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Kidney function estimating equations in patients with chronic kidney disease
1Department of Nephrology, Clinic of Internal Medicine, University Medical center Maribor, Maribor, Slovenia.
Insights
Serum cystatin C equations reliably estimate kidney function in chronic kidney disease (CKD) patients. These cystatin C formulas show higher accuracy than some creatinine-based equations for assessing glomerular filtration rate (GFR).
Area of Science:
- Nephrology
- Biomarkers
- Kidney Function Assessment
Background:
- Current guidelines recommend predictive equations for kidney function assessment over serum creatinine alone.
- This study evaluates cystatin C-based equations against creatinine-based equations in chronic kidney disease (CKD).
Purpose of the Study:
- To compare the diagnostic accuracy of serum cystatin C-based equations versus serum creatinine-based equations for estimating glomerular filtration rate (GFR) in CKD patients.
- To assess the reliability of different GFR estimation formulas.
Main Methods:
- Seven hundred sixty-four adult CKD patients were enrolled.
- Glomerular filtration rate (GFR) was estimated using three creatinine-based equations (Cockcroft-Gault, MDRD, CKD-EPI) and two cystatin C-based equations.
- Measured GFR was determined using (51)CrEDTA clearance.
Main Results:
- Both cystatin C formulas demonstrated higher diagnostic accuracy than the Cockcroft-Gault formula for GFR estimation.
- Cystatin C formulas showed a statistically significant higher ability to predict GFR above or below 60 ml/min/1.73m² compared to the MDRD formula.
- All formulas, except the simple cystatin C formula, underestimated measured GFR at a GFR cut-off of 60 ml/min/1.73m².
Conclusions:
- Serum cystatin C-based equations are reliable markers for estimating GFR in CKD patients.
- Cystatin C-based equations offer comparable or superior performance to traditional creatinine-based formulas for GFR assessment.
Background:
The current guidelines emphasise the need to assess kidney function using predictive equations rather than just serum creatinine. The present study compares serum cystatin C-based equations and serum creatinine-based equations in patients with chronic kidney disease (CKD).
Methods:
Seven hundred and sixty-four adult patients with CKD were enrolled. In each patient serum creatinine and serum cystatin C were determined. Their glomerular filtration rate (GFR) was estimated using three serum creatinine-based equations [Cockcroft-Gault (C&G), modification of diet in renal disease (MDRD) and the Chronic Kidney Disease Epidemiology Collaboration equation (CKD-EPI)] and two serum cystatin C-based equations [our own cystatin C formula (GFR=90.63 × cystatin C(-1.192) ) and simple cystatin C formula (GFR=100/cystatin C)]. The GFR was measured using (51) CrEDTA clearance.
Results:
Statistically significant correlation between (51) CrEDTA clearance with serum creatinine, serum cystatin C and all observed formulas was found. The receiver operating characteristic curve analysis (cut-off for GFR 60 ml/min/1.73m(2)) showed that serum cystatin C and both cystatin C formulas had a higher diagnostic accuracy than C&G formula. Bland and Altman analysis for the same cut-off value showed that all formulas except simple cystatin C formula underestimated measured GFR. The accuracy within 30% of estimated (51) CrEDTA clearance values differs according to stages of CKD. Analysis of ability to correctly predict patient's GFR below or above 60 ml/min/1.73m(2) showed statistically significant higher ability for both cystatin C formulas compared to MDRD formula.
Conclusion:
Our results indicate that serum cystatin C-based equations are reliable markers of GFR comparable with creatinine-based formulas.
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