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Published on: February 26, 2013
Changes in Renal Function in Patients With Atrial Fibrillation: An Analysis From the RE-LY Trial
Michael Böhm1, Michael D Ezekowitz2, Stuart J Connolly3
1Klinik für Innere Medizin III, Universitätsklinikum des Saarlandes, Homburg, Germany.
Insights
Warfarin use in patients with atrial fibrillation led to a greater decline in glomerular filtration rate (GFR) compared to dabigatran etexilate (DE). Renal function decline was worsened by diabetes and prior vitamin K antagonist use.
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- Vitamin K-dependent factors play a role in preventing vascular calcification.
- Vitamin K antagonists have been linked to reduced glomerular filtration rate (GFR).
Purpose of the Study:
- To compare changes in GFR during long-term treatment with warfarin versus dabigatran etexilate (DE).
- To analyze renal function changes in patients with atrial fibrillation receiving oral anticoagulation.
Main Methods:
- Analysis of GFR changes over 30 months in 16,490 patients from the RE-LY trial.
- Patients with atrial fibrillation received warfarin, DE 110 mg, or DE 150 mg twice daily.
- Creatinine values were measured at baseline and follow-up visits.
Main Results:
- GFR declined in all treatment groups.
- Warfarin was associated with a significantly greater mean GFR decline (-3.68 ml/min) compared to DE 110 mg (-2.57 ml/min) and DE 150 mg (-2.46 ml/min).
- A >25% GFR decrease was less likely with DE than warfarin, especially after 18 months. Poor international normalized ratio control, prior warfarin use, and diabetes amplified GFR decline.
Conclusions:
- Oral anticoagulation in atrial fibrillation patients leads to GFR decline.
- Warfarin use resulted in a greater decline in renal function compared to dabigatran etexilate.
- Diabetes and previous vitamin K antagonist use exacerbated the decline in renal function.
Background:
Vitamin K-dependent factors protect against vascular and renovascular calcification, and vitamin K antagonists may be associated with a decreased glomerular filtration rate (GFR).
Objectives:
This study analyzed changes in GFR during long-term treatment with warfarin or dabigatran etexilate (DE) in patients enrolled in the RE-LY (Randomized Evaluation of Long Term Anticoagulation Therapy) trial.
Methods:
Of the 18,113 patients in the RE-LY study randomized to receive DE (110 mg or 150 mg twice daily) or warfarin, 16,490 patients with atrial fibrillation had creatinine values measured at baseline and at least 1 follow-up visit. Changes in GFR for up to 30 months were evaluated.
Results:
GFR declined in all treatment groups. After an average of 30 months, the mean ± SE decline in GFR was significantly greater with warfarin (-3.68 ± 0.24 ml/min) compared with DE 110 mg (-2.57 ± 0.24 ml/min; p = 0.0009 vs. warfarin) and DE 150 mg (-2.46 ± 0.23 ml/min; p = 0.0002 vs. warfarin). A decrease in GFR >25% was less likely with DE 110 mg (hazard ratio: 0.81 [95% confidence interval: 0.69 to 0.96]; p = 0.017) or DE 150 mg (hazard ratio: 0.79 [95% confidence interval: 0.68 to 0.93]; p = 0.0056) than with warfarin in the observation period >18 months. Patients with poor international normalized ratio control (i.e., time in therapeutic range <65%) exhibited a faster decline in GFR. A more pronounced decline in GFR was associated with previous warfarin use and with the presence of diabetes.
Conclusions:
Patients with atrial fibrillation receiving oral anticoagulation exhibited a decline in renal function that was greater in those taking warfarin versus DE, and it was amplified by diabetes and previous vitamin K antagonist use. (Randomized Evaluation of Long Term Anticoagulant Therapy [RE-LY] With Dabigatran Etexilate; NCT00262600).
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