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New evidence of direct oral anticoagulation therapy on cardiac valve calcifications, renal preservation and inflammatory modulation.

Authors :
Di Lullo, Luca
Lavalle, Carlo
Magnocavallo, Michele
Mariani, Marco Valerio
Della Rocca, Domenico Giovanni
Severino, Paolo
Di Iorio, Biagio Raffaele
Russo, Domenico
Summaria, Francesco
Forleo, Giovanni Battista
Ronco, Claudio
Mancone, Massimo
Chimenti, Cristina
Miraldi, Fabio
Natale, Andrea
Bellasi, Antonio
Source :
International Journal of Cardiology. Dec2021, Vol. 345, p90-97. 8p.
Publication Year :
2021

Abstract

Rivaroxaban is a direct inhibitor of activated Factor X (FXa), an anti-inflammatory protein exerting a protective effect on the cardiac valve and vascular endothelium. We compare the effect of Warfarin and Rivaroxaban on inflammation biomarkers and their contribution to heart valve calcification progression and renal preservation in a population of atrial fibrillation (AF) patients with chronic kidney disease (CKD) stage 3b – 4. This was an observational, multicenter, prospective study enrolling 347 consecutive CKD stage 3b – 4 patients newly diagnosed with AF: 247 were treated with Rivaroxaban and 100 with Warfarin. Every 12 months, we measured creatinine levels and cardiac valve calcification via standard trans-thoracic echocardiogram, while plasma levels of inflammatory mediators were quantified by ELISA at baseline and after 24 months. Over a follow-up of 24 months, long-term treatment with Rivaroxaban was associated with a significative reduction of cytokines. Patients treated with Rivaroxaban experienced a more frequent stabilization/regression of valve calcifications comparing with patients treated with Warfarin. Rivaroxaban use was related with an improvement in kidney function in 87.4% of patients, while in those treated with Warfarin was reported a worsening of renal clearance in 98% of cases. Patients taking Rivaroxaban experienced lower adverse events (3.2% vs 49%, p -value <0.001). Our findings suggest that Rivaroxaban compared to Warfarin is associated with lower levels of serum markers of inflammation. The inhibition of FXa may exert an anti-inflammatory effect contributing to reduce the risk of cardiac valve calcification progression and worsening of renal function. • Higher cytokines levels were associated with reduction of eGFR and augmented severity of cardiac valve calcification. • A significant reduction of cytokines was observed only in the Rivaroxaban group. • Patients treated with Rivaroxaban experienced a stabilization/regression of mitral valve and aortic valve calcifications. • Rivaroxaban use was related with an improvement/stabilization in kidney function. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01675273
Volume :
345
Database :
Academic Search Index
Journal :
International Journal of Cardiology
Publication Type :
Academic Journal
Accession number :
153597558
Full Text :
https://doi.org/10.1016/j.ijcard.2021.10.025