Key result
Initiation of statin treatment in vitamin K antagonist users was associated with a minor but statistically significant long-term decrease in VKA dosage, suggesting potential anticoagulant properties.
Why the study?
Does statin initiation reduce VKA dosage requirements in patients on vitamin K antagonists?
Observational (n=738)
Yes
Does statin initiation reduce VKA dosage requirements in patients on vitamin K antagonists?
Mean Difference: -0.07 (95% CI -0.09–-0.04)
Absolute Event Rate: 1.81% vs 1.91%
Initiation of statin therapy in patients on vitamin K antagonists is associated with a minor, likely clinically insignificant, decrease in required VKA dosage, suggesting mild anticoagulant properties of statins.
Statin initiation warrants no VKA dosing change in practice; leaves open mild anticoagulant effects for prospective trials.
PURPOSE: The purpose of the study is to determine the immediate and long-term effect of statins on coagulation in patients treated with vitamin K antagonists (VKAs). METHODS: We selected patients on VKAs of two Dutch anticoagulation clinics who initiated treatment with a statin between 2009 and 2013. Patients who initiated or stopped concomitant drugs that interact with VKAs or were hospitalised during follow-up were excluded. The VKA dosage (mg/day) after statin initiation was compared with the last VKA dosage before the statin was started. Immediate and long-term differences in VKA dosage (at 6 and 12 weeks) were calculated with a paired student t test. RESULTS: Four hundred thirty-five phenprocoumon users (mean age 70 years, 60 % men) and 303 acenocoumarol users (mean age 69 years, 58 % men) were included. After start of statin use, the immediate phenprocoumon dosage was 0.02 mg/day (95 % CI, 0.00 to 0.03) lower. At 6 and 12 weeks, these phenprocoumon dosages were 0.03 (95 % CI, 0.01 to 0.05) and 0.07 mg/day (95 % CI, 0.04 to 0.09) lower as compared with the dosage before first statin use. In acenocoumarol users, VKA dosage was 0.04 mg/day (95%CI, 0.01 to 0.07) (immediate effect), 0.10 (95 % CI, 0.03 to 0.16) (at 6 weeks), and 0.11 mg/day (95 % CI, 0.04 to 0.18) (after 12 weeks) lower. CONCLUSIONS: Initiation of statin treatment was associated with an immediate and long-term minor although statistically significant decrease in VKA dosage in both phenprocoumon and acenocoumarol users, which suggests that statins may have anticoagulant properties.
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Rein et al. (2016) conducted an observational in Patients treated with vitamin K antagonists (VKAs) (n=738). Statin initiation vs. Last VKA dosage before statin initiation (self-controlled) was evaluated on Difference in daily phenprocoumon dosage at 12 weeks after statin initiation (MD -0.07 mg/day, 95% CI -0.09 to -0.04). Initiation of statin treatment in vitamin K antagonist users was associated with a minor but statistically significant long-term decrease in VKA dosage, suggesting potential anticoagulant properties.
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