Pleiotropic Effects of Direct Oral Anticoagulants in Chronic Heart Failure and Atrial Fibrillation: Machine Learning Analysis.

Journal: Molecules (Basel, Switzerland)
PMID:

Abstract

Oral anticoagulant therapy (OAT) for managing atrial fibrillation (AF) encompasses vitamin K antagonists (VKAs, such as warfarin), which was the mainstay of anticoagulation therapy before 2010, and direct-acting oral anticoagulants (DOACs, namely dabigatran etexilate, rivaroxaban, apixaban, edoxaban), approved for the prevention of AF stroke over the last thirteen years. Due to the lower risk of major bleeding associated with DOACs, anticoagulant switching is a common practice in AF patients. Nevertheless, there are issues related to OAT switching that still need to be fully understood, especially for patients in whom AF and heart failure (HF) coexist. Herein, the effective impact of the therapeutic switching from warfarin to DOACs in HF patients with AF, in terms of cardiac remodeling, clinical status, endothelial function and inflammatory biomarkers, was assessed by a machine learning (ML) analysis of a clinical database, which ultimately shed light on the real positive and pleiotropic effects mediated by DOACs in addition to their anticoagulant activity.

Authors

  • Marco Mele
    Department of Political Sciences, Roma Tre University, Roma, Italy.
  • Antonietta Mele
    Department of Pharmacy-Drug Sciences, University of Bari, Via Orabona 4, 70125 Bari, Italy.
  • Paola Imbrici
    Dipartimento di Farmacia-Scienze del Farmaco, Università degli Studi di Bari Aldo Moro, 70125 Bari, Italy.
  • Francesco Samarelli
    Department of Pharmacy-Drug Sciences, University of Bari, Via Orabona 4, 70125 Bari, Italy.
  • Rosa Purgatorio
    Department of Pharmacy-Drug Sciences, University of Bari, Via Orabona 4, 70125 Bari, Italy.
  • Giorgia Dinoi
    Department of Pharmacy-Drug Sciences, University of Bari, Via Orabona 4, 70125 Bari, Italy.
  • Michele Correale
    Cardiology Department, Policlinico Riuniti University Hospital Foggia, Viale Pinto, 1 71100 Foggia, Italy.
  • Orazio Nicolotti
    Department of Pharmacy- Drug Sciences, University of Bari "Aldo Moro", Via Orabona 4, 70125 Bari, Italy.
  • Annamaria De Luca
    Dipartimento di Farmacia-Scienze del Farmaco, Università degli Studi di Bari Aldo Moro, 70125 Bari, Italy.
  • Natale Daniele Brunetti
    Department of Medical and Surgical Sciences, University of Foggia, Via Antonio Gramsci, 89, 71122 Foggia, Italy.
  • Antonella Liantonio
    Dipartimento di Farmacia-Scienze del Farmaco, Università degli Studi di Bari Aldo Moro, 70125 Bari, Italy.
  • Nicola Amoroso
    Dipartimento Interateneo di Fisica "M. Merlin", Università degli studi di Bari "A. Moro", Bari, Italy; Istituto Nazionale di Fisica Nucleare, Sezione di Bari, Bari, Italy. Electronic address: nicola.amoroso@ba.infn.it.