Natriuretic peptides to classify risk of atrial fibrillation detection after stroke: analysis of the BIOSIGNAL and PRECISE cohort studies (original) (raw)

Cameron, A. et al. (2024) Natriuretic peptides to classify risk of atrial fibrillation detection after stroke: analysis of the BIOSIGNAL and PRECISE cohort studies.Neurology, 103(3), e209625. (doi: 10.1212/WNL.0000000000209625) (PMID:38950311) (PMCID:PMC11226326)

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Abstract

Background and Objectives: Prolonged cardiac monitoring (PCM) increases atrial fibrillation (AF) detection after ischemic stroke, but access is limited, and it is burdensome for patients. Our objective was to assess whether midregional proatrial natriuretic peptide (MR-proANP) and N-terminal pro-B-type natriuretic peptide (NT-proBNP) could classify people who are unlikely to have AF after ischemic stroke and allow better targeting of PCM. Methods: We analyzed people from the Biomarker Signature of Stroke Aetiology (BIOSIGNAL) study with ischemic stroke, no known AF, and ≥3 days cardiac monitoring. External validation was performed in the Preventing Recurrent Cardioembolic Stroke: Right Approach, Right Patient (PRECISE) study of 28 days of cardiac monitoring in people with ischemic stroke or transient ischemic attack and no known AF. The main outcome is no AF detection. We assessed the discriminatory value of MR-proANP and NT-proBNP combined with clinical variables to identify people with no AF. A decision curve analysis was performed with combined data to determine the net reduction in people who would undergo PCM using the models based on a 15% threshold probability for AF detection. Results: We included 621 people from the BIOSIGNAL study. The clinical multivariable prediction model included age, NIH Stroke Scale score, lipid-lowering therapy, creatinine, and smoking status. The area under the receiver-operating characteristic curve (AUROC) for clinical variables was 0.68 (95% CI 0.62–0.74), which improved with the addition of log10MR-proANP (0.72, 0.66–0.78; p = 0.001) or log10NT-proBNP (0.71, 0.65–0.77; p = 0.009). Performance was similar for the models with log10MR-proANP vs log10NT-proBNP (p = 0.28). In 239 people from the PRECISE study, the AUROC for clinical variables was 0.68 (0.59–0.76), which improved with the addition of log10NT-proBNP (0.73, 0.65–0.82; p < 0.001) or log10MR-proANP (0.79, 0.72–0.86; p < 0.001). Performance was better for the model with log10MR-proANP vs log10NT-proBNP (p = 0.03). The models could reduce the number of people who would undergo PCM by 30% (clinical and log10MR-proANP), 27% (clinical and log10NT-proBNP), or 20% (clinical only). Discussion: MR-proANP and NT-proBNP help classify people who are unlikely to have AF after ischemic stroke. Measuring MR-proANP or NT-proBNP could reduce the number of people who need PCM by 30%, without reducing the amount of AF detected.

Item Type: Articles
Additional Information: The BIOSIGNAL study was supported by the Swiss National Science Foundation (grant 142422), the Swiss Heart Foundation, the USZ-Foundation and the Baasch Medicus Foundation. The kits for the measurement of MR-proANP in the BIOSIGNAL study were provided by B.R.A.H.M.S. Gmbh, which produces the assay. However, B.R.A.H.M.S. was not involved in the study design or analyses. The PRECISE study is supported by the Heart Research UK (Scotland) Grant (RG2700/21/24), the Royal College of Physicians and Surgeons of Glasgow Ritchie Trust Research Award, the Mason Medical Research Trust, the University of Glasgow and NHS Greater Glasgow and Clyde. Measurement of NT-proBNP levels was supported by funding from a Pfizer Quality Improvement Grant (67452629).
Status: Published
Refereed: Yes
Glasgow Author(s) Enlighten ID: Docherty, Dr Kieran and Dawson, Professor Jesse and Cameron, Dr Alan and Campbell, Dr Ross and Abdul-Rahim, Dr Azmil and Quinn, Professor Terry
Authors: Cameron, A., Arnold, M., Katsas, G., Yang, J., Quinn, T. J., Abdul-Rahim, A. H., Campbell, R., Docherty, K., De Marchis, G. M., Arnold, M., Kahles, T., Nedeltchev, K., Cereda, C., Kaegi, G., Bustamante, A., Montaner, J., Ntaios, G., Foerch, C., Spanaus, K., Von Eckardstein, A., Dawson, J., and Katan, M.
College/School: College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health
Journal Name: Neurology
Publisher: American Academy of Neurology
ISSN: 0028-3878
ISSN (Online): 1526-632X
Published Online: 01 July 2024
Copyright Holders: Copyright © 2024 American Academy of Neurology
First Published: First published in Neurology 103(3):e209625
Publisher Policy: Reproduced in accordance with the publisher copyright policy

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Deposit and Record Details

ID Code: 327133
Depositing User: Dr Mary Donaldson
Datestamp: 30 May 2024 10:40
Last Modified: 03 Jul 2025 01:31
Date of acceptance: 24 May 2024
Date of first online publication: 1 July 2024
Date Deposited: 30 May 2024
Data Availability Statement: Yes