The clinical significance of interleukin-6 in heart failure: results from the BIOSTAT-CHF study.


Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
08 2019
Historique:
received: 19 11 2018
revised: 12 03 2019
accepted: 12 04 2019
pubmed: 16 5 2019
medline: 2 10 2020
entrez: 16 5 2019
Statut: ppublish

Résumé

Inflammation is a central process in the pathophysiology of heart failure (HF), but trials targeting tumour necrosis factor (TNF)-α were largely unsuccessful. Interleukin (IL)-6 is an important inflammatory mediator and might constitute a potential pharmacologic target in HF. However, little is known regarding the association between IL-6 and clinical characteristics, outcomes and other inflammatory biomarkers in HF. We thus aimed to identify and characterize these associations. Interleukin-6 was measured in 2329 patients [89.4% with a left ventricular ejection fraction (LVEF) ≤ 40%] of the BIOSTAT-CHF cohort. The primary outcome was all-cause mortality and HF hospitalization during 2 years, with all-cause, cardiovascular (CV), and non-CV death as secondary outcomes. Approximately half (56%) of all included patients had plasma IL-6 values greater than the previously determined 95th percentile of normal values at baseline. Elevated N-terminal pro-brain natriuretic peptide, procalcitonin and hepcidin, younger age, TNF-α/IL-1-related biomarkers, or having iron deficiency, atrial fibrillation and LVEF > 40% independently predicted elevated IL-6 levels. IL-6 independently predicted the primary outcome [HR (95% confidence interval) per doubling: 1.16 (1.11-1.21), P < 0.001], all-cause mortality [1.22 (1.16-1.29), P < 0.001] and CV as well as non-CV mortality [1.16 (1.09-1.24), P < 0.001; 1.31 (1.18-1.45), P < 0.001], but did not improve discrimination in previously published risk models. In a large, heterogeneous cohort of HF patients, elevated IL-6 levels were found in more than 50% of patients and were associated with iron deficiency, reduced LVEF, atrial fibrillation and poorer clinical outcomes. These findings warrant further investigation of IL-6 as a potential therapeutic target in specific HF subpopulations.

Identifiants

pubmed: 31087601
doi: 10.1002/ejhf.1482
doi:

Substances chimiques

Biomarkers 0
Interleukin-6 0

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

965-973

Informations de copyright

© 2019 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Auteurs

George Markousis-Mavrogenis (G)

Department of Cardiology, University of Groningen, Groningen, The Netherlands.

Jasper Tromp (J)

Department of Cardiology, University of Groningen, Groningen, The Netherlands.
National Heart Centre Singapore, Singapore.

Wouter Ouwerkerk (W)

Department of cardiology, national heart center Singapore.
Department of Dermatology, Amsterdam UMC, University of Amsterdam, Amsterdam Infection and Immunity Institute, Amsterdam, The Netherlands.

Matt Devalaraja (M)

Corvidia Therapeutics, 35 Gatehouse Dr., Waltham, MA, USA.

Stefan D Anker (SD)

Division of Cardiology and Metabolism - Heart Failure, Cachexia & Sarcopenia, Charité University Medicine, Berlin, Germany.
Department of Cardiology (CVK), Charité University Medicine, Berlin, Germany.
Berlin-Brandenburg Center for Regenerative Therapies (BCRT), Charité University Medicine, Berlin, Germany.
Department of Cardiology and Pneumology, University Medicine Göttingen (UMG), Göttingen, Germany.
DZHK (German Center for Cardiovascular Research), University Medicine Göttingen (UMG), Göttingen, Germany.

John G Cleland (JG)

National Heart & Lung Institute, Royal Brompton & Harefield Hospitals, Imperial College, London, UK.

Kenneth Dickstein (K)

Stavanger University Hospital, University of Bergen, Stavanger, Norway.

Gerasimos S Filippatos (GS)

School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Department of Cardiology, Heart Failure Unit, Athens University Hospital Attikon, Athens, Greece.

Pim van der Harst (P)

Department of Cardiology, University of Groningen, Groningen, The Netherlands.

Chim C Lang (CC)

Division of Molecular & Clinical Medicine, University of Dundee, Dundee, UK.

Marco Metra (M)

Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, Institute of Cardiology, University of Brescia, Brescia, Italy.

Leong L Ng (LL)

Department of Cardiovascular Sciences, Glenfield Hospital, University of Leicester, Leicester, UK.
NIHR Leicester Biomedical Research Centre, Glenfield Hospital, Leicester, UK.

Piotr Ponikowski (P)

Department of Heart Diseases, Wroclaw Medical University, Wroclaw, Poland.
Poland and Cardiology Department, Military Hospital, Wroclaw, Poland.

Nilesh J Samani (NJ)

Division of Molecular & Clinical Medicine, University of Dundee, Dundee, UK.

Faiez Zannad (F)

Inserm CIC 1433, Université de Lorrain, CHU de Nancy, Nancy, France.

Aeilko H Zwinderman (AH)

Department of Epidemiology, Biostatistics & Bioinformatics, Academic Medical Center, Amsterdam, The Netherlands.

Hans L Hillege (HL)

Department of Cardiology, University of Groningen, Groningen, The Netherlands.

Dirk J van Veldhuisen (DJ)

Department of Cardiology, University of Groningen, Groningen, The Netherlands.

Rahul Kakkar (R)

Corvidia Therapeutics, 35 Gatehouse Dr., Waltham, MA, USA.

Adriaan A Voors (AA)

Department of Cardiology, University of Groningen, Groningen, The Netherlands.

Peter van der Meer (P)

Department of Cardiology, University of Groningen, Groningen, The Netherlands.

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