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Published on: August 9, 2019
Factors other than glomerular filtration rate affect serum cystatin C levels
Lesley A Stevens1, Christopher H Schmid, Tom Greene
1Division of Nephrology, Clinical Care Research, Tufts Medical Center, Boston, Massachusetts 02111, USA. lstevens1@tuftsmedicalcenter.org
Insights
Serum cystatin C levels are influenced by factors beyond glomerular filtration rate (GFR), including age, gender, diabetes, and inflammation. These non-GFR factors must be considered when estimating GFR using cystatin C.
Area of Science:
- Nephrology
- Clinical Chemistry
- Biomarker Research
Background:
- Serum cystatin C is a recognized endogenous marker for glomerular filtration rate (GFR).
- Understanding factors influencing cystatin C beyond GFR is crucial for accurate clinical interpretation.
Purpose of the Study:
- To investigate non-GFR-related factors affecting serum cystatin C levels.
- To compare the influence of these factors on cystatin C versus creatinine.
Main Methods:
- Cross-sectional analysis of 3418 patients from clinical trials and chronic kidney disease populations.
- GFR measured using urinary clearance of 125I-iothalamate and 51Cr-EDTA.
- Errors-in-variables models used to account for measurement errors in GFR.
Main Results:
- Adjusted for GFR, cystatin C decreased with age and in females, with minimal difference in Black individuals.
- Diabetes was associated with higher cystatin C and lower creatinine.
- Inflammatory markers (CRP, WBC) and lower albumin correlated with higher cystatin C and lower creatinine.
Conclusions:
- Serum cystatin C levels are significantly affected by age, gender, diabetes, and inflammation, independent of GFR.
- These non-GFR influences are more pronounced for cystatin C than for creatinine.
- Clinical estimation of GFR using cystatin C requires consideration of these additional influencing factors.
Abstract:
Cystatin C is an endogenous glomerular filtration marker hence its serum level is affected by the glomerular filtration rate (GFR). To study what other factors might affect it blood level we performed a cross-sectional analysis of 3418 patients which included a pooled dataset of clinical trial participants and a clinical population with chronic kidney disease. The serum cystatin C and creatinine levels were related to clinical and biochemical parameters and errors-in-variables models were used to account for errors in GFR measurements. The GFR was measured as the urinary clearance of 125I-iothalamate and 51Cr-EDTA. Cystatin C was determined at a single laboratory while creatinine was standardized to reference methods and these were 2.1+/-1.1 mg/dL and 1.8+/-0.8 mg/L, respectively. After adjustment for GFR, cystatin C was 4.3% lower for every 20 years of age, 9.2% lower for female gender but only 1.9% lower in blacks. Diabetes was associated with 8.5% higher levels of cystatin C and 3.9% lower levels of creatinine. Higher C-reactive protein and white blood cell count and lower serum albumin were associated with higher levels of cystatin C and lower levels of creatinine. Adjustment for age, gender and race had a greater effect on the association of factors with creatinine than cystatin C. Hence, we found that cystatin C is affected by factors other than GFR which should be considered when the GFR is estimated using serum levels of cystatin C.
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