D.</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mc Causland, Finnian R.</au><au>Lefkowitz, Martin P.</au><au>Claggett, Brian</au><au>Anavekar, Nagesh S.</au><au>Senni, Michele</au><au>Gori, Mauro</au><au>Jhund, Pardeep S.</au><au>McGrath, Martina M.</au><au>Packer, Milton</au><au>Shi, Victor</au><au>Van Veldhuisen, Dirk J.</au><au>Zannad, Faiez</au><au>Comin-Colet, Josep</au><au>Pfeffer, Marc A.</au><au>McMurray, John J.V.</au><au>Solomon, Scott D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Angiotensin-Neprilysin Inhibition and Renal Outcomes in Heart Failure With Preserved Ejection Fraction</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><stitle>CIRCULATION</stitle><date>2020-09-29</date><risdate>2020</risdate><volume>142</volume><issue>13</issue><spage>1236</spage><epage>1245</epage><pages>1236-1245</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><abstract>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 versus >= 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.</abstract><cop>PHILADELPHIA</cop><pub>by the American College of Cardiology Foundation and the American Heart Association, Inc</pub><pmid>32845715</pmid><doi>10.1161/CIRCULATIONAHA.120.047643</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-0299-0533</orcidid><orcidid>https://orcid.org/0000-0003-4306-5317</orcidid><orcidid>https://orcid.org/0000-0001-8780-720X</orcidid><orcidid>https://orcid.org/0000-0003-1828-2387</orcidid><orcidid>https://orcid.org/0000-0003-3876-7568</orcidid><oa>free_for_read</oa></addata></record> |
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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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