The role of sacubitril/valsartan in the treatment of chronic heart failure with reduced ejection fraction in hypertensive patients with comorbidities: From clinical trials to real-world settings.


Journal

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 16 04 2020
revised: 13 07 2020
accepted: 28 07 2020
entrez: 29 7 2021
pubmed: 30 7 2021
medline: 13 8 2021
Statut: ppublish

Résumé

Sacubitril/valsartan, the first agent to be approved in a new class of drugs called angiotensin receptor neprilysin inhibitors (ARNIs), has been shown to reduce cardiovascular mortality and morbidity compared to enalapril in outpatient subjects with chronic heart failure (HF) and reduced left ventricular ejection fraction (HFrEF). However, there is little real-world evidence about the efficacy of ARNIs in elderly hypertensive patients with HFrEF and comorbidities. In this prospective open-label study, 108 subjects, 54 of them (mean age 78.6 ± 8.2 years, 75.0 % male), with HFrEF (29.8 ± 4.3 %) and New York Heart Association (NYHA) class II-III symptoms were assigned to receive ARNIs twice daily, according to the recommended dosage of 24/26, 49/51, 97/103 mg. Patients were gender- and age-matched with a control arm of patients with HFrEF receiving the optimal standard therapy for HF. The clinic blood pressure (BP), N-terminal pro-B-type natriuretic peptide (NT-proBNP), estimated glomerular filtration rate (eGFR), blood glucose and glycated hemoglobin (HbA1c), uric acid (UA), left ventricular ejection fraction (LVEF) and NYHA class were evaluated at a mean follow-up of 12 months. During the follow-up, the clinical outcomes, including mortality and re-hospitalization for HF, were collected. NYHA class significantly improved in the ARNI arm compared to the control (24.9 vs. 6.4 %, shifting from class III to II, and 55.4 vs. 25.2 %, from class II to I, p < 0.05 for all). A significant improvement in LVEF and eGFR levels was found in the ARNI arm compared to controls (42.4 vs. 34.2 %, 73.8 vs. 61.2 mL/min, respectively; p < 0.001 for all). NT-proBNP, clinic systolic and diastolic BP, blood glucose, HbA1c and UA values were reduced in both treatment arms, but they were lower in the ARNI arm compared controls (3107 vs. 4552 pg/mL, 112.2 vs. 120.4 and 68.8 vs. 75.6 mmHg, 108.4 vs. 112.6 mg/dL, 5.4 vs. 5.9 % and 5.9 vs. 6.4 mg/dL, respectively, p < 0.05). Mortality and re-hospitalization for HF was lower in the ARNI arm than controls (20.1 vs. 33.6 % and 27.7 vs. 46.3 % respectively; p < 0.05 for all). Gender differences were not found in either arm. No patients refused to continue the study, and no side effects to the ARNI treatment were observed. In elderly patients with HFrEF and comorbidities, ARNI treatment seems effective and safe. The improvement in LVEF and cardiac remodeling, BP, eGFR, serum glucose, UA and HbA1c could be the mechanisms by which ARNIs play their beneficial role on clinical outcomes. However, these results need to be confirmed in studies involving a greater number of subjects, and with a longer follow-up.

Sections du résumé

BACKGROUND BACKGROUND
Sacubitril/valsartan, the first agent to be approved in a new class of drugs called angiotensin receptor neprilysin inhibitors (ARNIs), has been shown to reduce cardiovascular mortality and morbidity compared to enalapril in outpatient subjects with chronic heart failure (HF) and reduced left ventricular ejection fraction (HFrEF). However, there is little real-world evidence about the efficacy of ARNIs in elderly hypertensive patients with HFrEF and comorbidities.
METHODS METHODS
In this prospective open-label study, 108 subjects, 54 of them (mean age 78.6 ± 8.2 years, 75.0 % male), with HFrEF (29.8 ± 4.3 %) and New York Heart Association (NYHA) class II-III symptoms were assigned to receive ARNIs twice daily, according to the recommended dosage of 24/26, 49/51, 97/103 mg. Patients were gender- and age-matched with a control arm of patients with HFrEF receiving the optimal standard therapy for HF. The clinic blood pressure (BP), N-terminal pro-B-type natriuretic peptide (NT-proBNP), estimated glomerular filtration rate (eGFR), blood glucose and glycated hemoglobin (HbA1c), uric acid (UA), left ventricular ejection fraction (LVEF) and NYHA class were evaluated at a mean follow-up of 12 months. During the follow-up, the clinical outcomes, including mortality and re-hospitalization for HF, were collected.
RESULTS RESULTS
NYHA class significantly improved in the ARNI arm compared to the control (24.9 vs. 6.4 %, shifting from class III to II, and 55.4 vs. 25.2 %, from class II to I, p < 0.05 for all). A significant improvement in LVEF and eGFR levels was found in the ARNI arm compared to controls (42.4 vs. 34.2 %, 73.8 vs. 61.2 mL/min, respectively; p < 0.001 for all). NT-proBNP, clinic systolic and diastolic BP, blood glucose, HbA1c and UA values were reduced in both treatment arms, but they were lower in the ARNI arm compared controls (3107 vs. 4552 pg/mL, 112.2 vs. 120.4 and 68.8 vs. 75.6 mmHg, 108.4 vs. 112.6 mg/dL, 5.4 vs. 5.9 % and 5.9 vs. 6.4 mg/dL, respectively, p < 0.05). Mortality and re-hospitalization for HF was lower in the ARNI arm than controls (20.1 vs. 33.6 % and 27.7 vs. 46.3 % respectively; p < 0.05 for all). Gender differences were not found in either arm. No patients refused to continue the study, and no side effects to the ARNI treatment were observed.
CONCLUSIONS CONCLUSIONS
In elderly patients with HFrEF and comorbidities, ARNI treatment seems effective and safe. The improvement in LVEF and cardiac remodeling, BP, eGFR, serum glucose, UA and HbA1c could be the mechanisms by which ARNIs play their beneficial role on clinical outcomes. However, these results need to be confirmed in studies involving a greater number of subjects, and with a longer follow-up.

Identifiants

pubmed: 34321170
pii: S0753-3322(20)30789-7
doi: 10.1016/j.biopha.2020.110596
pmc: PMC8963534
mid: NIHMS1742441
pii:
doi:

Substances chimiques

Aminobutyrates 0
Biphenyl Compounds 0
Drug Combinations 0
Valsartan 80M03YXJ7I
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110596

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM103542
Pays : United States

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Références

Ig Sanita Pubbl. 2015 Sep-Oct;71(5):499-513
pubmed: 26722827
Recenti Prog Med. 2019 Jan;110(1):23-32
pubmed: 30720014
Curr Atheroscler Rep. 2016 Aug;18(8):48
pubmed: 27324636
Eur J Heart Fail. 2010 Oct;12(10):1076-84
pubmed: 20805094
Diabetes. 2018 Aug;67(8):1616-1626
pubmed: 29941448
Eur J Heart Fail. 2016 Oct;18(10):1228-1234
pubmed: 27283779
Biomed Pharmacother. 2017 Aug;92:826-835
pubmed: 28599248
Hypertens Res. 2017 Apr;40(4):329-335
pubmed: 27853165
Heart. 2010 Jan;96(2):148-52
pubmed: 19858141
Am J Physiol. 1988 Sep;255(3 Pt 2):F415-20
pubmed: 2970796
Diabetologia. 2012 May;55(5):1400-5
pubmed: 22159910
Arterioscler Thromb Vasc Biol. 2017 Jun;37(6):1241-1249
pubmed: 28408375
Int J Cardiol. 2016 Jun 15;213:20-2
pubmed: 26386814
Eur J Heart Fail. 2017 Nov;19(11):1401-1409
pubmed: 28597606
Eur J Heart Fail. 2013 Jun;15(6):671-8
pubmed: 23397577
J Am Coll Cardiol. 2019 Mar 26;73(11):1264-1272
pubmed: 30846338
J Am Geriatr Soc. 2016 Jul;64(7):1469-74
pubmed: 27348135
J Am Coll Cardiol. 2003 Oct 1;42(7):1226-33
pubmed: 14522486
Eur J Heart Fail. 2018 Jun;20(6):973-977
pubmed: 29603541
BMC Med Inform Decis Mak. 2018 Jun 22;18(1):44
pubmed: 29929496
Eur J Heart Fail. 2017 Sep;19(9):1095-1104
pubmed: 28470962
Eur J Heart Fail. 2016 Apr;18(4):386-93
pubmed: 26749570
Int Heart J. 2005 May;46(3):419-31
pubmed: 16043938
Eur Heart J. 2015 Oct 7;36(38):2576-84
pubmed: 26231885
PLoS Med. 2014 Aug 12;11(8):e1001699
pubmed: 25117081
Eur Heart J. 2016 Jul 14;37(27):2129-2200
pubmed: 27206819
J Am Coll Cardiol. 1993 Jun;21(7):1687-96
pubmed: 8496538
Clin Exp Hypertens. 2015;37(3):192-6
pubmed: 25051056
Am J Physiol. 1997 Oct;273(4):R1457-64
pubmed: 9362312
Drug Res (Stuttg). 2016 Dec;66(12):628-632
pubmed: 27643410
J Am Coll Cardiol. 1992 Jul;20(1):112-9
pubmed: 1607511
Eur J Heart Fail. 2016 Apr;18(4):402-10
pubmed: 26754527
Circulation. 1998 Nov 10;98(19):2037-42
pubmed: 9808602
Drugs. 2003;63(20):2185-202
pubmed: 14498755
Cholesterol. 2014;2014:261878
pubmed: 24672715
Int J Cardiol. 2018 Mar 1;254:240-241
pubmed: 29407098
J Gen Intern Med. 2018 Oct;33(10):1700-1707
pubmed: 29992429
Mol Immunol. 2010 Aug;47(13):2161-9
pubmed: 20580091
JACC Heart Fail. 2018 Jun;6(6):489-498
pubmed: 29655829
N Engl J Med. 2001 Dec 6;345(23):1667-75
pubmed: 11759645
Lancet. 2004 Jun 19;363(9426):2022-31
pubmed: 15207952
Pharmacol Res. 2018 Feb;128:315-321
pubmed: 29080798
Lancet Diabetes Endocrinol. 2018 Jul;6(7):547-554
pubmed: 29661699
Am Heart J. 1991 Mar;121(3 Pt 1):864-71
pubmed: 2000754
Clin Chim Acta. 1998 Jul 6;275(1):9-18
pubmed: 9706839
Jpn Heart J. 1998 Sep;39(5):639-51
pubmed: 9925995
Int J Cardiol. 2011 Oct 6;152(1):88-94
pubmed: 21397348
Indian Heart J. 2016 Apr;68 Suppl 1:S22-8
pubmed: 27056649
Circulation. 1984 Oct;70(4):657-62
pubmed: 6478568
JAMA. 2002 Dec 18;288(23):2998-3007
pubmed: 12479764
J Am Heart Assoc. 2016 Jun 17;5(6):
pubmed: 27317347
Adv Physiol Educ. 2017 Jun 1;41(2):179-185
pubmed: 28377431
Circulation. 1978 Dec;58(6):1072-83
pubmed: 709763
Circulation. 1977 Apr;55(4):613-8
pubmed: 138494
J Am Coll Cardiol. 2013 Jan 29;61(4):391-403
pubmed: 23219302
N Engl J Med. 2014 Sep 11;371(11):993-1004
pubmed: 25176015
Am J Cardiovasc Dis. 2017 Dec 20;7(6):108-113
pubmed: 29348971
Clin Chim Acta. 2006 Jul 15;369(1):95-9
pubmed: 16515777
Lancet Diabetes Endocrinol. 2017 May;5(5):333-340
pubmed: 28330649
Am J Physiol. 1989 Dec;257(6 Pt 2):F1146-57
pubmed: 2532476
Heart. 2003 Jan;89(1):49-53
pubmed: 12482791
Intern Emerg Med. 2019 Nov;14(8):1287-1297
pubmed: 31147823
Biomed Res Int. 2017;2017:4391920
pubmed: 28116308
Expert Opin Investig Drugs. 2017 May;26(5):651-659
pubmed: 28388237
J Am Coll Cardiol. 1996 Apr;27(5):1214-8
pubmed: 8609345
BMJ. 1998 Feb 21;316(7131):628
pubmed: 9518931
Eur J Heart Fail. 2018 Mar;20(3):514-522
pubmed: 29193563
Diabetologia. 2017 Apr;60(4):701-708
pubmed: 27933334
Trends Pharmacol Sci. 2011 Dec;32(12):734-9
pubmed: 21880378

Auteurs

Alberto Mazza (A)

ESH Excellence Hypertension Centre, Internal Medicine Unit, S. Maria della Misericordia General Hospital, AULSS 5 Polesana, Rovigo, Italy. Electronic address: Xalberto.mazza@aulss5.veneto.it.

Danyelle M Townsend (DM)

Department of Drug Discovery and Biomedical Sciences, Medical University of South Carolina, USA.

Gioia Torin (G)

ESH Excellence Hypertension Centre, Internal Medicine Unit, S. Maria della Misericordia General Hospital, AULSS 5 Polesana, Rovigo, Italy; Unit of Internal Medicine, S. Maria della Misericordia General Hospital, AULSS 5 Polesana, Rovigo, Italy.

Laura Schiavon (L)

ESH Excellence Hypertension Centre, Internal Medicine Unit, S. Maria della Misericordia General Hospital, AULSS 5 Polesana, Rovigo, Italy; Unit of Internal Medicine, S. Maria della Misericordia General Hospital, AULSS 5 Polesana, Rovigo, Italy.

Alessandro Camerotto (A)

Department of Diagnosis and Care, Clinical Laboratory, S. Maria della Misericordia General Hospital, Rovigo, Italy.

Gianluca Rigatelli (G)

Interventional Cardiology Unit, Division of Cardiology, S. Maria della Misericordia General Hospital, AULSS 5 Polesana, Rovigo, Italy.

Stefano Cuppini (S)

Unit of Internal Medicine, S. Maria della Misericordia General Hospital, AULSS 5 Polesana, Rovigo, Italy.

Pietro Minuz (P)

Unit of Internal Medicine C, Department of Medicine, University of Verona, Verona, Italy.

Domenico Rubello (D)

Nuclear Medicine Unit, Santa Maria della Misericordia Hospital, Rovigo, Italy. Electronic address: domenico.rubello@libero.it.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH