Screening of Multiple Biomarkers Associated With Ischemic Stroke in Atrial Fibrillation.

dc.contributor.author

Hijazi, Ziad

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Wallentin, Lars

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Lindbäck, Johan

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Alexander, John H

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Connolly, Stuart J

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Eikelboom, John W

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Ezekowitz, Michael D

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Granger, Christopher B

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Lopes, Renato D

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Pol, Tymon

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Yusuf, Salim

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Oldgren, Jonas

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Siegbahn, Agneta

dc.date.accessioned

2021-05-10T18:05:18Z

dc.date.available

2021-05-10T18:05:18Z

dc.date.issued

2020-12-09

dc.date.updated

2021-05-10T18:05:15Z

dc.description.abstract

Background To explore the pathophysiological features of ischemic stroke in patients with atrial fibrillation (AF), we evaluated the association between 268 plasma proteins and subsequent ischemic stroke in 2 large AF cohorts receiving oral anticoagulation. Methods and Results A case-cohort sample of patients with AF from the ARISTOTLE (Apixaban for Reduction in Stroke and Other Thromboembolic Events in Atrial Fibrillation) trial, including 282 cases with ischemic stroke or systemic embolism and a random sample of 4124 without these events, during 1.9 years of follow-up was used for identification. Validation was provided by a similar case-cohort sample of patients with AF from the RE-LY (Randomized Evaluation of Long-Term Anticoagulation Therapy) trial, including 149 cases with ischemic stroke/systemic embolism and a random sample of 1062 without these events. In plasma obtained before randomization, 268 unique biomarkers were measured with OLINK proximity extension assay panels (CVD II, CVD III, and Inflammation) and conventional immunoassays. The association between biomarkers and outcomes was evaluated by random survival forest and adjusted Cox regression. According to random survival forest or Cox regression analyses, the biomarkers most strongly and consistently associated with ischemic stroke/systemic embolism were matrix metalloproteinase-9, NT-proBNP (N-terminal pro-B-type natriuretic peptide), osteopontin, sortilin, soluble suppression of tumorigenesis 2, and trefoil factor-3. The corresponding hazard ratios (95% CIs) for an interquartile difference were as follows: 1.18 (1.00-1.38), 1.55 (1.28-1.88), 1.28 (1.07-1.53), 1.19 (1.02-1.39), 1.23 (1.05-1.45), and 1.19 (0.97-1.45), respectively. Conclusions In patients with AF, of 268 unique biomarkers, the 6 biomarkers most strongly associated with subsequent ischemic stroke/systemic embolism represent fibrosis/remodeling (matrix metalloproteinase-9 and soluble suppression of tumorigenesis 2), cardiac dysfunction (NT-proBNP), vascular calcification (osteopontin), metabolism (sortilin), and mucosal integrity/ischemia (trefoil factor-3). Registration URL: https://www.clinicaltrials.gov. Unique Identifiers: NCT00412984 and NCT00262600.

dc.identifier.issn

2047-9980

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2047-9980

dc.identifier.uri

https://hdl.handle.net/10161/22862

dc.language

eng

dc.publisher

Ovid Technologies (Wolters Kluwer Health)

dc.relation.ispartof

Journal of the American Heart Association

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10.1161/jaha.120.018984

dc.subject

Humans

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Atrial Fibrillation

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Embolism

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Thromboembolism

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Pyrazoles

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Pyridones

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Natriuretic Peptide, Brain

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Peptide Fragments

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Adaptor Proteins, Vesicular Transport

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Anticoagulants

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Aged

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Aged, 80 and over

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Middle Aged

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Female

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Male

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Matrix Metalloproteinase 9

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Osteopontin

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Stroke

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Patient Outcome Assessment

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Factor Xa Inhibitors

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Biomarkers

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Trefoil Factor-3

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Interleukin-1 Receptor-Like 1 Protein

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Ischemic Stroke

dc.title

Screening of Multiple Biomarkers Associated With Ischemic Stroke in Atrial Fibrillation.

dc.type

Journal article

duke.contributor.orcid

Alexander, John H|0000-0002-1444-2462

duke.contributor.orcid

Granger, Christopher B|0000-0002-0045-3291

duke.contributor.orcid

Lopes, Renato D|0000-0003-2999-4961

pubs.begin-page

e018984

pubs.issue

24

pubs.organisational-group

School of Medicine

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Duke Clinical Research Institute

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Medicine, Cardiology

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Duke

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Institutes and Centers

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Medicine

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Clinical Science Departments

pubs.organisational-group

Nursing

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School of Nursing

pubs.publication-status

Published

pubs.volume

9

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