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

Author:

Tancin Lambert Anna12ORCID,Ratajczak‐Tretel Barbara12,Al‐Ani Riadh3,Arntzen Kathrine4,Bakkejord Grete Kristin4,Bekkeseth Hanna Marie Otterholt5,Bjerkeli Vigdis6,Eldøen Guttorm7,Gulsvik Anne Kristine8,Halvorsen Bente26,Høie Gudrun Anette3,Ihle‐Hansen Hege9,Ihle‐Hansen Håkon10ORCID,Ingebrigtsen Susanne11,Johansen Henriette12,Kremer Christine1314,Krogseth Siv Bohne15,Kruuse Christina16,Kurz Martin17,Nakstad Ingvild18,Novotny Vojtech19,Næss Halvor19,Qazi Rehman8,Rezai Mehdi Kallaj17,Rørholt Dag Marius7,Steffensen Linn Hofsøy11,Sømark Jesper512,Tobro Håkon20,Truelsen Thomas Clement21,Wassvik Lejla22,Ægidius Karen Lehrmann22,Pesonen Maiju23,de Melis Mirko24,Atar Dan225,Aamodt Anne Hege12ORCID,

Affiliation:

1. Department of Neurology Østfold Hospital Trust Grålum Norway

2. Institute of Clinical Medicine University of Oslo Oslo Norway

3. Department of Cardiology Østfold Hospital Trust Grålum Norway

4. Department for Neurology Nordlandssykehuset Bodø Norway

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

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

7. Department of Neurology Molde Hospital Molde Norway

8. Department of Internal Medicine Diakonhjemmet Hospital Oslo Norway

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

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

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

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

13. Department of Neurology Skåne University Hospital Malmö Sweden

14. Department of Clinical Sciences Lund University Malmö Sweden

15. Department of Neurology Vestfold Hospital Tønsberg Norway

16. Department of Neurology Herlev Gentofte Hospital Herlev Denmark

17. Department of Neurology Stavanger University Hospital Stavanger Norway

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

19. Department of Neurology Haukeland University Hospital Bergen Norway

20. Department of Neurology Telemark Hospital Skien Norway

21. Department of Neurology Rigshospitalet University Hospital Copenhagen Denmark

22. Department of Neurology Bispebjerg University Hospital Copenhagen Denmark

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

24. Bakken Research Center Maastricht The Netherlands

25. Department of Cardiology Oslo University Hospital, Ullevål Oslo Norway

Abstract

AbstractBackground and purposeThere 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.MethodsEligible 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.ResultsB‐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).ConclusionSeveral 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.

Funder

Medtronic

Nasjonalforeningen for Folkehelsen

Sykehuset Østfold

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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