Variation in Renal Function Following Transition to Sacubitril/Valsartan in Patients With Heart Failure

被引:15
作者
Chatur, Safia [1 ]
Claggett, Brian L. [1 ]
McCausland, Finnian R. [2 ]
Rouleau, Jean [3 ]
Zile, Michael R. [4 ,5 ]
Packer, Milton [6 ]
Pfeffer, Marc A. [1 ]
Lefkowitz, Martin [7 ]
McMurray, John J. V. [8 ]
Solomon, Scott D. [1 ,9 ]
Vaduganathan, Muthiah [1 ]
机构
[1] Brigham & Womens Hosp, Harvard Med Sch, Cardiovasc Div, Boston, MA USA
[2] Brigham & Womens Hosp, Harvard Med Sch, Renal Div, Boston, MA USA
[3] Univ Montreal, Inst Cardiol Montreal, Montreal, PQ, Canada
[4] Med Univ South Carolina, Charleston, SC USA
[5] Ralph H Johnson Dept Vet Affairs Med Ctr, Charleston, SC USA
[6] Baylor Univ, Med Ctr, Dallas, TX USA
[7] Novartis Pharmaceut, E Hanover, NJ USA
[8] Univ Glasgow, BHF Cardiovasc Res Ctr, Glasgow, Scotland
[9] Brigham & Womens Hosp, Harvard Med Sch, Dept Med, Cardiovasc Div, 75 Francis St, Boston, MA 02115 USA
关键词
KEY WORDS heart failure; kidney function; sacubitril; valsartan; THERAPY; INHIBITION; INITIATION;
D O I
10.1016/j.jacc.2023.02.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Some patients with heart failure may experience transient changes in kidney function upon transition to sacubitril/valsartan. Whether such changes portend adverse outcomes or influence long-term treatment benefits with sacubitril/valsartan continuation is unknown.OBJECTIVES This investigation aimed to evaluate the association between the occurrence of moderate estimated glomerular filtration rate (eGFR) decline (>15%) after initial exposure to sacubitril/valsartan and subsequent cardiovascular outcomes and its treatment benefits in PARADIGM-HF and PARAGON-HF.METHODS In sequential run-in phases, patients were titrated to enalapril 10 mg twice daily and then sacubitril/val-sartan 97 mg/103 mg twice daily (in PARADIGM-HF) or valsartan 80 mg twice daily and then sacubitril/valsartan 49 mg/ 51 mg twice daily (in PARAGON-HF). RESULTS Among randomized participants, 11% in PARADIGM-HF and 10% in PARAGON-HF experienced eGFR decline (>15%) during sacubitril/valsartan run-in. eGFR partially recovered (from nadir to postrandomization week 16) regardless of sacubitril/valsartan continuation or switch to renin-angiotensin system inhibitor (RASi) postrandomization. Initial eGFR decline was not consistently associated with clinical outcomes in either trial. Treatment benefits of sacubitril/valsartan vs RASi on primary outcomes were similar irrespective of run-in eGFR decline in PARADIGM-HF (eGFR decline, HR: 0.69; 95% CI: 0.53-0.90; and no eGFR decline, HR: 0.80; 95% CI: 0.73-0.88; Pinteraction = 0.32) and PARAGON-HF (eGFR decline, rate ratio [RR]: 0.84; 95% CI: 0.52-1.36 and no eGFR decline, RR: 0.87; 95% CI: 0.75-1.02, Pinteraction = 0.92). The treatment effect of sacubitril/valsartan remained consistent across a range of eGFR declines.CONCLUSIONS Moderate eGFR decline when transitioning from RASi to sacubitril/valsartan is not consistently associated with adverse outcomes, and its long-term benefits are retained in heart failure across a broad range of eGFR declines. Early eGFR changes should not deter continuation of sacubitril/valsartan or stall uptitration. (Efficacy and Safety of LCZ696 Compared to Valsartan, on Morbidity and Mortality in Heart Failure Patients With Preserved Ejection Fraction [PARAGON-HF]; NCT01920711; Prospective Comparison of Angiotensin Receptor-Neprilysin Inhibitors with Angiotensin-Converting Enzyme Inhibitors to Determine Impact on Global Mortality and Morbidity in Heart Failure [PARADIGM-HF]; NCT01035255) (J Am Coll Cardiol 2023;81:1443-1455) (c) 2023 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/).
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收藏
页码:1443 / 1455
页数:13
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