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Rivaroxaban is a direct oral anticoagulant (DOAC) that directly inhibits coagulation factor Xa and exerts its anticoagulant effects. Although rivaroxaban generally exhibits predictable pharmacokinetic (PK) and pharmacodynamic (PD) profiles, significant interindividual variability in therapeutic responses exists. Research on the role of genetic factors in the clinical variability of rivaroxaban is relatively new and extensive. In this review, 12 pharmacogenetic studies on rivaroxaban were summarised, and 25 reported gene polymorphic sites were summarised, including (rs1045642, rs4148738, rs1128503, rs2032582, rs4728709, rs3789243 and rs3213619, (rs2231142, rs2231137, rs3114018, rs2622604 and rs1481012), (rs35599367, rs2242480, rs4646437 and rs12333983), (rs776746, rs15524, rs4646450), (rs890293), (rs4244285 and rs12248560), (rs7212506), (rs1738023 and rs1738025). The review provided an overview of the current state of research on rivaroxaban gene polymorphisms. However, due to the significant heterogeneity of existing studies and the lack of consistency in results, the evidence to date has limited impact. Therefore, larger-scale, global, multi-centre clinical trials are needed in the future to validate potential gene loci for testing.
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http://dx.doi.org/10.2147/DDDT.S534569 | DOI Listing |
Phlebology
September 2025
Department of Orthopeadics, DongGuan Tungwah Hospital, DongGuan, China.
ObjectiveLower extremity varicose veins are a common chronic venous disorder, affecting approximately 23% of adults globally. Although endovenous thermal ablation, particularly radiofrequency ablation (RFA), has become the preferred treatment, post-procedural deep vein thrombosis (DVT) remains a concern. The necessity of pharmacologic prophylaxis following RFA remains controversial.
View Article and Find Full Text PDFBackground: Data on the levels of rivaroxaban-specific anti-factor Xa activity (AFXaA) within three weeks of starting high-dose rivaroxaban therapy in patients with cancer-associated thromboembolism (CAT) is limited. This study aimed to determine initial levels of rivaroxaban-specific AFXaA in patients with CAT to assist with drug monitoring.
Methods: This study included a total of 33 patients from December 2017 through January 2019.
Cancer Med
September 2025
School of Pharmacy, Sungkyunkwan University, Suwon, South Korea.
Introduction: Venous thromboembolism (VTE) is a leading cause of mortality in cancer patients, and a substantial number of patients are being treated with oral anticoagulants. We aim to assess the comparative effectiveness of direct oral anticoagulants (DOACs) compared to warfarin for VTE treatment in cancer patients.
Methods: In this retrospective cohort study, we included 2,367 cancer patients who are new users of oral anticoagulants (OACs) for VTE treatment from 2009 to 2021 in NHS Scotland.
Circulation
September 2025
Department of Vascular Surgery, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Circulation
September 2025
Faculty of Chinese Medicine, Macau University of Science and Technology, Taipa, Macau, China (C.W., H.T.).