Bone morphogenetic protein 10: a novel risk marker of ischaemic stroke in patients with atrial fibrillation.
Atrial fibrillation
BMP10
Biomarker
Heart failure
Risk stratification
Stroke
Journal
European heart journal
ISSN: 1522-9645
Titre abrégé: Eur Heart J
Pays: England
ID NLM: 8006263
Informations de publication
Date de publication:
14 01 2023
14 01 2023
Historique:
received:
09
03
2022
revised:
31
08
2022
accepted:
24
10
2022
pubmed:
17
11
2022
medline:
18
1
2023
entrez:
16
11
2022
Statut:
ppublish
Résumé
Biomarkers specifically related to atrial tissue may increase the understanding of the pathophysiology of atrial fibrillation (AF) and further improve risk prediction in this setting. Bone morphogenetic protein 10 (BMP10) is a protein expressed in the atrial myocardium. We evaluated the association between BMP10 and the risk of ischaemic stroke and other cardiovascular events in large cohorts of patients with AF, treated with and without oral anticoagulation (OAC). BMP10 was measured in plasma samples collected at randomisation in patients with AF without OAC in the ACTIVE A and AVERROES trials (n = 2974), and with OAC in the ARISTOTLE trial (n = 13 079). BMP10 was analysed with a prototype Elecsys immunoassay. Associations with outcomes were evaluated by Cox-regression models adjusted for clinical characteristics, kidney function, and N-terminal pro-B-type natriuretic peptide (NT-proBNP). Median concentrations of BMP10 were 2.47 and 2.44 ng/mL, in the non-OAC and OAC cohort, respectively. Increasing BMP10 was associated with lower body mass index, older age, female sex, kidney dysfunction, and AF rhythm. BMP10 was consistently associated with ischaemic stroke. In the non-OAC cohort, BMP10 increased the concordance index of the multivariable model from 0.713 to 0.733 (P = 0.004) and in the OAC cohort from 0.673 to 0.694 (P < 0.001). Additionally, BMP10 maintained a significant prognostic value after additionally adjusting for NT-proBNP. BMP10 was not independently associated with bleeding or with death. The novel atrial biomarker BMP10 was independently associated with ischaemic stroke in patients with AF irrespective of OAC treatment. BMP10 seems to be more specifically related to the risk of ischaemic stroke in AF. In this study, BMP10 may be a novel specific biomarker of ischaemic stroke in patients with atrial fibrillation, irrespective of oral anticoagulation.
Identifiants
pubmed: 36380569
pii: 6830621
doi: 10.1093/eurheartj/ehac632
pmc: PMC9839419
doi:
Substances chimiques
Anticoagulants
0
Biomarkers
0
BMP10 protein, human
0
Bone Morphogenetic Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
208-218Subventions
Organisme : Sanofi
Organisme : Bristol Myers Squibb (BMS) Co.
Organisme : Population Health Research Institute
Organisme : Duke Clinical Research Institute
Organisme : Uppsala Clinical Research Center
Organisme : Roche Diagnostics International
Organisme : Swedish Society for Medical Research
Organisme : Hjärt-Lungfonden
Organisme : Swedish Heart Lung Foundation
Organisme : Uppsala University Hospital
Commentaires et corrections
Type : CommentIn
Informations de copyright
© The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology.
Déclaration de conflit d'intérêts
Conflict of interest: Dr Hijazi reports lecture and consulting fees from Boehringer Ingelheim, Bristol Myers Squibb, Pfizer and Roche Diagnostics International. Dr Benz has nothing to disclose. Mr Lindbäck reports institutional research grant from Roche Diagnostics International. Dr Alexander reports institutional research grants from Artivion/CryoLife, Bayer, Bristol Myers Squibb, CSL Behring, Ferring, Humacyte, and XaTek and consulting or honoraria payments from AbbVie, Akros, Artivion/CryoLife, AtriCure, Bristol Myers Squibb, Ferring, GlaxoSmithKline, Janssen, Pfizer, Portola, and Quantum Genomics. Dr Connolly reports institutional research grants and honoraria from Boehringer Ingelheim, Portola/Alexion Pharmaceuticals, Bristol Myers Squibb/Pfizer, Bayer, and Daiichi Sankyo. Dr Eikelboom reports institutional research grants and honoraria from AstraZeneca, Bayer, Boehringer Ingelheim, Bristol Myers Squibb/Pfizer, Daiichi Sankyo, Eli Lilly, GlaxoSmithKline, Janssen, and Sanofi. Dr Granger reports grants and consulting fees from Boehringer Ingelheim, Bristol Myers Squibb, Pfizer, Janssen Pharmaceutica Products, L.P., Medtronic Foundation, Novartis; grants from Daiichi Sankyo, AKROS, Apple, GlaxoSmithKline, AstraZeneca, the U.S. Food and Drug Administration; consulting fees from Abbvie, Abiomed, Athos Therapeutic, LLC, Bayer Corporation US, Boston Scientific Corporation, Espero BioPharma, National Institutes of Health, Philips, Rhoshan Pharmaceuticals, Roche Diagnostics, CeleCor Therapeutics, Correvio, Merck, NovoNordisk. Drs. Kastner and Ziegler are employees of Roche Diagnostics GmbH. Dr Lopes reports institutional research grants and consulting fees from Bristol Myers Squibb, GlaxoSmithKline, Medtronic, Pfizer, and Sanofi; consulting fees from Amgen, Bayer, Boehringer Ingelheim, Daiichi Sankyo, Merck, and Portola. Dr Oldgren reports institutional research grants and fees paid to his institution for advisory boards and lectures from Roche Diagnostics International; fees paid to his institution for advisory boards, study steering committees, and lectures from AstraZeneca, Bayer, Bristol Myers Squibb, Boehringer Ingelheim, Pfizer, and Sanofi; fees paid to his institution for advisory boards, safety committees, and lectures from Daichii Sankyo. Dr Siegbahn reports institutional research grants from AstraZeneca, Boehringer Ingelheim, Bristol Myers Squibb/Pfizer, GlaxoSmithKline, and Roche Diagnostics International. Dr Wallentin reports institutional research grants from AstraZeneca, Boehringer Ingelheim, Bristol Myers Squibb/Pfizer, GlaxoSmithKline, Roche Diagnostics International, Merck & Co; consulting fees from Abbott; holds two patents involving GDF-15 licensed to Roche Diagnostics (EP2047275B1 and US8951742B2).
Références
Am Heart J. 2010 Mar;159(3):331-9
pubmed: 20211292
JAMA. 1982 May 14;247(18):2543-6
pubmed: 7069920
Eur Heart J. 2018 Feb 7;39(6):477-485
pubmed: 29069359
Eur Heart J. 2016 Oct 07;37(38):2869-2878
pubmed: 27071819
N Engl J Med. 2011 Mar 3;364(9):806-17
pubmed: 21309657
Clin Cardiol. 2019 Oct;42(10):1003-1009
pubmed: 31490011
Clin Chem. 2017 Jan;63(1):152-164
pubmed: 27811208
Eur Heart J. 2021 Feb 1;42(5):373-498
pubmed: 32860505
Circulation. 2014 Nov 18;130(21):1847-58
pubmed: 25294786
J Am Coll Cardiol. 2016 Oct 25;68(17):1881-1894
pubmed: 27765191
Circulation. 2021 May 11;143(19):1863-1873
pubmed: 33849281
Stroke. 2010 Sep;41(9):1850-7
pubmed: 20671249
Circulation. 2004 Feb 10;109(5):594-600
pubmed: 14769680
Nat Genet. 2018 Sep;50(9):1225-1233
pubmed: 29892015
J Am Coll Cardiol. 2013 Jun 4;61(22):2274-84
pubmed: 23563134
J Am Coll Cardiol. 2014 Jan 7-14;63(1):52-61
pubmed: 24055845
Open Heart. 2018 Nov 1;5(2):e000908
pubmed: 30487982
Lancet. 2016 Jun 4;387(10035):2302-2311
pubmed: 27056738
N Engl J Med. 2011 Sep 15;365(11):981-92
pubmed: 21870978
Eur Heart J. 2013 May;34(20):1475-80
pubmed: 23386711
JCI Insight. 2020 Aug 20;5(16):
pubmed: 32814717
Eur Heart J. 2016 May 21;37(20):1582-90
pubmed: 26920728
N Engl J Med. 2009 May 14;360(20):2066-78
pubmed: 19336502
Clin Chem. 2006 Apr;52(4):680-5
pubmed: 16497939
Circ Cardiovasc Genet. 2011 Apr;4(2):123-33
pubmed: 21282332
J Am Coll Cardiol. 2010 Feb 23;55(8):747-53
pubmed: 20170812