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Biological variation of cystatin C and creatinine
Mark Reinhard1, Erland J Erlandsen, Else Randers
1Department of Internal Medicine, Viborg Regional Hospital, Viborg, Denmark. m.reinhard@dadlnet.dk
Insights
Serum creatinine is preferred for monitoring kidney function due to lower day-to-day biological variation compared to cystatin C. This study found greater intra-individual variance for cystatin C in healthy and impaired renal function groups.
Area of Science:
- Biochemistry
- Nephrology
- Clinical Chemistry
Background:
- Cystatin C and creatinine are biomarkers used to assess renal function.
- Understanding the biological variation of these markers is crucial for accurate interpretation of serial measurements.
Purpose of the Study:
- To compare the day-to-day biological variation of serum cystatin C and serum creatinine.
- To evaluate these variations in both healthy individuals and patients with impaired renal function.
Main Methods:
- Eight weekly blood samples were collected from 20 healthy subjects and 19 patients with renal impairment.
- Serum cystatin C was measured using the Dade Behring N Latex Cystatin C assay.
- Serum creatinine was measured using an enzymatic method.
Main Results:
- Intra-individual variance was significantly greater for cystatin C (8.6% in healthy, 16.0% in renal impairment) than for creatinine (4.7% in healthy, 8.9% in renal impairment).
- Analytical variance was low for both markers (2.0% for cystatin C, 1.6% for creatinine in healthy subjects).
- Inter-individual variance was similar for cystatin C and creatinine.
Conclusions:
- Serum creatinine exhibits less day-to-day biological variation than cystatin C.
- Serum creatinine is the preferred biomarker for serial monitoring of renal function in individuals with stable muscle mass.
- The higher intra-individual variability of cystatin C may limit its utility for routine serial renal function assessment.
Objective:
To evaluate the day-to-day biological variation of cystatin C in comparison with creatinine in healthy subjects and in patients with impaired renal function.
Material And Methods:
Eight weekly morning blood samples were taken from 20 healthy subjects (13 females and 7 males, median age 44 years, range 25-61) and 19 patients with impaired renal function (8 females and 11 males, median age 61 years, range 35-70). Serum cystatin C was measured using Dade Behring N Latex Cystatin C assay and serum creatinine by an enzymatic method (Roche).
Results:
In the healthy subjects mean serum cystatin C was 0.70 mg/L (range 0.44-1.09) and mean serum creatinine 77 micromol/L (range 54-100). The analytical variance was 2.0% for cystatin C and 1.6% for creatinine. The intra-individual variance was greater for cystatin C than for creatinine (8.6% vs. 4.7%). The inter-individual variance was similar for both analytes (cystatin C 15.1% vs. creatinine 14.4%). In the patients with impaired renal function mean serum cystatin C was 1.86 mg/L (range 0.45-3.31) and mean serum creatinine 224 micromol/L (range 103-430). The analytical variance was 1.8% for cystatin C and 1.4% for creatinine. The intra-individual variance was greater for cystatin C than for creatinine (16.0% vs. 8.9%).
Conclusion:
In the present study, the intra-individual variance was greater for cystatin C than for creatinine in both healthy subjects and in patients with impaired renal function. Accordingly, serum creatinine is the preferred marker for serial monitoring of renal function in individuals with stable muscle mass.
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