Increased concentrations of bioactive adrenomedullin subsequently to angiotensin-receptor/neprilysin-inhibitor treatment in chronic systolic heart failure.


Journal

British journal of clinical pharmacology
ISSN: 1365-2125
Titre abrégé: Br J Clin Pharmacol
Pays: England
ID NLM: 7503323

Informations de publication

Date de publication:
03 2021
Historique:
received: 22 11 2019
revised: 09 05 2020
accepted: 14 05 2020
pubmed: 1 7 2020
medline: 27 7 2021
entrez: 30 6 2020
Statut: ppublish

Résumé

The clinically investigated rationale for neprilysin (NEP)-inhibition by angiotensinreceptor-NEPinhibitor (ARNi) therapy is to induce elevations in endogenous natriuretic peptides. NEP, however, cleaves a broad spectrum of substrates, which partially hold significant implications in heart failure with reduced ejection fraction (HFrEF). The effect of NEP inhibition on these peptides has not been investigated thoroughly. This study explored the response of adrenomedullin (ADM) regulation to the initiation of ARNi. Seventy-four patients with stable HFrEF and initiation of ARNi were prospectively enrolled, 67 patients on continuous angiotensin-converting-enzyme inhibitor(ACEi)/angiotensin-receptor blocker (ARB) therapy served as control. Plasma bioactive-ADM (bio-ADM), mid-regional-pro-ADM (MR-proADM), B-typenatriuretic peptide (BNP) and N-terminal-pro-BNP (NT-proBNP) were determined at baseline, short-term, 1-year and 2-year follow up. Following ARNi initiation both bio-ADM and MR-proADM concentrations were significantly increased at early and long-term follow up (bio-ADM [pg/mL]: 26.0 [interquartile range {IQR}: 17.7-37.5] vs. 50.8 [IQR: 36.5-78.1] vs. 54.6 [IQR: 42.0-97.1] vs. 57.4 [IQR: 48.5-161.6]; MR-proADM [nmol/L]: 0.87 [IQR: 0.64-1.12] vs. 1.25 [IQR: 0.93-1.79] vs. 1.42 [IQR: 0.95-1.90] vs. 1.60 [IQR: 1.12-2.46], P < .0001 for all). The ratios bio-ADM/MR-proADM and BNP/NT-proBNP increased during ARNi-therapy proving improved availability of bioactive peptides. The proportional increase of bio-ADM markedly exceeded BNP increase. Patients converted to ARNi showed similar biomarker patterns irrespective of baseline renin-angiotensin system blocker therapy, i.e. ACEi or ARB (P > .05 for all), indicating that activation of the ADM-axis arises particularly from NEPinhibition. The significant increase of MR-proADM and bio-ADM together with an elevated bioADM/MR-proADM ratio suggest both enhanced formation and reduced breakdown of bioactive ADM following the initiation of ARNi. Activation of the ADM-axis represents a so far unrecognized effect of ARNi.

Identifiants

pubmed: 32598074
doi: 10.1111/bcp.14442
pmc: PMC9328655
doi:

Substances chimiques

Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
Angiotensins 0
Biomarkers 0
Peptide Fragments 0
Receptors, Angiotensin 0
Natriuretic Peptide, Brain 114471-18-0
Adrenomedullin 148498-78-6
Neprilysin EC 3.4.24.11

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

916-924

Subventions

Organisme : Sphingotec GmbHAssays for BNP
Organisme : bio-ADM
Organisme : MR-proADM

Informations de copyright

© 2020 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

Références

Br J Clin Pharmacol. 2001 Aug;52(2):159-64
pubmed: 11488772
J Am Coll Cardiol. 2019 Mar 26;73(11):1264-1272
pubmed: 30846338
Eur Heart J. 2016 Jul 14;37(27):2129-2200
pubmed: 27206819
Thromb Haemost. 2007 Nov;98(5):944-51
pubmed: 18000597
Eur J Heart Fail. 2009 Apr;11(4):361-6
pubmed: 19190023
Eur J Heart Fail. 2019 Jun;21(6):732-743
pubmed: 30843353
J Hypertens. 1998 Dec;16(12 Pt 2):2057-62
pubmed: 9886897
Eur J Heart Fail. 2017 Jun;19(6):710-717
pubmed: 28326642
Crit Care. 2014 Feb 17;18(1):R34
pubmed: 24533868
Eur J Heart Fail. 2010 May;12(5):484-91
pubmed: 20215339
Sci Rep. 2016 Sep 19;6:33495
pubmed: 27640364
Ann Intensive Care. 2017 Dec;7(1):6
pubmed: 28050899
Nat Rev Cardiol. 2017 Mar;14(3):171-186
pubmed: 27974807
Am Heart J. 2018 May;199:130-136
pubmed: 29754651
Br J Clin Pharmacol. 1997 Jul;44(1):57-60
pubmed: 9241097
N Engl J Med. 2014 Sep 11;371(11):993-1004
pubmed: 25176015
Eur J Heart Fail. 2020 Apr;22(4):683-691
pubmed: 31797505
Circulation. 1997 Sep 16;96(6):1983-90
pubmed: 9323090
Ann Transl Med. 2016 Sep;4(17):329
pubmed: 27713887
J Am Coll Cardiol. 2016 Aug 9;68(6):639-653
pubmed: 27491909
Am J Emerg Med. 2016 Feb;34(2):257-62
pubmed: 26577429
Diabetes Care. 2009 Oct;32(10):1890-5
pubmed: 19564455
Heart Fail Clin. 2018 Jan;14(1):49-55
pubmed: 29153200
Eur J Heart Fail. 2019 May;21(5):598-605
pubmed: 30520545
JAMA Cardiol. 2018 Dec 1;3(12):1232-1243
pubmed: 30484834
Br J Clin Pharmacol. 2018 Sep;84(9):2129-2141
pubmed: 29856470
Br J Clin Pharmacol. 2001 Aug;52(2):165-8
pubmed: 11488773
Br J Clin Pharmacol. 2021 Mar;87(3):916-924
pubmed: 32598074
Circ Res. 2002 Oct 4;91(7):618-25
pubmed: 12364390
Hypertension. 2002 Nov;40(5):667-72
pubmed: 12411460
Eur J Heart Fail. 2019 Feb;21(2):163-171
pubmed: 30592365

Auteurs

Henrike Arfsten (H)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Georg Goliasch (G)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Philipp E Bartko (PE)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Suriya Prausmüller (S)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Georg Spinka (G)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Anna Cho (A)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Johannes Novak (J)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Helmuth Haslacher (H)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Guido Strunk (G)

Complexity Research, Vienna, Austria.

Joachim Struck (J)

Sphingotec GmbH, Hennigsdorf, Germany.

Martin Hülsmann (M)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

Noemi Pavo (N)

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.

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