Biomarker panels for improved risk prediction and enhanced biological insights in patients with atrial fibrillation.

Journal: Nature communications
Published Date:

Abstract

Atrial fibrillation (AF) increases the risk of adverse cardiovascular events, yet the underlying biological mechanisms remain unclear. We evaluate a panel of 12 circulating biomarkers representing diverse pathophysiological pathways in 3817 AF patients to assess their association with adverse cardiovascular outcomes. We identify 5 biomarkers including D-dimer, growth differentiation factor 15 (GDF-15), interleukin-6 (IL-6), N-terminal pro-B-type natriuretic peptide (NT-proBNP), and high-sensitivity troponin T (hsTropT) that independently predict cardiovascular death, stroke, myocardial infarction, and systemic embolism, significantly enhancing predictive accuracy. Additionally, GDF-15, insulin-like growth factor-binding protein-7 (IGFBP-7), NT-proBNP, and hsTropT predict heart failure hospitalization, while GDF-15 and IL-6 are associated with major bleeding events. A biomarker model improves predictive accuracy for stroke and major bleeding compared to established clinical risk scores. Machine learning models incorporating these biomarkers demonstrate consistent improvements in risk stratification across most outcomes. In this work, we show that integrating biomarkers related to myocardial injury, inflammation, oxidative stress, and coagulation into both conventional and machine learning-based models refine prognosis and guide clinical decision-making in AF patients.

Authors

  • Pascal B Meyre
    Department of Cardiology, University Heart Center, University Hospital Basel, Basel, Switzerland. pascal.meyre@usb.ch.
  • Stefanie Aeschbacher
    Department of Cardiology, University Heart Center, University Hospital Basel, Basel, Switzerland.
  • Steffen Blum
    Department of Cardiology, University Heart Center, University Hospital Basel, Basel, Switzerland.
  • Tobias Reichlin
    Department of Cardiology, Bern University Hospital, University of Bern, Freiburgstrassse 3, 3010, Bern, Switzerland.
  • Moa Haller
    Institute of Primary Health Care (BIHAM), University of Bern, Bern, Switzerland.
  • Nicolas Rodondi
    Institute of Primary Health Care (BIHAM), University of Bern, Bern, Switzerland.
  • Andreas S Müller
    Department of Cardiology, Triemli Hospital Zurich, Zurich, Switzerland.
  • Alain Bernheim
    Department of Cardiology, Triemli Hospital Zurich, Zurich, Switzerland.
  • Jürg Hans Beer
    Department Internal Medicine, Baden Switzerland and Center of Molecular Cardiology, Cantonal Hospital Baden, University of Zürich, Zürich, Switzerland.
  • Giorgio Moschovitis
    Divison of Cardiology, Regional Hospital of Lugano, Ente Ospedaliero Cantonale (EOS), Lugano, Switzerland.
  • André Ziegler
    Roche Diagnostics International, Rotkreuz, Switzerland.
  • Bianca Wahrenberger
    Department of Cardiology, University Heart Center, University Hospital Basel, Basel, Switzerland.
  • Elia Rigamonti
    Divison of Cardiology, Regional Hospital of Lugano, Ente Ospedaliero Cantonale (EOS), Lugano, Switzerland.
  • Giulio Conte
    Division of Cardiology, Fondazione Cardiocentro Ticino, Via Tesserete 48, Lugano 6900, Switzerland; Centre for Computational Medicine in Cardiology, Faculty of Informatics, Università della Svizzera Italiana, Via la Santa 1, Lugano 6900, Switzerland.
  • Philipp Krisai
    Department of Cardiology, University Heart Center, University Hospital Basel, Basel, Switzerland.
  • Leo H Bonati
    Neurologic Clinic and Policlinic, Departments of Neurology and Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Stefan Osswald
    Department of Cardiology, University Hospital Basel, Basel, Switzerland.
  • Michael Kühne
    University Hospital Basel, Basel, Switzerland.
  • David Conen
    Population Health Research Institute, McMaster University, Hamilton, ON, Canada.