Key result
Ex-vivo rivaroxaban linked to greater suppression of endogenous thrombin potential in elderly versus young subjects.
Why the study?
Elderly patients taking direct oral anticoagulants face the greatest risk of bleeding, but it remains unclear whether age intrinsically affects anticoagulation response.
Does age intrinsically affect the ex-vivo anticoagulation response to rivaroxaban in fit subjects?
Observational (n=66)
No
Does age intrinsically affect the ex-vivo anticoagulation response to rivaroxaban in fit subjects?
Ex-vivo rivaroxaban effect may be enhanced in elderly; leaves open age-specific dosing relevance in patients.
According to both trial and clinical data on direct oral anticoagulants (DOACs) elderly patients are at greatest risk of bleeding. It is unclear whether age intrinsically affects anticoagulation response. To investigate the age-related sensitivity to DOACs, we compared the pharmacological activity of the direct factor Xa inhibitor, rivaroxaban, between young and elderly subjects ex-vivo. 36 fit elderly and 30 fit young subjects [median (IQR) age: 83(75-87) vs 30(26-38) years] provided a blood sample. Clotting parameters were measured in the resultant plasma samples incubated with rivaroxaban (100-500 ng/ml). Parametric, non-parametric tests and regression lines adjusted for rivaroxaban concentration and baseline values were used to compare data. Rivaroxaban produced a greater prolongation of both Prothrombin Time (PT) and modified Prothrombin Time (mPT) (both p < 0.001) in the elderly compared to young subjects (with difference in mean PT increasing from 1.6 to 6.1s and for mPT from 23.5 to 71.1s at 100 ng/ml and 500 ng/ml plasma rivaroxaban concentration, respectively). Factor X and factor II activity was significantly lower in the elderly in the presence of rivaroxaban (p < 0.001 for both). Rivaroxaban prolonged time-based parameters and suppressed the amount of thrombin generation to a significantly greater extent in the elderly compared to young subjects [%change from baseline for Endogenous Thrombin Potential (ETP): - 35.0 ± 4.4 vs - 29.8 ± 7.4 nM*min; p = 0.002]. The use of validated DOAC assays will be of considerable benefit for monitoring elderly patients who, because of their increased sensitivity to rivaroxaban, may require lower doses of the drug for therapeutic anticoagulation.
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Kampouraki et al. (2020) conducted an observational in Healthy subjects (n=66). Rivaroxaban vs. Young subjects was evaluated on Percentage change from baseline for Endogenous Thrombin Potential (ETP) (p=0.002). Ex-vivo exposure to rivaroxaban suppressed endogenous thrombin potential to a significantly greater extent in elderly subjects compared to young subjects (-35.0% vs -29.8%).
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