Key result
Moderate renal dysfunction linked to ~115% higher edoxaban trough anti-factor Xa levels versus normal function.
Why the study?
The impact of renal function on anti-factor Xa activity concentrations with edoxaban use in patients with non-valvular atrial fibrillation has not been fully assessed.
Does renal function impact anti-factor Xa activity concentrations in patients with non-valvular atrial fibrillation taking edoxaban?
Observational (n=93)
No
Does renal function impact anti-factor Xa activity concentrations in patients with non-valvular atrial fibrillation taking edoxaban?
Absolute Event Rate: 0.28% vs 0.13%
p-value: p=<0.01
Creatinine clearance is negatively correlated with trough anti-factor Xa activity concentrations in patients with non-valvular atrial fibrillation taking edoxaban, suggesting renal function impacts drug exposure at trough but not peak levels.
Associated with higher edoxaban exposure in moderate renal impairment; leaves open whether AXA levels predict outcomes or warrant dose adjustment in AF.
BACKGROUND: Chromogenic anti-factor Xa activity (AXA) assay is used to measure the pharmacodynamics of factor Xa inhibitors, including edoxaban. Although AXA concentrations in patients with non-valvular atrial fibrillation using edoxaban have been reported, the impact of renal function on AXA concentrations with edoxaban use in patients with non-valvular atrial fibrillation has not been fully assessed. METHODS: Trough and peak AXA concentrations were measured in 93 patients with non-valvular atrial fibrillation taking edoxaban (73.6 ± 11.2 years, 48 were male). The patients were divided into three groups: patients with moderate renal dysfunction (creatinine clearance 15-49 mL/min), mild renal dysfunction (creatinine clearance 50-95 mL/min), and normal renal function (creatinine clearance > 95 mL/min). Both trough and peak AXA concentrations were assessed among the groups according to the edoxaban dose (30 or 60 mg). RESULTS: At a 30-mg dose, patients with moderate renal dysfunction showed significantly higher trough AXA concentrations than patients with mild renal dysfunction or normal renal function. At a 60-mg dose, patients with mild renal dysfunction showed significantly higher trough AXA concentrations than patients with normal renal function. Peak AXA concentrations were not significantly different between the groups. Creatinine clearance was significantly and negatively correlated with trough AXA concentrations at a 60-mg dose, whereas the correlation of creatinine clearance with AXA concentrations was borderline significant at a 30-mg dose. No correlation was found between creatinine clearance and peak AXA concentrations at either dose. CONCLUSIONS: Creatinine clearance tends to be negatively correlated with trough AXA concentrations in patients with non-valvular atrial fibrillation taking edoxaban, while renal function is not correlated with peak AXA concentrations.
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Ono et al. (2022) conducted an observational in Non-valvular atrial fibrillation (n=93). Edoxaban vs. Normal renal function (CrCl > 95 mL/min) was evaluated on Trough anti-factor Xa activity (AXA) concentrations (IU/mL) (p=<0.01). Edoxaban trough anti-factor Xa activity concentrations were significantly higher in patients with moderate renal dysfunction compared to those with normal renal function (0.28 vs 0.13 IU/mL, p < 0.01).
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