Biomarkers predictive of atrial fibrillation in patients with cryptogenic stroke. Insights from the Nordic Atrial Fibrillation and Stroke (NOR-FIB) study.


Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
05 2023
Historique:
revised: 31 01 2023
received: 10 11 2022
accepted: 09 02 2023
medline: 6 4 2023
pubmed: 15 2 2023
entrez: 14 2 2023
Statut: ppublish

Résumé

There are currently no biomarkers to select cryptogenic stroke (CS) patients for monitoring with insertable cardiac monitors (ICMs), the most effective tool for diagnosing atrial fibrillation (AF) in CS. The purpose of this study was to assess clinically available biomarkers as predictors of AF. Eligible CS and cryptogenic transient ischaemic attack patients underwent 12-month monitoring with ICMs, clinical follow-up and biomarker sampling. Levels of cardiac and thromboembolic biomarkers, taken within 14 days from symptom onset, were compared between patients diagnosed with AF (n = 74) during monitoring and those without AF (n = 185). Receiver operating characteristic curves were created. Biomarkers reaching area under the receiver operating characteristic curve ≥ 0.7 were dichotomized by finding optimal cut-off values and were used in logistic regression establishing their predictive value for increased risk of AF in unadjusted and adjusted models. B-type natriuretic peptide (BNP), N-terminal pro-brain natriuretic peptide (NT-proBNP), creatine kinase, D-dimer and high-sensitivity cardiac troponin I and T were significantly higher in the AF than non-AF group. BNP and NT-proBNP reached the predefined area under the curve level, 0.755 and 0.725 respectively. Optimal cut-off values were 33.5 ng/l for BNP and 87 ng/l for NT-proBNP. Regression analysis showed that NT-proBNP was a predictor of AF in both unadjusted (odds ratio 7.72, 95% confidence interval 3.16-18.87) and age- and sex-adjusted models (odds ratio 4.82, 95% confidence interval 1.79-12.96). Several clinically established biomarkers were associated with AF. NT-proBNP performed best as AF predictor and could be used for selecting patients for long-term monitoring with ICMs.

Sections du résumé

BACKGROUND AND PURPOSE
There are currently no biomarkers to select cryptogenic stroke (CS) patients for monitoring with insertable cardiac monitors (ICMs), the most effective tool for diagnosing atrial fibrillation (AF) in CS. The purpose of this study was to assess clinically available biomarkers as predictors of AF.
METHODS
Eligible CS and cryptogenic transient ischaemic attack patients underwent 12-month monitoring with ICMs, clinical follow-up and biomarker sampling. Levels of cardiac and thromboembolic biomarkers, taken within 14 days from symptom onset, were compared between patients diagnosed with AF (n = 74) during monitoring and those without AF (n = 185). Receiver operating characteristic curves were created. Biomarkers reaching area under the receiver operating characteristic curve ≥ 0.7 were dichotomized by finding optimal cut-off values and were used in logistic regression establishing their predictive value for increased risk of AF in unadjusted and adjusted models.
RESULTS
B-type natriuretic peptide (BNP), N-terminal pro-brain natriuretic peptide (NT-proBNP), creatine kinase, D-dimer and high-sensitivity cardiac troponin I and T were significantly higher in the AF than non-AF group. BNP and NT-proBNP reached the predefined area under the curve level, 0.755 and 0.725 respectively. Optimal cut-off values were 33.5 ng/l for BNP and 87 ng/l for NT-proBNP. Regression analysis showed that NT-proBNP was a predictor of AF in both unadjusted (odds ratio 7.72, 95% confidence interval 3.16-18.87) and age- and sex-adjusted models (odds ratio 4.82, 95% confidence interval 1.79-12.96).
CONCLUSION
Several clinically established biomarkers were associated with AF. NT-proBNP performed best as AF predictor and could be used for selecting patients for long-term monitoring with ICMs.

Identifiants

pubmed: 36786305
doi: 10.1111/ene.15746
doi:

Substances chimiques

Biomarkers 0
Natriuretic Peptide, Brain 114471-18-0
Peptide Fragments 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1352-1363

Informations de copyright

© 2023 European Academy of Neurology.

Références

Noubiap JJ, Agbaedeng TA, Kamtchum-Tatuene J, et al. Rhythm monitoring strategies for atrial fibrillation detection in patients with cryptogenic stroke: a systematic review and meta-analysis. IJC Heart Vasc. 2021;34:100780.
Ratajczak-Tretel B, Tancin Lambert A, Al-Ani R, et al. Atrial fibrillation in cryptogenic stroke and TIA patients in the Nordic Atrial Fibrillation and Stroke (NOR-FIB) study: main results. Eur Stroke J. 2022.
Brachmann J, Morillo CA, Sanna T, et al. Uncovering atrial fibrillation beyond short-term monitoring in cryptogenic stroke patients: three-year results from the cryptogenic stroke and underlying atrial fibrillation trial. Circ Arrhythm Electrophysiol. 2016;9(1):e003333.
Ziegler PD, Rogers JD, Ferreira SW, et al. Long-term detection of atrial fibrillation with insertable cardiac monitors in a real-world cryptogenic stroke population. Int J Cardiol. 2017;244:175-179.
Sposato LA, Cipriano LE, Saposnik G, Ruiz Vargas E, Riccio PM, Hachinski V. Diagnosis of atrial fibrillation after stroke and transient ischaemic attack: a systematic review and meta-analysis. Lancet Neurol. 2015;14(4):377-387.
Cuadrado-Godia E, Benito B, Ois A, et al. Ultra-early continuous cardiac monitoring improves atrial fibrillation detection and prognosis of patients with cryptogenic stroke. Eur J Neurol. 2020;27(2):244-250.
Triantafyllou S, Katsanos AH, Dilaveris P, et al. Implantable cardiac monitoring in the secondary prevention of cryptogenic stroke. Ann Neurol. 2020;88(5):946-955.
Dilaveris PE, Antoniou CK, Caiani EG, et al. ESC working group on e-cardiology position paper: accuracy and reliability of electrocardiogram monitoring in the detection of atrial fibrillation in cryptogenic stroke patients: In collaboration with the Council on Stroke, the European Heart Rhythm Association, and the Digital Health Committee. Eur Heart J Dig Health. 2022;3(3):341-358.
Healey JS, Alings M, Ha A, et al. Subclinical atrial fibrillation in older patients. Circulation. 2017;136(14):1276-1283.
Fonseca AC, Coelho P. Update on biomarkers associated to cardioembolic stroke: a narrative review. Life (Basel, Switzerland). 2021;11(5):448.
Chua W, Law JP, Cardoso VR, et al. Quantification of fibroblast growth factor 23 and N-terminal pro-B-type natriuretic peptide to identify patients with atrial fibrillation using a high-throughput platform: a validation study. PLoS Med. 2021;18(2):e1003405.
Staerk L, Preis SR, Lin H, et al. Protein biomarkers and risk of atrial fibrillation: the FHS. Circ Arrhythm Electrophysiol. 2020;13(2):e007607.
Cameron A, Cheng HK, Lee R-P, et al. Biomarkers for atrial fibrillation detection after stroke. Neurology. 2021;97(18):e1775.
Harpaz D, Bajpai R, Ng GJL, et al. Blood biomarkers to detect new-onset atrial fibrillation and cardioembolism in ischemic stroke patients. Heart Rhythm. 2021;18(6):855-861.
Bai Y, Guo SD, Liu Y, Ma CS, Lip GYH. Relationship of troponin to incident atrial fibrillation occurrence, recurrence after radiofrequency ablation and prognosis: a systematic review, meta-analysis and meta-regression. Biomarkers. 2018;23(6):512-517.
Scheitz JF, Erdur H, Haeusler KG, et al. Insular cortex lesions, cardiac troponin, and detection of previously unknown atrial fibrillation in acute ischemic stroke: insights from the troponin elevation in acute ischemic stroke study. Stroke. 2015;46(5):1196-1201.
Beaulieu-Boire I, Leblanc N, Berger L, Boulanger JM. Troponin elevation predicts atrial fibrillation in patients with stroke or transient ischemic attack. J Stroke Cerebrovasc Dis. 2013;22(7):978-983.
Ward F, McGovern R, Cotter PE. Troponin-I is a predictor of a delayed diagnosis of atrial fibrillation in acute ischemic stroke and transient ischemic attack. J Stroke Cerebrovasc Dis. 2015;24(1):66-72.
Tomich C, Liegey JS, Sagnier S, et al. Contribution of routine cardiac biological markers to the etiological workup of ischemic stroke. Am J Emerg Med. 2019;37(2):194-198.
Montaner J, Perea-Gainza M, Delgado P, et al. Etiologic diagnosis of ischemic stroke subtypes with plasma biomarkers. Stroke. 2008;39(8):2280-2287.
Ratajczak-Tretel B, Lambert AT, Johansen H, et al. Atrial fibrillation in cryptogenic stroke and transient ischaemic attack-the Nordic Atrial Fibrillation and Stroke (NOR-FIB) study: rationale and design. Eur Stroke J. 2019;4(2):172-180.
Xia J, Broadhurst DI, Wilson M, Wishart DS. Translational biomarker discovery in clinical metabolomics: an introductory tutorial. Metabolomics. 2012;9(2):280-299.
Palà E, Pagola J, Juega J, et al. B-type natriuretic peptide over N-terminal pro-brain natriuretic peptide to predict incident atrial fibrillation after cryptogenic stroke. Eur J Neurol. 2021;28(2):540-547.
Fonseca AC, Brito D, Pinho e Melo T, et al. N-terminal pro-brain natriuretic peptide shows diagnostic accuracy for detecting atrial fibrillation in cryptogenic stroke patients. Int J Stroke. 2014;9(4):419-425.
Kneihsl M, Gattringer T, Bisping E, et al. Blood biomarkers of heart failure and hypercoagulation to identify atrial fibrillation-related stroke. Stroke. 2019;50(8):2223-2226.
Rodríguez-Yáñez M, Arias-Rivas S, Santamaría-Cadavid M, Sobrino T, Castillo J, Blanco M. High pro-BNP levels predict the occurrence of atrial fibrillation after cryptogenic stroke. Neurology. 2013;81(5):444-447.
Werhahn SM, Becker C, Mende M, et al. NT-proBNP as a marker for atrial fibrillation and heart failure in four observational outpatient trials. ESC Heart Fail. 2022;9(1):100-109.
Bahit MC, Sacco RL, Easton JD, et al. Predictors of atrial fibrillation development in patients with embolic stroke of undetermined source: an analysis of the RE-SPECT ESUS trial. Circulation. 2021;144(22):1738-1746.
Zhao J, Zhang Y, Yuan F, et al. Diagnostic value of N-terminal pro B-type natriuretic peptide for nonvalvular atrial fibrillation in acute ischemic stroke patients: a retrospective multicenter case-control study. J Neurol Sci. 2020;414:116822.
Miyazaki Y, Toyoda K, Iguchi Y, et al. Atrial fibrillation after ischemic stroke detected by chest strap-style 7-day Holter monitoring and the risk predictors: EDUCATE-ESUS. J Atheroscler Thromb. 2021;28(5):544-554.
García-Berrocoso T, Giralt D, Bustamante A, et al. B-type natriuretic peptides and mortality after stroke: a systematic review and meta-analysis. Neurology. 2013;81(23):1976-1985.
Zhang K, Kamtchum-Tatuene J, Li M, Jickling GC. Cardiac natriuretic peptides for diagnosis of covert atrial fibrillation after acute ischaemic stroke: a meta-analysis of diagnostic accuracy studies. Stroke Vasc Neurol. 2021;6(1):128-132.
Tancin Lambert A, Kong XY, Ratajczak-Tretel B, et al. Biomarkers associated with atrial fibrillation in patients with ischemic stroke: a pilot study from the NOR-FIB study. Cerebrovasc Dis Extra. 2020;10(1):11-20.
Lind L, Sundstrom J, Stenemo M, Hagstrom E, Arnlov J. Discovery of new biomarkers for atrial fibrillation using a custom-made proteomics chip. Heart. 2017;103(5):377-382.
Fonseca AC, Matias JS, e Melo TP, et al. Time course of NT-proBNP levels after acute ischemic stroke. Acta Neurol Scand. 2013;128(4):235-240.
Jensen JK, Mickley H, Bak S, Korsholm L, Kristensen SR. Serial measurements of N-terminal pro-brain natriuretic peptide after acute ischemic stroke. Cerebrovasc Dis. 2006;22(5-6):439-444.
Purroy F, Suárez-Luis I, Mauri-Capdevila G, et al. N-terminal pro-brain natriuretic peptide level determined at different times identifies transient ischaemic attack patients with atrial fibrillation. Eur J Neurol. 2014;21(4):679-683.
Giannakoulas G, Hatzitolios A, Karvounis H, et al. N-terminal pro-brain natriuretic peptide levels are elevated in patients with acute ischemic stroke. Angiology. 2005;56(6):723-730.
Llombart V, Antolin-Fontes A, Bustamante A, et al. B-type natriuretic peptides help in cardioembolic stroke diagnosis: pooled data meta-analysis. Stroke. 2015;46(5):1187-1195.

Auteurs

Anna Tancin Lambert (A)

Department of Neurology, Østfold Hospital Trust, Grålum, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Barbara Ratajczak-Tretel (B)

Department of Neurology, Østfold Hospital Trust, Grålum, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Riadh Al-Ani (R)

Department of Cardiology, Østfold Hospital Trust, Grålum, Norway.

Kathrine Arntzen (K)

Department for Neurology, Nordlandssykehuset, Bodø, Norway.

Grete Kristin Bakkejord (GK)

Department for Neurology, Nordlandssykehuset, Bodø, Norway.

Hanna Marie Otterholt Bekkeseth (HMO)

Department of Neurology, Innlandet Hospital Trust, Lillehammer Hospital, Lillehammer, Norway.

Vigdis Bjerkeli (V)

Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.

Guttorm Eldøen (G)

Department of Neurology, Molde Hospital, Molde, Norway.

Anne Kristine Gulsvik (AK)

Department of Internal Medicine, Diakonhjemmet Hospital, Oslo, Norway.

Bente Halvorsen (B)

Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.

Gudrun Anette Høie (GA)

Department of Cardiology, Østfold Hospital Trust, Grålum, Norway.

Hege Ihle-Hansen (H)

Department of Neurology, Stroke Unit, Oslo University Hospital, Ullevål, Oslo, Norway.

Håkon Ihle-Hansen (H)

Department of Internal Medicine, Vestre Viken Hospital Trust, Baerum Hospital, Gjettum, Norway.

Susanne Ingebrigtsen (S)

Department of Neurology, University Hospital of North Norway, Tromsø, Norway.

Henriette Johansen (H)

Department of Neurology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.

Christine Kremer (C)

Department of Neurology, Skåne University Hospital, Malmö, Sweden.
Department of Clinical Sciences, Lund University, Malmö, Sweden.

Siv Bohne Krogseth (SB)

Department of Neurology, Vestfold Hospital, Tønsberg, Norway.

Christina Kruuse (C)

Department of Neurology, Herlev Gentofte Hospital, Herlev, Denmark.

Martin Kurz (M)

Department of Neurology, Stavanger University Hospital, Stavanger, Norway.

Ingvild Nakstad (I)

Department of Neurology, Vestre Viken Hospital Trust, Drammen Hospital, Drammen, Norway.

Vojtech Novotny (V)

Department of Neurology, Haukeland University Hospital, Bergen, Norway.

Halvor Naess (H)

Department of Neurology, Haukeland University Hospital, Bergen, Norway.

Rehman Qazi (R)

Department of Internal Medicine, Diakonhjemmet Hospital, Oslo, Norway.

Mehdi Kallaj Rezai (MK)

Department of Neurology, Stavanger University Hospital, Stavanger, Norway.

Dag Marius Rørholt (DM)

Department of Neurology, Molde Hospital, Molde, Norway.

Linn Hofsøy Steffensen (LH)

Department of Neurology, University Hospital of North Norway, Tromsø, Norway.

Jesper Sømark (J)

Department of Neurology, Innlandet Hospital Trust, Lillehammer Hospital, Lillehammer, Norway.
Department of Neurology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.

Håkon Tobro (H)

Department of Neurology, Telemark Hospital, Skien, Norway.

Thomas Clement Truelsen (TC)

Department of Neurology, Rigshospitalet University Hospital, Copenhagen, Denmark.

Lejla Wassvik (L)

Department of Neurology, Bispebjerg University Hospital, Copenhagen, Denmark.

Karen Lehrmann AEgidius (KL)

Department of Neurology, Bispebjerg University Hospital, Copenhagen, Denmark.

Maiju Pesonen (M)

Center for Biostatistics and Epidemiology, Oslo University Hospital, Oslo, Norway.

Mirko de Melis (M)

Bakken Research Center, Maastricht, The Netherlands.

Dan Atar (D)

Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Department of Cardiology, Oslo University Hospital, Ullevål, Oslo, Norway.

Anne Hege Aamodt (AH)

Department of Neurology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH