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

Author:

Mele Marco12ORCID,Mele Antonietta1,Imbrici Paola1ORCID,Samarelli Francesco1ORCID,Purgatorio Rosa1ORCID,Dinoi Giorgia1,Correale Michele2ORCID,Nicolotti Orazio1ORCID,De Luca Annamaria1ORCID,Brunetti Natale Daniele3ORCID,Liantonio Antonella1,Amoroso Nicola14ORCID

Affiliation:

1. Department of Pharmacy—Drug Sciences, University of Bari, Via Orabona 4, 70125 Bari, Italy

2. Department of Cardiology, “Ospedali Riuniti” University Hospital, Viale Pinto 1, 71100 Foggia, Italy

3. Department of Medical and Surgical Sciences, University of Foggia, Viale Pinto 1, 71100 Foggia, Italy

4. National Institute of Nuclear Physics, Section of Bari, Via Orabona 4, 70125 Bari, Italy

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.

Funder

PRIN-MIUR

Publisher

MDPI AG

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