Angiotensin Receptor Antagonist-Neprilysin Inhibitor (ARNI) therapy as a new hope in the population of people with heart failure with reduced ejection fraction (HFrEF)
DOI:
https://doi.org/10.12775/JEHS.2022.12.09.068Keywords
ARNI, neprilysin inhibition, HFrEF, heart failureAbstract
Introduction: Heart failure affects an estimated 23 million people, as many as 50% of whom suffer from a heart failure with reduced ejection fraction (HFrEF), in which the left ventricle ejection fraction is <40% and is accompanied by clinical symptoms. Given the high mortality rate in this group of patients and the continuous suboptimal control of the condition, novel pharmacotherapy regimens are needed to slow the progression of the disease. Preliminary studies report a positive effect of including an angiotensin receptor antagonist and neprilysin inhibitors (ARNIs) in this group of patients.
Aim of the study: The aim of the study was to summarize the benefits of ARNI in a group of patients with HFrEF.
Methods and materials: This article is based on the literature found in PubMed Database with use of keywords such as “ARNI”, “neprilysin inhibition”, HFrEF”, “heart failure”
Results: The benefits of ARNI therapy in patients with HFrEF originate from reversing myocardial remodeling and increasing left ventricular ejection fraction. ARNI therapy is associated with reduced number of hospitalizations and a lower need for intensive treatment. In addition, ARNI use reduces the risk of cardiovascular death and is responsible for lower overall mortality rate compared to pharmacotherapy with angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor antagonists (ARBs).
Conclusion: ARNIs in patients with HFrEF have a positive effect on the rate of cardiovascular hospitalization, as well as reducing cardiovascular-related mortality and total mortality. Future research studies should evaluate the predictive factors of response to treatment with this group of drugs using larger groups of patients.
References
Murphy SP, Ibrahim NE, Januzzi JL Jr. Heart Failure With Reduced Ejection Fraction: A Review. JAMA. 2020 Aug 4;324(5):488-504. doi: 10.1001/jama.2020.10262. Erratum in: JAMA. 2020 Nov 24;324(20):2107. PMID: 32749493.
Špinar J, Špinarová L, Vítovec J. Pathophysiology, causes and epidemiology of chronic heart failure. Vnitr Lek. 2018 Fall;64(9):834-838. English. PMID: 30441995.
Orso F, Fabbri G, Maggioni AP. Epidemiology of Heart Failure. Handb Exp Pharmacol. 2017;243:15-33. doi: 10.1007/164_2016_74. PMID: 27718059.
Kuchulakanti PK. ARNI in cardiovascular disease: current evidence and future perspectives. Future Cardiol. 2020 Sep;16(5):505-515. doi: 10.2217/fca-2019-0089. Epub 2020 Apr 22. PMID: 32319309.
Edelmann F, Knosalla C, Mörike K et al., Chronic Heart Failure. Dtsch Arztebl Int. 2018 Feb 23;115(8):124-130. doi: 10.3238/arztebl.2018.0124. PMID: 29526184; PMCID: PMC5852309.
Khalil P, Kabbach G, Said S et al., Entresto, a New Panacea for Heart Failure? Cardiovasc Hematol Agents Med Chem. 2018;16(1):5-11. doi: 10.2174/1871525716666180313121954. PMID: 29532764.
Hubers SA, Brown NJ. Combined Angiotensin Receptor Antagonism and Neprilysin Inhibition. Circulation. 2016 Mar 15;133(11):1115-24. doi: 10.1161/CIRCULATIONAHA.115.018622. PMID: 26976916; PMCID: PMC4800749.
Hayashi D, Kudoh S, Shiojima I et al., Atrial natriuretic peptide inhibits cardiomyocyte hypertrophy through mitogen-activated protein kinase phosphatase-1. Biochem Biophys Res Commun. 2004 Sep 10;322(1):310-9. doi: 10.1016/j.bbrc.2004.07.119. PMID: 15313208.
Tham YK, Bernardo BC, Ooi JY et al., Pathophysiology of cardiac hypertrophy and heart failure: signaling pathways and novel therapeutic targets. Arch Toxicol. 2015 Sep;89(9):1401-38. doi: 10.1007/s00204-015-1477-x. Epub 2015 Feb 24. PMID: 25708889.
McMurray JJ, Packer M, Desai AS et al.; PARADIGM-HF Investigators and Committees. Angiotensin-neprilysin inhibition versus enalapril in heart failure. N Engl J Med. 2014 Sep 11;371(11):993-1004. doi: 10.1056/NEJMoa1409077. Epub 2014 Aug 30. PMID: 25176015.
McMurray J, Packer M, Desai A et al.; PARADIGM-HF Committees and Investigators. A putative placebo analysis of the effects of LCZ696 on clinical outcomes in heart failure. Eur Heart J. 2015 Feb 14;36(7):434-9. doi: 10.1093/eurheartj/ehu455. PMID: 25416329; PMCID: PMC4328198.
Jianqing She,Bowen Lou,Hui Liu et al. ARNI versus ACEI/ARB in Reducing Cardiovascular Outcomes after Myocardial Infarction, 19 October 2021, doi: 10.1002/ehf2.13644
Bertero E, Maack C. Metabolic remodelling in heart failure. Nat Rev Cardiol. 2018 Aug;15(8):457-470. doi: 10.1038/s41569-018-0044-6. PMID: 29915254.
Porter KE, Turner NA. Cardiac fibroblasts: at the heart of myocardial remodeling. Pharmacol Ther. 2009 Aug;123(2):255-78. doi: 10.1016/j.pharmthera.2009.05.002. Epub 2009 May 19. PMID: 19460403.
De Diego C, Gonzalez-Torres L, Centurion ER et al. P787 Angiotensin-neprilysin inhibition further reverses cardiac remodeling as compared to angiotensin inhibition in reduced heart failure patients. Europace.2018;20:i139. doi: 10.1093/europace/euy015.391.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2022 Przemysław Żelazny, Joanna Filipczak, Oliwer Sygacz, Sebastian Bróż, Sara Dankiewicz, Aleksandra Swora, Joanna Borowik, Wojciech Brodowski, Piotr Pawłowski, Katarzyna Basta-Arciszewska

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
The periodical offers access to content in the Open Access system under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0
Stats
Number of views and downloads: 702
Number of citations: 0