2015
DOI: 10.1016/j.atherosclerosis.2015.03.023
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Rivaroxaban, a novel oral anticoagulant, attenuates atherosclerotic plaque progression and destabilization in ApoE-deficient mice

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Cited by 147 publications
(135 citation statements)
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“…6A–D) in contrast to the 50% decrease in plaque macrophages reported by Hara et al after 5 months of Xa inhibition. 37 However, despite our shorter 1-month time window of therapeutic intervention that may not have allowed for reduced plaque macrophage content, our observations of rapid downregulation of NF-kB in macrophage-rich regions and downstream inflammatory markers (TF, TAT complexes, sVCAM) (Fig. 4E–H), is consistent with the similar observations of Kadoglou et al in dabigatran-treated ApoE-null mice.…”
Section: Discussionsupporting
confidence: 91%
“…6A–D) in contrast to the 50% decrease in plaque macrophages reported by Hara et al after 5 months of Xa inhibition. 37 However, despite our shorter 1-month time window of therapeutic intervention that may not have allowed for reduced plaque macrophage content, our observations of rapid downregulation of NF-kB in macrophage-rich regions and downstream inflammatory markers (TF, TAT complexes, sVCAM) (Fig. 4E–H), is consistent with the similar observations of Kadoglou et al in dabigatran-treated ApoE-null mice.…”
Section: Discussionsupporting
confidence: 91%
“…Furthermore, both valvular and arterial calcification have been reported in animals on warfarin treatment 17. By contrast, limited data from experimental animal studies have indicated a potentially beneficial effect of novel, direct‐acting anticoagulants on the development and progression of atherosclerosis 18, 19, 20…”
Section: Discussionmentioning
confidence: 99%
“…During that study, Hara et al were able to show a resulting decrease in plaque burden and they also suggested a PARmediated effect. 10 The COMPASS trial will now evaluate whether rivaroxaban plays a role in secondary prevention of major cardiovascular events in patients with known coronary or peripheral artery disease. 11 A main limitation of studies using atherosclerosis models in mice is the comparison of merely plaque development in mice that have been fed a Western diet and unstable plaques in humans where exacerbation is causing ACS.…”
Section: Editorial Friebel J Et Almentioning
confidence: 99%