» Articles » PMID: 29921166

Sacubitril/valsartan in Cardiovascular Disease: Evidence to Date and Place in Therapy

Overview
Publisher Sage Publications
Date 2018 Jun 21
PMID 29921166
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Cardiovascular (CV) disease is a major cause of morbidity and mortality in the developing and the developed world. Mortality from CV disease had plateaued in the recent years raising concerning alarms about the sustained efficacy of available preventive and treatment options. Heart failure (HF) is among the major contributors to the CV-related health care burden, a persisting concern despite the use of clinically proven guideline-directed therapies. A requirement for more efficient medical therapies coupled with recent advances in bio-innovation led to the creation of sacubitril/valsartan, an angiotensin receptor-neprilysin inhibitor (ARNI), which demonstrated substantial CV benefit when compared with the standard of care, enalapril, in patients with HF and reduced ejection fraction. Further investigations of this novel combination ARNI at the tissue level shed light into the anti-remodeling and cardioprotective effects of sacubitril/valsartan, while clinical studies in the phenotypes of HF with preserved ejection fraction, hypertension and subsets, coronary outcomes, postmyocardial infarction, and renal disease suggested that this combination could be beneficial across a wide spectrum of CV disease. Sacubitril/valsartan is a much-needed therapeutic advance in the avenue of CV disease.

Citing Articles

Sacubitril/valsartan reverses cardiac structure and function in experimental model of hypertension-induced hypertrophic cardiomyopathy.

Jeremic J, Govoruskina N, Bradic J, Milosavljevic I, Srejovic I, Zivkovic V Mol Cell Biochem. 2023; 478(12):2645-2656.

PMID: 36997815 DOI: 10.1007/s11010-023-04690-7.


Sacubitril/valsartan mitigated intermittent hypoxia related intestinal microbiota alteration and aortic injury.

Wang J, Zhang H, Wu L, Lu D Sleep Breath. 2023; 27(5):1769-1777.

PMID: 36719525 DOI: 10.1007/s11325-023-02781-9.


Biomarkers of Volume Overload and Edema in Heart Failure With Reduced Ejection Fraction.

Chiorescu R, Lazar R, Buksa S, Mocan M, Blendea D Front Cardiovasc Med. 2022; 9:910100.

PMID: 35783848 PMC: 9247259. DOI: 10.3389/fcvm.2022.910100.


Our Experience With Sacubitril/Valsartan in Chronic Heart Failure Management - HFrEF in the Ambulatory Setting.

Naser N, Kulic M, Jatic Z Med Arch. 2022; 76(2):101-107.

PMID: 35774049 PMC: 9233466. DOI: 10.5455/medarh.2022.76.101-107.


Sacubitril Ameliorates Cardiac Fibrosis Through Inhibiting TRPM7 Channel.

Jia T, Wang X, Tang Y, Yu W, Li C, Cui S Front Cell Dev Biol. 2021; 9:760035.

PMID: 34778271 PMC: 8586221. DOI: 10.3389/fcell.2021.760035.


References
1.
Hubers S, Brown N . Combined Angiotensin Receptor Antagonism and Neprilysin Inhibition. Circulation. 2016; 133(11):1115-24. PMC: 4800749. DOI: 10.1161/CIRCULATIONAHA.115.018622. View

2.
Jhund P, Claggett B, Voors A, Zile M, Packer M, Pieske B . Elevation in high-sensitivity troponin T in heart failure and preserved ejection fraction and influence of treatment with the angiotensin receptor neprilysin inhibitor LCZ696. Circ Heart Fail. 2014; 7(6):953-9. DOI: 10.1161/CIRCHEARTFAILURE.114.001427. View

3.
Sagnella G . Vasopeptidase inhibitors. J Renin Angiotensin Aldosterone Syst. 2002; 3(2):90-5. DOI: 10.3317/jraas.2002.023. View

4.
Yandrapalli S, Andries G, Biswas M, Khera S . Profile of sacubitril/valsartan in the treatment of heart failure: patient selection and perspectives. Vasc Health Risk Manag. 2017; 13:369-382. PMC: 5634378. DOI: 10.2147/VHRM.S114784. View

5.
Jordan J, Stinkens R, Jax T, Engeli S, Blaak E, May M . Improved Insulin Sensitivity With Angiotensin Receptor Neprilysin Inhibition in Individuals With Obesity and Hypertension. Clin Pharmacol Ther. 2016; 101(2):254-263. DOI: 10.1002/cpt.455. View