Bioactive adrenomedullin for assessment of venous congestion in heart failure.

Bioactive adrenomedullin Biomarker Congestion Haemodynamics Heart failure Prognosis

Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
10 2022
Historique:
revised: 08 05 2022
received: 30 11 2021
accepted: 03 06 2022
pubmed: 30 7 2022
medline: 6 12 2022
entrez: 29 7 2022
Statut: ppublish

Résumé

Bioactive adrenomedullin (bio-ADM) is a vascular-derived peptide hormone that has emerged as a promising biomarker for assessment of congestion in decompensated heart failure (HF). We aimed to evaluate diagnostic and prognostic performance of bio-ADM for HF in comparison to amino-terminal pro-B-type natriuretic peptide (NT-proBNP), with decision thresholds derived from invasive haemodynamic and population-based studies. Normal reference ranges for bio-ADM were derived from a community-based cohort (n = 5060). Correlations with haemodynamic data were explored in a cohort of HF patients undergoing right heart catheterization (n = 346). Mortality and decision cutoffs for bio-ADM was explored in a cohort of patients presenting in the ER with acute dyspnoea (n = 1534), including patients with decompensated HF (n = 570). The normal reference range was 8-39 pg/mL. The area under the receiver operating characteristic curve (AUROC) for discrimination of elevated mean right atrial pressure (mRAP) and pulmonary arterial wedge pressure (PAWP) was 0.74 (95% CI = 0.67-0.79) and 0.70 (95% CI = 0.64-0.75), respectively, with optimal bio-ADM decision cutoff of 39 pg/mL, concordant with cubic spline analyses. NT-proBNP discriminated PAWP slightly better than mRAP (AUROC 0.73 [95% CI = 0.68-0.79] and 0.68 [95% CI = 0.61-0.75]). Bio-ADM correlated with (mRAP, r = 0.55) while NT-proBNP correlated with PAWP. Finally, a bio-ADM decision cutoff of 39 pg/mL associated with 30 and 90 day mortality and conferred a two-fold increased odds of HF diagnosis, independently from NT-proBNP. Bio-ADM tracks with mRAP and associates with measures of systemic congestion and with mortality in decompensated HF independently from NT-proBNP. Our findings support utility of bio-ADM as a biomarker of systemic venous congestion in HF and nominate a decision threshold.

Identifiants

pubmed: 35903845
doi: 10.1002/ehf2.14018
pmc: PMC9715871
doi:

Substances chimiques

Adrenomedullin 148498-78-6
Biomarkers 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

3543-3555

Informations de copyright

© 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

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Auteurs

Anna Egerstedt (A)

Department of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.
Wallenberg Center for Molecular Medicine and Lund University Diabetes Center, Lund University, Lund, Sweden.

Tomasz Czuba (T)

Department of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.
Wallenberg Center for Molecular Medicine and Lund University Diabetes Center, Lund University, Lund, Sweden.
The Wallenberg Laboratory/Department of Molecular and Clinical Medicine, Institute of Medicine, Gothenburg University and the Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Kevin Bronton (K)

Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden.

Carl Lejonberg (C)

Department of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.
Wallenberg Center for Molecular Medicine and Lund University Diabetes Center, Lund University, Lund, Sweden.
Department of Cardiology, Helsingborg Hospital, Helsingborg, Sweden.

Thoralph Ruge (T)

Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden.

Torgny Wessman (T)

Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden.

Göran Rådegran (G)

Department of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.
Department of Heart Failure and Valvular Disease, Skåne University Hospital, Lund, Sweden.

Janin Schulte (J)

SphingoTec GmbH, Hennigsdorf, Germany.

Oliver Hartmann (O)

SphingoTec GmbH, Hennigsdorf, Germany.

Olle Melander (O)

Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden.

J Gustav Smith (JG)

Department of Cardiology, Clinical Sciences, Lund University, Lund, Sweden.
Wallenberg Center for Molecular Medicine and Lund University Diabetes Center, Lund University, Lund, Sweden.
The Wallenberg Laboratory/Department of Molecular and Clinical Medicine, Institute of Medicine, Gothenburg University and the Department of Cardiology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department of Heart Failure and Valvular Disease, Skåne University Hospital, Lund, Sweden.

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