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Stable cystatin C serum levels confirm normal renal function in patients with dronedarone-associated increase in
David Duncker1, Hanno Oswald, Ajmal Gardiwal
1Department of Cardiovascular Medicine, Hannover Medical School, D-30625 Hannover, Germany. duncker.david@mh-hannover.de
Insights
Dronedarone may elevate serum creatinine, masking true kidney function in atrial fibrillation patients. Cystatin C offers a reliable alternative marker for assessing renal health during dronedarone treatment.
Area of Science:
- Pharmacology
- Nephrology
- Cardiology
Background:
- Dronedarone is an antiarrhythmic medication prescribed for nonpermanent atrial fibrillation (AF).
- Elevated serum creatinine is a common side effect of dronedarone, potentially confounding renal function assessment.
- Dronedarone's interaction with renal organic cation transporters may affect creatinine levels independently of actual kidney function.
Purpose of the Study:
- To evaluate alternative biomarkers for assessing true renal function in patients treated with dronedarone.
- To compare serum cystatin C and creatinine clearance as indicators of kidney function in this patient group.
Main Methods:
- Prospective study of 20 patients with nonpermanent AF starting dronedarone therapy.
- Measurements of serum creatinine, serum cystatin C, and creatinine clearance were taken at baseline, day 10, and day 90.
- Patients were categorized based on serum creatinine level changes to analyze biomarker stability.
Main Results:
- Serum creatinine levels showed a significant increase in a subgroup of patients (n=5) within 10 days.
- Serum cystatin C levels remained stable across all patients and subgroups, unaffected by dronedarone treatment.
- Creatinine clearance data was also collected but not detailed in the abstract's main findings.
Conclusions:
- Serum creatinine is an unreliable marker for renal function in patients taking dronedarone.
- Serum cystatin C is a stable and reliable biomarker for estimating true renal function in patients on dronedarone.
- Cystatin C provides a more accurate assessment of kidney health compared to creatinine in this context.
Abstract:
Dronedarone is a new antiarrhythmic drug for patients with nonpermanent atrial fibrillation (AF). A relatively consistent finding in all trials studying dronedarone was a moderate but significant elevation of serum creatinine. Since dronedarone competes for the same organic cation transporter in the distal renal tubule with creatinine, serum creatinine and its derived estimated glomerular filtration rate might not reflect true renal function in patients on dronedarone. We therefore investigated alternative markers for renal function in these patients. We prospectively included 20 patients with nonpermanent AF in whom dronedarone 400 mg twice daily was started. Patients had normal renal function and serum creatinine; serum cystatin C and creatinine clearance were measured before treatment and 10 and 90 days after treatment started. Mean serum creatinine level for all 20 patients at baseline (day 0) was 84.55 ± 12.14 and 87.8 ± 17.59 µmol/L on day 10. This slight increase in all patients was not significant. Patients were now divided into the predefined groups of "increased creatinine" (increase in serum creatinine level > 1 standard deviation) and "not increased creatinine." Patients with increased creatinine levels (n = 5) showed a significant elevation of serum creatinine levels from day 0 to day 10 (82.4 ± 9.18 to 104.4 ± 12.74 µmol/L; P = .003), whereas change in serum creatinine levels in the not increased creatinine group (n = 15) was not significant. Serum cystatin C levels remained stable in both of these groups (increased creatinine group: 0.76 ± 0.08 to 0.78 ± 0.08 mg/L; P = .65; not increased creatinine group: 0.77 ± 0.108 to 0.77 ± 0.107 mg/L; P = .906). In conclusion, cystatin C represents an easily available and reliable biomarker for estimation of true renal function in patients on dronedarone treatment.
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