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Cystatin C vs creatinine as markers of renal function in patients on digoxin treatment
Pär Hallberg1, Håkan Melhus, Lars-Olof Hansson
1Department of Medical Sciences, Clinical Chemistry and Pharmacology, University Hospital, Uppsala, Sweden.
Insights
Serum cystatin C better correlates with digoxin levels than serum creatinine. Improved glomerular filtration rate (GFR) monitoring using cystatin C can optimize digoxin treatment, especially in elderly patients.
Area of Science:
- Pharmacology
- Nephrology
- Clinical Chemistry
Background:
- Digoxin elimination is primarily renal, making kidney function crucial for its serum concentration.
- Glomerular filtration rate (GFR) declines with age, impacting digoxin pharmacokinetics in the elderly.
- Serum cystatin C is a potential alternative to creatinine for GFR estimation.
Purpose of the Study:
- To compare the correlation between serum digoxin levels and two markers of kidney function: serum creatinine and serum cystatin C.
- To determine which marker, creatinine or cystatin C, better reflects GFR for digoxin monitoring.
Main Methods:
- A comparative study involving 149 patients undergoing therapeutic drug monitoring for digoxin.
- Serum levels of digoxin, creatinine, and cystatin C were measured and compared.
- Statistical analysis was used to assess the correlation between digoxin and the GFR markers.
Main Results:
- Serum cystatin C showed a significantly stronger correlation with serum digoxin concentrations than serum creatinine.
- A notable percentage of patients with elevated digoxin levels had normal serum creatinine levels, highlighting potential underestimation of impaired GFR.
- Fewer patients with elevated digoxin levels had normal serum cystatin C levels, suggesting its superior sensitivity.
Conclusions:
- Serum cystatin C is a more reliable marker than serum creatinine for monitoring kidney function in patients treated with digoxin.
- Enhanced GFR monitoring, particularly with cystatin C, can lead to better control of digoxin serum concentrations.
- Optimizing digoxin therapy through improved GFR assessment is essential, especially in aging populations.
Background:
The kidney function is a major determinant of the serum concentration of digoxin as this drug is mainly eliminated unchanged through the kidneys. Since digoxin is widely prescribed among the elderly, and the glomerular filtration rate (GFR) declines with age, it is important that the clinician takes the patient's GFR into account when prescribing digoxin. Serum cystatin C has been suggested to be superior to creatinine for estimation of GFR, which may have relevance for the optimization of treatment with digoxin.
Methods:
To evaluate which of the two GFR markers serum creatinine and serum cystatin C that best correlates with serum digoxin, we compared the serum levels of digoxin with the serum levels of creatinine and cystatin C in 149 patients on therapeutic drug monitoring of digoxin at our hospital.
Results:
Overall, there was a stronger correlation between serum digoxin concentrations and cystatin C (p=0.00001) as compared to creatinine (p= 0.00003). Interestingly, of the patients with a serum digoxin concentration > or = 1.5 nmol/L, 29% had a serum creatinine level within normal limits, as compared to 20% with normal cystatin C levels.
Conclusions:
In this study, serum cystatin C correlated better to serum digoxin than did serum creatinine. With improved GFR monitoring, digoxin concentrations should be better controlled.
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